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Fluorescence control on panchromatic spectra via c-alkylation on arylated quinoxalines
Ho-Jin Son1, Won-Sik Han, Dae-Hwan Yoo
1Department of Materials Chemistry, Sejong Campus, Korea University, Chung-Nam 339-700, South Korea.
Abstract:
A coherent green fluorescence was obtained by butylation at the 2-position of panchromatic 2,3-diaryl-5,8-diarylquinoxalines (2) to give corresponding 2-butyl-2,3-diaryl-5,8-diaryl-1H-quinoxalines (3). Full color quinoxaline derivatives (2) were prepared from electronic modification at either the 2,3- or 5,8-positions at the peripheral ArX group or X group (X = -H, -OMe, -NPh(2), -NMe(2), -NMePh) of the quinoxalines. 2-Butylation converted one imine unit of the pyrazine ring to an amine group, which effectively altered the electron donor and acceptor functions to produce a coherent green fluorescence.
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