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Photophysics of benzazole derived push–pull butadienes: A highly sensitive fluorescence probes

Paper ID Volume ID Publish Year Pages File Format Full-Text
28682 44085 2006 10 PDF Available
Title
Photophysics of benzazole derived push–pull butadienes: A highly sensitive fluorescence probes
Abstract

Two new homologues of 1,4-diphenylbutadiene, namely, 1-(2-benzazolyl)-4-(p-dimethylaminophenyl)buta-1,3-diene have been synthesized and their absorption and fluorescence properties have been investigated in different organic solvents. The absorption spectra are less sensitive to the solvent polarity than the corresponding fluorescence spectra, which show dual emission and high solvatochromic effect in polar solvents. Using an efficient solvatochromic method, a large excited state dipole moment parallel to the smaller ground state dipole moment was calculated. Other properties of the lowest excited state such as the planar ICT Bu nature, fluorescence quantum yield and the basicity of the two nitrogen atoms (of the benzoxazole or benzothiazole ring as well as the amino group) were studied by spectroscopic techniques and semiempirical AM1 quantum chemical calculations. The findings have been presented and discussed along with the promising fluorescence probing and pH-sensing properties of these two dienes. The main spectroscopic properties of the two derivatives have been also compared.

Keywords
Diphenylbutadiene; Fluorescence probing; ICT; Benzoxazole; Benzothiazole; Semiempirical; Dipole moment; Viscosity
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Photophysics of benzazole derived push–pull butadienes: A highly sensitive fluorescence probes
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Publisher
Database: Elsevier - ScienceDirect
Journal: Journal of Photochemistry and Photobiology A: Chemistry - Volume 177, Issues 2–3, 25 January 2006, Pages 238–247
Authors
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Subjects
Physical Sciences and Engineering Chemical Engineering Bioengineering
Get Full-Text Now
Don't Miss Today's Special Offer
Price was $35.95
You save - $31
Price after discount Only $4.95
100% Money Back Guarantee
Full-text PDF Download
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