Before 2010

(A * indicates work performed at UT Austin)

(A indicates work performed as joint appointee at Yonsei University)


1981


1.Collman, J. P.; Brauman, J. I.; Collins, T. J.; Iverson, B.; Sessler, J. L. “The 'Pocket' Porphyrin:  A Hemoprotein Model with Lowered CO Affinity,” J. Am. Chem. Soc. 1981, 103, 2450-2452.  DOI: 10.1021/ja00399a070. 


2.Collman, J. P.; Basolo, F.; Bunnenberg, E.; Collins, T. J.; Dawson, J. H.; Ellis, P. E., Jr.; Marrocco, M. L.; Moscowitz, A.; Sessler, J. L.; Syzmanski, T. “Use of Magnetic Circular Dichroism to Determine Axial Ligation for Some Sterically Encumbered Iron(II) Porphyrins,” J. Am. Chem. Soc. 1981, 103, 5636-5648.  DOI: 10.1021/ja00409a003


3.Collman, J. P.; Anson, F. C.; Bencosme, S.; Chong, A.; Collins, T.; Denisevich, P; Evitt, E.; Geiger, T.; Ibers, J. A.; Jameson, G.; Konai, Y.; Koval, C.; Meier, K.; Oakley, R.; Pettman, R.; Schmittou, E.; Sessler, J. “Molecular Engineering:  The Design and Synthesis of Catalysts for the Rapid 4-Electron Reduction of Molecular Oxygen to Water,” Organic Synthesis Today and Tomorrow; Trost, B. M.; Hutchinson, C. R., Eds.; Pergamon:  Oxford, 1981; pp 29-45.



1982


4.Perutz, M. F.; Hasnain, S. S.; Duke, P. J.; Sessler, J. L.; Hahn, J. E. “Stereochemistry of Iron in Deoxhaemoglobin,” Nature 1982, 295, 535-538.



1983


5.Collman, J. P.; Brauman, J. I.; Collins, T. J.; Iverson, B. I.; Sessler, J. L.; Morris, R.; Gibson, Q. H. “The 'Pocket' Porphyrins:  Hemoprotein Models with Lowered CO Affinities,” Inorg. Chim. Acta 1983, 79, 101-102.


6.Collman, J. P.; Brauman, J. I.; Doxsee, K. M.; Sessler, J. L.; Morris, R.; Gibson, Q. H. “Effect of Axial Base on Dioxygen and Carbon Monoxide Affinities of Iron(II) Porphyrins.  Imidazole vs. Pyridine,” Inorg. Chem. 1983, 22, 1427-1432.


7.Collman, J. P.; Brauman, J. I.; Collins, T. J.; Iverson, B. L.; Lang, G.; Pettman, R. B.; Sessler, J. L.; Walters, M. A. “Synthesis and Characterization of the 'Pocket' Porphyrins,” J. Am. Chem. Soc. 1983, 105(10), 3038-3052.  DOI: 10.1021/ja00348a018


8.Collman, J. P.; Brauman, J. I.; Iverson, B. L.; Sessler, J. L.; Morris, R.; Gibson, Q. H. “Dioxygen and Carbonyl Binding to Iron(II) Porphyrins:  A Comparison of the 'Picket Fence' and 'Pocket' Porphyrins,” J. Am. Chem. Soc. 1983, 105(10), 3052-3064. DOI: 10.1021/ja00348a019


9.Collman, J. P.; Brauman, J. I.; Iverson, B. L.; Sessler, J. L.; Morris, R.; Gibson, Q. H. “Comparison of O2 and CO Binding to Iron(II) 'Picket Fence' and 'Pocket' Porphyrins,” Biomimetic Chemistry; Yoshida, Z.-I.; Ise, N., Eds.; Kodansha:  Tokyo, 1983; pp 37-49.



1984


10.Gückel, F.; Schweitzer, D.; Collman, J. P.; Bencosme, S.; Evitt, E.; Sessler, J. L. “ODMR of Triplet States of Cofacial Dimeric Zinc Porphyrins,” Chem. Phys. 1984, 86, 161-179.


11.Hamilton, A. D.; Lehn, J.-M.; Sessler, J. L. “Mixed Substrate Supermolecules: Binding of Organic Substrates and of Metal Ions to Heterotopic Coreceptors Containing Porphyrin Subunits,” J. Chem. Soc., Chem. Commun. 1984, 311-313. DOI: 10.1039/C39840000311.


12.Powers, L.; Sessler, J. L.; Woolery, G. L.; Chance, B. “CO Bond Angle Changes in Photolysis of Carboxymyoglobin,” Biochemistry 1984, 23, 5519-5523.  Funding: National Institutes of Health Grant No. GM17880-14


13.Sessler, J. L.; Collman, J. P. “The 'Pocket' Porphyrins:  Hemoprotein Models with Lowered CO Affinities,” Kagaku 1984, 39, 805-806.



1986


14.*Sessler, J. L.; Johnson, M. R.; Hugdahl, J. “A Convenient Synthesis of a 'Gable'-Type Porphyrin,” J. Org. Chem. 1986, 51, 2838-2840.  Funding: Robert A. Welch Foundation Grant No. AP-868


15.Hamilton, A.; Lehn, J.-M.; Sessler, J. L. “Coreceptor Molecules.  Synthesis of Metalloreceptors Containing Porphyrin Subunits and Formation of Mixed Substrate Supermolecules by Binding of Organic Substrates and of Metal Ions,” J. Am. Chem. Soc. 1986, 108, 5158-5167.  DOI: 10.1021/ja00277a021. This work was subsequently featured on the cover of Prof. Lehn’s Nobel Award lecture writeup in Angew. Chem.



1987


16.*Sessler, J. L.; Johnson, M. R. “New Photosynthetic Model Systems:  Quinone Substituted Porphyrin Dimers,” Recueil des Travaux Chimiques des Pays-Bas 1987, 106, 222.


17.*Sessler, J. L.; Johnson, M. R. “The Synthesis of 1,3- and 1,4-Phenylene-Linked Bisquinone Substituted Porphyrin Dimers,” Angew. Chem. 1987, 99, 679-680; Angew. Chem. Int. Ed. Engl. 1987, 26, 678-680.

    17a.*“Progress Made in Synthesizing Enzyme Mimics,” C & E News October 19, 1987, 30-34.


18.*Sessler, J. L.; Piering, S. “The Synthesis and Optical Properties of the First Quinone-linked Porphyrin Dimer,” Tetrahedron Lett. 1987, 28, 6569-6572.


19.*Sessler, J. L.; Lynch, V.; Johnson, M. R. “Synthesis and Crystal Structure of a Novel Tripyrrane-Containing Porphyrinogen-like Macrocycle,” J. Org. Chem. 1987, 52, 4394-4397.  DOI: 10.1021/jo00228a048


20.*Sessler, J. L. “How to Avoid Getting into Medical School,” The Scapel, 1987, 56, 16-17.



1988


21.Gubelmann, M.; Harriman, A.; Lehn, J.-M.; Sessler, J. L. “Photoinduced Charge Separation Within a Polymetallic Supramolecular System,” J. Chem. Soc., Chem. Commun. 1988, 77-79.  DOI: 10.1039/C39880000077.


22.*Sessler, J. L.; Johnson, M. R.; Lin, T.-Y., Creager, S. E. “Quinone Substituted Monometallated Porphyrin Dimers:  Models for Photoinduced Charge Separation at Fixed Orientation and Energy,” J. Am. Chem. Soc. 1988, 110, 3659-3661.


23.*Sessler, J. L.; Murai, T.; Lynch, V.; Cyr., M. “An 'Expanded Porphyrin':  The Synthesis and Structure of a New Aromatic Pentadentate Ligand,” J. Am. Chem. Soc. 1988, 110, 5586-5588. DOI: 10.1021/ja00224a062

    23a.*“Unusual Porphyrin Analog Promises Many Applications,” C & E News August 8, 1988, 26-27.

    23b.*“How Big Can Aromatic Compounds Grow?” New Scientist, 1989, 32.

    23c.*“Texaphyrin,” Kagaku to Kogyo, 1989, 42, 116-118.


24.*Sessler, J. L.; Hugdahl, J. D.; Kurosaki, H.; Sasaki, Y. “Synthesis and Binding Properties of a Triazamacrocyclic Ligand Bearing Pendant Pyridyl Groups,” J. Coord. Chem. 1988, 18, 93-98.


25.*Sessler, J. L.; Johnson, M. R.; Lynch, V.; Murai, T. “Expanded Porphyrins:  The Synthesis and Metal Binding Properties of Novel Tripyrrane-Containing Macrocycles,” J. Coord. Chem. 1988, 18, 99-104.


26.*Sessler, J. L.; Cyr, M.; Murai, T. “The Coordination Chemistry of Planar Pentadentate Porphyrin-like Ligands,” Comm. Inorg. Chem., 1988, 7, 333-350.



1989


27.*Sessler, J. L.; Magda, D. M.; Hugdahl, J. “The Preparation of Ribose-free 'Artificial Dinucleotides':  A New Approach to Molecular Recognition?” J. Incl. Phenomen. 1989, 7, 19-26.


28.*Kim, K.; Fettinger, J.; Sessler, J.; Cyr, M.; Hugdahl, J.; Collman, J. P.; Ibers, J. “Structural Characterization of a Sterically Encumbered Iron(II) Porphyrin CO Complex,” J. Am. Chem. Soc. 1989, 111, 403-405.  Funding: National Science Foundation Presidential Young Investigator Award 1986 and Robert A. Welch Foundation Grant No. F-1018


29.*Harriman, A.; Maiya, B. G.; Murai, T.; Hemmi, G.; Sessler, J. L.; Mallouk, T. E. “Metallotexaphyrins:  A New Family of Photosensitizers for Efficient Generation of Singlet Oxygen,” J. Chem. Soc., Chem. Commun. 1989, 314-316. DOI: 10.1039/C39890000314.


30.*Sessler, J. L.; Magda, D. J.; Lynch, V.; Schiff, G. M.; Bernstein, D. “The Synthesis of 2-Amino 7-Substituted Purines,” Nucleotides and Nucleosides 1989, 8, 431-448. DOI: 10.1080/07328318908054186


31.*Regev, A.; Berman, A.; Levanon, H.; Murai, T.; Sessler, J. L. “Principal ZFS Tensor Axes Versus Optical Transition Moments of Novel Expanded Porphyrins (Texaphyrins).  Time-Resolved Triplet EPR Spectroscopy,” Chem. Phys. Lett. 1989, 160, 401-409.


32.*Sessler, J. L.; Murai, T.; Lynch, V. “Binding of Pyridine and Benzimidazole to a Cadmium ‘Expanded Porphyrin’:  Solution and X-ray Structural Studies,” Inorg. Chem. 1989, 28(7), 1333-1341.  DOI: 10.1021/ic00306a025.  Funding: Texas Advanced Research Program, Camille and Henry Dreyfus Foundation New Faculty Award 1984 and the National Science Foundation Presidential Young Investigator Award 1986


33.*Sessler, J. L.; Sibert, J. W.; Hugdahl, J.D.; Lynch, V. “Synthesis and Characterization of a New Potentially Ditopic Receptor, 1,4,7,10-Tetraoxa-13,16,19,22-tetraazacyclotetracosane, and the X-ray Crystal Structure of Its Mononuclear Copper(II) Complex,” Inorg. Chem. 1989, 28(7), 1417-1419.  DOI: 10.1021/ic00306a042


34.*Sessler, J. L.; Johnson, M. R.; Lin, T.-Y. “Absorption and Static Emision Properties of Monometalated Quinone-substituted Porphyrin Dimers:  Evidence for ‘Superexchange’ Mediated Electron Transfer in Multicomponent Photosynthetic Model Systems,” Tetrahedron, 1989, 45, 4767-4784.


35.*Sessler, J. L.; Murai, T.; Hemmi, G. “A Water-Stable Gadolinium(III) Complex Derived from a New Pentadentate 'Expanded Porphyrin' Ligand,” Inorg. Chem. 1989, 28, 3390-3393.  DOI: 10.1021/ic00316a030.  Funding: Texas Advanced Research Program, Camille and Henry Dreyfus Foundation New Faculty Award 1984 and the National Science Foundation Presidential Young Investigator Award 1986


36.*Maiya, B. G; Harriman, A.; Sessler, J. L.; Hemmi, G.; Murai, T.; Mallouk, T. E. “Ground- and Excited-State Spectral and Redox Properties of Cadmium(II) Texaphyrin,” J. Phys. Chem. 1989, 93, 8111-8115.  Funding: Texas Advanced Research Program


37.*Won, Y.; Friesner, R. A.; Johnson, M. R.; Sessler, J. L., “Exciton Interactions in Synthetic Porphyrin Dimers,” Photosynthesis Research 1989, 22, 201-210.  Funding: Robert A. Welch Foundation Grant No. F-1018



1990


38.*Sessler, J. L.; Magda, D. “Artificial Oligonucleotides:  Molecular Recognition by Base-Pairing,” Inclusion Phenomena and Molecular Recognition; Atwood, J., Ed.; Plenum Press:  New York, 1990; pp 17-26.


39.Gubelmann, M.; Harriman, A.; Lehn, J.-M.; Sessler, J. L. “Quenching of Porphyrin Excited States by Silver(I) Ions and Charge Separation in Bimolecular Systems and in Macropolycyclic Coreceptors,” J. Phys. Chem. 1990, 94, 308-315. DOI: 10.1021/j100364a052. 


40.*Levanon, H.; Regev, A.; Michaeli, S.; Galili, T.; Cyr, M.; Sessler, J. L. “The Photoexcited State of Sapphyrin Dication.  Unusual Spin Alignment in Monomers and Spin Delocalization in Dimers,” Chem. Phys. Lett. 1990, 174, 235-240.

40a.*“ACS Award Winners,” C & E News  November 19, 1990, 31-35.


41.*Sessler, J. L.; Cyr, M.; Maiya, B. G.; Judy, M. L.; Newman, J. T.; Skiles, H.; Boriack, R.; Matthews, J. L.; Chanh, T. C. “Photodynamic Inactivation of Enveloped Viruses Using Sapphyrin, a 22 pi-Electron ‘Expanded Porphyrin’:  Possible Approaches to Prophylactic Blood Purification Protocols,” Proc. SPIE Int. Opt. Eng. 1990, 1203 (Photodynamic Therapy:  Mechanisms II), 233-245.  DOI: 10.1117/12.17669.  Funding: Texas Advanced Research Program Grant No. 1581, National Science Foundation Presidential Young Investigator Award (1986), Alfred P. Sloan Foundation Research Fellowship and Camille and Henry Dreyfus Foundation Teacher-Scholar Award


42.*Kennedy, M. A.; Sessler, J. L.; Murai, T.; Ellis, P. D. “Cadmium-113 Shielding Tensors of the Cadmium Complex of Texaphyrin, a Novel Expanded Porphyrin, and Its Pyridine and Benzimidazole Adducts,” Inorg. Chem. 1990, 29(5), 1050-1054.  DOI: 10.1021/ic00330a027.  Funding: Texas Advanced Research Program Grant No. 1581 and National Science Foundation Presidential Young Investigator Award (1986)


43.*Maiya, B. G.; Cyr, M.; Harriman, A.; Sessler, J. L. “In Vitro Photodynamic Activity of Diprotonated Sapphyrin:  A 22-π-Electron Pentapyrrolic Porphyrin-like Macrocycle,” J. Phys. Chem. 1990, 94, 3597-3601.  DOI: 10.1021/j100372a043.  Texas Advanced Research Program Grant No. 1581


44.*Sessler, J. L.; Cyr, M. J.; Lynch, V.; McGhee, E.; Ibers, J. A. “Synthetic and Structural Studies of Sapphyrin, a 22 π-Electron Pentapyrrolic 'Expanded Porphyrin',” J. Am. Chem. Soc. 1990, 112, 2810-2813.  DOI: 10.1021/ja00163a059.  Funding: Texas Advanced Research Program Grant No. 1581, National Science Foundation Presidential Young Investigator Award (1986), Alfred P. Sloan Foundation Research Fellowship and Camille and Henry Dreyfus Foundation Teacher-Scholar Award


45.*Sessler, J. L.; Capuano, V. L. “Phenyl-linked Quinone-Substituted Porphyrin Trimers,” Angew. Chemie 1990, 102, 1162-1164; Angew. Chemie, Int. Ed. Engl. 1990, 29, 1134-1137.


46.*Maiya, B. G.; Mallouk, T. E.; Hemmi, G.; Sessler, J. L. “Effect of Substitutuents on the Spectral and Redox Properties of Cadmium(II) Texaphyrins,” Inorg. Chem. 1990, 29, 3738-3745.  DOI: 10.1021/ic00344a021.  Funding: Texas Advanced Research Program Grant No. 1581, National Science Foundation Presidential Young Investigator Award (1986), Alfred P. Sloan Foundation Research Fellowship and Camille and Henry Dreyfus Foundation Teacher-Scholar Award


47.*Regev, A.; Levanon, H.; Murai, T.; Sessler, J. L. “Triplet Electron Paramagnetic Resonance Detection of Porphyrinoids in Fluid Liquid Crystals at Elevated Temperatures,” J. Chem. Phys. 1990, 92, 4718-4723.


48.*Sessler, J. L.; Sibert, J. W.; Lynch, V. “Model Studies Related to Hemerythrin:  Synthesis and Characterization of a Bridged Tetranuclear Iron(III) Complex,” Inorg. Chem. 1990, 29, 4143-4146.  Funding: National Science Foundation Presidential Young Investigator Award (1986), Alfred P. Sloan Foundation Research Fellowship and Camille and Henry Dreyfus Foundation Teacher-Scholar Award


49.*Sessler, J. L.; Johnson, M. R.; Creager, S. F.; Fettinger, J. C.; Ibers, J. A. “Synthesis and Characterization of Quinone-Substituted Octaalkyl Porphyrin Monomers and Dimers,” J. Am. Chem. Soc. 1990, 112, 9310-9329.  Funding: Robert A. Welch Foundation Grant No. F-1018, National Science Foundation Presidential Young Investigator Award (1986), National Institutes of Health Grant No. GM41657



1991


50.*Burrell, A. K.; Sessler, J. L.; Cyr, M.; McGhee, E.; Ibers, J. A. “Metal Carbonyl Complexes of Sapphyrins,” Angew. Chem. 1991, 103, 83-85; Angew. Chem., Int. Ed. Engl. 1991, 30, 91-93.


51.*Judy, M. M.; Matthews, J. L.; Newman, J. T.; Skiles, H. L.; Boriack, R.; Sessler, J. L.; Cyr, M.; Maiya, B. G.; Nichol, S.T. “In vitro Photodynamic Inactivation of Herpes simplex Virus with Sapphyrins:  22 π-Electron Porphyrin-like Macrocycles,” Photochem. Photobiol. 1991, 53, 101-107.


52.*Sessler, J. L.; Hugdahl, J. D.; Lynch, V.; Davis, B. “Synthesis and Characterization of a Tetranuclear Iron(III) Complex Derived From a New m-Xylyl-Bridged Tetraimidazole Ligand,” Inorg. Chem. 1991, 30(2), 334-336.  DOI: 10.1021/ic00002a035. 


53.*Furuta, H.; Magda, D.; Sessler, J. L. “Molecular Recognition via Base Pairing:  Amine-Containing, Cytosine-Based Ditopic Receptors that Complex Guanosine Monophosphate,” J. Am. Chem. Soc. 1991, 113(3), 978-985.  DOI: 10.1021/ja00003a035.  Funding: Camille and Henry Dreyfus Foundation Teacher-Scholar Award, Alfred P. Sloan Foundation Research Fellowship and National Science Foundation Presidential Young Investigator Award (1986)


54.*Rodriguez, J.; Kirmaier, C.; Johnson, M. R.; Friesner, R. A.; Holten, D.; Sessler, J. L. “Picosecond Studies of Quinone-Substituted Monometalated Porphyrin Dimers:  Evidence for Superexchange-Mediated Electron Transfer in a Photosynthetic Model System,” J. Am. Chem. Soc. 1991, 113, 1652-1659. DOI: 10.1021/ja9835436.  Funding: Robert A. Welch Foundation Grant No. F-1018, Camille and Henry Dreyfus Foundation Teacher-Scholar Award, National Science Foundation Presidential Young Investigator Award (1986) and National Institutes of Health Grant No. GM41657


55.*Harriman, A.; Magda, D.; Sessler, J. L. “Energy Transfer across a Hydrogen-bonded, Cytosine-derived, Zinc-Free-base Porphyrin Conjugate,” J. Chem. Soc., Chem. Commun. 1991, 345-348. DOI: 10.1039/C39910000345.  Funding: National Institutes of Health Grant No. GM41657, Robert A. Welch Foundation Grant No. F-1018 and Texas Advanced Research Program Grant No. 1581


56.*Waluk, J.; Hemmi, G.; Sessler, J. L.; Michl, J. “Magnetic Circular Dichroism of Metallotexaphyrins,” J. Org. Chem. 1991, 56(8), 2735-2742.  DOI: 10.1021/jo00008a030.  Funding:  National Institutes of Health Grant No. AI28845


57.*Lynch, V. M.; Sibert, J. W.; Sessler, J. L.; Davis, B. E. “Structure of Aqua-hexakis(µ2-benzoato)-bis(methanol)-µ3-oxo-triiron(III) Benzoate Ethanol Methanol Solvate,” Acta Cryst. 1991, C47, 866-869.  DOI: 10.1107/S010827019001085X.  Funding: National Science Foundation Presidential Young Investigator Award (1986), Alfred P. Sloan Foundation Research Fellowship and Camille and Henry Dreyfus Foundation Teacher-Scholar Award


58.*Harriman, A.; Magda, D. J.; Sessler, J. L. “Photon Antennae Assembled by Nucleic Acid Base Pairing,” J. Phys. Chem. 1991, 95(4), 1530-1532.  DOI: 10.1021/j100157a005.  Funding: National Science Foundation Presidential Young Investigator Award (1986), Camille and Henry Dreyfus Foundation Teacher-Scholar Award, Alfred P. Sloan Foundation Research Fellowship, Robert A. Welch Foundation Grant No. F-1018 and National Institutes of Health Grant No. GM41657

59.*Sessler, J. L.; Cyr, M. J.; Burrell, A. K. “Sapphyrins:  New Life for an Old 'Expanded Porphyrin',” SynLett  1991, 127-133.


60.*Sessler, J. L.; Hemmi, G.; Maiya, B. G.; Harriman, A.; Judy, M. L.; Boriak, R.; Matthews, J. L.; Ehrenberg, B.; Malik, Z.; Nitzan, Y. Rück, A. “Tripyrroledimethine-derived (“Texaphyrin”-type) Macrocycles:  Potential Photosensitizers which Absorb in the Far-red Spectral Region,” Proc. SPIE Int. Opt. Eng. 1991, 1426, 318-329.


