Excitation Energy-Dependent, Excited-State Intramolecular Proton Transfer-Based Dual Emission in Poor Hydrogen-Bonding Solvents

被引:8
|
作者
Hurley, Joseph J. M. [1 ]
Zhu, Lei [1 ]
机构
[1] Florida State Univ, Dept Chem & Biochem, Tallahassee, FL 32306 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY A | 2022年 / 126卷 / 34期
基金
美国国家科学基金会;
关键词
SKELETAL DEFORMATIONS; O-HYDROXYBENZALDEHYDE; WHITE-LIGHT; N-OXIDE; FLUORESCENCE; MECHANISM; PHOTOPHYSICS; DYNAMICS; BREAKING; COHERENT;
D O I
10.1021/acs.jpca.2c03668
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
2-(2'-Hydroxyphenyl)benzoxazole (HBO) substituted at the 5'-position with bipyridylvinylene phenylenevinylene (compound 2) produces both normal and, via an excited-state intramolecular proton transfer (ESIPT) reaction, tautomer emissions in solvents that preserve intramolecular hydrogen bonds. The abundance of the tautomer emission from compound 2 in a poor hydrogen-bonding solvent increases in response to the application of a higher excitation energy. Based on quantum chemical calculations, the excitation-dependent dual emission is consistent with a model in which the ESIPT reaction is more favored in the S-2 than in the S-1 electronically excited state.
引用
收藏
页码:5711 / 5720
页数:10
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