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Synthesis of porphyrin dimers fused with a benzene unit
Authors:Uno Hidemitsu  Nakamoto Ken-Ichi  Kuroki Kenji  Fujimoto Akiko  Ono Noboru
Affiliation:Division of Synthesis and Analysis, Department of Molecular Science, Integrated Center for Sciences (INCS), Ehime University, Matsuyama 790-8577, Japan. uno@dpc.ehime-u.ac.jp
Abstract:Bicyclo[2.2.2]octadiene-connected pyrrolo-porphyrins have been prepared by an inverse-type [3+1] porphyrin synthesis of a bicyclo[2.2.2]octadiene-fused dipyrrole with a tripyrrane dicarbaldehyde. Another [3+1] porphyrin synthesis of pyrrole-connected porphyrins with the same or other tripyrrane dicarbaldehydes gave bicyclo[2.2.2]octadiene-bridged diporphyrins, the central metals and/or peripheral substituents of which were different. Thermal decomposition of the bicyclo[2.2.2]octadiene skeleton to a benzene moiety gave pi-system-fused porphyrin dimers in a highly pure form.
Keywords:conjugation  dimerization  porphyrinoids  retro‐ Diels–Alder reaction  stacking interactions
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