61.*Furuta, H.; Furuta, K.; Sessler, J. L. “Enhanced Transport of Nucleosides and Nucleoside Analogues with Complementary Base-Pairing Agents,” J. Am. Chem. Soc. 1991, 113, 4706-4707.


62.*Burrell, A. K.; Hemmi, G.; Lynch, V.; Sessler, J. L. “Uranylpentaphyrin:  An Actinide Complex of an Expanded Porphyrin,” J. Am. Chem. Soc. 1991, 113, 4690-4692.  Funding: National Institutes of Health Grant No. AI28845, National Science Foundation  Presidential Young Investigator Award (1986), Alfred P. Sloan Foundation Research Fellowship and Camille and Henry Dreyfus Foundation Teacher-Scholar Award

63.*Furuta, H.; Cyr, M. J.; Sessler, J. L. “Phosphate Anion Binding:  Enhanced Transport of Nucleotide Monophosphates Using a Sapphyrin Carrier,” J. Am. Chem. Soc. 1991, 113, 6677-6678.  DOI: 10.1021/ja00017a051.  Funding: National Science Foundation  Presidential Young Investigator Award (1986), Camille and Henry Dreyfus Foundation Teacher-Scholar Award and Alfred P. Sloan Foundation Research Fellowship

64.*Sessler, J. L.; Mozaffari, A.; Johnson, M. R. “3,4-Diethylpyrrole and 2,3,7,8,12,13,17,18-Octaethylporphyrin,” Organic Syntheses 1991, 70, 68-77.


65.*Sessler, J. L.; Morishima, T.; Lynch, V. “Rubyrin:  A New Hexapyrrolic Expanded Porphyrin,” Angew. Chem. 1991, 103, 1018-1020; Angew. Chem., Intl. Ed. Engl. 1991, 30, 977-980.


66.*Sessler, J. L.; Johnson, M. R.; Creager, S. E.; Fettinger, J.; Ibers, J. A.; Rodriguez, J.; Kirmaier, C.; Holten, D. “Quinone Substituted Porphyrin Dimers:  New Photosynthetic Model Systems,” PHOTOBIOLOGY:  The Science and its Applications; Riklis, E., Ed.; Plenum Press:  New York, 1991; pp 391-399.


67.*Regev, A.; Michaeli, S.; Levanon, H.; Cyr, M.; Sessler, J. L. “Solvent Effect in Randomly and Partially Oriented Triplets of Sapphyrin Dication.  Optical and Fast EPR-Magnetophotoselection Measurements,” J. Phys. Chem. 1991, 95, 9121-9129.


68.*Sessler, J. L.; Burrell, A. K. “Expanded Porphyrins,” Top. Curr. Chem. 1991, 161, 177-273.  DOI: 10.1007/3-540-54348-1_10.  Funding: National Institutes of Health Grant No. AI28845, National Science Foundation  Presidential Young Investigator Award (1986), Camille and Henry Dreyfus Foundation Teacher-Scholar Award and Alfred P. Sloan Foundation Research Fellowship

69.*Burrell, A. K.; Cyr, M.; Lynch, V.; J.; Sessler, J. L. “Nucleophilic Attack at the meso Position of a Uranyl Sapphyrin Complex,” J. Chem. Soc., Chem. Commun. 1991, 1710-1713.  DOI: 10.1039/C39910001710.  Funding: National Institutes of Health Grant No. AI28845, National Science Foundation  Presidential Young Investigator Award (1986), Alfred P. Sloan Foundation Research Fellowship, and Camille and Henry Dreyfus Foundation Teacher-Scholar Award

70.*Sessler, J. L.; Ford, D.; Cyr, M. J.; Furuta, H. “Enhanced Transport of Fluoride Anion Effected using Protonated Sapphyrin as a Carrier,” J. Chem. Soc., Chem. Commun. 1991, 1733-1735.  DOI: 10.1039/C39910001733.  Funding: National Science Foundation  Presidential Young Investigator Award (1986), Camille and Henry Dreyfus Foundation Teacher-Scholar Award and Alfred P. Sloan Foundation Research Fellowship



1992


71.*Harriman, A.; Kubo, Y.; Sessler, J. L. “Molecular Recognition via Base Pairing:  Photoinduced Electron Transfer in Hydrogen-Bonded Zinc Porphyrin-Benzoquinone Conjugates,” J. Am. Chem. Soc. 1992, 114, 388-390.  DOI: 10.1021/ja00027a074.  Funding: National Science Foundation Presidential Young Investigator Award (1986), Camille and Henry Dreyfus Foundation Teacher-Scholar Award, Alfred P. Sloan Foundation Research Fellowship, Robert A. Welch Foundation Grant No. F-1018 and National Institutes of Health Grant No. GM 41657


72.*Sessler, J. L.; Magda, D.; Furuta, H. “Synthesis and Binding Properties of Monomeric and Dimeric Guanine and Cytosine Amine Derivatives,” J. Org. Chem. 1992, 57, 818-826.  DOI: 10.1021/jo00029a008.  National Science Foundation Presidential Young Investigator Award (1986), Camille and Henry Dreyfus Foundation Teacher-Scholar Award and Alfred P. Sloan Foundation Research Fellowship


73.*Sessler, J. L.; Mody, T. D.; Lynch, V. “Synthesis and X-ray Characterization of a Uranyl(VI) Schiff Base Complex Derived from a 2:2 Condensation Product of 3,4-Diethylpyrrole-2,5-dicarbaldehyde and 1,2-Diamino-4,5-dimethoxybenzene,” Inorg. Chem. 1992, 31, 529-531.  DOI: 10.1021/ic00030a001.  Funding: National Institutes of Health Grant No. AI28845, National Science Foundation Presidential Young Investigator Award (1986), Alfred P. Sloan Foundation Research Fellowship, and Camille and Henry Dreyfus Foundation Teacher-Scholar Award


74.*Sessler, J. L.; Mody, T. D.; Ford, D. A.; Lynch, V. “A Nonaromatic Expanded Porphyrin Derived from Anthracene — A Macrocycle which Unexpectedly Binds Anions,” Angew. Chem. 1992, 104, 461-464; Angew. Chem., Int. Ed. Engl. 1992, 31, 452-455.


75.*Tohda, K.; Tange, M.; Odashima, K.; Umezawa, Y.; Furuta, H.; Sessler, J. L. “Liquid Membrane Electrode for Guanosine Nucleotides Using a Cytosine-Pendant Triamine Host as the Sensory Element,” Anal. Chem. 1992, 64, 960-964.  DOI: 10.1021/ac00032a023.  Funding: Texas Advanced Research Program, National Science Foundation Presidential Young Investigator Award (1986), Alfred P. Sloan Foundation Research Fellowship, and Camille and Henry Dreyfus Foundation Teacher-Scholar Award


76.*Sessler, J. L.; Mody, T. D.; Ramasamy, R.; Sherry, A. D. “Synthesis, Characterization, and 23Na NMR Shift Studies of a Dysprosium(III) Crown Ether Texaphyrin,” New J. Chem. 1992, 16, 541-544.


77.*Shionoya, M.; Furuta, H.; Lynch, V.; Harriman, A.; Sessler, J. L. “Diprotonated Sapphyrin:  A Fluoride Selective Halide Anion Receptor,” J. Am. Chem. Soc. 1992, 114, 5714-5722.  Funding: National Institutes of Health Grant No. AI28845, National Science Foundation Presidential Young Investigator Award (1986), Alfred P. Sloan Foundation Research Fellowship, and Camille and Henry Dreyfus Foundation Teacher-Scholar Award

78.*Sessler, J. L.; Weghorn, S. J.; Morishima, T.; Rosingana, M.; Lynch, V.; Lee, V. “Rosarin:  A New, Easily Prepared Hexapyrrolic Expanded Porphyrin,” J. Am. Chem. Soc. 1992, 114, 8306-8307.  Funding: National Institutes of Health Grant No. AI28845, Pharmacyclics Inc. and Camille and Henry Dreyfus Foundation Teacher-Scholar Award


79.*Král, V; Sessler, J. L.; Furuta, H. “Synthetic Sapphyrin-Cytosine Conjugates:  Carriers for Selective Nucleotide Transport at Neutral pH,” J. Am. Chem. Soc. 1992, 114, 8704-8705.  DOI: 10.1021/ja00048a056.  Funding: Texas Advanced Research Program, Camille and Henry Dreyfus Foundation Teacher-Scholar Award and Alfred P. Sloan Foundation Research Fellowship


80.*Sessler, J. L.; Kubo, J.; Harriman, A. “The Photochemistry of Pyrene-cytosine Conjugates:  Modelling the Carcinogenic Action of Aromatic Hydrocarbons,” J. Phys. Org. Chem. 1992, 5, 644-648.  DOI: 10.1002/poc.610051005. 


81.*Sessler, J. L.; Cyr, M. J.; Burrell, A. K. “Sapphyrin and Heterosapphyrins,” Tetrahedron 1992, 48, 9661-9672.


82.*Ehrenberg, B.; Lavi, A.; Nitzan, Y.; Malik, Z.; Ladan, H.; Johnson, F. M.; Sessler, J. L. “Spectroscopy, Photokinetics and Cellular Effect of Far-red and Near Infrared Absorbing Photosensitizers,” Proc. SPIE 1992, 1645, 259-263DOI: 10.1117/12.60947  

    82a.*"Who Was That Masked Molecule?  Dr. Sessler Puts Texaphyrin In The Lone Star State," The Vector  1992, 40 (5), 8.


83.*Sessler, J. L.; Capuano, V. L.; Kubo, Y.; Johnson, M. R.; Magda, D. J.; Harriman, A. H. “Examining Long-distance Biological Electron Transfer with Synthetic Model Systems,” Photoprocesses in Transition Metal Complexes, Biosystems, and Other Molecules.  Experiment and Theory; Kochanski, E., Ed.; Kluwer:  Dorderecht; NATO ASI Series 1992, Series C, Vol. 376, 375-401.


84.*Bixon, M.; Fajer, J.; Feher, G.; Freed, J. H.; Gamliel, D.; Hoff, A. J.; Levanon, H.; Möbius, K.; Nechushtai, R.; Norris, J. R.; Scherz, A.; Sessler, J. L.; Stehlik, D.  “Primary Events in Photosynthesis:  Problems, Speculations, Controversies, and Future Trends,” Isr. J. Chem. 1992, 32, 369-518 (dedicated issue with highlight on the cover).


1993


85.*Sessler, J. L.; Capuano, V. L.; Burrell, A. K. “Orthogonal RuII(bpy)3 Complexes in meso- Substituted Porphyrins,” Inorg. Chim. Acta. 1993, 204, 93-101.


86.*Sessler, J. L. “Texas-size Molecules,” Discovery 1993, 13, 44-49.

    86a.*“Focus on Research,” Focus on Science  1993, 5, 6-7.


87.*Sessler, J. L.; Cyr, M.; Furuta, H.; Král, V.; Mody, T.; Morishima, T.; Shionoya, M.; Weghorn, S. “Anion Binding:  A New Direction in Porphyrin-related Research,” Pure Appl. Chem. 1993, 65, 393-398.  Funding: National Institutes of Health Grant No. AI28845, Pharmacyclics, Inc. and Camille and Henry Dreyfus Foundation Teacher-Scholar Award


88.*Sessler, J. L.; Sibert, J. W.; Lynch, V. “Synthesis and Crystal Structure Of The 1:1 Pd(II) Complex Of 1,4,7,10-tetraoxa-13,16,19,22-tetraazacyclotetracosane,” Inorg. Chim. Acta 1993, 206, 63-67.


89.*Sessler, J. L.; Sibert, J. W.; Lynch, V.; Markert, J. T.; Wooten, C. L. “Structure and Properties of a Tetranuclear Iron(III) Cage Complex.  A Model for Hemerythrin,” Inorg. Chem. 1993, 32, 621-626.  Funding: National Institutes of Health Grant No. GM36348, National Science Foundation Presidential Young Investigator Award (1986) and Camille and Henry Dreyfus Foundation Teacher-Scholar Award


90.*Sessler, J. L.; Capuano, V. L. “Selective Insertion of Ni(II) into the Outer Porphyrin Suunits of a Trimeric Porphyrin Array,” Tetrahedron Lett. 1993, 34, 2287-2290.


91.*Ikeda, H.; Sessler, J. L. “Synthesis of the First a-linked Quaterpyrrole,” J. Org. Chem. 1993, 58, 2340-42.


92.*Sessler, J. L.; Mody, T. D.; Lynch, V. “Neutral Substrate Complexation by an ‘Expanded Porphyrin’,” J. Am. Chem. Soc. 1993, 115, 3346-3347.  Funding: National Institutes of Health Grant No. AI28845, National Science Foundation Grant No. CHE- 9122161, Camille and Henry Dreyfus Foundation Teacher-Scholar Award and Pharmacyclics, Inc.


93.*Sessler, J. L.; Capuano, V. L.; Harriman, A. “Electronic Energy Migration and Trapping in Quinone-Substituted, Phenyl-Linked Dimeric and Trimeric Porphyrins,” J. Am. Chem. Soc. 1993, 115, 4618-4628.  Funding: Robert A. Welch Foundation Grant No. F-1018, Camille and Henry Dreyfus Foundation Teacher-Scholar Award, National Institutes of Health Grant No. GM41657


94.*Sessler, J. L.; Furuta, H.; Král, V. “Phosphate Anion Chelation and Base-pairing.  Design of Receptors and Carriers for Nucleotides and Nucleotide Analogs,” Supramolec. Chem. 1993 1, 209-220.  DOI: 10.1080/10610279308035164. 


95.*Sessler, J. L.; Mody, T. D.; Hemmi, G. W.; Lynch, V. “Synthesis and Structural Characterization of Lanthanide(III) Texaphyrins,” Inorg. Chem. 1993, 32, 3175-3187.  DOI: 10.1021/ic00066a032.  Funding: National Institutes of Health Grant No. AI28845, National Science Foundation Grant No. CHE- 9122161, Camille and Henry Dreyfus Foundation Teacher-Scholar Award and Pharmacyclics, Inc.


96.*Tohda, K.; Naganawa, R.; Lin, X. M.; Tange, M.; Umezawa, K.; Odashima, K.; Umezawa, Y.; Furuta, H.; Sessler, J. L. “Liquid Membrane Electrodes for Nucleotides Based on Sapphyrin, Cytosine-pendant Triamine and Neutral Cytosine Derivative as Sensory Elements,” Sensors Actuators B 1993, 13-14, 669-672.


97.*Sessler, J. L.; Sibert, J. W.; Burrell, A. K.; Lynch, V.; Markert, J. T.; Wooten, C. L. “Oxo-bridged Iron Clusters.  The Synthesis of 1,3-Bis(1,4,7-triaza-1-cyclononyl)-2-hydroxypropane and Its Stabilixation of the Fe4O6 Core,” Inorg. Chem. 1993, 32, 4277-4283.  DOI: 10.1021/ic00072a020.  Funding: National Institutes of Health Grant No. GM36348, National Science Foundation Presidential Young Investigator Award (1986), Camille and Henry Dreyfus Foundation New Faculty Award and Teacher-Scholar Award


98.*Sessler, J. L.; Sibert, J. W. “On the Synthesis of Unsymmetrical Bis(Macrocyclic) Ligands,” Tetrahedron 1993, 49, 8727-8738.


99.*Furuta, H.; Morishima, T.; Král, V.; Sessler, J. L. “Protonated Rubyrin and C-Tips:  Co-carriers for the Transport of Guanosine 5’- Monophosphate at Neutral pH,” Supramolec. Chem. 1993, 3, 5-8.


100.*Sessler, J. L.; Wang, B.; Harriman, A. “Long-Range Photoinduced Electron Transfer in an Associated but Noncovalently Linked Photosynthetic Model System,” J. Am. Chem. Soc. 1993, 115, 10418-10419.  DOI: 10.1021/ja00075a091.  Funding: Robert A. Welch Foundation Grant No. F-1018 and National Institutes of Health Grant No. GM41657


101.*Sessler, J. L.; Mody, T. D.; Hemmi, G. W.; Lynch, V.; Young, S. W.; Miller, R. A. “Gadolinium(III) Texaphyrin:  A Novel MRI Contrast Agent,” J. Am. Chem. Soc. 1993, 115, 10368-10369.  DOI: 10.1021/ja00075a066.  Funding: National Institutes of Health Grant No. AI28845 and National Science Foundation Grant No. CHE-9122161


102.*Iverson, B. L.; Shreder, K.; Král, V.; Sessler, J. L. “Phosphate Recognition by Sapphyrin.  A New Approach to DNA Binding,” J. Am. Chem. Soc. 1993, 115, 11022-11023.  DOI: 10.1021/ja00076a083.  Funding: Pharmacyclics, Inc. and National Institutes of Health Grant Nos. AI28845 and AI/DK33577


103.*Ehrenberg, B.; Malik, Z.; Nitzan, Y.; Laden, H.; Johnson, F. M.; Hemmi, G.; Sessler, J. L. “The Binding and Photosensitization Effects of Tetrabenzoporphyrins and Texaphyrin in Bacterial Cells,” Lasers Med. Sci. 1993, 8, 197-203.



1994


104.*Sessler, J. L.; Sibert, J. W.; Lynch, V. “Bulky substituent effects on the iron(III) complexation of 1,4,7-triazacyclononane,” Inorg. Chim. Acta 1994, 216, 89-95.


105.*Ray, G. B.; Li, X.-Y.; Ibers, J. A.; Sessler, J. L.; Spiro, T. G. “How Far Can Proteins Bend the FeCO Unit?  Distal Polar and Steric Effects in Heme Proteins and Models,” J. Am. Chem. Soc. 1994, 116, 162-176.


106.*Sessler, J. L.; Hemmi, G.; Mody, T. D.; Murai, T.; Burrell, A.; Young, S. W. “Texaphyrins:  Synthesis and Applications,” Acc. Chem. Res. 1994, 27, 43-50.  DOI: 10.1021/ar00038a002.  Funding: National Institutes of Health Grant No. AI28845, National Science Foundation Presidential Young Investigator Award (1986) and Grant No. CHE-9122161, Camille and Henry Dreyfus Foundation, Alfred P. Sloan Foundation and Pharmacyclics, Inc.


107.*Sessler, J. L.; Hoehner, M. C. “An Efficient, High-Yield Preparation of Substituted 2,2’-Bipyrroles,” SYNLETT 1994, 211-212.  Funding: National Science Foundation Grant No. CHE-9122161


108.*Iverson, B. L.; Thomas, R. E.; Král, V.; Sessler, J. L. “Molecular Recognition of Anionic Species by Silica Gel Bound Sapphyrin,” J. Am. Chem. Soc. 1994, 116, 2663-2664.  DOI: 10.1021/ja00085a074.  Funding: Pharmacyclics, Inc. and National Institutes of Health Grant No. AI33577


109.*Young, S. W.; Sidhu, M. K.; Qing, F.; Muller, H. H.; Neuder, M.; Zanassi, G.; Mody, T. D.; Hemmi, G.; Dow, W.; Mutch, J. D.; Sessler, J. L.; Miller, R. A. “Preclinical Evaluation of Gd-Tex:  A New Paramagnetic Contrast Agent for Magnetic Resonance Imaging,” Invest. Radiol. 1994, 29, 330-338.


110.*Iverson, B. L.; Shreder, K.; Král, V.; Smith, D. A.; Smith, J.; Sessler, J. L. “Interactions Between Expanded Porphyrins and Nucleic Acids,” Pure Appl. Chem. 1994, 66, 845-850.  Funding: Pharmacyclics, Inc. and National Institutes of Health Grant No. AI33577


111.*Sessler, J. L.; Weghorn, S. J.; Lynch, V.; Fransson, K. “5,15,25-tris-nor-Hexapyrrin:  The First Structurally Characterized Linear Hexpyrrin,” J. Chem. Soc., Chem. Commun. 1994, 1289-1290. DOI: 10.1039/C39940001289


112.*Sessler, J. L.; Weghorn, S.; Lynch, V.; Johnson, M. R. “Turcasarin, The Largest Expanded Porphyrin Prepared to Date,” Angew. Chem. 1994, 106, 1572-1575; Angew. Chem. Int. Ed. Engl. 1994, 33, 1509-1512. This work was highlighted on the front cover.


113.*Sessler, J. L. “New Porphyrin Isomers,” Angew. Chem. 1994, 106, 1410-1412; Angew. Chem. Int. Ed. Engl. 1994, 33, 1348-1350.


114.*Magda, D.; Miller, R. A.; Sessler, J. L.; Iverson, B. L. “Site-Specific Hydrolysis of RNA by Europium(III)-Texaphyrin Conjugated to a Synthetic Oligodeoxynucleotide,” J. Am. Chem. Soc. 1994, 116, 7439-7440.  DOI: 10.1021/ja00095a070.  Funding: National Institutes of Health Grant No. AI28845


115.*Endeward, B.; Regev, A.; Plato, M.; Levanon, H.; Sessler, J. L.; Möbius, K. "Structure of Expanded Porphyrins:  Electron-Nuclear Multiple Resonance and Molecular Orbital Studies of Texaphyrin Anion Radicals in Solution," Chem. Phys. Lett. 1994, 226, 151-158.


116.*Sessler, J. L.; Brucker, E. A.; Král, V.; Harriman, A.  “A Face-to-Face Porphyrin-Sapphyrin Pseudo Dimer,” Supramolecular Chem. 1994, 4, 35-41.


117.*Sessler, J. L.; Burrell, A. K.; Furuta, H.; Hemmi, G. W.; Iverson, B. L.; Král, V.; Magda, D. J.; Mody, T. D.; Shreder, K.; Smith, D.; Weghorn, S. J. “Expanded Porphyrins.  Receptors for Cationic, Anionic, and Neutral Substrates”, Transition Metals in Supramolecular Chemistry; Fabbrizzi, L.; Poggi, A., Eds.; Kluwer:  Dorderecht; NATO ASI Series; 1994, Series C, Vol. 448, pp 391-408.


118.*Sessler, J. L.; Brucker, E. A.; Weghorn, S. J.; Kisters, M.; Schäfer, M.; Lex, J.; Vogel, E. “Corrphycene:  A New Porphyrin Isomer,” Angew. Chem. 1994, 106, 2402-2406; Angew. Chem. Int. Ed. Engl. 1994, 33, 2308-2312.

    118a.* “Broad Efforts Focus On Synthesis And Characterization Of Porphyrins,” C & E News  June 26, 1995, 30-31.


119.*Roitman, L.; Ehrenberg, B.; Nitzan, Y.; Král, V.; Sessler, J. L. “Spectroscopy and Photosensitization of Sapphyrins in Solutions and Biological Membranes,” Photochem. Photobiol. 1994, 60, 421-426.  DOI: 10.1111/j.1751-1097.1994.tb05127.x. 


