Azaphthalocyanines with fused triazolo rings: formation of sterically stressed constitutional isomers
Language English Country Great Britain, England Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
22441509
DOI
10.1039/c2cc30942d
Knihovny.cz E-resources
- MeSH
- Indoles chemistry MeSH
- Isoindoles MeSH
- Isomerism MeSH
- Spectrum Analysis MeSH
- Triazoles chemistry MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Indoles MeSH
- Isoindoles MeSH
- phthalocyanine MeSH Browser
- Triazoles MeSH
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 C(4h) isomer.
References provided by Crossref.org
Tuning Electron-Accepting Properties of Phthalocyanines for Charge Transfer Processes
