The renaissance in optical spectroscopy of phthalocyanines and other tetraazaporphyrins

Author:

Nyokong Tebello1,Isago Hiroaki2

Affiliation:

1. Department of Chemistry, Rhodes University, Grahamstown 6140, South Africa

2. National Institute for Materials Science (NIMS), 1-2-1, Sengen, Tsukuba, Ibaraki, 305-0047, Japan

Abstract

Spectral properties of metallophthalocyanines and other tetraazaporphyrins are governed mainly by the Q band which originates from the π-π* transitions within the ring. The position and intensity of the Q band is important in tailoring new phthalocyanine derivatives for particular applications. Aggregation, the nature of the central metal, π conjugation, symmetry of the molecules, and axial, peripheral or non-peripheral substitutions affect the spectra and hence the properties of the phthalocyanine molecule. This review gives a brief outline on how optical spectroscopy provides useful informations on molecular and electronic structures, chemistry and physics of phthalocyanines and other tetraazaporphyrins.

Publisher

World Scientific Pub Co Pte Lt

Subject

General Chemistry

Reference70 articles.

1. M. J. Stillman and T. Nyokong, Phthalocyanines: Properties and Applications 1, eds. C. C. Leznoff and A. B. P. Lever (VCH, New York, 1989) pp. 133–291.

2. Phthalocyanines

3. Electronic Structures of Metal Phthalocyanine and Porphyrin Complexes from Analysis of the UV–Visible Absorption and Magnetic Circular Dichroism Spectra and Molecular Orbital Calculations

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