120.*Odashima, K.; Naganawa, R.; Radecka, H.; Kataoka, M.; Kimura, E.; Koike, T.; Tohda, K.; Tange, M.; Furuta, H.; Sessler, J. L.; Yagi, K.; Umezawa, Y. “Chemical Sensing Based on Membrane Potential Change Induced by Host-Guest Complexation at Membrane Surface,” Supramolec. Chem. 1994, 4, 101-113.  DOI: 10.1080/10610279408029869.


121.*Ehrenberg, B.; Roitman, L.; Lavi, A.; Nitzan, Y.; Sessler, J. L. “Spectroscopic studies of photosensitization in solutions and in cells,” In: Photodynamic Therapy of Cancer II, SPIE 1994, 2325, 68-79. DOI: 10.1117/12.199180


122.*Amani, S.; Sessler, J. “Synthesis of Binuclear Copper(II) Complexes with Expanded Porphyrins,” Iran. J. Chem. & Chem. Eng. 1994, 13, 83-90.



1995


123.*Sessler, J. L.; Wang, B.; Harriman, A. “Photoinduced Energy Transfer in Associated but Non-covalently Linked Photosynthetic Model Systems,” J. Am. Chem. Soc 1995, 117, 704-714.  Funding: Robert A. Welch Foundation Grant No. F-1018 and National Institutes of Health Grant No. GM41657


124.*Sessler, J. L.; Weghorn, S. J.; Hisaeda, Y.; Lynch, V. “Hexaalkyl Terpyrrole.  A New Building Block For the Preparation of Expanded Porphyrins,” Chem. Eur. J. 1995, 1, 56-67.  DOI: 10.1002/chem.19950010110.  Funding: National Science Foundation Grant No. CHE-9122161


125.*Král, V.; Sessler, J. L. “Molecular Recognition via Base-pairing and Phosphate Chelation.  Ditopic and Tritopic Sapphyrin-based Receptors for the Recognition and Transport of Nucleotide Monophosphates,” Tetrahedron 1995, 51, 539-554.


126.*Sessler, J. L.; Brucker, E. A. “The First "Crowned" Expanded Porphyrin,” Tetrahedron Lett. 1995, 36, 1175-1176.


127.* Lisowski, J.; Sessler, J. L.; Lynch, V.; Mody, T. D. “1H NMR Spectroscopic Study of Paramagnetic Lanthanide(III) Texaphyrins.  Effect of Axial Ligation,” J. Am. Chem. Soc. 1995, 117, 2273-2285.  Funding: National Institutes of Health Grant No. AI28845 and Pharmacyclics, Inc.


128.*Král, V.; Andrievsky, A.; Sessler, J. L. “A Covalently Linked Sapphyrin Dimer.  A  New Receptor for Dicarboxylate Anions,” J. Am. Chem. Soc. 1995, 117, 2953-2954.  Funding: National Institutes of Health Grant No. AI33577 and Pharmacyclics, Inc.


129.*Magda, D.; Wright, M.; Miller, R. A.; Sessler, J. L.; Sansom, P. I.; “Sequence-Specific Photocleavage of DNA by an Expanded Porphyrin with Irradiation Above 700 nm,” J. Am. Chem. Soc. 1995, 117, 3629-3630.  Funding: National Institutes of Health Grant No. AI28845


130.*Král, V.; Brucker, E. A.; Hemmi, G.; Sessler, J. L.; Králová, J.; Bose, H., Jr. “A Non-ionic Water Soluble Pentaphyrin Derivative.  Synthesis and Cytotoxicity,” Bioorg. Med. Chem. 1995, 3, 573-578.

130a.*“UT trying to invent more commercial licensing, patent revenues,” The Daily Texan, April 17, 1995, 94, 1-2.


131.*Lisowski, J.; Sessler, J. L.; Lynch, V. “Synthesis and X-ray Structure of Selenasapphyrin,” Inorg. Chem. 1995, 34, 3567-3572.  Funding: National Science Foundation Grant No. CHE- 91221610, National Institutes of Health Grant Nos. AI28845 and AI33577

132.*Weghorn, S. J.; Lynch, V.; Sessler, J. L. “[22]Dehydropentaphyrin-(2.1.0.0.1) and [22]Pentaphyrin-(2.1.0.0.1):  Novel Sapphyrin Analogues,” Tetrahedron Lett. 1995, 36, 4713-4716.


133.*Lisowski, J.; Sessler, J. L.; Mody, T. D. “13C and 31P NMR Study of Paramagnetic Lanthanide(III) Texaphyrins,” Inorg. Chem. 1995, 34, 4336-4342. DOI: 10.1021/ic00121a011.  Funding: National Institutes of Health Grant No. AI28845 and Pharmacyclics, Inc.


134.*Iverson, B. L.; Shreder, K.; Morishima, T.; Rosingana, M.; Sessler, J. L. “Synthesis of a Sapphyrin-EDTA Conjugate and Preliminary Cleavage Results Using a Supercoiled Plasmid DNA Assay,” J. Org. Chem. 1995, 60, 6616-6620.  DOI: 10.1021/jo00125a062.  Funding: National Institutes of Health Grant No. AI33577 and Texas Advanced Technology Program Grant No. 003658-280


135.*Sessler, J. L.; Lisowski, J.; Boudreaux, K. A.; Lynch, V.; Barry, J.; Kodadek, T. J. “Synthesis and Characterization of DiAryl Sapphyrins Prepared under Lindsey-type Conditions,” J. Org. Chem. 1995, 60, 5975-5978.  DOI: 10.1021/jo00123a043.  Funding: Texas Advanced Technology Program Grant No. 003658-280, National Institutes of Health Grant No. AI33577, and National Science Foundation Grant No. CHE-912216


136.*Berman, A.; Izraeli, E. S.; Levanon, H.; Wang, B.; Sessler, J. L. “Photoinduced Intraensemble Electron Transfer in a Base-paired Porphyrin-quinone System.  Time-resolved EPR Spectroscopy,” J. Am. Chem. Soc. 1995, 117, 8252-8257.  DOI: 10.1021/ja00136a024.  Funding: Robert A. Welch Foundation Grant No. F-1018 and National Institutes of Health Grant No. GM41657


137.*Král, V.; Springs, S. L.; Sessler, J. L. “A Noncovalent  Assembly for Energy Transfer Based on Anion Chelation,” J. Am. Chem. Soc. 1995, 117, 8881-8882.  DOI: 10.1021/ja00139a034.  Funding: National Institutes of Health Grant No. GM41657 and Robert A. Welch Foundation Grant No. F-1018


138.*Král, V.; Andrievsky, A.; Sessler, J. L. “Oligosapphyrins:  Receptors for the Recognition and Transport of Nucleotide Di-, and Triphosphates,” J. Chem. Soc., Chem. Commun. 1995, 2349-2351. DOI: 10.1039/C39950002349.  Funding: National Institutes of Health Grant No. AI33577, Texas Advanced Technology Program Grant No. 003658-280 and Pharmacyclics, Inc.


139.*Sessler, J. L. “Texaphyrins,” McGraw-Hill Yearbook of Science & Technology 1996, Parker, S. B., Ed.; McGraw-Hill, New York, 1995, pp. 341-343.


140.*Geraldes, C. F. G. C.; Sherry, A. D.; Vallet, P.; Maton, F.; Muller, R. N.; Mody, T. D.; Hemmi, G.; Sessler, J. L. “Nuclear Magnetic Relaxation Dispersion Studies of a Water-Soluble Gadolinium(III)-Texaphyrin Complex,” J. Magn. Res. Imaging. 1995, 5, 725-729.



1996


141.*Král, V.; Furuta, H.; Shreder, K.; Lynch, V.; Sessler, J. L. “Protonated Sapphyrins.  Highly Effective Phosphate Anion Receptors,” J. Am. Chem. Soc. 1996, 118, 1595-1607.  DOI: 10.1021/ja9529605.  Funding: Texas Advanced Technology Program Grant No. 003658-280, National Institutes of Health Grant No. AI33577, Pharmacyclics, Inc. and Howard Hughes Medical Institute


142.*Iverson, B. L.; Shreder, K.; Král, V.; Sansom, P.; Lynch, V.; Sessler, J. L. “Interaction of Sapphyrin with Phosphorylated Species of Biological Interest,” J. Am. Chem. Soc. 1996, 118, 1608-1616.  DOI: 10.1021/ja952961x.  Funding: National Institutes of Health Grant No. AI33577, Pharmacyclics, Inc. and Howard Hughes Medical Institute


143.*Steven J. Weghorn, Jonathan L. Sessler, Vincent Lynch, Theodore F. Baumann, John W. Sibert “Bis-[(m-chloro)copper(II)] Amethryin:  A Bimetallic Copper(II) Complex of an Expanded Porphyrin,” Inorg. Chem. 1996, 35, 1089-1090.  DOI: 10.1021/ic9509692.  Funding: National Science Foundation Grant No. CHE-9122161


144.*Sessler, J. L.; Genge, J. W.; Urbach, A. “A 3 + 1 Approach to Monofunctionalized Alkyl Porphyrins,” SynLett. 1996, 187-188.  DOI: 10.1055/s-1996-5350.  Funding: Texas Advanced Technology Program Grant No. 003658-280


145.*Young, S. W.; Woodburn, K. W.; Wright, M.; Mody, T. D.; Fan, Q.; Sessler, J. L.; Dow, W. C.; Miller, R. A. “Lutetium Texaphyrin (PCI-0123):  A Near-Infrared, Water-Soluble Photosensitizer,” Photochem. Photobiol. 1996, 63(6), 892-897.  DOI: 10.1111/j.1751-1097.1996.tb09647.x  Funding: National Institutes of Health Grant No. CA68682


146.*Sessler, J. L.; Andrievsky, A. “Sapphyrin-Lasalocid Conjugate:  A Novel Carrier for Aromatic Amino Acid Transport,” Chem. Commun. 1996, 1119-1120. DOI: 10.1039/CC9960001119.  Funding:


147.*Young, S. W.; Quing, F.; Harriman, A.; Sessler, J. L.; Dow, W. C.; Mody, T. D.; Hemmi, G.; Hao, Y.; Miller, R. A. “Gadolinium(III) texaphyrin:  A tumor selective radiation sensitizer that is detectable by MRI,” Proc. Natl. Acad. Sci. USA 1996, 93, 6610-6615.  Funding: National Institutes of Health Grant Nos. AI28845 and CA68682.    Correction: Proc. Natl. Acad. Sci. USA 1999, 96, 2569.


148.*Gale, P. A.; Sessler, J. L.; Král, V.; Lynch, V. “Calix[4]pyrroles:  Old Yet New Anion Binding Agents,” J. Am. Chem. Soc. 1996, 118, 5140-5141.  Funding: National Institutes of Health Grant No. AI33577 and National Science Foundation Grant No. CHE-9122161


149.*Sessler, J. L.; Mody, T. D.; Dulay, M. T.; Espinoza, R.; Lynch, V. “The Template Synthesis and X-ray Characterization of Pyrrole-derived Hexadentate Uranyl(VI) Schiff Base Macrocyclic Complexes,” Inorg. Chim. Acta 1996, 246, 23-30.


150.*Magda, D.; Miller, R. A.; Wright, M.; Rao, J.; Sessler, J. L.; Iverson, B. L.; Sansom, P. I. “Texaphyrin-Based Nuclease Analogs.  Rationally Designed Approaches to the Catalytic Cleavage of RNA and DNA Targets,” in DNA  and RNA Cleavers and Chemotherapy of Cancer and Viral Disease, Meunier, B., Ed., NATO ASI Series C, Vol 479, Kluwer: Amsterdam, 1996, pp. 337-353.


151.*Vögtle, F.; Ahuis, F.; Baumann, S.; Sessler, J. L. “Porphyrin Blocking Groups in Amide-based Rotaxanes,” Liebigs Ann. 1996, 921-926.  DOI: 10.1002/jlac.199619960609.


152.*Sessler, J. L.; Král, V.; Hoehner, M. C.; Chin, K. O. A.; Dávila, R. “New texaphyrin-type expanded porphyrins,” Pure and Appl. Chem. 1996, 68, 1291-1295.  Funding: Pharmacyclics, Inc., National Institutes of Health Grant Nos. AI28845 and National Science Foundation Grant No. CHE-9122161


153.*Sessler, J. L.; Wang, B.; Springs, S. L.; Brown, C. T. “Electron and Energy Transfer Reactions in Non-covalently Linked, Supramolecular Model Systems,” Comprehensive Supramolecular Chemistry, Vol. 4; Murakami, Y., Ed.; Pergamon:  Oxford UK; Chapter 9, 1996.


154.*Sessler, J. L.; Burrell, A. H.; Lisowski, J.; Gebauer, A.; Cyr, M. J.; Lynch, V. “Cobalt(II) and rhodium(I) complexes of thia- and oxasapphyrins,” Bull. Soc. Chem. Fr. 1996, 133, 725-734.


155.*Sessler, J. L.; Dávila, R. M.; Král, V. “Polypyrroles in Three Dimensions.  The Synthesis of Tripyrrane-strapped 2-Aminophenylporphyrins,” Tetrahedron Lett. 1996, 37, 6469-6472.


156.*Sessler, J. L.; Wang, R. “Self-Assembly of an 'Artificial Dinucleotide Duplex',” J. Am. Chem. Soc. 1996, 118, 9808-9809.  Funding: Robert A. Welch Foundation Grant No. F-1018


157.*Sessler, J. L.; Hoehner, M. C.; Johnson, D. W.; Gebauer, A. Lynch, V. “Synthesis and Characterization of a Novel Three Dimensional Oligopyrrole:  Tris(bipyrro)methane,” Chem. Commun. 1996, 2311-2312. DOI: 10.1039/CC9960002311.  Funding: National Science Foundation Grant No. CHE-9122161


158.*Arimura, T.; Brown, C. T.; Springs, S. L.; Sessler, J. L. “Intracomplex Electron Transfer in a Hydrogen-Bonded Calixarene-Porphyrin System,” Chem. Commun. 1996, 2293-2294. DOI: 10.1039/CC9960002293.  Funding: National Institutes of Health Grant No. GM 41657 and Robert A. Welch Foundation Grant No. F-1018


159.*Gale, P. A.; Sessler, J. L.; Lynch, V.; Sansom, P. I. “Synthesis of a New Cylindrical Calix[4]arene-Calix[4]pyrrole Pseudo Dimer,” Tetrahedron Lett. 1996, 44, 7881-7884.


160.*Sessler, J. L.; Gebauer, A.; Král, V.; Lynch, V. “Synthesis and Characterization of a Tripyrrane-Copper(II)-Complex,” Inorg. Chem. 1996, 35, 6636-6637.  DOI: 10.1021/ic9606789.  Funding: National Science Foundation Grant No. CHE-9122161


161.*Sessler, J. L.; Sansom, P. I.; Král, V.; O'Connor, D.; Iverson, B. L. “Sapphyrin-Oligonucleotide Conjugates.  Novel Sequence-Specific DNA Photomodifying Agents with Increased Binding Affinity,” J. Am. Chem. Soc. 1996, 118, 12322-12330.  DOI: 10.1021/ja961672l.  Funding: National Institutes of Health Grant No. AI33577 and Howard Hughes Medical Institute


162.*Allen, W. E.; Gale, P. A.; Brown, C. T.; Lynch, V. M.; Sessler, J. L. “Binding of Neutral Substrates by Calix[4]pyrroles,” J. Am. Chem. Soc. 1996, 118, 12471-12472.  DOI: 10.1021/ja9632217.  Funding: National Institutes of Health Grant No. AI33577, National Science Foundation Grant No. CHE-9122161, State of Texas Coordinating Board TD&T-023 and Pharmacyclics, Inc.


163.*Sessler, J. L.; Genge, J. W.; Král, V.; Iverson, B. L. “Separation of Mono-, Di-, and Triphosphate Nucleotides by Cytosine-substituted, Silica-bound Sapphyrin Solid Supports,” Supramolec. Chem. 1996, 8, 45-52 (cover).  DOI: 10.1080/10610279608233967


164.*Sessler, J. L.; Brucker, E. A.; Lynch, V.; Choe, M.; Sorey, S.; Vogel, E. “Solution Phase and Single Crystal Diffraction X-ray Analyses of Diprotonated Porphyrin Isomers:  Etioporphyrin, Etioporphycene, and Etiocorrphycene Bishydroperchlorate Salts,” Chem. Eur. J. 1996, 2, 1527-1532.  DOI: 10.1002/chem.19960021209.  Funding: National Science Foundation Grant No. CHE-9122161 and Alexander von Humboldt-Stiftung Senior Scientist Award


165.*Woodburn, K. W.; Fan, Q.; Kessel, D.; Wright, M.; Mody, T. D.; Hemmi, G.; Magda, D.; Sessler, J. L.; Dow, W. C.; Miller, R. A.; Young, S. W. “Phototherapy of Cancer and Atheromatous Plaque with Texaphyrins,” J. Clin. Laser Med. & Surg. 1996, 14, 343-348.


166.Sessler, J. L.; Andrievsky, A.; Gale, P. A.; Lynch, V. “Anion Binding:  Self-Assembly of Polypyrrolic Macrocycles,” Angew. Chem. 1996, 108, 2954-2957; Angew. Chem. Int. Ed. Engl. 1996, 35, 2782-2785.


167.*Sessler, J. L.; Brown, C. T.; Wang, R.; Hirose, T. “A Rigid Cytidine-RuII (bpy)3 Conjugate.  A Potential Precursor for Non-Covalent Electron Transfer Modeling,” Inorg. Chim. Acta 1996, 251, 135-140.



1997


168.*Magda, D.; Crofts, S.; Lin, A.; Miles, D.; Wright, M.; Sessler, J. L. “Synthesis and Kinetic Properties of Ribozyme Analogues Prepared Using Phosphramidite Derivatives of Dysprosium(III) Texaphyrin,” J. Am. Chem. Soc. 1997, 119, 2293-2294.


169.*Gale, P. A.; Sessler, J. L.; Allen, W. E.; Tvermoes, N. A.; Lynch, V. “Calix[4]pyrroles:  C-rim Substitution and Tunability of Anion Binding Strength,” Chem. Commun., 1997, 665-666. DOI: 10.1039/a700685c.  Funding: National Institutes of Health Grant No. AI33577, National Science Foundation Grant No. CHE-9122161 and Pharmacyclics, Inc.


170.*Sessler, J. L.; Dow, W. C.; O'Connor, D.; Harriman, A.; Hemmi, G.; Mody, T. D.; Miller, R. A.; Qing, F.; Springs, S.; Woodburn, K.; Young, S. W. “Biomedical applications of lanthanide(III) texaphyrins.  Lutetium(III) texaphyrins as potential photodynamic therapy photosensitizers,” J. Alloys & Compounds 1997, 249, 146-152.

    170a.*“It’s not real big, but Texas takes to it,” New York Times, February 12, 1997, A11.

    170b.*“Watch out, buckyball – Texaphyrin proves mettle,” Austin American-Statesman, September 27, 1997, A1.

    170c.*“Resolution proposed for official molecule,” Daily Texan, February 14, 1997, 1.

    170d.*Buckyball, UT entry collide in bid to be state molecule,” February 19, 1997, Austin American Statesman, B1.


171.*Magda, D. M.; Wright, M.; Crofts, S.; Lin, A.; Sessler, J. L. “Metal Complex Conjugates of Antisense DNA Which Display Ribozyme-like Activity,” J. Am. Chem. Soc. 1997, 119, 6947-6948.


172.*Sessler, J. L.; Andrievsky, A.; Sansom, P. I.; Král, V.; Iverson, B. L. “Enhanced DNA Photocleavage and Binding Properties of Sapphyrin-polyamine Conjugates,” Bioorg. & Med. Chem. Lett. 1997, 7, 1433-1436.


173.*Vogel, E.; Bröring, M.; Scholz, P.; Deponte, R.; Lex, J.; Schmickler, H.; Schaffner, K.; Braslavsky, S.; Müller, M. Pörting, S.; Weghorn, S. J.; Fowler, C. L.; Sessler, J. L. “Octaethylhemiporphycene:  Synthesis, Molecular Structure, and Photophysics,” Angew. Chem., Intl. Ed. Engl. 1997, 36, 1651-1654.


174.*Magda, D.; Crofts, S.; Sessler, J. L.; Sansom, P.; Springs, S. L.; Ohya, Y. “Energy Transfer Assemblies Composed of Expanded Porphyrin-Oligonucleotide Conjugates,” Tetrahedron Letters 1997, 38, 5759-5762.


175.*Sessler, J. L.; Andrievsky, A.; Genge, J. W. “Anion Binding by Sapphyrins,” in Advances in Supramolecular Chemistry Vol. 4, Gokel, G. W., Ed., JAI Press Inc., Greenwich, Connecticut, 1997, pp 97-142.


176.*Sessler, J. L.; Sansom, P. I.; Andrievsky, A.; Král, V. “Application Aspects Involving the Supramolecular Chemistry of Anions,” in Supramolecular Chemistry of Anions, Bianchi, A.; Bowman-James, K.; Garcia-Espana, E., Eds. VCH Verlag, Weinheim, 1997, pp. 355-419.


177.*Sessler, J. L.; Andrievsky, A.; Král, V.; Lynch, V. “Chiral Recognition of Dicarboxylate Anions by Sapphyrin-based Receptors,” J. Am. Chem. Soc. 1997, 119, 9385-9392.  DOI: 10.1021/ja971614f.  Funding: National Institutes of Health Grant Nos. AI33577 and TW06282 and Howard Hughes Medical Institute


178.*Scherer, M.; Sessler, J. L.; Gebauer, A.; Lynch, V. “Synthesis and Properties of Pyrrole Substituted Cyclopentadienes,” J. Org. Chem. 1997, 62, 7877-7881.  DOI: 10.1021/jo970818b.  Funding: National Science Foundation Grant No. CHE-9122161


179.*Morosini, P.; Scherer, M.; Meyer, S.; Lynch, V.; Sessler, J. L. “5,10,20,25,35,40-Hexanornonapyrrin: The Largest Structurally Characterized Oligopyrrole Prepared to Date,” J. Org. Chem. 1997, 62, 8848-8853.  DOI: 10.1021/jo971430j.  Funding: National Science Foundation Grant No. CHE-9122161


180.*Sessler, J. L.; Hoehner, M.; Gebauer, A.; Andrievsky, A.; Lynch, V. “Synthesis and Characterization of All-Alkyl-Substituted Mono-, Di- and Trioxasapphyrins,” J. Org. Chem. 1997, 62, 9251-9260.  DOI: 10.1021/jo9715736.  Funding: National Science Foundation Grant Nos. CHE-9122161 and CHE- 9725399


181.*Gale, P. A.; Genge, J. W.; Král, V.; McKervey, M. A.; Sessler, J. L.; Walker, A. “First Synthesis of an Expanded Calixpyrrole,” Tetrahedron Lett. 1997, 38, 8443-8444.


