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Issue 36, 2012
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Azaphthalocyanines with fused triazolo rings: formation of sterically stressed constitutional isomers

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Abstract

The presented work deals with synthesis and isolation of constitutional isomers of triazolo-fused azaphthalocyanines. Distribution of the isomers did not follow the statistical calculations due to steric effects of the substituents preferring the least sterically stressed C4h isomer.

Graphical abstract: Azaphthalocyanines with fused triazolo rings: formation of sterically stressed constitutional isomers

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Publication details

The article was received on 09 Feb 2012, accepted on 09 Mar 2012 and first published on 09 Mar 2012


Article type: Communication
DOI: 10.1039/C2CC30942D
Citation: Chem. Commun., 2012,48, 4326-4328
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    Azaphthalocyanines with fused triazolo rings: formation of sterically stressed constitutional isomers

    V. Novakova, J. Roh, P. Gela, J. Kuneš and P. Zimcik, Chem. Commun., 2012, 48, 4326
    DOI: 10.1039/C2CC30942D

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