5,10,15,20-Tetrakis(2-amino-6-methoxycarbonylphenyl)porphyrin. Synthesis and Separation of Atropisomers Useful for Porphyrin Architecture
Norikazu Nishino, Toshiaki Sakamoto, Hiroshi Kiyota, Hisakazu Mihara, Tomoko Yanai, Tsutomu Fujimoto
Abstract
Norikazu Nishino, Toshiaki Sakamoto, Hiroshi Kiyota, Hisakazu Mihara, Tomoko Yanai, Tsutomu Fujimoto
Abstract
Abstract 5,10,15,20-Tetrakis(2-amino-6-methoxycarbonylphenyl)porphyrin was synthesized and three atropisomers in four were successfully separated. Different from the related mono-substituted tetraphenylporphyrins (2-amino- and 2-methoxycarbonylphenylporphyrins), the rotation of the bond between phenyl and porphyrin rings was totally prohibited under thermal isomerization.
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Abstract 5,10,15,20-Tetrakis(2-amino-6-methoxycarbonylphenyl)porphyrin was synthesized and three atropisomers in four were successfully separated. Different from the related mono-substituted tetraphenylporphyrins (2-amino- and 2-methoxycarbonylphenylporphyrins), the rotation of the bond between phenyl and porphyrin rings was totally prohibited under thermal isomerization.
Key concepts: Atropisomer, Porphyrin, Chemistry, Isomerization, Photochemistry, Stereochemistry, Medicinal chemistry, Polymer chemistry