182.*Sessler, J. L.; Gale, P. A.; Král, V.; Lynch, V.; Genge, J. W.; Allen, W. E.; Brown, C. T.; Gebauer, A.; Tvermoes, N. A.; Sansom, P. I. “New Aspects of Calixpyrrole Chemistry,” Electronic Conference on Trends in Organometallic Chemistry, Royal Society of Chemistry, ISBN 0 85404 889 8, 1997.


183.*Sessler, J. L.; Gebauer, A.; Gale, P. A. “Anion Binding and Electrochemical Properties of Calix[4]pyrrole Ferrocene Conjugates,” Gazz. Chim. Ital. 1997, 127, 723-726.



1998


184.*Gale, P. A.; Sessler, J. L.; Král, V. “Calixpyrroles,” Chem. Commun. 1998, 1-8 (cover). DOI: 10.1039/a706280j.  Funding:  National Institutes of Health Grant Nos. AI 33577 and TW00682, National Science Foundation Grant Nos. CHE-9122161 and CHE-9725399 and Howard Hughes Medical Institute


185.*Král, V.; Gale, P. A.; Anzenbacher, P., Jr.; Jusiková, K.; Lynch, V.; Sessler, J. L. “Calix[4]pyridine:  A New Arrival in the heterocalixarene family,” Chem. Commun. 1998, 9-10. DOI: 10.1039/a706018a.  Funding: National Institutes of Health Grant Nos. AI 33577 and TW00682, National Science Foundation Grant No. CHE-9725399 and Howard Hughes Medical Institute

185a.*“Calixarene Family Embraces New Cousins,” C&EN, February 16, 1998, 31.


186.*Scherer. M.; Sessler, J. L.; Moini, M.; Gebauer, A.; Lynch, V. “Self-Assembly of Pyrrole-Ferrocene Hybrids; Determined Inter Alia by a New Chemically Induced Electrospray Mass Spectrometry Technique,” Chem. Eur. J. 1998, 4, 152-158 (cover).  DOI: 10.1002/(SICI)1521-3765(199801)4:1<152::AID-CHEM152>3.0.CO;2-E. Funding: National Science Foundation Grant Nos. CHE-9122161 and CHE-9725399


187.*Sessler, J. L.; Andrievsky, A. “Efficient Transport of Aromatic Amino Acids by Sapphyrin-Lasalocid Conjugates,” Chem. Eur. J. 1998, 4, 159-167.  DOI: 10.1002/(SICI)1521-3765(199801)4:1<159::AID-CHEM159>3.0.CO;2-N.  Funding: National Institutes of Health Grant No. AI33577 and Pharmacyclics, Inc.


188.*Scherer, M.; Sessler, J. L.; Gebauer, A.; Lynch, V. “A Bridged Pyrrolic Ansa-ferrocene.  A New Anion Receptor,” Chem. Commun. 1998, 85-86.


189.*Guldi, D. M.; Heger, A.; Vogel, E.; Sessler, J. L. “Octaethylcorrphycene and its Metal Complexes.  Radiolytic Reduction Studies,” J. Phys. Chem. A. 1998, 102, 960-967.  DOI: 10.1021/jp973341g.  Funding: National Science Foundation Grant No. CHE-9122161


190.*Ito, T.; Radecka, H.; Umezawa, K.; Kimura, T.; Yashiro, A.; Lin, X. M.; Kataoka, M.; Kimura, E.; Sessler, J. L.; Odashima, K.; Umezawa, Y. “A Variety of Lipophilic Amines Incorporated in Liquid Membranes Exhibit Potentiometric Responses to Neutral Phenols,” Analytical Sciences 1998, 14, 89-98.


191.*Lin, X. M.; Umezawa, K.; Tohda, K.; Furuta, H.; Sessler, J. L.; Umezawa, Y. “Potentiometric Responses of Expanded Porphyrin Incorporated Liquid Membrane Electrodes toward a Series of Inorganic and Organic Anions,” Analytical Sciences, 1998, 14, 99-108.


192.*Sessler, J. L.; Gebauer, A.; Guba, A.; Scherer, M.; Lynch, V. “Synthesis and X-ray Crystallography of Rh(I) Carbonyl Complexes of Amethyrin,” Inorg. Chem., 1998, 8, 2073-2076.  DOI: 10.1021/ic971018m.  Funding: National Science Foundation Grant No. CHE-9725399


193.*Kavenova, I.; Holakovsky, R.; Hovorka, M.; Kriz, V.; Anzenbacher, P., Jr.; Matejka, P.; Král, V.; Genge, J. W.; Sessler, J. L. “Molecular Recognition with Novel Chromatographic Phases Based on Combination of Porphyrins and Expanded Porphyrins with Chiral Binaphthyl Derivatives:  Application for the Separation of Biologically Important Substrates,” Chem. Listy, 1998, 92, 147-148.


194.*Sessler, J. L.; Wang, R. “Design, Synthesis, and Self-assembly of 'Artificial Dinucleotides',” J. Org. Chem. 1998, 63, 4079-4091.  DOI: 10.1021/jo980194p.  Funding: Robert A. Welch Foundation Grant No. F-1018


195.*Sessler, J. L; Gale, P. A.; Genge, J. W. “Calix[4]pyrroles:  New Solid Phase HPLC Supports for the Separation of Anions,” Chem. Eur. J. 1998, 4, 1095-1099.  DOI: 10.1002/(SICI)1521-3765(19980615)4:6<1095::AID-CHEM1095>3.0.CO;2-1.


196.*Sessler, J. L.; Wang, R. “A New Base Pairing Motif Based on Modified Dimeric Guanosines,” Angew. Chem. 1998, 110, 1818-1821; Angew. Chem. Intl. Ed. Engl. 1998, 37, 1726-1729.


197.*Sessler, J. L.; Král, V.; Genge, J. W.; Thomas, R. L.; Iverson, B. L. “Anion Selectivity of a Sapphyrin-Modified Silica Gel HPLC Support,”Analytical Chem. 1998, 70, 2516-2522.  DOI: 10.1021/ac971214a.  Funding: National Institutes of Health Grant No. AI33577, National Science Foundation Grant No. CHE-9725399 and Texas Advanced Technologies Program


198.*Meyer, S.; Andrioletti, B.; Sessler, J. L.; Lynch, V. “Synthesis and Structural Characterization of the First Schiff-base Macrocycles Containing Terpyrrole Subunits,” J. Org. Chem. 1998, 63, 6752-6756.  DOI: 10.1021/jo980628g.  Funding: National Science Foundation Grant No. CHE-9725399 


199.*Andrievsky, A.; Ahuis, F.; Sessler, J. L.; Vögtle, F.; Gudat, D.; Moini, M. “Bipyrrole-Based [2]Catenane:  A New Type of Anion Receptor,” J. Am. Chem. Soc. 1998, 120, 9712-9713.  DOI: 10.1021/ja980755u.  Funding: Alexander Von Humboldt Senior Scientist Award, National Science Foundation Grant No. CHE-9725399 and National Institutes of Health Grant No. AI33577


200.*Springs, S. L.; Andrievsky, A.; Král, V.; Sessler, J. L. “Energy Transfer in a Supramolecular Complex Assembled via Sapphyrin Dimer-mediated Dicarboxylate Anion Chelation,” J. Porph. Phthalocy. 1998, 2, 315-325.


201.*Sessler, J. L.; Davis, J. M.; Lynch, V. “Synthesis and Characterization of a Stable Smaragdyrin Isomer,” J. Org. Chem. 1998, 63, 7062-7065.  DOI: 10.1021/jo981019b.  Funding: National Science Foundation Grant No. CHE-9725399


202.*Sessler, J. L.; Gebauer, A.; Hoehner, M.; Lynch, V. “Synthesis and Characterization of an Oxasapphyrin-uranyl Complex,” Chem. Commun. 1998, 1835-1836. DOI: 10.1039/a803975e.  Funding: National Science Foundation Grant Nos. CHE-9122161 and CHE-9725399


203.*Sessler, J. L.; Brown, C. T.; O’Connor, D.; Springs, S.; Wang, R.; Sathiosatham, M.; Hirose, T. A “Rigid Chlorin-Naphthalene Diimide Conjugate. A Possible New Noncovalent Electron Transfer Model System,” J. Org. Chem. 1998, 63, 7370-7374. DOI: 10.1021/jo9810112.  Funding: National Institutes of Health Grant No. GM41657 and Robert A. Welch Foundation Grant No. F-1018


204.*Sessler, J. L.; Anzenbacher, P., Jr.; Jursíková, K.; Miyaji, H.; Genge, J. W.; Tvermoes, N. A.; Allen, W. E.; Shriver, J.; Gale, P. A.; Král, V. “Functionalized Calix[4]pyrroles,” Pure and Applied Chemistry 1998, 70, 2401-2408.  Funding: National Institutes of Health Grant Nos. AI33577 and TW00682, National Science Foundation Grant No. CHE-9725399 and Howard Hughes Foundation


205.* Asano-Someda, M.; Levanon, H.; Sessler, J. L.; Wang, R. “Intramolecular Photoinduced Electron Transfer in a Hydrogen Bonded Zinc(II) Porphyrin - Dinitrobenzene Complex by Time-resolved Electron Paramagnetic Resonance Spectroscopy,” Molec. Phys. 1998, 95, 935-942.  DOI: 10.1080/00268979809483227.  Funding: National Institutes of Health Grant No. GM41657 and Robert A. Welch Foundation Grant No. F-1018



1999


206.*Sessler, J. L.; Tvermoes, N. A.; Guldi, D. M.; Mody, T. D. Allen, W. A. “One-Electron Reduction and Oxidation Studies of the Radiation Sensitizer Gadolinium(III) Texaphyrin (PCI-0120) and Other Water Soluble Metallotexaphyrins,” J. Phys. Chem. A 1999, 103, 787-794. DOI: 10.1021/jp9838588.  Funding: National Institutes of Health Grant No. CA68682

    206a.“10-Gallon molecule stomps tumors,” Science, February 27, 1998, 279.

    206b.“Texas-sized molecule battles cancer,” Science News February 28, 1998, 153, 137.


207.*Meyer, S.; Hoehner, M. C.; Lynch, V.; Sessler, J. L. “Synthesis and Characterization of New Non-aromatic Texaphyrin-type Expanded Porphyrins,” J. Porph. Phthalocy. 1999, 3, 148-158.


208.*Shuali, Z.; Berg, A.; Levanon, H.; Vogel, E.; Bröring, M.; Sessler, J. L.; Fowler, C.; Weghorn, S. J. “Photoexcited triplet-state dynamics of novel porphyrinoids:  octaethylcorrphycene and octaethylhemiporphycene.  Time-resolved electron paramagnetic resonance study,” Chem. Phys. Lett. 1999, 300, 687-694.


209.*Springs, S. L.; Gosztola, D.; Wasielewski, M.; Král, V.; Andrievsky, A.; Sessler, J. L. “Picosecond Dynamics of Energy Transfer in Porphyrin-Sapphyrin Noncovalent Assemblies,”  DOI: 10.1021/ja9835436 J. Am. Chem. Soc. 1999, 121, 2281-2289.  Funding: National Institutes of Health Grant No. GM41657


210.*Mody, T. D.; Sessler, J. L. “Porphyrin- and Expanded Porphyrin-based Diagnostic and Therapeutic Agents,” in Supramolecular Materials and Technologies, Reinhoudt, D. N., Ed., Wiley, New York, 1999 (pp 245-294).


211.*Miyaji, H.; Anzenbacher, P., Jr.; Sessler, J. L.; Bleasdale, E. R.; Gale, P. A. “Anthracene-linked calix[4]pyrroles:  fluorescent chemosensors for anions,” Chem. Commun. 1999, 1723-1724. DOI: 10.1039/a905054j.  Funding: National Institutes of Health Grant No. GM58907 and Texas Advanced Research Program Grant No. 3658


212.*Berg, A.; Shuali, Z.; Asano-Someda, M.; Levanon, H.; Fuhs, M.; Möbius, K.; Wang, R.; Brown, C. T.; Sessler, J. L. “A First High-Field EPR Study of Photoinduced Electron Transfer in a Base-Paired Porphyrin-Dinitrobenzene Supramolecular Complex,” J. Am. Chem. Soc. 1999, 121, 7433-7434.  DOI: 10.1021/ja990734f.  Funding: National Institutes of Health Grant No. GM41657 and Robert A. Welch Foundation Grant No. F-1018


213.*Král, V.; Sessler, J. L.; Shishkanova, T. V.; Gale, P. A.; Volf, R. “Molecular Recognition at an Organic-Aqueous Interface: Heterocalixarenes as Anion Binding Agents in Liquid Polymeric Membrane Ion-Selective Electrodes,” J. Am. Chem. Soc. 1999, 121, 8771-8775.  DOI: 10.1021/ja991044e.  Funding: National Institutes of Health Grant Nos. GM58097 and TW00682 and the Howard Hughes Foundation


214.*Allen, W. E.; Sessler, J. L. “Anion Carriers:  New Tools for Crossing Membranes,” ChemTech 1999, 29, 16-24.


215.*Gale, P. A.; Twyman, L. J.; Handlin, C. I.; Sessler, J. L. “A colourimetric calix[4]pyrrole-4-nitrophenolate based anion sensor,” Chem. Commun., 1999, 1851-1852. DOI: 10.1039/a905743i.  Funding: National Institutes of Health Grant No. GM58097 and Texas Advanced Research Program Grant No. 003658-102


216.*Rachlewicz, K.; Latos-Graynski, L.; Gebauer, A.; Vivian, A.; Sessler, J. L. “NH tautomerization of 2,7,18,23-tetramethyl-3,8,12,13,17,22-hexaethylsapphyrin,” J. Chem. Soc. Perkin Trans. 2 1999, 2189-2195. DOI: 10.1039/a901983i.  Funding: National Science Foundation Grant No. CHE-9725399


217.*Miller, R. A.; Woodburn, K.; Fan, Q.; Renschler, M.; Sessler, J. L.; Koutcher, J. A. “In Vivo Animal Studies with Gadolinium(III) Texaphyrin as a Radiation Enhancer,” Int. J. Biol. Radiat Oncol. 1999, 45, 981-989.


218.*Lament, B.; Dobkowski, J.; Sessler, J. L.; Weghorn, S. J.; Waluk, J. “Spectroscopy and Photophysics of a Highly Nonplanar Expanded Porphyrin:  4,9,13,18,22,27-Hexaethyl-5,8,14,17,23,26-hexamethyl-2,11,20-triphenylrosarin,” Chem. Eur. J. 1999, 5, 3039-3045.  3   Funding: National Science Foundation Grant No. CHE-9725399


219.*Arimura, T.; Ide, S.; Sugihara, H.; Murata, S.; Sessler, J. L. “A non-covalent assembly for electron transfer based on a calixarene-porphyrin conjugate:  tweezers for a quinone,” New. J. Chem, 1999, 23 977-979. DOI: 10.1039/a906474e.


220.*Black, C. B.; Andrioletti, B.; Try, A. C.; Ruiperez, C.; Sessler, J. L. “Dipyrrolylquionoxalines.  Efficient Sensors for Fluoride Anion in Organic Solution,” J. Am. Chem. Soc. 1999, 121, 10438-10439. DOI: 10.1021/ja992579a.  Funding: National Institutes of Health Grant No. GM58907, National Science Foundation Grant No. CHE-9725399 and Texas Advanced Research Program Grant No. 003658-102


221.*Sessler, J. L.; Seidel, D.; Lynch, V. “Synthesis of [28]Heptaphyrin(1.0.0.1.0.0.0) and [32]Octaphyrin(1.0.0.0.1.0.0.0) via a Directed Oxidative Ring Closure: The First Expanded Porphyrins Containing a Quaterpyrrole Subunit,” J. Am.Chem. Soc. 1999, 121, 11257-11258.  DOI: 10.1021/ja992934x.  Funding: National Science Foundation Grant No. CHE-9725399 and National Institutes of Health Grant No. CA68682   


222.*Anzenbacher, P. Jr.; Jursíková, K.; Lynch, V. M.; Gale, P. A.; Sessler, J. L. “Calix[4]pyrroles Containing Deep Cavities and Fixed Walls.  Synthesis, Structural Studies and Anion Binding Properties of the Isomeric Products Derived from the Condensation of p-Hydroxyacetophenone and Pyrrole,” J. Am. Chem. Soc. 1999, 121, 11020-11021.  DOI: 10.1021/ja993195n.  Funding: National Science Foundation Grant No. CHE-9725399 and National Institutes of Health Grant No. GM58907


223.*Sessler, J. L.; Tvermoes, N. A.; Davis, J.; Anzenbacher, P., Jr.; Jursíková, K.; Sato, W.; Seidel, D.; Lynch, V.; Black, C. B.; Try, A.; Andrioletti, B.; Hemmi, G.; Mody, T. D.; Magda, D. J.; Král, V. “Expanded Porphyrins.  Synthetic Materials with Potential Medical Utility,” Pure and Applied Chemistry 1999, 71, 2009-2018.  Funding: National Institutes of Health Grant Nos. CA68682, GM58907, and TW00682, National Science Foundation Grant No. CHE-9725399, Pharmacyclics, Inc., Texas Advanced Research Program Grant No. 003658-102 and the Howard Hughes Foundation



2000


224.*Sessler, J. L.; Gebauer, A.; Weghorn, S. J. “Expanded Porphyrins,” in The Porphyrin Handbook, K. M. Kadish, K. M. Smith and R. Guilard, Eds.; Academic Press:  San Diego, CA and Burlington, MA, 2000.


225.*Sessler, J. L.; Gebauer, A.; Vogel, E. “Porphyrin Isomers,” in The Porphyrin Handbook, K. M. Kadish, K. M. Smith and R. Guilard, Eds.; Academic Press:  San Diego, CA and Burlington, MA, 2000.


226.*Sessler, J. L.; Gale, P. A. “Calixpyrroles:  Novel Anion and Neutral Substrate Receptors,” in The Porphyrin Handbook, K. M. Kadish, K. M. Smith and R. Guilard, Eds.; Academic Press:  San Diego, CA and Burlington, MA, 2000.


227.*Sessler, J. L.; Miller, R. A. “Texaphyrins.  New Drugs with Diverse Clinical Applications in Radiation and Photodynamic Therapy,” Biochemical Pharmacology 2000, 59, 733-739.


228.*Miyaji, H.; Sato, W.; Sessler, J. L.; Lynch, V. M. “A ‘Building Block’ Approach to Functionalized Calix[4]pyrroles,” Tetrahedron Lett. 2000, 41, 1369–1373.


229.*Král, V.; Sessler, J. L.; Zimmerman, R. S.; Seidel, D.; Lynch, V.; Andrioletti, B. “Calixphyrins:  Novel Macrocycles at the Intersection Between Porphyrins and Calixpyrroles,” Angew. Chem. 2000, 112, 1097-1100; Angew. Chem., Int. Ed. 2000, 39, 1055–1058.


230.*Sessler, J. L.; Sathiosatham, M.; Doerr, K.; Lynch, V.; Abboud, K. A. “A G-quartet Formed in the Absence of a Templating Metal Cation:  A New 8-(N,N-dimethylaniline)guanosine Derivative,” Angew. Chem. 2000, 112, 1356-1359; Angew. Chem. Int. Ed. 2000, 39, 1300–1303.


231.*Sessler, J. L.; Genge, J. W.; Gale, P. A.; Král, V. “Calix[4]pyrrole-Functionalized Silica Gels.  Novel Supports for the HPLC-Based Separation of Anions,” in Calixarene-based Separations, Lummetta, G. J.; Rogers, R. D.; Gopalan, A. S., Eds., ACS Symposium Series 757, American Chemical Society, Washington, D.C., 2000; Chapter 18; pp 238-254.


232.*Sessler, J. L. “Porphyrin Analogues,” J. Porph. Phthalocy. 2000, 4, 331-336.


233.*Gisselbrecht, J. P.; Gross, M.; Vogel, E.; Sessler, J. L. “Electrochemical Studies of Corrphycenes and Metallocorrphycenes,” Inorg. Chem. 2000, 39, (13), 2850-2854. DOI: 10.1021/ic9913031.  Funding: National Science Foundation Grant No. CHE-9725399


234.*Sessler, J. L.; Seidel, D.; Bucher, C.; Lynch, V. “[26]Hexaphyrin(1.1.1.1.0.0):  An all-aza isomer of rubyrin with an inverted pyrrole subunit,” Chem. Commun. 2000, 1473-1474. DOI: 10.1039/b003777j.  Funding: National Science Foundation Grant No. CHE-9725399


235.*Synytsya, A.; Synytsya, A.; Král, V.; Volka, K.; Copíková, J; Sessler, J. L. “Interaction of metallotexaphyrins with mono- and polysaccharides,” J. C. S. Perkin 2 2000, 1876-1884. DOI: 10.1039/b003263h.  Funding: Howard Hughes Medical Institute Grant No. 75195-541101, National Institutes of Health Grant No. CA 68682


236.*Miyaji, H.; Sato, W.; Sessler, J. L. “Naked-Eye Detection of Anions in Dichloromethane:  Colorimetric Anion Sensors Based on Calix[4]pyrrole,” Angew. Chem. 2000, 112, 1847-1850; Angew. Chem. Int. Ed. 2000, 39, 1777-1780.


237.*Guldi, D. M.; Mody, T. D.; Gerasimchuk, N. N.; Magda, D.; Sessler, J. L. “Influence of Large Metal Cations on the Photophysical Properties of Texaphyrin, a Rigid Aromatic Chromophore,” J. Am. Chem. Soc. 2000, 122, 8289-8298.  DOI: 10.1021/ja001578b.  Funding: National Institutes of Health Grant No. CA 68682


238.*Sato, W.; Miyaji, H.; Sessler, J. L. “Calix[4]pyrrole Dimers Bearing Rigid Spacers.  Towards the Synthesis of Cooperative Anion Binding Agents,” Tetrahedron Letters 2000, 41, 6731-6736.


