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“Preparation, Photophysics, and Electrochemistry of Segmented Co-Monomers Consisting of Thiophene and Pyrimidine Units: New Monomers for Hybrid Co-Polymers”

Dufresne, S., Hanan, G.H, and Skene, W.G. “Preparation, Photophysics, and Electrochemistry of Segmented Co-Monomers Consisting of Thiophene and Pyrimidine Units: New Monomers for Hybrid Co-Polymers” J. Phys. Chem. B, 111, 11407-11418 (2007).

“Spectral Characterization of Thiophene Acylhydrazides”

Skene, W. G. and Pérez Guarin, S. A. “Spectral Characterization of Thiophene Acylhydrazides” J. Fluores., 17, 540-546 (2007).

“Thermal, Photophysical, and Electrochemical Characterization of a Conjugated Polyazomethine Prepared by Anodic Electropolymerization of a Thiophenoazomethine Co-Monomer”

Pérez Guarìn, S., Skene, W. G. “Thermal, Photophysical, and Electrochemical Characterization of a Conjugated Polyazomethine Prepared by Anodic Electropolymerization of a Thiophenoazomethine Co-Monomer” Mater. Lett., 61, 5102-5106 (2007).

“A Highly Conjugated p- and n-Type Polythiophenoazomethine: Synthesis, Spectroscopic, and Electrochemical Investigation”

Bourgeaux, M., Skene, W. G. “A Highly Conjugated p- and n-Type Polythiophenoazomethine: Synthesis, Spectroscopic, and Electrochemical Investigation” Macromolecules, 40, 1792-1795 (2007).

“Photophysics and Electrochemistry of Conjugated Oligothiophenes Prepared Using Azomethine Connections”

Bourgeaux, M. and Skene, W.G “Photophysics and Electrochemistry of Conjugated Oligothiophenes Prepared Using Azomethine Connections” J. Org. Chem., 72, 8882-8892 (2007).

“Convergent Preparation and Photophysical Characterization of Dimaleimide Dansyl Fluorogens: Elucidation of the Maleimide Fluorescence Quenching Mechanism”

Guy, J., Caron, K., Dufresne, S., Michnick, S.W., Skene, W.G., Keillor, J.W. “Convergent Preparation and Photophysical Characterization of Dimaleimide Dansyl Fluorogens: Elucidation of the Maleimide Fluorescence Quenching Mechanism” J. Am. Chem. Soc., 129, 11969-11977 (2007).

“Disodium 5,5′-Diamino-2,2′-Ethylenedibenzenesulfonate Tetrahydrate”

Dufresne, S., Gaultois, M., Skene, W.G. “Disodium 5,5′-Diamino-2,2′-Ethylenedibenzenesulfonate Tetrahydrate” Acta Cryst., E63, 11, m2714 (2007).

“Bis(triethylammonium) 4,4′-Diamino-trans-Stilbene-2,2′-Disulfonate”

Dufresne, S., Gaultois, M., Skene, W.G. “Bis(triethylammonium) 4,4′-Diamino-trans-Stilbene-2,2′-Disulfonate” Acta Cryst., E63, 10, o3926 (2007).

“Demystifying the Triplet State and the Quenching Mechanism of Self-Assembled Fluorenoazomethines”

Tsang, D., Bourgeaux, M., Skene. W.G. “Demystifying the Triplet State and the Quenching Mechanism of Self-Assembled Fluorenoazomethines” J. Photochem. Photobiol. A, 192, 122-129 (2007).

“Synthesis and properties of 6,6′-dithienyl-4,4′-bipyrimidine and its hetero- and homo-leptic Ru(II) complexes”

Hanan, G. S, M., Ioachim, E., Medlycott, E.A., Skene, W.G. “Synthesis and properties of 6,6′-dithienyl-4,4′-bipyrimidine and its hetero- and homo-leptic Ru(II) complexes” Polyhedron, 26, 4929–4935 (2007).

“Photophysical, Electrochemical, and Crystallographic Investigation of Self-Assembled Conjugated Fluoreno Azomethines and Their Precursors”

Pérez, S., Dufresne, S., Tsang, D., Sylla, A., Skene, W. G. “Photophysical, Electrochemical, and Crystallographic Investigation of Self-Assembled Conjugated Fluoreno Azomethines and Their Precursors” J. Mater. Chem., 17, 2801-2811 (2007).

“Fluoresceinophane: 2-(6-Hydroxy-3-oxo-3H-xanthen-9-yl)-benzoic acid undecanoic acid”

Dufresne, S., Pérez Guarin, S., Skene, W.G. “Fluoresceinophane: 2-(6-Hydroxy-3-oxo-3H-xanthen-9-yl)-benzoic acid undecanoic acid” Acta Cryst., C63, o350-o352 (2007).

“Ethyl 2-aminothiophene-3-carboxylate”

Bourgeaux, M., and Skene, W. G. “Ethyl 2-aminothiophene-3-carboxylate” Acta Cryst., E63, o1603–o1605 (2007).

“Tunable spectroscopic and electrochemical properties of conjugated push-push, push-pull and pull-pull thiopheno azomethines”

Dufresne, S., Bourgeaux, M., Skene, W. G. “Tunable spectroscopic and electrochemical properties of conjugated push-push, push-pull and pull-pull thiopheno azomethines” J. Mater. Chem., 17, 1166-1177 (2007).

“Photophysical, crystallographic, and Electrochemical Characterization of Symmetric and Unsymmetric Self-Assembled Conjugated Thiopheno Azomethines”

Pérez Guarin, S., Bourgeaux, M., Dufresne, S., Skene, W. G. “Photophysical, crystallographic, and Electrochemical Characterization of Symmetric and Unsymmetric Self-Assembled Conjugated Thiopheno Azomethines” J. Org. Chem., 72, 2631-2643 (2007).

“Photophysical, crystallographic, and electrochemical characterization of novel conjugated thiopheno azomethines”

Bourgeaux, M., Pérez Guarin, S., Skene, W. G. “Photophysical, crystallographic, and electrochemical characterization of novel conjugated thiopheno azomethines” J. Mater. Chem., 17, 972-979 (2007).

“Spectroscopic Studies of a Fluorescent Fluoresceinophane Formed via a Practical Synthetic Route”

Pérez Guarin, S. A., Tsang, D., Skene, W. G. “Spectroscopic Studies of a Fluorescent Fluoresceinophane Formed via a Practical Synthetic Route” New J. Chem., 31, 210-217 (2007).

“Diethyl 2,5-bis[(E)-thiophen-2-ylmethyleneamino]thiophene-3,4-dicarboxylate”

Dufresne, S., Bourgeaux, M., Skene, W. G. “Diethyl 2,5-bis[(E)-thiophen-2-ylmethyleneamino]thiophene-3,4-dicarboxylate” Acta Cryst., E62, o5602-o5604 (2006).

“A naphthalene–thiophene–naphthalene diazomethine triad solvated with dichloromethane”

Skene, W.G and Dufresne, S. “A naphthalene–thiophene–naphthalene diazomethine triad solvated with dichloromethane”, Acta Cryst., E62, o1116-o1117, (2006).

“Selective product amplification of thymine photodimer by recognition-directed supramolecular assistance”

Skene, W. G., Berl, V., Risler, H. Khoury, R., and Lehn, J.-M. “Selective product amplification of thymine photodimer by recognition-directed supramolecular assistance” Org. Biomol. Chem., 19, 3652-3663, (2006).