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A kinetically protected pyrene: molecular design, bright blue emission in the crystalline state and aromaticity relocation in its dicationic species†
Akinobu Matsumoto,Mitsuharu Suzuki,Daiki Kuzuhara,Junpei Yuasa,Tsuyoshi Kawai,Naoki Aratani
Chemical Communications Pub Date : 07/03/2014 00:00:00 , DOI:10.1039/C4CC03645J
Abstract

Sterically congested tetraarylpyrenes exhibited emission in both solution and the solid state. The monocationic species of pyrene 1 could be isolated because of the reasonably protected system. The aromaticity of 1 relocates from the biphenyl part to the naphthalene unit upon two-electron oxidation.

Graphical abstract: A kinetically protected pyrene: molecular design, bright blue emission in the crystalline state and aromaticity relocation in its dicationic species
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