Intense fluorescence from light-driven self-assembled aggregates of nonionic azobenzene derivative

被引:180
作者
Han, M
Hara, M
机构
[1] RIKEN, Frontier Res Syst, Local Spatio Temporal Funct Lab, Wako, Saitama 3510198, Japan
[2] Tokyo Inst Technol, Dept Elect Chem, Midori Ku, Yokohama, Kanagawa 2268502, Japan
关键词
D O I
10.1021/ja0509275
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We describe here the highly fluorescent self-assembled spherical aggregates of an azobenzene molecule without a specific ionic component in organic solution under UV light illumination. The first stage of trans-to-cis photoisomerization by UV light at 365 nm was followed by a significant enhancement, up to about 1000 times, of the emission from an azobenzene molecule (CN2Azo) with a long alkyl chain, which is due to the spontaneous formation of spherical organic aggregates. Fluorescence emission was further enhanced in the dark, and the quantum yield increased to about 0.3. We also report the significant size and structural changes of the aggregates, from nanometer-scale micelle-like aggregates to micrometerscale vesicular aggregates, obtained only from the variation in the concentration of an azobenzene derivative. The light-driven azobenzene aggregates show the size and structure dependences of emission wavelength from violet-blue to green-yellow.
引用
收藏
页码:10951 / 10955
页数:5
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