Excited state behavior of benzoxazole derivatives in a confined environment afforded by a water soluble octaacid capsule

被引:54
作者
Santos, Fabiano S. [1 ,2 ]
Ramasamy, Elamparuthi [1 ]
Ramamurthy, V. [1 ]
Rodembusch, Fabiano S. [2 ]
机构
[1] Univ Miami, Dept Chem, 1301 Mem Dr,Cox Sci Bldg 230, Coral Gables, FL 33146 USA
[2] Univ Fed Rio Grande do Sul, Grp Pesquisa Fotoquim Organ Aplicada, Inst Quim, Ave Bento Goncalves 9500, BR-91501970 Porto Alegre, RS, Brazil
基金
美国国家科学基金会;
关键词
Supramolecular photochemistry; ESIPT; Proton transfer; Octaacid; Benzazoles; Fluorescence; INTRAMOLECULAR PROTON-TRANSFER; FLUORESCENCE QUANTUM YIELDS; CONTROLLING FREE-SPACE; CHARGE-TRANSFER; TRANSFER ESIPT; TRANSFER SPECTROSCOPY; TRANSIENT ABSORPTION; ORGANIC CAPSULE; SOLVENT; PHOTOCHEMISTRY;
D O I
10.1016/j.jphotochem.2015.08.019
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
This feature article presents a brief description of the excited state intramolecular proton transfer mechanism (ESIPT), describes the solvent dependence of the ESIPT phenomenon and present the potential applications that can be envisaged for these fluorophores. Photophysics of three dye molecules exhibiting ESIPT were examined free in solution and within a water soluble supramolecular host, octaacid (OA) by steady-state and time resolved fluorescence emission techniques. Inclusion of the above dyes within OA was confirmed by H-1 NMR spectra. The free and octaacid complexed dyes had electronic absorption in the UV region. Within the OA container the fluorophores showed fluorescence emission similar to that in benzene, dichloromethane and acetonitrile. Moreover, the observed large Stokes' shift in the emission of the dyes when confined within OA capsule was unlike that in aqueous medium. The results suggest that a confined medium is a powerful tool to tailor the fluorescence emission of ESIPT compounds in aqueous media. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:175 / 185
页数:11
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