Kumar Naresh, Kumar Jagdeep, Hota Prasanta Kumar
Department of Chemistry, School of Sciences, Hemvati Nandan Bahuguna Garhwal University, Srinagar Garhwal, Pauri Garhwal, Uttarakhand, 246174, India.
J Fluoresc. 2017 Sep;27(5):1729-1738. doi: 10.1007/s10895-017-2111-5. Epub 2017 May 5.
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.
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。