Journal
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY
Volume 187, Issue 2-3, Pages 305-310Publisher
ELSEVIER SCIENCE SA
DOI: 10.1016/j.jphotochem.2006.10.027
Keywords
the charge transfer mechanism; the hydrogen bond; the heptamethine cyanine dye; the absorption and fluorescence spectra
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The charge transfer mechanism of a synthesized near-infrared (NIR) heptamethine cyanine dye has been studied with 3D real space analysis method. Anew phenomenon about the intramolecular charge transfer (ICT) process is observed: the sulfonate (-SO3-) groups are mainly concerned with the ICT process. The electrons can transfer from the sulfonate (-SO3-) groups to the bridgehead amine and the electron-defect conjugated system. And the absorption and fluorescence spectra of the ICT state in alcoholic and aprotic solvents are analyzed. The spectral regularities are explained by the Kamlet and Taft (pi*, alpha, beta) scale and the ICT mechanism. Specific hydrogen-bonding interactions between the solute and solvent are considered to explain the different spectral regularities of the dye in alcoholic and aprotic solvents. (C) 2006 Elsevier B.V. All rights reserved.
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