Synthesis of highly fluorescent diketopyrrolopyrrole derivative and two-step response of fluorescence to acid
摘要:
A highly fluorescent diketopyrrolopyrrole derivative with amino groups was synthesized from Pigment Red 254 by a Pd-catalyzed amination reaction. The amino-substituted diketopyrrolopyrrole exhibits a two-step response Of fluorescence depending oil acidity. This optical property can be applied to a colorimetric detection of acids in the gas phase. (C) 2010 Elsevier Ltd. All rights reserved.
Solid-state structure and optical properties of highly fluorescent diketopyrrolopyrrole derivatives synthesized by cross-coupling reaction
作者:Junpei Kuwabara、Takuya Yamagata、Takaki Kanbara
DOI:10.1016/j.tet.2010.03.067
日期:2010.5
Diketopyrrolopyrrole (DPP) derivatives with four different substituents were synthesized by cross-coupling reactions. The DPP derivatives were investigated in terms of their solid-state structure, absorption, emission, and electrochemistry. The electron-donating property of each substituent causes a redshift of UV/vis absorption and emission in the solution state. Although all of the DPP derivatives have high quantum yields in solution, only butoxyphenyl-substituted DPP exhibits strong emission in the solid state. (C) 2010 Elsevier Ltd. All rights reserved.