作者:Radomir Myśliborski、Lechosław Latos-Grażyński、Ludmiła Szterenberg
DOI:10.1002/ejoc.200600364
日期:2006.7
Pyriporphyrin 1 (6,11,16,21-tetraaryl-22-aza-m-benziporphyrin), the simplest homologue of 5,10,15,20-tetraarylporphyrin can be constructed by replacement of one of the pyrrole rings of 5,10,15,20-tetraarylporphyrin with a pyridine moiety, linked to the macrocycle through α,α′-carbon atoms. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006)
Pyriporphyrin 1 (6,11,16,21-tetraaryl-22-aza-m-benziporphyrin) 是 5,10,15,20-tetraarylporphyrin 最简单的同系物,可以通过替换 5,10 的吡咯环之一来构建,15,20-四芳基卟啉,带有吡啶部分,通过 α,α'-碳原子与大环相连。(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006)