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Cation-responsive turn-on fluorescence and absence of heavy atom effects of pyridyl-substituted triarylmethyl radicals
Chemical Communications ( IF 4.9 ) Pub Date : 2018-01-04 00:00:00 , DOI: 10.1039/c7cc08568k
Yohei Hattori 1, 2, 3, 4, 5 , Shun Kimura 1, 2, 3, 4, 5 , Tetsuro Kusamoto 1, 2, 3, 4, 5 , Hiroaki Maeda 1, 2, 3, 4, 5 , Hiroshi Nishihara 1, 2, 3, 4, 5
Affiliation  

Pyridyl-substituted triarylmethyl radicals exhibited cation-responsive turn-on fluorescence when additional pyridyl rings were incorporated at an appropriate position; the mechanism of fluorescence enhancement is examined. Reduced quenching by internal and external heavy atom effects is proposed as a unique property of fluorescent radicals, which can be utilized in different environments to conventional closed-shell fluorescent molecules.

中文翻译:

阳离子响应的开启荧光,吡啶基取代的三芳基甲基自由基不具有重原子效应

当在合适的位置引入另外的吡啶基环时,吡啶基取代的三芳基甲基自由基显示出阳离子响应的开启荧光。检查了荧光增强的机理。提出通过内部和外部重原子效应减少淬灭是荧光自由基的独特性质,可以与常规的闭壳荧光分子在不同的环境中使用。
更新日期:2018-01-16
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