Solvent Effects on Linear and Multi-branched Bithiazole-based Derivatives Fluorescence Studied by Steady-state and Time-resovled Spectroscopy

Steady-state absorption, emission, and time-resolved spectroscopy were utilized to study the dynamics of excited states of linear and multi-branched bithiazole derivatives in different solvents at room temperature. In the studied compounds, triphenylamine and bithiazole groups act as donor and accep...

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Published inRussian Journal of Physical Chemistry A Vol. 95; no. 8; pp. 1641 - 1645
Main Authors Shi, Fuwen, Ni, Minghao, Wang, Zhiquan, He, Nannan, Li, Xiang, Hua, Jianli, Li, Bo, Chen, Ye
Format Journal Article
LanguageEnglish
Published Moscow Pleiades Publishing 01.08.2021
Springer Nature B.V
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ISSN0036-0244
1531-863X
DOI10.1134/S0036024421080215

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Abstract Steady-state absorption, emission, and time-resolved spectroscopy were utilized to study the dynamics of excited states of linear and multi-branched bithiazole derivatives in different solvents at room temperature. In the studied compounds, triphenylamine and bithiazole groups act as donor and acceptor, respectively. BTZ-I and II have similar linear molecular structures, while BTZ-III and BTZ-IV have multi-branched structures. The difference is that the donor and acceptor units are connected by a single bond or a triple bond, respectively. With increase in solvent polarity, the fluorescence spectra exhibit a red shift and the fluorescence lifetime increases. Our results suggest there is intra-molecular charge transfer (ICT) processes in these four samples.
AbstractList Steady-state absorption, emission, and time-resolved spectroscopy were utilized to study the dynamics of excited states of linear and multi-branched bithiazole derivatives in different solvents at room temperature. In the studied compounds, triphenylamine and bithiazole groups act as donor and acceptor, respectively. BTZ-I and II have similar linear molecular structures, while BTZ-III and BTZ-IV have multi-branched structures. The difference is that the donor and acceptor units are connected by a single bond or a triple bond, respectively. With increase in solvent polarity, the fluorescence spectra exhibit a red shift and the fluorescence lifetime increases. Our results suggest there is intra-molecular charge transfer (ICT) processes in these four samples.
Author Li, Bo
Ni, Minghao
Wang, Zhiquan
He, Nannan
Hua, Jianli
Li, Xiang
Chen, Ye
Shi, Fuwen
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Snippet Steady-state absorption, emission, and time-resolved spectroscopy were utilized to study the dynamics of excited states of linear and multi-branched bithiazole...
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StartPage 1641
SubjectTerms Charge transfer
Chemical bonds
Chemistry
Chemistry and Materials Science
Doppler effect
Emission analysis
Fluorescence
Molecular structure
Physical Chemistry
Red shift
Room temperature
Solvent effect
Solvents
Spectroscopic analysis
Spectrum analysis
Steady state
Structure of Matter and Quantum Chemistry
Title Solvent Effects on Linear and Multi-branched Bithiazole-based Derivatives Fluorescence Studied by Steady-state and Time-resovled Spectroscopy
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