239.*Anzenbacher, P., Jr.; Jurisíková, K.; Sessler, J. L. “Second Generation Calixpyrrole Anion Sensors,” J. Am. Chem. Soc. 2000, 122, 9350-9351.  DOI: 10.1021/ja001308t.  Funding: National Science Foundation Grant No. CHE-9725399, National Institutes of Health Grant No. GM58907, and Texas Advanced Research Program Grant No. 3658


240.*Sessler, J. L.; Anzenbacher, P., Jr.; Miyaji, H.; Jursíková, K.; Bleasdale, E. R.; Gale, P. A. “Modified Calix[4]pyrroles,” Industr. Engin. Chem. Res. 2000, 39, 3471-3478. DOI: 10.1021/ie000102y.  Funding: National Institutes of Health Grant No. 58907, and Texas Advanced Research Program Grant No. 3658


241.*Bucher, C.; Seidel, D.; Sessler, J. L.; Král, V.; Lynch, V. “Novel Synthesis of Hybrid Calixphyrin Macrocycles,” Org. Lett. 2000, 2, 3103-3106. DOI: 10.1021/ol006316t.  Funding: National Science Foundation Grant No. CHE-9725399


242.*Anzenbacher, P., Jr.; Try, A. C.; Miyaji, H.; Jurisíková, K.; Lynch, V. M.; Marquez, M.; Sessler, J. L. “Fluorinated Calix[4]pyrrole and Dipyrrolylquinoxaline: Neutral Anion Receptors with Augmented Affinites and Enhanced Selectivities,” J. Am. Chem. Soc. 2000, 122, 10268-10272.  DOI: 10.1021/ja002112w.  Funding: National Science Foundation Grant No. CHE-9725399, National Institutes of Health Grant No. 58907, and Texas Advanced Research Program Grant No. 3658


243.*Anzenbacher, P., Jr.; Jurisíková, K.; Shriver, J.; Miyaji, H.; Lynch, V. M.; Sessler, J. L.; Gale, P. A. “Lithiation of meso-Octamethylcalix[4]pyrrole:  A General Route to C-Rim Monosubstituted Calix[4]pyrroles,” J. Org. Chem. 2000, 65, 7641-7645. DOI: 10.1021/jo005610w. Funding: National Science Foundation Grant No. CHE-9725399, National Institutes of Health Grant No. 58907, and Texas Advanced Research Program Grant No. 3658


244.*Sessler, J. L.; Anzenbacher, P., Jr.; Shriver, J. A.; Jurisíková, K.; Miyaji, H.; Lynch, V. M.; Marquez, M. “Direct Synthesis of Expanded Fluorinated Calix[n]pyrroles: Decafluorocalix[5]pyrrole and Hexadecafluorocalix[8]pyrrole,” J. Am. Chem. Soc. 2000, 122, (48), 12061-12062.  DOI: 10.1021/ja005650h.  Funding: National Science Foundation Grant No. CHE-9725399, National Institutes of Health Grant No. 58907, and Texas Advanced Research Program Grant No. 3658


245.*Sessler, J. L. “Expanded Porphyrin Chemistry:  A Personal Overview,” Ernst Schering Research Foundation Lecture Publication Series, vol. 39.  Hellmich PrePress & Print GmbH: Berlin, 2000, pp. 7-22.  ISSN 1431-5033.



2001


246.*Umezawa, K.; Tohda, K.; Lin, X. M.; Sessler, J. L.; Umezawa, Y. “Expanded porphyrin incorporated solvent polymeric membrane electrodes:  protonation and interaction with an analyte anion at organic/water interface as studied by optical second harmonic generation and Fourier transform infrared attenuated total reflectance spectrometry,” Anal. Chim. Acta 2001, 426, 19-32.


247.*Miyaji, H.; Sessler, J. L. “Off the Shelf Anion Sensors,” Angew. Chem. 2001, 113, 158-161; Angew. Chem. Int. Ed., Engl. 2001, 40, 154-157.


248.*Allen, W. E.; Fowler, C. J.; Lynch, V. M.; Sessler, J. L. “Self-assembly of Helices from 2,2’-Biimidazoles,” Chem. Eur. J. 2001, 7, 721-729 (cover).


249.*Sessler, J. L.; Seidel, D.; Vivian, A. E.; Lynch, V.; Scott, B. L.; Keogh, D. W. “Hexaphyrin(1.0.01.0.0):  An Expanded Porphyrin Ligand for the Actinide Cations Uranyl (UO22+) and Neptunyl (NpO2+),” Angew. Chem. 2001, 113, 611-614; Angew. Chem. Int. Ed., Engl. 2001, 40, 591-594.

249a.*“Expanded Porphyrin Forms Stable Complexes with Actinide yl Cations,” Chemical Engineering News, February 5, 2001, p. 26.


250.*Mody, T. D.; Sessler, J. L. “Texaphyrins:  A new approach to drug development,” J. Porphyrins & Phthalocyanines 2001, 5, 134-142.  DOI: 10.1002/jpp.326


251.*Sessler, J. L.; Tvermoes, N. A.; Guldi, D. M.; Hug, G. L.; Mody, T. D.; Magda, D. “Pulse Radiolytic Studies of Metallotexaphyrins in the presence of Oxygen:  Relevance of the Equilibrium with Superoxide Anion to the Mechanism of Action of the Radiation Sensitizer Motexafin Gadolinium (Gd-Tex2+, Xcytrin®),” J. Phys. Chem. B 2001, 105, 1452-1457.  DOI: 10.1021/jp0035131.  Funding: National Institutes of Health Grant No. CA68685


252.*Bucher, C.; Zimmerman, R. S.; Lynch, V.; Král, V.; Sessler, J. L. “Synthesis of Novel Expanded Calixphyrins:  Anion Binding Properties of a Calix[6]phyrin with a Deep Cavity,”:  J. Am. Chem. Soc. 2001, 123, 2099-2100. DOI: 10.1021/ja005842c. Correction:  J. Am. Chem. Soc. 2001, 123, 12744-12744.  DOI: 10.1021/ja0151347.  Funding: National Science Foundation Grant No. CHE-9725399 and National Institutes of Health Grant No. 58907


253.*Shevchuk, A.; Davis, J.; Sessler, J. L. “Synthesis of sapphyrins via a ‘3+1+1’ Procedure,” Tetrahedron Lett. 2001, 42, 2447-2450.


254.*Mody, T. D.; Fu, L.; Sessler, J. L. “Texaphyrins:  Synthesis and Development of a Novel Class of Therapeutic Agents,” in Progr. Inorg. Chem., 2001, 49, 551-598; Karlin, K. D., ed., J. Wiley & Sons, New York.


255.*Sessler, J. L. “New Opportunities in Drug Development,” Chemical & Engineering News March 26, 2001, 223.


256.*Shimanovich, R.; Hannah, S.; Lynch, V.; Gerasimchuk, N.; Mody, T. D.; Magda, D.; Sessler, J. L.; Groves, J. T. “Mn(II)-Texaphyrin as a Catalyst for the Decomposition of Peroxynitrite,” J. Am. Chem. Soc. 2001, 123, 3613-3614.  DOI: 10.1021/ja005856i.  Funding: National Institutes of Health Grant No. CA68682


257.*Sessler, J. L.; Muhunthan, S.; Brown, C. T.; Rhodes, T. A.; Wiederrecht, G. “Hydrogen-Bond-Mediated Photoinduced Electron-Transfer: Novel Dimethylaniline-Anthracene Ensembles Formed via Watson-Crick Base-Pairing,” J. Am. Chem. Soc. 2001, 123, 3655-3660. DOI: 10.1021/ja005547s.  Funding: National Institutes of Health Grant No. GM41657 and Robert A. Welch Foundation Grant No. F-1018


258.*Gorski, A.; Lament, B.; Davis, J. M.; Sessler, J.; Waluk, J. “Electronic States of a Novel Smaragdyrin Isomer:  Polarized Spectroscopy and Theoretical Studies,” J. Phys. Chem. A 2001, 105, 4992-4999.  DOI: 10.1021/jp004255a.  Funding: National Science Foundation Grant No. CHE-9725399 and National Institutes of Health Grant No. CA68682


259.*Sessler, J. L.; Seidel, D.; Lynch, V. “Isosamagdyrins.  New Aromatic Expanded Porphyrins,” Tetrahedron 2001, 57, 3743-3752.


260.*Hrdlicka, J.; Matejka, P.; Volf, R.; Volka, K.; Král, V.; Try, A. C.; Sessler, J. L. “Comparison of FT Raman Spectra of Some 5-Nitroquinoxalines and Their Electropolymers,” J. Mol. Struct. 2001, 565/566, 101-105.


261.*Sessler, J. L.; Shevchuk, S. V.; Callaway, W.; Lynch, V. “A one step synthesis of a free base secochlorin from a 2,3-dimethoxyporphyrin,” Chem. Commun. 2001, 968-969. DOI: 10.1039/b102139g.  Funding: National Institutes of Health Grant No. CA68682


262.*Sessler, J. L.; Tvermoes, N. A.; Guldi, D. M.; Mody, T. D. “Probing the Reactivity of the Radiation Sensitizer Motexafin Gadolinium (Xcytrin) and a Series of Lanthanide(III) Analogues in the Presence of Both Hydroxyl Radicals and Aqueous Electrons,” J. Porphyrins & Phthalocyanines 2001, 5, 593-599.  DOI: 10.1002/jpp.369.  Funding: National Institutes of Health Grant No. CA68682


263.*Sessler, J. L.; Vivian, A. E.; Sessler, J. L.; Seidel, D.; Burrell, A. K.; Hoehner, M.; Mody, T. D.; Gebauer, A.; Weghorn, S. J.; Lynch, V. “Actinide Complexes of Expanded Porphyrins,” Coord. Chem. Rev. 2001, 216, 411-434.


264.*Hannah, S.; Seidel, D.; Lynch, V. M.; Sessler, J. L. “New Chemistry of Amethyrin,” Inorg. Chimica Acta 2001, 317, 211-217.


265.*Camiolo, S.; Coles, S. J.; Gale, P. A.; Hursthouse, M. B.; Sessler, J. L. “Tetrabutylammonium meso-octamethylcalix[4]pyrrole fluoride dichloromethane solvate” Acta Cryst. 2001, E57, o816-o818.  DOI: 10.1107/S1600536801012880.


266.*Wu, Y.-D.; Wang, D.-F.; Sessler, J. L. “Conformational Features and Anion-Binding Properties of Calix[4]pyrrole:  A Theoretical Study,” J. Org. Chem. 2001, 66 (11), 3739-3746.  DOI: 10.1021/jo0016273.  Funding: National Science Foundation Grant No. CHE-9725399


267.*Hayashi, T.; Okazaki, K.; Urakawa, N.; Shimakoshi, H.; Sessler, J. L.; Vogel, E.; Hisaeda, Y. “Cobalporphycenes as Catalysts.  The Oxidation of Vinyl Ethers via the Formation and Dissociation of Cobalt-Carbon Bonds,” Organometallics 2001, 20, 3074-3078. DOI: 10.1021/om010141p.  Funding: National Science Foundation Grant No. CHE-9725399


268.*Gisselbrecht, J. P.; Gross, M.; Vogel, E.; Scholz, P.; Bröring, M.; Sessler, J. “Redox properties of hemiporphyceneand and isoporphycene.  Comparison with those of porphyrin and other porphyrin isomers, porphycene and corrphycene,” J. Electroanal. Chem. 2001, 507, 244-249.


269.*Bucher, C.; Zimmerman, R. S.; Lynch, V.; Sessler, J. L. “First Cryptand-like Calixpyrrole: Synthesis, X-ray Structure and Anion Binding Properties of a Bicyclic[3,3,3]nonapyrrole,” J. Am. Chem. Soc. 2001, 123, 9716-9717. DOI: 10.1021/ja016629z.  Funding: National Science Foundation Grant No. CHE-9725399

269a.*Congress Report:  “IUPAC in Australia,” Chemical & Engineering News, August 20, 2001, 42-43.


270.*Gale, P. A.; Hursthouse, M. B.; Light, M. E.; Sessler, J. L.; Warriner, C.; Zimmerman, R. “Ferrocene substituted calix[4]pyrrole:  A new electrochemical sensor for anions involving CH---O hydrogen bonds,” Tetrahedron Lett. 2001, 42, 6759-6762.


271.*Sessler, J. L.; Zimmerman, R. S.; Bucher, C.; Král, V.; Andioletti, B. “Calixphyrins:  Hybrid Macrocycles at the Structural Crossroads between Porphyrins and Calixpyrroles,” Pure and Applied Chemistry 2001, 73, 1041-1057.  Funding: National Science Foundation Grant No. CHE-9725399, and National Institutes of Health Grant Nos. CA68682 and GM58907


272.*Gale, P. A.; Anzenbacher, P. Jr.; Sessler, J. L. “Calixpyrroles II,” Coord. Chem. Rev. 2001, 222, 57-102 (featured on cover).


273.*Miyaji, H.; An, D.; Sessler, J. L. “Mono Halogen Substituted Calix[4]pyrroles:  Fine-tuning the Anion Binding Properties of Calix[4]pyrrole,” Supramolecular Chemistry 2001, 13, 661-669.


274.*Magda, D.; Lepp, C.; Gerasimchuk, N.; Lee, I.; Sessler, J. L.; Lin, A.; Biaglow, J.; Miller, R. A. “Redox Cycling by Motexafin Gadolinium Enhances Cellular Response to Ionizing Radiation by Forming Reactive Oxygen Species,” Int. J. Radiat. Biol. Oncol. Phys. 2001, 51 1025-1036.


275.*Sessler, J. L.; Davis, J. M. “Sapphyrins:  Versatile Anion-binding Agents,” Acc. Chem. Res. 2001, 34, 989-997 (cover). DOI: 10.1021/ar980117g


276.*Hannah, S.; Lynch, V. M.; Gerasimchuk, N.; Magda, D.; Sessler, J. L. ”Synthesis of a Metal-Free Texaphyrin,” Org. Lett. 2001, 3, 3911-3914. DOI: 10.1021/ol016757s.  Funding: National Institutes of Health Grant No. CA66885


277.*Sessler, J. L. Zimmerman, R. S.; Kirkovits, G. J.; Gebauer, A.; Scherer, M. “Synthesis and Dihydrogen Phosphate Binding Properties of Pyrrole-containing ansa-Ferrocenes,” J. Organometallic Chem. 2001, 637, 343-348.


278.*Lynch, V. M.; Gale, P. A.; Sessler, J. L.; Madeeiros, D. “Room-temperature monoclinic and low-temperature triclinic phase-transition structures of meso-octamethylcalix[4]pyrrole-dimethyl sulfoxide (1:1),” Acta Cryst. 2001, C57, 1426-1428. DOI: 10.1107/S0108270101015931.  Funding: Robert A. Welch Foundation Grant No. F-1018 and the National Institutes of Health


279.*Sessler, J. L.; Seidel, D.; Gebauer, A.; Lynch, V.; Abboud, K. A. “Dioxa-[40]decaphyrin(1.0.1.0.0.1.0.1.0.0):  An Analogue of Turcasarin with a “Figure–Eight” Structure,” J. Heterocycl. Chem. 2001, 38, 1419-1429.  Funding: National Science Foundation Grant No. CHE-9725399


280.*Kirkovits, G. J.; Shriver, J. A.; Gale, P. A.; Sessler, J. L. “Synthetic Ditopic Receptors,” J. Incl. Phenom.  2001, 41, 69-75.  Funding: National Institutes of Health Grant No. GM 58907



2002


281.*Sessler, J. L.; Cho, W.-S.; Lynch, V. Král, V. “Missing link macrocycles:  Hybrid heterocalixarene analogues formed from several different building blocks,” Chem. Eur. J. 2002, 8, 1134-1143.  Funding: National Institutes of Health Grant No. GM 58907


282.*Bucher, C.; Seidel, D.; Lynch, V.; Sessler, J. L. “[30]Heptaphyrin(1.1.1.1.1.0.0): an aromatic expanded porphyrin with a “figure eight” like structure,” Chem. Commun. 2002, 323-329. DOI: 10.1039/b109877b.  Funding: National Science Foundation Grant No. CHE-0107732


283.*Král, V.; Davis, J.; Andreivsky, A.; Kralová, J.; Aynytsya, A.; Poucková, P.; Sessler, J. L. “Synthesis and Biolocalization of Water Soluble Sapphyrins,” J. Med. Chem. 2002, 45, 1073-1078.  DOI: 10.1021/jm0104320.  Funding: Howard Hughes Medical Institute Grant No 75195- 541101 and National Institutes of Health Grant No. CA68682


284.*Mizuno, T.; Wei, W. H. Eller, L. R.; Sessler, J. L. “Phenanthroline Complexes Bearing Fused Dipyrrolylquinoxaline Anion Recognition Sites: Efficient Fluoride Anion Receptors,” J. Am. Chem. Soc. 2002, 124, 1134-1135.  DOI: 10.1021/ja017298t.  Funding: National Institutes of Health Grant No. GM 58907 and Robert A. Welch Foundation Grant No. F-1018


285.*Sessler, J. L.; Maeda, H.; Mizuno, T.; Lynch, V. M.; Furuta, H. “Quinoxaline-oligopyrroles:  Improved pyrrole-based anion receptors,” Chem. Commun. 2002, 862-863. DOI: 10.1039/b111708d.  Funding: National Institutes of Health Grant No. GM 58907 and Robert A. Welch Foundation Grant No. F-1018 


286.*Sessler, J. L.; Seidel, D.; Lynch, V. “Cyclo[8]pyrrole:  A Simple-to-make Expanded Porphyrin with No Meso Bridges,” Angew. Chem. 2002, 114, 1480-1483 (cover); Angew. Chem. Int. Ed. 2002, 41, 1422-1425 (cover).

286a.*“Simple-to-make Heteroannulene,” Chemical & Engineering News, April 15, 2002, p. 39.


287.*Sessler, J. L.; Král, V.; Shishkanova, T. V.; Gale, P. A. “Cytosine substituted calix[4]pyrroles: Neutral receptors for 5’-guanosine monophosphate,“ Proc. Natl. Acad. Sci. 2002, 99, 4848-4853.  DOI: 10.1073/pnas.062633799.  Funding: National Institutes of Health Grant No. GM 58907 and Texas Advanced Research Program Grant No. 0059


288.*Sessler, J. “Editorial” Supramolec. Chem. 2002, 14, 5-6.


289.*Dukh, M; Drasar, P.; Cerny, I.; Pouzar, V.; Shriver, J. A.; Král, V.; Sessler, J. L. “Novel Deep Cavity Calix[4]pyrroles Derived from Steroidal Ketones,” Supramolec. Chem. 2002, 14, 237-244. DOI: 10.1080/10610270290026149. Funding: National Institutes of Health Grant No. GM58907 and Texas Advanced Research Program Grant No. 0059


290.*Hannah, S.; Lynch, V.; Guldi, D. M.; Gerasimchuk, N.; MacDonald, C. L. B.; Magda, D.; Sessler, J. L. “Late First-row Transition-Metal Complexes of Texaphyrin,” J. Am. Chem. Soc. 2002, 124 (28), 8416-8427.  DOI: 10.1021/ja012747a.  Funding:  National Institutes of Health Grant No. CA68682


291.*Shishkanova, T. V.; Volf, R.; Král, V.; Sessler, J. L. “Formation of Porphyrin- and Sapphyrin-Containing Monolayers on Electrochemically Prepared Gold Substrates:  A FT Raman Spectroscopic Study,” Langmuir, 2002, 18(18), 6896-6906. DOI: 10.1021/la025766m.  Funding: National Institutes of Health Grant No. GM58907


292.*Gorski, A.; Vogel, E.; Sessler, J. L.; Waluk, J. “Magnetic Circular Dichroism of Octaethylcorrphycene and its Doubly Protonated and Deprotonated Forms,” J. Phys. Chem. 2002, 106, 8139-8145.  DOI: 10.1021/jp0201579.  Funding: National Science Foundation Grant No. CHE-9725399


293.*Gorski, A.; Vogel, E.; Sessler, J. L.; Waluk, J. “Magnetic Circular Dichroism of Neutral and Ionic Forms of Octaethylhemiporphycene,”Chem. Phys. 2002, 282, 37-49.


294.*Sessler, J. L.; Fowler, C. J.; Gebauer, A.; Hegar, A.; Scholz, P.; Lex, J.; Vogel, E. “Characterization of main group metal complexes of porphycene, corrphycene, and hemiporphycene:  X-ray Structures, Stability and Coordination Chemical Properties,” Chem. Eur. J. 2002, 8, 3485-3496.


