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

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
Externally published	Yes

ASJC Scopus subject areas

Chemistry(all)

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10.1246/cl.1999.1303

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title = "A novel naphthalocyanine isomer: A dinaphthophthalocyanine with C2v symmetry",

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.",

author = "Hideya Miwa and Nagao Kobayashi",

year = "1999",

doi = "10.1246/cl.1999.1303",

language = "English",

pages = "1303--1304",

journal = "Chemistry Letters",

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publisher = "Chemical Society of Japan",

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T2 - A dinaphthophthalocyanine with C2v symmetry

AU - Miwa, Hideya

AU - Kobayashi, Nagao

PY - 1999

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N2 - 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.

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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DO - 10.1246/cl.1999.1303

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JO - Chemistry Letters

JF - Chemistry Letters

SN - 0366-7022

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ER -

A novel naphthalocyanine isomer: A dinaphthophthalocyanine with C_2v symmetry

Abstract

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