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供体-受体取代的乙烯基噻吩的取代基依赖性电荷转移和光化学性质

Substituent Dependence Charge Transfer and Photochemical Properties of Donor-Acceptor Substituted Ethenyl Thiophenes.

作者信息

Kumar Naresh, Kumar Jagdeep, Hota Prasanta Kumar

机构信息

Department of Chemistry, School of Sciences, Hemvati Nandan Bahuguna Garhwal University, Srinagar Garhwal, Pauri Garhwal, Uttarakhand, 246174, India.

出版信息

J Fluoresc. 2017 Sep;27(5):1729-1738. doi: 10.1007/s10895-017-2111-5. Epub 2017 May 5.

Abstract

Donor-acceptor conjugated molecules with efficient light induced properties represent interesting material for electronic device application. In this context, we have calculated excited state dipole moment of three ethenyl thiophenes (1-3) bearing varied electron donor-acceptor substituent in p-phenyl unit using Lippert-Mataga, Bakhshiev and Kawski method. It is found that 1 with strong electron-withdrawing nitro substituent, is exhibiting charge transfer and highly dipolar excited state as compared to 2 and 3. Photochemical studies of 1-3, indicate towards the charge transfer dependence trans-cis photoisomerization under direct irradiation condition. Compound 1 exhibits charge transfer and less efficient towards photoisomerization, whereas 2 and 3 undergo efficient photoisomerization. Graphical Abstract Substituent dependence charge transfer and photochemical properties of donor-acceptor substituted ethenyl thiophenes.

摘要

具有高效光诱导性质的供体-受体共轭分子是电子器件应用中有趣的材料。在此背景下,我们使用Lippert-Mataga、Bakhshiev和Kawski方法计算了在对苯基单元中带有不同电子供体-受体取代基的三种乙烯基噻吩(1-3)的激发态偶极矩。研究发现,与2和3相比,具有强吸电子硝基取代基的1表现出电荷转移和高度偶极激发态。对1-3的光化学研究表明,在直接辐照条件下,反式-顺式光异构化依赖于电荷转移。化合物1表现出电荷转移且光异构化效率较低,而2和3则发生高效光异构化。图形摘要:供体-受体取代的乙烯基噻吩的取代基依赖性电荷转移和光化学性质。

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