295.*Kerkovits, G. J.; Zimmerman, R. S.; Huggins, M. T.; Lynch, V. M.; Sessler, J. L. “Synthesis, Structural Characterization and Complexation Properties of the First ‘Crowned’-Dipyrrolylquinoxalines,” Eur. J. Org. Chem. 2002, 3768-3778 (cover).  DOI: 10.1002/1099-0690.  Funding: National Institutes of Health Grant No. GM58907


296.*Sessler, J. L.; Maeda, H.; Mizuno, T.; Lynch, V. M.; Furuta, H. “Quinoxaline-bridged Porphyrinoids,” J. Am. Chem. Soc. 2002, 123, 13474-13479. DOI: 10.1021/ja0273750.  Funding: National Institutes of Health Grant No. GM58907 and  Robert A. Welch Foundation Grant No. F-1018


297.*Magda, D.; Lepp, C.; Gerasimchuk, N.; Lecane, P.; Miller, R. A.; Biaglow, J. E.; Sessler, J. L. “Motexafin Gadolinium Reacts with Ascorbic Acid to Produce Reactive Oxygen Species,” Chem. Commun. 2002, 2730-2731. DOI: 10.1039/b208760j.  Funding: NIH-CA


298.*Blas, J. R.; Marquez, M.; Sessler, J. L.; Luque, F. J.; Orozco, M. “Theoretical Study of Anion Binding to Calix[4]pyrrole: the Effects of Solvent, Fluorine Substitution, Cosolute, and Water Traces,” J. Am. Chem. Soc. 2002, 124, 12796-12805. DOI: 10.1021/ja020318m.  Funding: National Institutes of Health Grant No. GM58907


299.*Sessler, J. L.; Gorden, A. E. V.; Seidel, D.; Hannah, S.; Lynch, V.; Gordon, P. J.; Scott, B. L.; Tait, C. D.; Keogh, D. W. “New Actinide Expanded Porphyrin Complexes,” Inorg. Chim. Acta 2002, 341, 54-70.  DOI: 10.1016/S0020-1693(02)01202-1.  Funding: DOE



2003


300.*Synytsya, A.; Král, V.; Synytsya, A.; Volka, K.; Sessler, J. L. “In vitro interaction of macrocyclic photosensitizers with intact mitochondria:  A spectroscopic study,” Biochem. Biophys. Acta. 2003, 1620, 85-96.  DOI: 10.1016/S0304-4165(02)00511-1. Funding:  NIH-CA


301.*Sessler, J. L.; Camiolo, S.; Gale, P. A. “Pyrrolic and Polypyrrolic Anion Binding Agents,” Coord. Chem. Rev. 2003, 240, 17-55. DOI: 10.1016/S0010-8545(03)00023-7. Funding: NIH-GM


302.*Sessler, J. L.; An, D.; Cho, W.-S.; Lynch, V. “Calix[n]bipyrroles:  Synthesis, Characterization, and Anion Binding Studies,” Angew. Chem., 2003, 115, 2380-2383; Angew. Chem. Int. Ed. 2003, 42, 2278-2281.  DOI: 10.1002/anie.200350941. Funding:  NIH-GM


303.*Sessler, J. L.; Cho, W.-S.; Dudek, S. P.; Hicks, L.; Lynch, V. M.; Huggins, M. T. “Synthesis and study of a calixpyrrole-texaphyrin  chimera.  A new oligopyrrolic chloride anion receptor,” J. Porph. Phthalocy. 2003, 7, 97-104.  Funding:  NIH-CA


304.*Köhler, T., Seidel, D.; Lynch, V.; Arp, F. O.; Ou, Z.; Kadish, K. M.; Sessler, J. L. “Formation and Properties of Cyclo[6]pyrrole and Cyclo[7]pyrrole,” J. Am. Chem. Soc. 2003, 125, 6872-6873. DOI: 10.1021/ja035089y Funding: National Science Foundation Grant No. CHE- 0107732


305.*Lee, C.-H.; Na, H.-K.; Yoon, D.-W.; Won, D.-H.; Cho, W.-S.; Lynch, V. M.; Shevchuk, S. V.; Sessler, J. L. “Single Side Strapping.  A New Approach to Fine Tuning the Anion Recognition Properties of Calix[4]pyrroles,” J. Am. Chem. Soc. 2003, 125, 7301-7306. DOI: 10.1021/ja029175u.  Funding: National Institutes of Health Grant No. GM58907


306.*Sessler, J. L.; Jayawickramarajah,  J.; Sathiosatham, M.; Sherman, C. L.; Brodbelt, J. S. “Novel Guanosine-Cytidine Dinucleoside that Self-Assembles into a Trimeric Supramolecule,” Org. Lett. 2003, 5, 2627-2630.  DOI: 10.1021/ol034765y Funding: Robert A. Welch Foundation Grant No. F-1018


307.*Bucher, C.; Zimmerman, R. S.; Lynch, V.; Sessler, J. L. “Synthesis and X-ray structure of a three-dimensional calixphyrin,” Chem. Comm. 2003, 1646-1647. DOI: 10.1039/b302508j. Funding:  National Science Foundation Grant No. CHE- 0107732


308.*Sargent, A. L.; Hawkins, I. C.; Allen, W. E.; Liu, H.; Sessler, J. L.; Fowler, C. J. “Global vs. Local Aromaticity in Porphyrinoid Macrocycles:  Experimental and Theoretical Study of “Imidacene”, an Imidazole-Containing Analogue of Porphycene,” Chem. Eur. J. 2003, 9, 3065-3072.  DOI: 10.1002/chem.200204694.  Funding: National Science Foundation Grant No. CHE- 0107732


309.*Levitskaia, T. G.; Marquez, M.; Sessler, J. L.; Shriver, J. A.; Vercouter, T.; Moyer, B. A., “Fluorinated calixpyrroles:  Anion-binding extractants that reduce the Hofmeister bias,” Chem. Comm. 2003, 2248-2249. DOI: 10.1039/b306385m.  Funding:  U.S. Department of Energy Grant No. DE-FG03-01ER15186


310.*Sessler, J. L.; Callaway, W.; Dudek, S. P.; Date, R. W.; Lynch, V.; Bruce, D. W. “The first liquid-crystalline, expanded porphyrins,” Chem. Commun. 2003 2422-2423. DOI: 10.1039/b307901p.  Funding: National Science Foundation Grant No. CHE- 0107732


311.*Sessler, J. L.; An, D.; Cho, W. S.; Lynch, V. “Calix[2]bipyrrole[2]furan and Calix[2]bipyrrole[2]thiophene:  New Pyrrolic Receptors Exhibiting a Preference for Carboxylate Anions,” J. Am. Chem. Soc. 2003, 125, 13646-13647.  DOI: 10.1021/ja038264j. Funding:  National Institutes of Health Grant No. GM58907


312.*Sessler, J. L.; Pantos, G. D.; Katayev, E.; Lynch, V. M. “Pyrazine Analogues of Dipyrrolylquinoxalines,” Org. Lett. 2003, 5, 4141-4144.  DOI: 10.1021/ol0355635. Funding:  National Institutes of Health Grant No. GM58907


313.*Sessler, J. L.; Berthon-Gelloz, G.; Gale, P. A.; Camiolo, S.; Anslyn. E. V.; Anzenbacher, P., Jr.; Furuta, H.; Kirkovits, G.; Lynch, V.; Maeda, H.; Morosini, P.; Scherer, M.; Shriver, J.; Zimmerman, R. S. “Oligopyrrole-based solid state self-assemblies,” Polyhedron, 2003, 22, 2963-2983.  DOI: 10.1016/S0277-5387(03)00436-4.  Funding: NSF; Welch


314.*Sessler, J. L.; Seidel, D. “Synthetic Expanded Porphyrin Chemistry,” Angew. Chem. 2003, 115, 5292-5333; Angew. Chem. Int. Ed. 2003, 42, 5134-5175 (frontpiece). DOI: 10.1002/anie.200200561. Funding:  NSF


315.*Sessler, J. L.; Davis, J. M.; Král, V.; Kimbrough, T.; Lynch, V. “Water-soluble sapphyrins: potential fluorescent phosphate anion sensors,” Org. Biomolec. Chem. 2003, 1, 4113 – 4123 (cover).  DOI: 10.1039/b306964h.  Funding: National Institutes of Health Grant No. GM58907


316.*Breznova, H; Volf, R.; Kral, V.; Sessler, J. L.; Try, A. C.; Shishkanova, T. V. “Monomer and polymer quinoxaline derivatives for cationic recognition,” Anal. Bioanal. Chem. 2003, 375, 1193-1198.  DOI: 10.1007/s00216-003-1816-2.  Funding: National Institutes of Health Grant No. GM58907



2004


317.*Gorden, A. E. V.; Davis, J.; Sessler, J. L.; Král, V.; Keogh, D. W.; Schroeder, N. L. “Monoprotonated Sapphyrin-Pertechnetate Anion Interactions in Aqueous Media,” Supramolec. Chem. 2004, 16, 91-100.  Funding: U.S. Department of Energy Grant No. DE-FG03-01ER15186


318.*Yu, M.; Pantos, G. D.; Sessler, J. L.; Pagenkopf, B. L. “Synthesis of 2,2'-Bipyrroles and 2,2'-Thienylpyrroles from Donor-Acceptor Cyclopropanes and 2-Cyanoheteroles,” Org. Lett. 2004, 6 (6), 1057-1059.  DOI: 10.1021/ol049857h.   Funding:  National Science Foundation


319.*Veauthier, J. M.; Cho, W.-S.; Lynch, V. M.; Sessler, J. L. “Calix[4]pyrrole Schiff Base Macrocycles. Novel Binucleating Ligands for µ-Oxo Iron Complexes,” Inorg. Chem. 2004, 43 (4), 1220-1228 (cover).  DOI: 10.1021/ic0352001  Funding: National Institutes of Health Grant No. CA68682


320.*Magda, D. J.; Wang, Z.; Gerasimchuk, N.; Wei, W.-h.; Anzenbacher,  P., Jr.; Sessler, J. L. “Synthesis of Texaphyrin Conjugates, Pure Appl. Chem. 2004, 76, 365-374.  Funding: National Institutes of Health Grant No. CA68682 


321.*Král, V.; Shishkanova, T. V.;  Sessler, J. L.; Brown,  C. T. “Cytosine-substituted metalloporphyrins: receptors for recognition of nucleotides in ion-selective electrodes,” Org. Biomolec. Chem. 2004, 1169–1175.  DOI: 10.1039/b400880d.  Funding: National Institutes of Health Grant No. GM58907


322.*Koehler, T.; Hodgson, M. C.; Seidel, D.; Veauthier, J. M.; Meyer, S.; Lynch, V.; Boyd, P. D. W.; Brothers, P. J.; Sessler, J. L.; “Octaethylporphyrin and expanded porphyrin complexes containing coordinated BF2 groups,” Chem. Commun. 2004, 1060-1061.  DOI: 10.1039/b400596a. Funding:  National Science Foundation Grant No. CHE 0107732 and U.S. Department of Energy Grant No. DE- FG03-01ER15186


323.*Sessler, J. L.; Katayev, E.; Pantos, G. D.; Ustynyuk, Y. A. “Synthesis and study of a new diamidodipyrromethane macrocycle.  An anion receptor with a high sulfate-to-nitrate binding selectivity,” Chem. Commun. 2004, 1276-1277.  DOI: 10.1039/b403665d.  Funding: U.S. Department of Energy Grant Nos. DE- FG03-01ER15186 and DE-FG02-04ER63741

323a.*“Macrocycle for Nuclear Waste,” Chemical Engineering News, June 7, 2004, p. 8.


324.*Sessler, J. L.; Andrioletti, B.; Anzenbacher, P. Jr., Black, C.; Eller, L.; Furuta, H.; Jursíková, K.; Maeda, H.; Marquez, M.; Mizuno, T.; Try, A. “2,3-Dipyrrolylquinozaline-based Anion Sensors,” in Fundamentals and Applications of Anion Separations, Singh, R. P.; Moyer, B. A., Eds. Kluwer Academic/Plenum Publishers:  New York, 2004, pp. 71-85. Funding:  NIH-GM


325.*Sessler, J. L.; Jayawickramarajah,  J.; Muhunthan, S. “Energy and Electron Transfer in Supramolecular Systems,” in Encyclopedia of Supramolecular Chemistry, Atwood, J. L.; Steed, J. W., Eds. Marcel Dekker:  New York, 2004; part E, pp. 535-545. Funding: Welch Foundation


325.*Camiolo, S.; Gale, P. A.; Sessler, J. L. “Pyrrolic and Polypyrrolic Anion Binding Agents,” in Encyclopedia of Supramolecular Chemistry, Atwood, J. L.; Steed, J. W., Eds. Marcel Dekker:  New York, 2004.  Funding:  NIH-GM


326.*Král, V.; Valik, M.; Shishkanova, T. V.; Sessler, J. L. “Nucleoside- and Nucleobase-Substituted Oligopyrrolic Macrocycles,” Dekker Encyclopedia of Nanoscience and Nanotechnology, 2004. Funding:  NIH-GM


327.*Miyaji, H.; Sato, W.; An, D. Sessler, J. L. “Optical anion sensors based on Alkyne-linked, functionalized calix[4]pyrroles,” Col. Czechoslovak Chem. Commun. 2004, 69, 1027-1049. DOI: 10.1135/cccc20041027.  Funding:  NIH-GM


328.*Synytsya, A.; Král, V.; Matejka, P.; Poucková, P. Volka, K.; Sessler, J. L. “Biodistribution Assessment of a Lutetium(III) Texaphyrin Analogue in Tumor-bearing Mice using NIR Fourier-transform Raman Spectroscopy,” PhotoChem. Photobiol. 2004, 79, 453-460.  DOI: 10.1111/j.1751-1097.2004.tb00034.x. Funding: National Institutes of Health Grant No. CA68682

                 

329.*Callaway, W. B.; Veauthier, J.; Sessler, J. L. “Schiff-base Porphyrin and Expanded Porphyrin Analogues,” J. Porph. Phthalocyan. 2004, 8, 1-25.  Funding:  NIH-NCI; DOE


330.*Sessler, J. L.; Jayawickramarajah, J.; Sherman, C. L.; Brodbelt, J. S. “Enhancing Hoogsteen Interactions:  A Pyrrole-containing Purine Nucleoside that Competes with Guanosine Self-Assembly,” J. Am. Chem. Soc. 2004, 126, 11460-11461.  DOI: 10.1021/ja046773v Funding: Robert A. Welch Foundation Grant No. F-1018


331.*Sessler, J. L.; Callaway, W.; Dudek, S. P.; Date, R. W.; Bruce, D. W. “Synthesis and Characterization of a Discotic Uranium-containing Liquid Crystal.” Inorg. Chem. 2004, 43, 6650-6653.  DOI: 10.1021/ic0492690  Funding: U.S. Department of Energy Grant No. DE- FG02-01ER15186


332.*Dolensky, B.; Kroulík, J.; Král, V.; Sessler, J. L.; Dvorakova, H.; Bour, P.; Bernatkova, M.; Bucher, C.; Lynch V. “Calix[4]phyrins.  Effect of Peripheral Substituents on Conformational Mobility and Structure within a Series of Related Systems,” J. Am. Chem. Soc. 2004, 126, 13714-13722. DOI: 10.1021/ja048075g Funding: National Institutes of Health Grant No. CA68682


333.*Sessler, J. L.; Melfi, P. J.; Seidel, D.; Gorden, A. V.; Ford, D. K.; Palmer, P. D.; Tait, C. D. “Hexaphyrin(1.0.1.0.0.0): A new colorimetric actinide sensors,” Tetrahedron, 2004, 60, 11089-11097.  DOI:10.1016/j.tet.2004.08.055 Funding:  DOE


334.*Shevchuk, S. V.; Lynch, V. M.; Sessler, J. L. “A new terpyrrolic analogue of dipyrrolylquinoxalines: An efficient optical-based sensor for anions in organic media,” Tetrahedron, 2004, 60, 11283-11291.  DOI: 10.1016/j.tet.2004.08.054 Funding: NIH-GM


335.*Piatek, P.; Lynch, V. M.; Sessler, J. L. “Calix[4]pyrrole[2]carbazole: A New Kind of Expanded Calixpyrrole,” J. Am. Chem. Soc. 2004, 126, 16073-16076. DOI: 10.1021/ja045218q  Funding:  National Institutes of Health Grant No. GM58907


336.*Nielsen, K. A.; Cho, W.-S.; Jeppesen, J. O.; Lynch, V. M.; Becher, J.; Sessler, J. L. “Tetra-TTF Calix[4]pyrrole: A Rationally Designed Receptor for Electron-Deficient Neutral Guests,” J. Am. Chem. Soc. 2004, 126, 16296-16297. DOI: 10.1021/ja044664a Funding: National Science Foundation Grant No. CHE- 01017732



2005


337.*Koehler, T.; Ou, Z.; Lee, J. T.; Seidel, D.; Lynch, V.; Kadish, K. M.; Sessler, J. L. Reductive per-N-alkylation of cyclo[8]pyrroles,” Angew. Chem. 2005, 117, 85-89; Angew. Chem. Intl. Ed., 2005, 44, 83-87.  DOI: 10.1002/anie.200461801.  Funding:  NSF


338.*Sessler, J. L.; An, D.; Cho, W.-S.; Lynch, V.; Marqez, M. “Calix[4]bipyrrole – A Big, Flexible Yet Effective Chloride-Selective Anion Receptor,” Chem. Commun. 2005, 540-542.  DOI: 10.1039/b412737d  Funding: National Institutes of Health Grant No. GM58907


339.*Sessler, J. L.; An, D.; Cho, W.-S.; Lynch, V.; Yoon, D.-W.; Hong, S.-J.; Lee, C.-H.; “Anion-Binding Behavior of Hybrid Calixpyrroles,” J. Org. Chem. 2005, 70, 1511-1517 (cover).  DOI: 10.1021/jo048480q  Funding: National Institutes of Health Grant No. GM58907


340.*Cho, W.-S.; Sessler, J. L. “Pyrrole-Based Artificial Anion Receptors,” in “Functional Synthetic Receptors,” Schrader, T; Hamilton, Eds., Wiley-VCH, Weinheim, 2005.  Chapter 4, pp. 165-256.  Funding:  NIH-GM


341.*Sessler, J. L.; An, D.; Cho, W.-S.; Lynch, V.; Marqeuz, M. “Calix[n]bispyrrolylbenzenes: Synthesis, Characterization, and Preliminary Anion Binding Studies.” Chem. Eur. J. 2005, 11, 2001-2011 (cover). DOI: 10.1002/chem.200400894 Funding: National Institutes of Health Grant No. GM58907


342.*Lee, C. H.; Lee, J.-S.; Na, H.-K.; Yoon, D.-W.; Miyaji, H.; Cho, W.-S.; Sessler, J. L. “Cis- and trans-Strapped calix[4]pyrroles Bearing Phthalimide Linkers: Synthesis and Anion Binding Properties,” J. Org. Chem. 2005, 70, 2067-2074. DOI: 10.1021/jo0487146  Funding: National Institutes of Health Grant No. GM58907


343.*Sessler, J.; Jayawickramarajah, J.; Gouloumis, A.; Torres, T.; Guldi, D. M.; Maldonado, S.; Stevenson, K. J. “Synthesis and photophysics of a porphyrin-fullerene dyad assembled through Watson-Crick hydrogen bonding,” Chem. Commun. 2005, 1892-1894. DOI: 10.1039/b418345b  Funding: Robert A. Welch Foundation Grant No. F-1018


344.*Sessler, J.; Jayawickramarajah, J. “Functionalized base-pairs: Versatile scaffolds for self-assembly,” Chem. Commun. 2005, 1939-1949 (Feature Article; inside cover). DOI: 10.1039/b418526a  Funding:  Robert A. Welch Foundation Grant No. F-1018


345.*Sessler, J. L.; Tomat, E.; Mody, T.; Lynch, V.; Veauthier, J. M. “A Schiff Base Expanded Porphyrin Macrocycle that Acts as a Versatile Binucleating Ligand for Late First-Row Transition Metals,” Inorg. Chem. 2005, 44, 2125-2127. DOI: 10.1021/ic048412m  Funding: National Science Foundation Grant No. CHE- 0107732


346.*Koehler, T.; Seidel, D.; Sanchez, D.; Lynch, V.; Sessler, J. L. “Straightforward synthesis of sulfur bridged oligopyrrole macrocycles,” Chem. Commun. 2005, 2122-2124. DOI: 10.1039/b500735f Funding:  NSF


347.*Custelcean, R.; Moyer, B. A.; Sessler, J. L.; Cho, W.-S.; Gross, D.; Bates, G. W.; Brooks, S. J.; Light, M. E.; Gale, P. A. “Calix[4]pyrrole : An Old yet New Ion-Pair Receptor,” Angew. Chem. Int. Ed. 2005, 44, 2537-2542; Angew. Chem. 2005, 117, 2513-2518 (cover). DOI: 10.1002/anie.200462945  Funding:  DOE


348.*Sessler, J. L.; Koehler, T.; Seidel, D.; Arp, F.; Sanchez, D.; Apolonio, A.; Lynch, V.; “Facile Syntheses of Quarter-, Penta-, and Sexipyrroles,” Org. Lett. 2005, 7(10), 1887-1890. DOI: 10.1021/ol050151c Funding: National Science Foundation Grant No. CHE- 0107732


349.*Gorski, A.; Köhler, T.; Seidel, D.; Lee, J. T.; Orzanowska, G.; Sessler, J. L.; Waluk, J. “Electronic Structure, Spectra and Magnetic Circular Dichroism of Cyclohexa-, Cyclohepta-, and Cyclooctapyrrole,” Chem. Eur. J. 2005, 11, 4179-4184. DOI: 10.1002/chem.200401343 Funding: National Science Foundation Grant No. CHE- 0107732


350.*Naumovski, L.; Ramos, J.; Sirisawad, M.; Chen, J.; Thieman, P.; Lecane, P.; Magda, D.; Wang, Z.; Cortez, C.; Boswell, G.; Cho, D. G.; Sessler, J.; Miller, R. “Sapphyrins Induce Apoptosis in Hematopoietic Tumor-Derived Cell Lines and Demonstrate In Vivo Anti-Tumor Activity,” Molecular Cancer Therapeutics 2005, 4, 968-976. Funding:  National Institutes of Health Grant No. CA68682


351.*Sessler, J. L.; Cho, W. S.; Gross, D. E.; Shriver, J. A.; Lynch, V. M.; Marquez, M.; “Anion Binding Studies of Fluorinated Expanded Calixpyrroles,” J. Org. Chem. 2005, 70, 5982-5986.  DOI: 10.1021/jo050662c  Funding:  U.S. Department of Energy Grant No. DE-F6-02-04ER63741


352.*Sessler, J. L.; Katayev, E.; Pantos, D. G.; Scherbakov, P.; Reshetova, M. D.; Khrustalev, V.  N.; Lynch, V. M.; Ustynyuk, Y. A. “Fine Tuning the Anion Binding Properties of 2,6-Diamidopyridine Dipyrromethane Hybrid Macrocycles,” J. Am. Chem. Soc. 2005, 127, 11442-11446.  DOI: 10.1021/ja0522938 Funding: U.S. Department of Energy Grant No. DE-F6-02-04ER63741 and National Science Foundation Grant No. CHE-0107732


353.*Wei, W.-H.; Fountain, M.; Magda, D.; Wang, Z.; Lecane, P.; Mesfin, M.; Miles, D.; Sessler, J. L. “Gadolinium Texaphyrin-Methotrexate Conjugates.  Towards Improved Anticancer Chemotherapeutic Agents,” Org. Biomol. Chem. 2005, 3, 3290-3296 (inside cover). DOI: 10.1039/b503664j Funding:  National Institutes of Health Grant No. CA68682


354.*Veauthier, J. M.; Tomat, E.; Lynch, V. M. Sessler, J. L.; Mirasaidov, U.; Markert, J. T. “Calix[4]pyrrole Schiff Base Macrocycles:  Novel Binucleating Ligands for Cu(I) and Cu(II),” Inorg. Chem. 2005, 44, 6736-6743. DOI: 10.1021/ic050690d Funding:  National Institutes of Health Grant No. CA68682 and Robert A. Welch Foundation Grant No. F-1018


355.*Miyaji, H.; Sim, E.-K.; Kim, H.-K.; Lee, C.-K.; Cho, W.-S.; Sessler, J. L.; Lee, C.-H. “Coumarin-strapped calix[4]pyrrole: A Fluorogenic Receptor Modulated By Cation and Anion Binding,” J. Am. Chem. Soc. 2005, 127, 12510-12512. DOI: 10.1021/ja053612y Funding:  National Institutes of Health Grant No. GM58907


356.*Magda, D. J.; Sessler, J. L.; Gerasimchuk, N.; Miller, R. A. “Gadolium(III) Texaphyrin (Xcytrin®):  A New Class of Redox Active Drug Leads,” in Medicinal Inorganic Chemistry, J.L. Sessler, S. Doctrow, T. McMurry, S.J. Lippard, Eds., American Chemical Society Symposium Series 903, Oxford University Press, 2005.  Featured on Cover. Funding:  NIH-CA


357.*Sessler, J. L.; Eller, L. R.; Cho, W.-S.; Nicolaou, S.; Aguilar, A.; Lee, J. T.; Lynch, V. M.; Magda, D. J. “Synthesis, Anion Binding Properties, and In Vitro Anticancer Activity of Prodigiosin Analogues,” Angew. Chem. 2005, 117, 6143-6146; Angew. Chem. Int. Ed. 2005, 44, 5989-5992.  DOI: 10.1002/ange.20050174  Funding:  NIH-GM


358.*Wei, W.-H.; Fountain, M. E.; Sessler, J. L.; Magda, D. J.; Wang, Z.; Miller, R. A. “Texaphyrin Conjugates.  Progress Towards Second Generation Diagnostic and Therapeutic Agents,” in Macrocyclic Chemistry, Gloe, K., Ed., Springer, Dordrecht, 2005. Funding:  NIH-NCI


