Shiraishi Yasuhiro, Maehara Hajime, Hirai Takayuki
Research Center for Solar Energy Chemistry, and Division of Chemical Engineering, Graduate School of Engineering Science, Osaka University, Toyonaka 560-8531, Japan.
Org Biomol Chem. 2009 May 21;7(10):2072-6. doi: 10.1039/b821466b. Epub 2009 Mar 26.
An indole-azadiene conjugate (1), synthesized by facile one-step condensation, behaves as a highly selective probe for detection of fluoride ion both in colorimetric and fluorometric analyses. The probe 1 shows F(-)-selective color change from colorless to yellow and appearance of green fluorescence. 1H NMR analysis and ab initio calculation reveal that the F(-)-induced colorimetric and fluorometric responses of 1 are simply driven by hydrogen bonding interaction between the indolic NH protons and F(-).
通过简便的一步缩合反应合成的吲哚 - 氮杂二烯共轭物(1),在比色分析和荧光分析中均表现为用于检测氟离子的高选择性探针。探针1显示出对F⁻具有选择性的颜色变化,从无色变为黄色,并出现绿色荧光。¹H NMR分析和从头算计算表明,1对F⁻诱导的比色和荧光响应仅仅是由吲哚NH质子与F⁻之间的氢键相互作用驱动的。