Locking the phenyl rings of tetraphenylethene step by step: understanding the mechanism of aggregation-induced emission

被引：227

作者：

Shi, Junqing ^{[1
]}

Chang, Ning ^{[1
]}

Li, Cuihong ^{[1
]}

Mei, Ju ^{[2
]}

Deng, Chunmei ^{[3
]}

Luo, Xiaoliang ^{[1
]}

Liu, Zhengping ^{[1
]}

Bo, Zhishan ^{[1
]}

Dong, Yong Qiang ^{[1
]}

Tang, Ben Zhong ^{[2
,4
]}

机构：

[1] Beijing Normal Univ, Dept Chem, Beijing Key Lab Energy Convers & Storage Mat, Beijing 100875, Peoples R China

[2] Zhejiang Univ, Dept Polymer Sci & Engn, MOE Key Lab Macromol Synth & Functionalizat, Inst Biomed Macromol, Hangzhou 310027, Zhejiang, Peoples R China

[3] Chinese Acad Sci, Inst Chem, Beijing 100190, Peoples R China

[4] Hong Kong Univ Sci & Technol, Dept Chem, Kowloon, Hong Kong, Peoples R China

来源：

CHEMICAL COMMUNICATIONS | 2012年 / 48卷 / 86期

基金：

美国国家科学基金会;

关键词：

CONJUGATED POLYMERS; FLUORESCENCE;

D O I：

10.1039/c2cc35641d

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Stepwise locking of phenyl rings of tetraphenylethene increases the emission efficiency of luminogen solutions gradually, thus verifying the restriction of intramolecular rotation (RIR) mechanism of the aggregation induced emission phenomenon. The emission of the luminogen with one "O" bridge could be tuned reversibly in solid state through repeated heating and grinding.

引用

页码：10675 / 10677

页数：3

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