A novel naphthalocyanine isomer: A dinaphthophthalocyanine with C2v symmetry

Hideya Miwa; Nagao Kobayashi

doi:10.1246/cl.1999.1303

A novel naphthalocyanine isomer: A dinaphthophthalocyanine with C_2v symmetry

Hideya Miwa, Nagao Kobayashi

SCI - Chemistry

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

18 Citations (Scopus)

Abstract

An adjacently dinaphtho-substituted phthalocyanine with C_2v symmetry, which is a structural isomer of naphthalocyanines in the sense that eight benzene units are fused to the tetraazaporphyrin skeleton, has been synthesized and characterized by electronic absorption and magnetic circular dichroism spectroscopy, and molecular orbital calculations within the framework of the ZINDO approximation.

Original language	English
Pages (from-to)	1303-1304
Number of pages	2
Journal	Chemistry Letters
Issue number	12
DOIs	https://doi.org/10.1246/cl.1999.1303
Publication status	Published - 1999 Jan 1

ASJC Scopus subject areas

Chemistry(all)

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abstract = "An adjacently dinaphtho-substituted phthalocyanine with C2v symmetry, which is a structural isomer of naphthalocyanines in the sense that eight benzene units are fused to the tetraazaporphyrin skeleton, has been synthesized and characterized by electronic absorption and magnetic circular dichroism spectroscopy, and molecular orbital calculations within the framework of the ZINDO approximation.",

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AB - An adjacently dinaphtho-substituted phthalocyanine with C2v symmetry, which is a structural isomer of naphthalocyanines in the sense that eight benzene units are fused to the tetraazaporphyrin skeleton, has been synthesized and characterized by electronic absorption and magnetic circular dichroism spectroscopy, and molecular orbital calculations within the framework of the ZINDO approximation.

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