Quadruply Bridging Strategy Intensifies Circularly Polarized Luminescence of Azapyrenophanes

四重桥联策略增强氮杂芘烷的圆偏振发光

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Abstract

Multibridged azapyrenophanes were synthesized as organic circularly polarized luminescence (CPL) emitters. The g(lum) reached +0.12 and the B(CPL) amounted to 2,600 M(-1) cm(-1) at -95 °C. The xylylene-bridging to the binaphthyl-bridged pyrenophane produced a quadruply bridged structure that prompted the pyrene excimer to adopt a D(2)-symmetric rigid conformation. This strategy maximized the latent CPL performance. Furthermore, these emitters functioned as temperature- and acid/base-triggered (+)/(-)- or on/off-CPL switches in which enantiospecific responses toward chiral solvents were also observed.

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