π-π Interactions: Influence on Molecular Packing and Solid-State Emission of ESIPT and non-ESIPT Motifs

被引:41
作者
Padalkar, Vikas S. [1 ]
Sakamaki, Daisuke [1 ]
Kuwada, Kenji [1 ]
Horio, Akifumi [1 ]
Okamoto, Haruka [1 ]
Tohnai, Norimitsu [2 ]
Akutagawa, Tomoyuki [3 ]
Sakai, Ken-ichi [4 ]
Seki, Shu [1 ]
机构
[1] Kyoto Univ, Dept Mol Engn, Katsura Campus, Kyoto 6158510, Japan
[2] Osaka Univ, Dept Mat & Life Sci, Suita Campus, Suita, Osaka 5650871, Japan
[3] Tohuku Univ, Inst Multidisciplinary Res Adv Mat, Sendai, Miyagi 9808577, Japan
[4] Chitose Inst Sci & Technol, Dept Bio & Mat Photon, Chitose 0668655, Japan
基金
日本学术振兴会;
关键词
aggregation-induced emission; excited-state intramolecular proton transfer; fluorescence; molecular packing; photophysics; INTRAMOLECULAR PROTON-TRANSFER; AGGREGATION-INDUCED EMISSION; SENSITIZED SOLAR-CELLS; EFFICIENT EMISSION; ENHANCED EMISSION; CRYSTAL PACKING; FLUORESCENCE; TRIPHENYLAMINE; DERIVATIVES; DONOR;
D O I
10.1002/ajoc.201600159
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Novel, triphenylamino benzothiazole-based excited-state intramolecular proton transfer (ESIPT) and non-ESIPT fluorophores were prepared by Suzuki coupling reactions. Their photophysical properties in solution, aqueous suspension, and in the solid state were systematically investigated. High fluorescence quantum efficiencies (phi(sol)approximate to 95%; phi(solid)approximate to 88%), moderate Stokes shifts (approximate to 8000cm(-1)), microenvironment-sensitive and molecular-framework-dependent emission are the striking features of the protocol described here. Solid-state emission was modulated and interpreted as a crossover effect of - interactions using single-crystal X-ray analyses. The nonplanar/twisted framework of the system helps to avoid noncovalent interactions, facilitating the suppression of fluorescence quenching in the solid state with high quantum efficiency over 88%.
引用
收藏
页码:938 / 945
页数:8
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