Intramolecular [3+2] annulation of 5-aryl-, 20-ethynyl-substituted [26]hexaphyrin(1.1.1.1.1.1) triggered by molecular compression through a dynamic conformational change

被引:24
|
作者
Suzuki, Masaaki [1 ]
Osuka, Atsuhiro [1 ]
机构
[1] Kyoto Univ, Grad Sch Sci, Dept Chem, Sakyo Ku, Kyoto 6068502, Japan
关键词
annulation; conformational dynamics; macrocyclic ligands; porphyrinoids; zinc;
D O I
10.1002/anie.200700958
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
(Figure Presented) Across the great divide: Substituents located opposite one another in meso positions on a [26]hexaphyrin scaffold are forced into close contact through a dynamic conformational change. A simple aryl group and an ethynyl group in these positions undergo a [3+2] annulation reaction either upon thermal activation or spontaneously to provide indenylene-bridged macrocycles that can serve as ligands for mixed-valence complexes (see structures). © 2007 Wiley-VCH Verlag GmbH & Co. KGaA.
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页码:5171 / 5174
页数:4
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