Visible-light induced photo-click and release strategy between monoarylsydnone and phenoxylfumarate

被引：7

作者：

Liu, Hui ^{[1
]}

Zheng, Tingting ^{[1
]}

Zheng, Yuanqin ^{[1
]}

Li, Baolin ^{[1
]}

Xie, Xinyu ^{[1
]}

Shen, Xin ^{[1
]}

Zhao, Xiaohu ^{[1
]}

Yu, Zhipeng ^{[1
]}

机构：

[1] Sichuan Univ, Coll Chem, Key Lab Green Chem & Technol Minist Educ, 29 Wangjiang Rd, Chengdu 610064, Peoples R China

来源：

CHEMICAL COMMUNICATIONS | 2021年 / 57卷 / 66期

基金：

中国国家自然科学基金;

关键词：

FLUOROGENIC PROBE; NITRILE IMINE; CHEMISTRY; CYCLOADDITIONS;

D O I：

10.1039/d1cc02841c

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

We report a visible-light induced photo-click and release platform between monoarylsydnone (MASyd) and phenoxylfumarates. The pyrazoline produced by the cycloaddition undergoes a photo-aromatization to form a fluorescent pyrazole. Meanwhile, the photo-aromatization also serves as the driving force to release fluorophores that are quenched in the form of phenoxylfumarates.

引用

收藏

页码：8135 / 8138

页数：5

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