Issue 36, 2012

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

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

Supplementary files

Article information

Article type
Communication
Submitted
09 Feb 2012
Accepted
09 Mar 2012
First published
09 Mar 2012

Chem. Commun., 2012,48, 4326-4328

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

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements