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Chinese Academy of Sciences Institutional Repositories Grid
Intramolecular charge transfer and solvation dynamics of push-pull dyes with different pi-conjugated linkers

文献类型:期刊论文

作者Niu, Xinmiao; Gautam, Prabhat; Kuang, Zhuoran; Yu, Craig P.; Guo, Yuanyuan; Song, Hongwei; Guo, Qianjin; Chan, Julian M. W.; Xia, Andong
刊名PHYSICAL CHEMISTRY CHEMICAL PHYSICS
出版日期2019-08-21
卷号21期号:31页码:17323-17331
ISSN号1463-9076
DOI10.1039/c9cp02559f
英文摘要The solvation-dependent excited state dynamics of two push-pull fluorophores with donor-pi-acceptor (D-pi-A) structures were investigated using steady-state and ultrafast transient absorption (TA) spectroscopy, backed by theoretical calculations. Identical D and A groups were present in both dyes, which differed only in the structure of their central pi-conjugated linkers. Dye 1 features a p-phenylenediethynyl linker, while dye 2 contains a 2,5-diethynylthiophene linker. From the steady-state spectra, no appreciable shifts in absorption bands were observed, whereas large red-shifts in emission were seen with increasing solvent polarity, which indicated that the excited states were more polar than the ground state. Theoretical calculations support charge transfer from the triphenylamine (TPA) donor to the pentafluorosulfanyl (SF5) acceptor via pi-conjugated linkers to form an intramolecular charge transfer (ICT) state. TA spectra revealed that a solvation-stabilized conformationally relaxed intramolecular charge transfer (ICT ') state was formed in polar solvents, but only an ICT state was observed in nonpolar solvent. The SE band was quenched within 1 ps in high-polarity solvent, which corresponds to the low fluorescence quantum yield. It can be concluded that the dye with the p-phenylenediethynyl pi-linker (i.e., dye 1) exhibits a larger degree of ICT than the thiophene analogue (i.e., dye 2). These findings demonstrate how solvation can fine-tune the photophysical properties of push-pull dyes, and this study highlights the importance of pi-conjugated linkers in the excited state ICT process.
语种英语
WOS记录号WOS:000479245800039
源URL[http://ir.iccas.ac.cn/handle/121111/82649]  
专题中国科学院化学研究所
作者单位Chinese Acad Sci, Inst Chem, Beijing 100190, Peoples R China
推荐引用方式
GB/T 7714
Niu, Xinmiao,Gautam, Prabhat,Kuang, Zhuoran,et al. Intramolecular charge transfer and solvation dynamics of push-pull dyes with different pi-conjugated linkers[J]. PHYSICAL CHEMISTRY CHEMICAL PHYSICS,2019,21(31):17323-17331.
APA Niu, Xinmiao.,Gautam, Prabhat.,Kuang, Zhuoran.,Yu, Craig P..,Guo, Yuanyuan.,...&Xia, Andong.(2019).Intramolecular charge transfer and solvation dynamics of push-pull dyes with different pi-conjugated linkers.PHYSICAL CHEMISTRY CHEMICAL PHYSICS,21(31),17323-17331.
MLA Niu, Xinmiao,et al."Intramolecular charge transfer and solvation dynamics of push-pull dyes with different pi-conjugated linkers".PHYSICAL CHEMISTRY CHEMICAL PHYSICS 21.31(2019):17323-17331.

入库方式: OAI收割

来源:化学研究所

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