N-confused porphine

Tatsuki Morimoto; Shozo Taniguchi; Atsuhiro Osuka; Hiroyuki Furuta

doi:10.1002/ejoc.200500485

N-confused porphine

Tatsuki Morimoto, Shozo Taniguchi, Atsuhiro Osuka, Hiroyuki Furuta

Research output: Contribution to journal › Article › peer-review

14 Citations (Scopus)

Abstract

A skeleton of N-confused porphyrin (NC-porphine) has been synthesized for the first time, through a [3+1] coupling reaction. A completely planar inner 3H tautomeric form was found in the crystals, and the molecular packing shows a sandwich herringbone structure similar to that of normal porphine, whilst some of the spectroscopic properties demonstrate systematic substituent effects by the meso-phenyl groups on the N-confused porphyrin.

Original language	English
Pages (from-to)	3887-3890
Number of pages	4
Journal	European Journal of Organic Chemistry
Issue number	18
DOIs	https://doi.org/10.1002/ejoc.200500485
Publication status	Published - Sept 12 2005

All Science Journal Classification (ASJC) codes

Physical and Theoretical Chemistry
Organic Chemistry

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10.1002/ejoc.200500485

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AU - Taniguchi, Shozo

AU - Osuka, Atsuhiro

AU - Furuta, Hiroyuki

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N-confused porphine

Abstract

All Science Journal Classification (ASJC) codes

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