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Issue 7, 1997
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Substituted α,β,γ-triazatetrabenzcorrole: an unusual reduction product of a phthalocyanine

Abstract

4,5-Dipentyldiiminoisoindoline 1 reacts with hexachlorodisilane (Si 2 Cl 6 ) to give the ring-contracted hydroxysilicon-α,β,γ-triazatetrabenzcorrole 4 which in solution photolyses giving the ring cleavage compounds 5 and 6; the stability of triazatetrabenzcorroles 4 and 7 with silicon and germanium as central elements is studied by UV–VIS spectroscopy.

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Article information


Chem. Commun., 1997, 679-680
Article type
Paper

Substituted α,β,γ-triazatetrabenzcorrole: an unusual reduction product of a phthalocyanine

J. Li, L. R. Subramanian and M. Hanack, Chem. Commun., 1997, 679
DOI: 10.1039/A700532F

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