359.*Sessler, J. L.; Katayev, E. A.; Pantos, G. D.; Reshetova, M. D.; Khrustalev, V. N.; Lynch, V. M.; Ustynyuk, Y. A. “Anion Induced Synthesis and Combinatorial Selection of Polypyrrolic Macrocycles,” Angew. Chem. 2005, 117, 7552-7556; Angew. Chem. Int. Ed. 2005, 44, 7386-7390.  DOI: 10.1002/anie.200502393  Funding:   NSF; DOE


360.*Sessler, J. L.; Roznyatovskiy, V.; Pantos, G. D.; Borisova, N. E.; Reshetova, M. D.; Lynch, V. M.; Khrustalev, V. N.; Ustynyuk, Y. A. “Synthesis and Anion Binding Properties of 2,5-Diamidothiophene Polypyrrole Schiff Base Macrocycles,” Org. Lett. 2005, 7, 5277-5280. DOI: 10.1021/ol052162b Funding: U.S. Department of Energy Grant Nos. DE-FG02-04ER63741


361.*Katayev E. A., Pantos, G. D., Lynch, V. M., Sessler, J. L., Reshetova, M. D., Ustynyuk Y. A. “New polydentate macrocyclic ligands of hybrid amine-imine and amide-imine types as artificial anion receptors. Synthesis and study of anion binding,” Russ. Chem. Bull. 2005, 54, 165-172. DOI: 10.1007/s11172-005-0233-4 Funding: U.S. Department of Energy Grant Nos. DE- FG02-04ER63741 and DE-FG03-01ER15186



2006


362.*Král, V.; Lang, K.; Králová, J.; Martásek, P.; Chin, K. O. A.; Andrievsky, A.; Lynch, V.; Sessler, J. L. “Polyhydroxylated Sapphyrins:  Multi-site Non-metallic Catalysts for Activated Phosphodiester Hydrolysis,” J. Am. Chem. Soc. 2006, 128, 432-437. DOI: 10.1021/ja0518474  Funding:  National Institutes of Health Grant No. CA68682


363.*Sessler, J. L.; Jayawickramarajah, J.; Gouloumis, A.; Pantos, G. D.; Torres, T.; Guldi, D. M. “Guanosine and fullerene derived de-aggregation of a new phthalocyanine-linked cytidine derivative,” Tetrahedron, 2006, 2121-2131. DOI: 10.1016/j.tet.2005.05.110 Funding:  Welch Foundation


364.*Baker, E. S.; Lee, J. T.; Sessler, J. L.; Bowers, M. T. “Cyclo[n]pyrroles: Size and Site-Specific Binding to G-Quadruplexes,” J. Am. Chem. Soc. 2006, 128, 2641-2648. DOI: 10.1021/ja0564968  Funding: National Institutes of Health Grant No. CA68682


365.*Nielsen, K.A.; Cho, W.-S.; Lyskawa, J.; Levillain, E.; Lynch, V. M.; Sessler, J.L.; Jeppesen, J. “Tetrathiafulvalene-Calix[4]pyrroles: Synthesis, Anion Binding, and Electrochemical Properties,” J. Am. Chem. Soc. 2006, 128, 2444-2451. DOI: 10.1021/ja057367u.  Funding:  National Science Foundation Grant No. CHE-0515670


366.*Sessler, J. L.; Tomat, E.; Lynch, V. M. “Positive Homotropic Allosteric Binding of Silver(I) Cations in a Schiff Base Oligopyrrolic Macrocycle,” J. Am. Chem. Soc. 2006, 128, 4184-4185. DOI: 10.1021/ja0582004 Funding: National Science Foundation Grant No. CHE- 0515670


367.*Sessler, J. L.; Rubin, B. L.; Camiolo, S.; Cho, W.-S.; Pantos, G. D.; Lynch, V. M. “Diamidopyrazoles:  A new class of anion receptors,” Supramolec. Chem. 2006, 18, 103-109.  Funding:  NSF


368.*Sessler, J. L.; Melfi, P. J.; Pantos, G. D.; Tomat, E. J. “Uranium complexes of multidentate N-donor Ligands” Coord. Chem. Rev. 2006, 250, 816-843. DOI: 10.1016/j.ccr.2005.10.007 Funding:  DOE


369.*Wei, W.-H.; Wang, Z.; Mizuno, T.; Cortez, C.; Fu, L.; Sirisawad, M.; Naumovski, L.; Magda, D.; Sessler, J. L. “New polyethyleneglycol-functionalized texaphyrins:  Synthesis and in vitro biological studies,” J. Chem. Soc., Dalton Trans. 2006, 1934-1942 (cover). DOI: 10.1039/b515636j.  Funding:  National Institutes of Health Grant No. CA68682


370.*Tomé, J. P. C.; Cho, D.-G.; Sessler, J. L.; Neves, M. G. P. M. S.; Tomé, A. F.; Silva, A. M. S.; Cavaleiro, J. A. S. “Synthesis and Diels-Alder reaction of a sapphyrin derivative,” Tetrahedron Lett. 2006, 47, 3131-3134.  DOI:10.1016/j.tetlet.2006.02.144.  Funding:  NSF


371.*Sessler, J. L.; Pantoş, G. D.; Gale, P. A.; Light, M. E. “Synthesis and anion binding properties of N, N’-bis-pyrrole-2-yl-2,5-diamidopyrrole,” Org. Lett. 2006, 8, 1593-1596. DOI: 10.1021/ol060193g.  Funding: National Institutes of Health Grant No. GM58907


372.*Şener, M. K.; Sanchez-Garcia, D.; Akkurt, M.; Yıldırım, S. O.; Fun, H.-K.; Sessler, J. L. “Synthesis and crystal structure of 1,3-bis(5-formylpyrrol-2-yl)benzene and its conversion to a macrocyclic derivative,” Turkish J. Chem. 2006, 243-251. Funding: National Science Foundation Grant No. CHE-0515670


373.*Pantoş, G. D.; Rodríguez-Morgade, M. S.; Torres, T.; Lynch, V. M.; Sessler, J. L. “2-Amino-3,4-diethylpyrrole: New building blocks for coiled structures,” Chem. Commun. 2006, 2132-2134. DOI: 10.1039/b602956f Funding: National Science Foundation Grant No. CHE-0515670


374.*Sessler, J. L.; Melfi, P. J.; Tomat, E. J.; Callaway, W. ; Huggins, M. T. ; Gordon, P. L. ; Keogh, D. W. ; Date, R.; Bruce, D.; Donnio, B. “Schiff Base Oligopyrrolic Macrocycles as Ligands for Lanthanides and Actinides,” J. Alloys Compds. 2006, 408, 171-177. DOI: 10.1016/j.jallcom.2005.06.089  Funding:  DOE


375.*Won, D. H.; Yoon, D.-W.; Hong, S. J.; Ha, K. S.; Sessler, J. L.; Lee, C. H. “Synthesis and structure of non-aromatic porphyrinoid Schiff-base macrocycles bearing thiophene,” Bull. Korean Chem. Soc. 2006, 27, 925-928.  Funding:  NSF


376.*Sessler, J. L.; Rubin, B. L.; Stępień, M. Köhler, T.; Pantos, G. D.; Roznyatovski, V. “Tetraazaoctaphyrin - A biimidazole-containing expanded porphyrin,” Can. J. Chem. 2006, 84, 1218-1225.  DOI: 10.1139/V06-068 Funding: National Science Foundation Grant No. CHE-0515670


377.*Bucher, C.; Devillers, C. H.; Moutet, J.-C.; Pécaut, J.; Sessler, J. L. “Electrochemical synthesis of cyclo[8]pyrrole,” Chem. Commun. 2006, 3891-3893. DOI: 10.1039/b606998c  Funding: National Science Foundation Grant No. CHE-0515670  


378.*Sessler, J. L.; Tomat, E.; Lynch, V. M. “Coordination of oxovanadium(V) in an expanded porphyrin macrocycle,” Chem. Commun. 2006, 4486 – 4488 (cover). DOI: 10.1039/b608143F Funding:  U.S. Department of Energy Grant No. DE-FG02-01ER15186


379.*Sessler, J. L.; Gross, D. E.; Cho, W.-S.; Lynch, V. M.; Schmidtchen, F. P.; Bates, G. W.; Light, M. E.; Gale, P. A. “Calix[4]pyrrole as a Chloride Anion Receptor:  Solvent and Countercation Effects,” J. Am. Chem. Soc. 2006, 128, 12281-12288. DOI: 10.1021/ja064012h  Funding:  National Institutes of Health Grant No. GM069492


380.*Yoon, Z. S.; Kwon, J. H.; Yoon, M.-C.; Koh, M. K.; Noh, S. B.; Sessler, J. L.; Lee, J. T.; Seidel, D.; Aguilar, A.;  Shimizu, S.; Suzuki, M.; Osuka, A.; Kim, D. “Nonlinear Optical Properties and Excited-State Dynamics of Highly Symmetric Expanded Porphyrins,” J. Am. Chem. Soc. 2006, 128, 14128-14134. DOI: 10.1021/ja064773k  Funding:  National Science Foundation Grant No. CHE-0515670


381.*Sessler, J. L.; Cho, D.-G.; Stepien, M.; Lynch,V. M. Waluk, J.; Yoon, S. Z.; Kim, D. “Inverted Sapphyrin: A New Family of Doubly N-Confused Expanded Porphyrins,” J. Am. Chem. Soc. 2006, 128, 12640-12641. DOI: 10.1021/ja064675z Funding: National Institutes of Health Grant No. 58907


382.*Katayev, E. A.; Ustynyuk, Y. A.; Lynch, V. M.; Sessler, J. L. “Mono-palladium(II) complexes of diamidopyridine-dipyrromethane hybrid macrocycles,” Chem. Commun. 2006, 4682-4684. DOI: 10.1039/b611946h Funding: U.S. Department of Energy Grant No. DE-FG02-01ER15186


383.*Nielsen, K. A.; Cho, W.-S.; Sarova, G.; Petersen, B. M.; Bond, A. D.; Becher, J.; Jensen, F.; Guldi, D. M.; Sessler, J. L.; Jeppesen, J. O. “Supramolecular Receptor Design -Anion-Triggered Binding of C60,” Angew. Chem. 2006, 118, 7002-7007; Angew. Chem. Int. Ed. 2006, 45, 6848-6853.  DOI: 10.1002/anie.200602724  Funding:  NIH-GM


384.*Sessler, J. L.; Cho, D.-G.; Lynch, V. “Diindolylquinoxalines: Effective Indole-Based Receptors for Phosphate Anion,” J. Am. Chem. Soc. 2006, 128, 16518-16519. DOI: 10.1021/ja067720b  Funding: National Institutes of Health Grant No. 58907


385.*Naumovski, L.; Sirisawad, M.; Lecane, P.; Ramos, J.; Wang, Z.; Cortez, C.; Magda, D. J.; Thiemann, P.; Boswell, G.; Cho, D. G.; Sessler, J. L.; Miller, R. A. “Tumor localization and antitumor efficacy of novel sapphyrin compounds,” Molecular Cancer Therapeutics, 2006, 5, 2798-2805.  DOI: 10.1158/1535-7163.MCT-06-0246 Funding: National Institutes of Health Grant No. 58907


386.*Sessler, J. L.; Lee, J. T.; Ou, Z.; Köhler, T.; Hargrove, A. E.; Cho, W.-S.; Lynch, V. M.; Kadish, K. M. “Chemical and electrochemical oxidation of N-alkyl cyclo[n]pyrroles,” J. Porphyr. Phthalocyan. 2006, 10, 1329-1336.  Funding:  NSF


387.*Katayev, E. A.; Ustynyuk, Y. A.; Sessler, J. L. “Receptors for tetrahedral oxyanions,” Coord. Chem. Rev. 2006, 250, 3004-3037. DOI: 10.1016/j.ccr.2006.04.013  Funding:  NIH-GM; DOE


388.*Moyer, B.A.; Delmau, L. H.; Fowler, C. J.; Ruas, A.; Bostick, D. A.; Sessler, J. L.; Katayev, E.; Pantos, G. D.; Llinares, J. M.; Hossain, M. A.; Kang, S. O.; Bowman-James, K. “Supramolecular Chemistry of Environmentally Relevant Anions,” Adv. Inorg. Chem, vol 59, Eldik, R. and Bowman-James, Eds, Elsevier, 2006, 175-204. DOI: 10.1016/S0898-8838(06)59005-1  Funding:  DOE



2007


389.*Blas, J. R.; López-Bes, J. M.; Márquez, N.; Sessler, J. L.; Luque, F. J.; Orozco, M. “Exploring the Dynamics of Calix[4]pyrrole:  Effect of Solvent and Fluoride Substitution,” Chem. Eur. J. 2007, 13, 1108-1116.  DOI: 10.1002/chem.200600757 Funding: National Institutes of Health Grant No. GM58907


390.*Torres, T.; Gouloumis, A.; Sanchez-Garcia, D.; Jayawickramarajah, J.; Seitz, W. Guldi, D. M.; Sessler, J. L. “Photophysical characterization of a cytidine–guanosine tethered phthalocyanine–fullerene dyad,” Chem. Commun. 2007, 292-294. DOI: 10.1039/b613086k Funding:  Robert A. Welch Foundation Grant No. F-1018


391.*Plitt, P.; Gross, D. E.; Lynch, V. M.; Sessler, J. L. “Dipyrrolyl-functionalized bipyridine-based anion receptors for emission-based selective detection of dihydrogen phosphate,” Chem. Eur. J., 200713, 1374-1381 (cover).  DOI: 10.1002/chem.200601514 Funding: National Institutes of Health Grant No. GM58907


392.*Sessler, J. L.; Lawrence, C. M.; Jayawickramarajah, J. “Molecular recognition via base-pairing,” Chem. Soc. Rev. 2007, 36, 314-325.  DOI: 10.1039/b604119c Funding: Robert A. Welch Foundation Grant No. F-1018


393.*Sessler, J. L.; Melfi, P. J.; Tomat, E.; Lynch, V. M. “Copper(II) and Oxovanadium(V) Complexes of Hexaphyrin(1.0.1.0.0.0),” Dalton Trans. 2007, 629-632. DOI: 10.1039/b617620h  Funding: U.S. Department of Energy Grant No. DE-FG02-01ER15186


394.*Stępień, M.; Donnio, B.; Sessler, J. L. “Self-assembly of a supramolecular liquid crystal induced by trinitrotoluene vapours.” Angew. Chem. Int. Ed. 2007, 46, 1431–1435.  DOI: 10.1002/anie.200603893  Funding:  NSF

394a.*Science 2007, 315, 303.


395.*Miyaji, H.; Na, H.-K.; Baeck, K.-K.; Sessler, J. L.; Lee, C.-H. “A binol-strapped calix[4]pyrrole as a model chirogenic receptor for the enantioselective recognition of carboxylate anions,” Angew. Chem. Int. Ed. 2007, 46, 2508-2511. DOI: 10.1002/anie.200604161 Funding:  NIH-GM


396.*Shishkanova, T. V.; Volf, R.; Král, V.; Sessler, J. L.; Camiolo, S.; Gale, P. A. “Heterocalixarenes as Novel Compounds for Salicylate-selective Electrodes,” Anal. Chem. Acta 2007, 587, 247-253.  DOI: 10.1016/j.aca.2007.01.044  Funding:  NIH-GM


397.*Katayev, E. A.; Boev, N. V.; Khrustalev, V. N.; Ustynyuk, Y. A.; Tananaev, I. G.; Sessler, J. L. “Bipyrrole- and Dipyrromethane-Based Amido-imine Hybrid Macrocycles. New Receptors for Oxoanions,” J. Org. Chem. 2007, 72, 2886-2896.  DOI: 10.1021/jo0624849 Funding:  U.S. Department of Energy Grant Nos. DE-FG02-01ER15186 and DE-FG02-04ER63741


398.*Boul, P. J.; Cho, D.-G.; Rahman, G. M. A.; Marquez, M.; Guldi, D. M.; Sessler, J. L. “Sapphyrin-Nanotube Assemblies,” J. Am. Chem. Soc. 2007, 129, 5683-5687. DOI: 10.1021/ja069266h. Funding:  National Institutes of Grant No. GM069492 and Robert A. Welch Foundation Grant No. F-1018


399.*E, W.; Ohkubo, K.; Sanchez-Garcia, D.; Shang, M.; Sessler, J. L.; Fukuzumi, S.; Kadish, K. M. “Electron-Transfer Oxidation Properties of Substituted Bi-, Ter-, and Quaterpyrroles,” J. Phys. Chem. B 2007, 111, 4320-4326.  DOI: 10.1021/jp068717h  Funding:  National Science Foundation Grant No. CHE-0515670


400.*Wang, Z.; Lecane, P.; Thiemann, P.; Fan, A.; Cortez, C.; Ma, X.; Tonev, D.; Miles, D.; Lin, A.; Hemmi, G.; Naumovski, L.; Miller, R. A.; Magda, D.; Cho, D.-G.; Sessler, J. L.; Pike, B. L.; Yeligar, S. M.; Karaman, M. W.; and Hacia, J. G. “Synthesis and Biologic Properties of Hydrophilic Sapphyrins, a New Class of Tumor Selective Drugs,” Molecular Cancer 2007, 6, 9-20.  DOI: 10.1186/1476-4598-6-9.  Funding:  NIH-GM


401.*Sessler, J. L.; Melfi, P. J.; Lynch, V. M. “Synthesis and characterization of a hexaphyrin(1.0.1.0.0.0) bearing both meso and -substituents,” J. Porph. Phthalocy. 2007, 11, 287-293.  Funding:  DOE


402.*Kim, D.; Zeok, S.; Cho, D.-G.; Sessler, J. L. “Evaluation of Planarity and Aromaticity in Sapphyrin and Inverted Sapphyrin Using a Bidirectional NICS (Nucleus-Independent Chemical Shift) Scan Method,” Chem.Commun. 2007, 2378-2380.  DOI: 10.1039/b618674b. Funding:  National Institutes of Health Grant No. GM58907


403.*Sessler, J. L.; Barkey, N. M.; Pantos, G. D.; Lynch, V. M. “Acyclic pyrrole-based anion receptors: Design, synthesis, and anion binding properties,” New. J. Chem. 2007, 646-654. DOI: 10.1039/b615673h (cover).  Funding: U.S. Department of Energy Grant No. DE-FG02-04ER63741 and National Institutes of Health Grant No. GM58907


404.*Melfi, P. J.; Kim, S. K.; Lee, J. T.; Bolze, F.; Seidel, D.; Lynch, V. M.; Veauthier, J. M.; Gaunt, A. J.; Neu, M. P.; Ou, Z.; Kadish, K. M.; Fukuzumi, S.; Ohkubo, K.; Sessler, J. L. “Redox Behavior of Cyclo[6]pyrrole in the Formation of a Uranyl Complex,” Inorg. Chem. 2007, 46, 5143-5145.  DOI: 10.1021/ic700781t.  Funding: U.S. Department of Energy Grant No. DE-FG02-01ER-15186 and Robert A. Welch Foundation Grant No. F-1018


405.*Sessler, J. L.; Tomat, E. “Transition Metal Complexes of Expanded Porphyrins,” Acc. Chem. Res. 2007, 40, 371-379.  DOI: 10.1021/ar600006n.  Funding:  NSF; NIH; DOE


406.*Tomat, E.; Cuesta, L.; Lynch, V. M.; Sessler, J. L. “Binuclear Fluoro-bridged Zinc and Cadmium Complexes of a Schiff-Base Expanded Porphyrin: Fluoride Abstraction from the Tetrafluoroborate Anion,” Inorg. Chem. 2007, 46, 6624-6626. DOI: 10.1021/ic700933p.  Funding: National Science Foundation Grant No. CHE-0515670


407.*Jeong, S.-D.; Hong, S.-J.; Park, K. J.; Ham, S.; Sessler, J. L.; Lynch, V.; Lee, C. H. “Core-Modified, meso-Alkylidenyl Porphyrins and Their Expanded Analogues: A New Family of Nonplanar Porphyrinoids,” J. Org. Chem. 2007, 72, 6232-6240. DOI: 10.1021/jo070872k.  Funding: National Science Foundation Grant No. CHE-0515670 


408.*Eller, L. R.; Stępień, M.; Fowler, C. J.; Lee, J. T. Sessler, J. L.; Moyer, B. A. “Octamethyl-octaundecylcyclo[8]pyrrole:  A Promising Sulfate Anion Extractant,” J. Am. Soc. 2007, 129, 11020-11021.  DOI: 10.1021/ja074568k. Correction: J. Am. Chem. Soc. 2007, 129, 14523.  DOI: 10.1021/ja077858+. Funding: U.S. Department of Energy Grant No. DE-FG02-04ER63741 and National Science Foundation Grant No. CHE-0515670 

408a.C & E  News, 2007, 85(35), 11.


