Title of article
Proton- and metal cation-enhanced excited state intramolecular proton transfers of 2-(2-hydroxyfluorophenyl)benzoxazole having imidazole moiety
Author/Authors
Tanaka، نويسنده , , Kiyoshi and Sano، نويسنده , , Kei-Ichi and Katoh، نويسنده , , Takuya and Iwata، نويسنده , , Satoru and Nemoto، نويسنده , , Kouhei and Kurushima، نويسنده , , Tohru، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2006
Pages
6
From page
1073
To page
1078
Abstract
2-(2-Hydroxyfluorophenyl)benzoxazole having an imidazole moiety 1 was synthesized by the two step reactions starting from 2-(pentafluorophenyl)benzoxazole. Protonation at the 3-imidazole nitrogen atom of 1 enhances the green emission around 500 nm, where the positive character caused by the protonation is inductively communicated to the hydroxy group, to recover its intramolecular hydrogen bonding, leading to the ESIPT process. Addition of Al3+ or Zn2+ to 1 enhances both the green emission and the blue emission around 450 nm in chloroform-acetonitrile.
Keywords
2-(2-Hydroxyfluorophenyl)benzoxazole , Heterocycles , excited state intramolecular proton transfer , Metal cation , fluorescence
Journal title
Journal of Fluorine Chemistry
Serial Year
2006
Journal title
Journal of Fluorine Chemistry
Record number
1609353
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