Abstract

Primary aryl amines reacted with aryl halides to give the secondary aryl amines by the catalysis of [Pd(dba)2/P(t-Bu)3] at 80 °C in toluene. Secondary aryl amines reacted with 1-bromo-pyrene and 9-bromo-phenanthrene and 2,7-dibromo-9H-fluorene to afford the OLED material of aminopyrene derivatives and aminophenanthrene derivatives and diamino-9H-fluorene type by the catalysis of [Pd(OAc)2/P(t-Bu)3] at 120 °C in o-xylene. The product structures were established by 1H NMR, 13C NMR, 13C(DEPT), HRMS spectra. Physical properties were examined by UV-vis, PL and DSC spectra.

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