409.*Stępień, M.; Donnio, B.; Sessler, J. L. “Discotic Liquid-Crystalline Materials Based on Porphycenes:  A Mesogenic Metalloporphycene–Tetracyanoquinodimethane (TCNQ) Adduct,” Chem. Eur. J. 2007, 13, 6853-6863.  DOI: 10.1002/chem.200700125.  Funding:  NSF


410.*Katayev, E. A.; Sessler, J. L.; Khrustalev, V. N.; Ustynyuk, Y. A. “Synthetic Model of the Phosphate Binding Protein: Solid State Structure and Solution Phase Anion Binding Properties of a Large Oligopyrrolic Macrocycle,” J. Org. Chem. 2007, 72, 7244-7252. DOI: 10.1021/jo071106g.  Funding:  National Institutes of Health Grant No. GM58907


411.*Cuesta, L.; Gross, D.; Lynch, V. M.; Ou, Z.; Kajonkijya, W.; Ohkubo, K.; Fukuzumi, S.; Kadish, K. M.; Sessler, J. L. “Design and Synthesis of Polymetallic Complexes Based on meso-Calix[4]pyrrole: Platforms for Multielectron Chemistry,” J. Am. Chem. Soc. 2007, 129, 11696-11697.  DOI: 10.1021/ja075613r.  Funding: Robert A. Welch Foundation Grant No. F-1018 and National Science Foundation Grant No. CHE-0515670 


412.*Stępień, M; Sessler, J. L. “A Facile Synthesis of Cyclononatripyrroles,” Org. Lett. 2007, 9, 4785-4787.  DOI: 10.1021/ol702119y.  Funding: Robert A. Welch Foundation Grant No. F-1018 and National Science Foundation Grant No. CHE-0515670 


413.*Martínez-García, H.; Morales, D.; Pérez, J.; Coady, D. J.; Bielawski, C. W.; Gross, D. E.; Cuesta, L.; Marquez, M.; Sessler, J. L. “Calix[4]pyrrole as a Promoter of the CuCl-Catalyzed Reaction of Styrene and Chloramine-T,” Organometallics 2007, 26, 6511-6514. DOI: 10.1021/om700958c.  Funding: National Institutes of Health Grant No. GM58907


414.*Hayes, N. W.; Tremlett, C. J.; Melfi, P. J.; Sessler, J. L.; Shaw, A. M. “Fibre Optic System for Detection of Uranyl Ions in the Solution Phase,” Proceedings of the SPIE, 2007, 6739, 673917. Funding:  DOE



2008


415.*Sanchez-Garcia, D.; Sessler, J. L. “Porphycenes :  Synthesis and derivatives, Chem. Soc. Rev. 2008, 37, 215-232 (front cover).  DOI: 10.1039/b704945e.  Funding: National Science Foundation Grant No. CHE- 0515670


416.*Lee, C.-H., Miyaji, H.; Yoon, D.-W.; Sessler, J. L. “Strapped and other topographically nonplanar calixpyrrole analogues. Improved Anion Receptors,” Chem. Commun. 2008, 24-34. DOI: 10.1039/b713183f (Feature Article highlighted on front cover).  Funding:  National Institutes of Health Grant No. GM58907


417.*Jeong, S.-D.; Sessler, J. L.; Lynch, V.; Lee, C.-H. “Dithiabenzisapphyrin: A Core-Modified Sapphyrin Bearing Excocyclic Double Bonds at the meso-Positions,” J. Am. Chem. Soc. 2008, 130, 390-391.  DOI: 10.1021/ja075800p.  Funding: National Science Foundation Grant No. CHE- 0515670 


418.*Sessler, J. L.; Cho, D.-G. “The Benzil Rearrangement Reaction: Trapping of a Hitherto Minor Product and Its Application to the Development of a Selective Cyanide Anion Indicator,” Org. Lett. 2008, 10, 73-75.  DOI: 10.1021/ol7027306. Funding: National Institutes of Health Grant No. GM58907


419.*Nielsen, K. A.; Sarova, G. H.; Martín-Gomis, L.; Fernández-Lázaro, F.; Stein, P. C.; Sanguit, L.; Levillain, E.; Sessler, J. L.; Guldi, D. M.; Sastre-Santos, A.; Jeppesen, J. O. “Chloride Anion Controlled Molecular “Switching”. Binding of 2,5,7-Trinitro-9-dicyanomethylenefluorene-C60 by Tetrathiafulvalene-Calix[4]pyrrole and Photophysical Generation of Two Different Charge-Separated States,” J. Am. Chem. Soc  2008, 130, 460-462.  DOI: 10.1021/ja0772243.  Funding: National Science Foundation Grant No. CHE- 0515670  


420.*Iordache, A.; Melfi, P. J.; Bucher, C.; Buda, M.; Moutet, J.-C.; Sessler, J. L. Electrochemically Driven Intramolecular Ring Closure of a Linear Hexapyrrole,” Org. Lett. 2008, 10, 425-428.  DOI: 10.1021/ol702798e.  Funding: National Science Foundation Grant No. CHE- 0515670   


421.*Zhang, M.; E, W.; Ohkubo, K.; Sanchez-Garcia, D.; Yoon, D.-W.; Sessler, J. L.; Fukuzumi, S.; Kadish, K. M. “Electron-Transfer and Acid-Base Properties of a Two-Electron Oxidized Form of Quaterpyrrole that Acts as Both an Electron Donor and an Acceptor,” J. Phys. Chem. A 2008, 112, 1633-1642.  DOI: 10.1021/jp0766306  Funding: National Science Foundation Grant No. CHE- 0515670 and Robert A. Welch Foundation Grant No. F-1018


422.*Pietrzak, M.; Try, A.; Andrioletti, B.; Sessler, J. L. Anzenbacher, P., Jr. Limbach, H.-H. “The largest 15N...15N coupling constant across an NHN-hydrogen bond,” Angew. Chem. 2008, 120, 1139-1142; Angew. Chem. 2008, 447, 1123-1126. DOI: 10.1002/anie.200704411.  Funding:  NIH-GM


423.*Furuta, H.; Nanami, H.; Morimoto, T.; Ogawa, T.; Král, V.; Sessler, J. L.; Lynch, V. “Halide Anion Mediated Dimerization of a meso-Unsubstituted N-Confused Porphyrin,” Chem. Asian J. 2008, 3, 592-599.  DOI: 10.1002/asia.200700130  Funding:  NIH-GM


424.*Wilson, J. J.; Kirkovits, G. J.; Sessler,  J. L.; Brodbelt, J. S. “Photodissociation of Non-Covalent Peptide-Crown Ether Complexes,” J. Am. Soc. Mass Spectrom. 2008, 19, 257–260. DOI:10.1016/j.jasms.2007.10.024  Funding: National Institutes of Health Grant No. GM58907 and Robert A. Welch Foundation Grant No. F-1018


425.*Plitt, P.; Lynch, V. M.; Sessler, J. L. “Oxidation-induced control of self-assembly using a bis-dipyrromethyl substituted phenanthroline building block,” New. J. Chem. 2008, 32, 777-779.  (Special Issue dedicated to Jerry Atwood)  DOI: 10.1039/b716796b   Funding:  National Science Foundation Grant No. CHE-0515670


426.*Aydogan, A.; Coady, D. J.; Lynch, V. M.; Akar, A.; Marquez, M.; Bielawski, C. W.; Sessler, J. L. “Poly(methyl methacrylate)s with pendant calixpyrroles: Polymeric extractants for halide anion salts,” Chem. Commun. 2008, 1455-1457. DOI: 10.1039/b718021g.  Funding:  National Institutes of Health Grant No. GM58907


427.*Shimizu, S.; Cho,W.-S.; Sessler, J. L.; Shinokubo, H.; Osuka, A. “Meso-Aryl Substituted Rubyrin and its Higher Homologs: Structural Characterization and Chemical Properties,” Chem. Eur. J. 2008, 14, 2668-2678 (front cover).  DOI: 10.1002/chem.200701909. Funding: National Institutes of Health Grant No. GM58907


428.*Katayev, E. A.; Melfi, P. J.; Sessler, J. L. “Anion-Binding Macrocycles,” in Modern Supramolecular Chemistry:  Strategies for Macrocycle Synthesis, Diederich, F.; Stang, P. J.; Tywinski, R. R., Eds.  Wiley-VCH, Weinheim, 2008, Chapt. 9, pp 315-347 (400 pp total).  ISBN 978-3-527-31826-1  Funding:  NIH-GM; DOE


429.*Hayes, N. W.; Tremlett, C. J.; Melfi, P. J.; Sessler, J.; Shaw, A. M. “Uranyl-specific binding at a functionalised interface: a chemophotonic fibre optic sensor platform,” Analyst, 2008133, 616 – 620.  DOI: 10.1039/b714625f.  Funding: U.S. Department of Energy Grant No. DE-FG02-01ER15186


430.*Aydogan, A.; Sessler, J. L.; Akar, A.; Lynch, V. “Calix[4]pyrroles with Long Alkyl Chains: Synthesis, Characterization, and Anion Binding Studies,” Supramolec. Chem. 2008, 20, 11-21. DOI: 10.1080/10610270701429789 Funding:  NIH-GM


431.*Melfi, P. J.; Camiolo, S.; Lee, J. T.; Ali, M. F.; McDevitt, J. T.; Lynch, V. M.; Sessler, J. L. “Immobilization of a hexaphyrin(1.0.1.0.0.0) derivative onto a tentagel-amino resin and its use in uranyl cation detection,” Dalton Trans 2008, 1538-1540. DOI: 10.1039/b718627d.  Funding: U.S. Department of Energy Grant No. DE-FG02-01ER15186 and Robert A. Welch Foundation Grant No. F-1018


432.*Wintergerst, M. P.; Levitskaia, T. G.; Moyer, B. A.; Sessler, J. L.; Delmau, L. H. Calix[4]pyrrole: A New Ion-Pair Receptor as Demonstrated by Liquid-Liquid Extraction,” J. Am. Chem. Soc. 2008, 130, 4129-4139. DOI: 10.1021/ja7102179 Funding: National Institutes of Health Grant No. GM58907


433.*Magda, D.; Lecane, P.; Wang, Z.; Hu, W.; Thiemann, P.; Ma, X.; Dranchak, P. K.; Wang, X.; Lynch, V.; Wei, W.; Csokai, V.; Hacia, J. G.; Sessler, J. L. “Synthesis and Anticancer Properties of Water-Soluble Zinc Ionophores,” Cancer Research 2008, 68, 5318-5325.  DOI: 10.1158/0008-5472.CAN-08-0601.  Funding: National Institutes of Health Grant No.  CA68682


434.*Yoon, D.-W.; Gross, D. E.; Lynch, V. M.; Sessler, J. L.; Hay, B. P.; Lee, C.-H. “Benzene-, pyrrole-, and furan-containing diametrically strapped calix[4]pyrroles. An experimental and theoretical study of hydrogen bonding effects in chloride anion recognition,” Angew. Chem. 2008, 47, 5038-5042; Angew. Chem. 2008, 120, 5116-5120.  DOI: 10.1002/anie.200801426.  Funding:  NIH-GM.


435.*Yoon, Z. S.; Cho, D.-G.; Kim, K. S.; Sessler, J. L.; Kim, D. “Nonlinear Optical Properties as a Guide to Aromaticity in Congeneric Pentapyrrolic Expanded Porphyrins: Pentaphyrin, Sapphyrin, Isosmaragdyrin, and Orangarin,” J. Am. Chem. Soc. 2008, 130, 6930-6931. DOI: 10.1021/ja801395y.  Funding: National Institutes of Health Grant No. CA68682


436.*Rodriguez-Morgade, M. S.; Pantos, G. D.; Caballero, E.; Sessler, J. L.; Torres, T. “Synthesis of Hemipyrazinoporphyrazines Bearing Peripheral Pyrrolic Substitutents,” Macroheterocycles 2008, 1, 40-43. Funding: National Science Foundation Grant No. CHE-0515670


437.*Nielsen, K. A.; Martín-Gomis, L.; Sarova, G. H.; Sanguinet, L.; Gross, D. E.; Fernández-Lázaro, F.; Stein, P. C; Levillain, E.; Sessler, J. L.; Guldi, D. M.; Sastre-Santos, Á.; Jeppesen, J. O. “Binding Studies of Tetrathiafulvalene-Calix[4]pyrroles with Electron Deficient Guests,” Tetrahedron 2008, 64, 8449-8463. DOI: 10.1016/j.tet.2008.05.141.  Funding:  NSF, Welch


438.*Cho, D.-G.; Plitt, P.; Kim, S. K.; Lynch, V.; Hong, S.-J.; Lee, C.-H.; Sessler, J. L. “Dioxabenzosapphyrin: A New Benzodifuran-Derived Sapphyrin Analogue,” J. Am. Chem. Soc. 2008, 130, 10502-10503. DOI: 10.1021/ja804090w. Funding: National Institutes of Health Grant No. GM58907 and Robert A. Welch Foundation Grant No. F-1018


439.*Cho, D.-G.; Kim, J.-H.; Sessler, J. L. “The Benzil-Cyanide Reaction and its Application to the Development of a Selective Cyanide Anion Indicator,” J. Am. Chem. Soc. 2008, 130, 12163-12167.   DOI: 10.1021/ja8039025.  Funding: National Institutes of Health Grant No. GM58907 and Robert A. Welch Foundation Grant No. F-1018


440.*Sessler, J. L.; Kim, S. K.; Gross, D. E.; Lee, C.-H.; Kim, J. S.; Lynch, V. M. “Crown-6-Calix[4]arene-Capped Calix[4]pyrrole: An Ion Pair Receptor for Solvent Separated CsF Ions,” J. Am. Chem. Soc. 2008, 130, 13162-13166.  DOI: 10.1021/ja804976f.  Funding:  National Institutes of Health Grant No. GM58907


441.*Cuesta, L.; Tomat, E.; Lynch, V. M.; Sessler, J. L. “Binuclear organometallic ruthenium complexes of a Schiff base expanded porphyrin,” Chem. Commun. 2008, 3744-3746. DOI: 10.1039/b807126h.  Funding: National Science Foundation Grant No. CHE-0515670


442.*Gross, D. E.; Schmidtchen, F. P.; Antonius, W.; Gale, P. A.; Lynch, V. M.; Sessler, J. L. “Cooperative Binding of Calix[4]pyrrole-Anion Complexes and Alkylammonium Cations in Halogenated Solvents,” Chem. Eur. J. 2008, 14, 7822-7827. DOI: 10.1002/chem.200800899.  Funding: National Institutes of Health Grant No. GM58907


443.*Cui, R.; Li, Q.; Gross, D. E.; Meng, X.; Li, B.; Marquez, M.; Yang, R.; Sessler, J. L.; Shao, Y. “Anion Transfer at a Micro-Water/1,2-Dichloroethane Interface Facilitated by β-Octafluoro-meso-octamethylcalix[4]pyrrole,” J. Am. Chem. Soc. 2008, 130, 14364-14365. DOI: 10.1021/ja804631p.  Funding: National Institutes of Health Grant No. GM58907


444.*Cuesta, L.; Karnas, E.; Lynch, V. M.; Sessler, J. L.; Kajonkijya, W.; Zhu, W.; Zhang, M.; Ou, Z.; Kadish, K. M.; Ohkubo, K.; Fukuzumi, S. “(Pentamethylcyclopentadienyl)ruthenium π-Complexes of Metalloporphyrins: Platforms with Novel Photo- and Electrochemical Properties,” Chem. Eur. J. 2008, 14, 10206-10210. DOI: 10.1002/chem.200801748.  Funding: National Science Foundation Grant No. CHE-0749571 and Robert A. Welch Foundation Grant No. F-1018


445.*Aydogan, A.; Coady, D. J.; Akar, A.; Bielawski, C. W.; Marquez, M.; Sessler, J. L. “Poly(Methyl Methacrylate)s with Pendant Calixpyrroles and Crown Ethers: A New Class of Polymeric Extractants for Potassium Halides,” Angew. Chem. 2008, 120, 9794-9798; Angew. Chem. Int. Ed. 2008, 47, 9648-9652 (frontpiece). DOI: 10.1002/anie.200803970 Funding:  NIH-GM

445a.C & E  News, 2008, 86(43), 9.


446.*Pierce, S. E.; Sherman, C. L.; Jayawickramarajah, J.; Lawrence, C. L.; Sessler, J. L.; Brodbelt, J. S. “ESI-MS characterization of a novel pyrrole–inosine nucleoside that interacts with guanine bases,” Analytica Chim. Acta 2008, 627, 129-135. DOI: 10.1016/j.aca.2008.04.018.  Funding: Robert A. Welch Foundation Grant No. F-1018


447.*Sessler, J. L.; Karnas, E.; Kim, S. K.; Ou, Z.; Zhang, M.; Kadish, K. M.; Ohkubo, K. Fukuzumi, S. “’Umpolung’ Photoinduced Charge Separation in an Anion-bound Supramolecular Complex,” J. Am. Chem. Soc. 2008, 130, 15256-15257. DOI: 10.1021/ja806813x.  Funding:  National Institutes of Health Grant No. GM58907 and Robert A. Welch Foundation Grant No. F-1018


448.*Fowler, C. J.; Moyer, B. A.; Shriver, J. A.; Gross, D. E.; Sessler, J. L.; Bowman-James, K. “Enhanced Anion Exchange for Selective Sulfate Extraction: Overcoming the Hofmeister Bias,” J. Am. Chem. Soc. 2008, 130, 14386-14387. DOI: 10.1021/ja806511b.  Funding: U. S. Department of Energy Grant No. DE-FG-02-04ER63741 and National Institutes of Health Grant No. GM58907


449.*Tong, C. C.; Quesada, R.; Sessler, J. L.; Gale, P. A. “meso-Octamethylcalix[4]pyrrole: an old yet new transmembrane ion-pair transporter,” Chem. Commun. 2008, 6321-6323. DOI: 10.1039/b814988g.  Funding: National Institutes of Health Grant No. GM58907



2009


450.*Nielsen, K. A.; Levillain, E.; Lynch, V. M.; Sessler, J. L.; Jeppesen, J. O. “Tetrathiafulvalene Porphyrins,” Chem. Eur. J. 2009, 15, 506-516. DOI: 10.1002/chem.200801636.  Funding: National Science Foundation Grant No. CHE-0749571


451.*Yoo, J.; Kim, M.-S.; Hong, S.-J.; Sessler, J. L.; Lee, C.-H. “Selective Sensing of Anions with Calix[4]pyrroles Strapped with Chromogenic Dipyrrolylquinoxalines,” J. Org. Chem. 2009, 74, 1065-1069.   DOI: 10.1021/jo802059c.  Funding: National Institutes of Health Grant No. GM58907


452.*Guimard, N. K. E.; Sessler, J. L.; Schmidt, C. E. “Toward a Biocompatible and Biodegradable Copolymer Incorporating Electroactive Oligothiophene Units,” Macromolecules 2009, 42, 502-511.  DOI: 10.1021/ma8019859.  Funding: National Institutes of Health Grant No. CA68682


453.*Yoon, D.-W.; Gross, D. E.; Lynch, V. M.; Lee, C.-H.; Bennett, P. C.; Sessler, J. L. “Real-time determination of chloride anion concentration in aqueous-DMSO using a pyrrole-strapped calixpyrrole anion receptor,” Chem. Commun., 2009, 1109-1111. DOI: 10.1039/b818077f.  Funding: National Institutes of Health Grant No. GM58907

453a.*Research Highlight in Nature Chemistry; Published online: 23 January 2009 | doi:10.1038/nchem.119


454.*Kim, D.-S.; Lynch, V. M.; Nielsen, K. A.; Johnsen, C.; Jeppesen, J. O.; Sessler, J. L. “A Chloride-Anion Insensitive Colorimetric Chemosensor for Trinitrobenzene and Picric Acid,” Anal. Bioanal. Chem. 2009, 395, 393-400. DOI: 10.1007/s00216-009-2819-4. Funding: National Science Foundation-CBET Grant No. 0730053


455.*Rio, Y.; Sánchez-Garcia, D.; Seitz, W.; Torres, T.; Sessler, J. L.; Guldi, D. M. “A bisfullerene-bis(dipyrrinato)zinc complex – electronic coupling and charge separation in an easy-to-assemble synthetic system,” Chem. Eur. J 2009, 15, 3956-3959.  Funding: National Science Foundation Grant No. CHE-0749571 and Robert A. Welch Foundation Grant No. F-1018


456.*Sessler, J. L.; Roznyatovskiy, V. V.; Lynch, V. M. “Novel β-substituted calix[4]pyrroles,” J. Porphyr. Phthalocy. 2009, 13, 322-325 (cover).  Funding: NSF.


457.*Kateyev, E. A.; Kolesnikov, G. V.; Sessler, J. L. “Molecular recognition of pertechnetate and perrhenate,” Chem. Soc. Rev. 2009, 38, 1572-1586 (featured on cover).  DOI: 10.1039/b806468g  Funding: U.S. Department of Energy Grant No. DE-FG02-01ER15186


458.*Fathalla, M.; Lawrence, C. M.; Zhang, N.; Sessler, J. L.; Jayawickramarajah Jayawickramarajah, J. “Base-pairing mediated non-covalent polymers,” Chem. Soc. Rev. 2009, 38, 1608-1620.  DOI: 10.1039/b806484a  Funding: Robert A. Welch Foundation Grant No. F-1018


459.*Cho, D.-G.; Sessler, J. L. “Modern reaction-based indicator systems,” Chem. Soc. Rev. 2009, 38, 1647 – 1662. DOI: 10.1039/b804436h  Funding: National Institutes of Health Grant No. GM58908


460.*Kim, S.-H.; Hong, S.-J.; Yoo, J.; Kim, S. K.; Sessler, J. L.; Lee, C.-H. “Strapped Calix[4]pyrroles Bearing a 1,3-Indanedion at a -Pyrrolic Position:  Chemodosimeters for the Cyanide Anion,” Org. Lett. 2009, 11, 3626-3629.  DOI: 10.1021/ol901361h  Funding: National Institutes of Health Grant No. GM58908


461.*Cuesta, L.; Sessler, J. L. “π-Metal complexes of tetrapyrrolic systems. A novel coordination mode in “porphyrin-like” chemistry, Chem. Soc. Rev. 2009, 38, 2716-2729 (inside cover).  DOI: 10.1039/b905850h. Funding: National Science Foundation Grant No. CHE-0749571


462.*Cuesta, L.; Karnas, E.; Lynch, V. M.; Chen, P.; Shen, J.; Kadish, K. M.; Ohkubo, K.; Fukuzumi, S.; Sessler, J. L. “Metalloporphycenes: Synthesis and Characterization of (Pentamethylcyclopentadienyl)ruthenium Sitting-Atop and π-Complexes,” J. Am. Chem. Soc. 2009, 131, 13538-13547.  DOI: 10.1021/ja905284d   Funding: National Science Foundation Grant No. CHE-0749571 and Robert A. Welch Foundation Grant No. F-1018


463.*Lin, Z.; Lawrence, C. M.; Xiao, D.; Kireev, V. V.; Skourtis, S. S.; Sessler, J. L.; Beratan, D. N.; Rubtsov, I. V. “Modulating Unimolecular Charge Transfer by Exciting Bridge Vibrations.” J. Am. Chem. Soc. 2009, 131, 18060-18062. DOI: 10.1021/ja907041t  Funding: National Science Foundation Grant No. CHE-0749571 and Robert A. Welch Foundation Grant No. F-1018

463a.*Research Highlight: Nature Chemistry, 11 December 2009 |DOI:10.1038/nchem.516

463b.*Science & Technology Concentrate, C & E News, December 7, 2009, p. 41.


464.*Arambula, J. F.; Sessler, J. L.; Fountain, M.; Wei, W.-h.; Magda, D.; Siddik, Z. H. “Gadolinium texaphyrin (Gd-Tex)-malonate-platinum conjugates: Synthesis and Comparison with carboplatin in normal and Pt-resistant cell lines,” Dalton Trans. 2009, 48, 10834-10840.  DOI: 10.1039/b912089k  Funding: National Institutes of Health Grant No. CA68682 and Robert A. Welch Foundation Grant No. F-1018


465.*Jensen, L. G.; Nielsen, K. A.; Breton, T.; Sessler, J. L.; Jeppesen, J. O.; Levillain, E.; Sanguinet, L. “Self-assembled Monolayers of Mono-Tetrathiafulvalene Calix[4]pyrroles and Their Electrochemical Sensing of Chloride,” Chem. Eur. J. 2009, 15, 8128-8133. DOI: 10.1002/chem.200901394  Funding: National Science Foundation Grant No. CHE-0749571 and Robert A. Welch Foundation Grant No. F-1018


466.*Katayev, E. A.; Sessler, J. L.; Ustynyuk, Y. A. “New strategy and methods for constructing artificial macrocyclic anion receptors. Selective binding of tetrahedral oxoanions,” Russian Chem. Bull., Int. Ed. 2009, 58, 1785—1798.

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Department of Chemistry, College of Natural Sciences

The University of Texas at Austin

The Sessler Group