A tricolor photochromic hybrid tetra-arylethene with > 99 % E-Z isomerization and photocyclization/cycloreversion

被引:0
|
作者
Lei, Wei [1 ]
Chen, Siyuan [1 ]
Zeng, Yan [1 ]
Wang, Xuewen [1 ]
Luo, Qianfu [1 ]
机构
[1] East China Univ Sci & Technol, Sch Chem & Mol Engn, Dept Chem, Shanghai 200237, Peoples R China
关键词
Z isomerization; Tricolor photochromism; Photo-gated thermal reversibility; AGGREGATION-INDUCED EMISSION; STEPWISE PHOTOCHROMISM; RUTHENIUM COMPLEX; MULTIPHOTOCHROMISM; DERIVATIVES;
D O I
10.1016/j.dyepig.2025.112766
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
We present the rational design and synthesis of an innovative tricolor photochromic switch featuring a unique molecular architecture combining an E-tetra-arylethene core with dual benzophenone moieties. The system demonstrates exceptional bidirectional photoresponsive behavior, achieving near-quantitative E-Z isomerization (yields >99%) and efficient photoinduced cyclization/cycloreversion reactions in tetrahydrofuran solution. This sophisticated photochromic interplay enables precise tricolor modulation through controlled light irradiation. Notably, the system exhibits light-regulated thermal reversibility, offering unprecedented control over its relaxation dynamics. The photochromic performance remains robust across different matrices, including PMMA polymer films and cellulose filter paper substrates. This multi-addressable color-switching platform demonstrates promising potential for advanced optical applications, particularly in dynamic information encryption systems and multi-level anti-counterfeiting technologies.
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页数:7
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