Solvent Effects on Spectral Property and Dipole Moment of the Lowest Excited State of Coumarin 343 Dye

被引:7
|
作者
Jiang, Li-lin [1 ,2 ]
Liu, Wei-long [1 ]
Song, Yun-fei [1 ]
He, Xing [1 ]
Wang, Yang [1 ]
Wu, Hong-lin [1 ]
Yang, Yan-qiang [1 ]
机构
[1] Harbin Inst Technol, Dept Phys, Ctr Condensed Matter Sci & Technol, Harbin 150001, Peoples R China
[2] Hezhou Univ, Dept Phys & Elect Informat Engn, Hezhou 542800, Peoples R China
基金
中国国家自然科学基金;
关键词
Time-resolved fluorescence; Dipole moment; Solvent polarity function; Quantum chemical calculation; Intermolecular hydrogen bonding interaction; DENSITY-FUNCTIONAL THEORY; DYE/SEMICONDUCTOR COLLOIDAL SYSTEMS; PHOTOINDUCED ELECTRON-TRANSFER; HYDROGEN-BOND DYNAMICS; SOLVATION DYNAMICS; FLUORESCENCE; DECAY; CHROMOPHORE;
D O I
10.1088/1674-0068/25/05/577-584
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
Steady-state absorption and fluorescence spectra, and time-resolved fluorescence spectra of coumarin 343 (C343) were measured in different solvents. The effect of the solvent on the spectral properties and dipole moment of the lowest excited state of C343 were investigated. It was found that the absorption and fluorescence spectra red-shifted slightly and strongly with increasing solvent polarity, respectively, because the charge distribution of the excited state leaded to the increasing difference between the absorption and fluorescence spectra with increasing solvent polarity. The dipole moment of the lowest excited state of C343 was determined from solvatochromic measurements and the quantum chemical calculation, and the results obtained from these two methods were fully consistent. Investigations of the time-resolved fluorescence of C343 in different solvents indicated that the fluorescence lifetimes increased nearly linearly with increasing solvent polarity from 3.09 ns in toluene to 4.45 ns in water. This can be ascribed to the intermolecular hydrogen bonding interactions between C343 and hydrogen donating solvents.
引用
收藏
页码:577 / 584
页数:8
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