An EPR analysis of β-dimerization in α-blocked pyrroles in oxidant conditions

Copyright © 2011 John Wiley & Sons, Ltd.

Bibliographische Detailangaben
Veröffentlicht in:Magnetic resonance in chemistry : MRC. - 1985. - 49(2011), 4 vom: 01. Apr., Seite 164-7
1. Verfasser: Julià, Luis (VerfasserIn)
Weitere Verfasser: Rius, Jordi, Torrelles, Xavier
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2011
Zugriff auf das übergeordnete Werk:Magnetic resonance in chemistry : MRC
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Fluoroacetates Free Radicals Oxidants Pyrroles thallium trifluoroacetate 23586-53-0 Thallium AD84R52XLF mehr... Trifluoroacetic Acid E5R8Z4G708
Beschreibung
Zusammenfassung:Copyright © 2011 John Wiley & Sons, Ltd.
Electron paramagnetic resonance (EPR) analysis of neutral and acidic solutions of 2,5-dimethyl-1-phenylpyrrol (1) and meta-, para-, and ortho-bis(2,5-dimethylpyrrol-1-yl)benzenes (4-6) in the presence of Tl(III) trifluoroacetate as oxidant reveals the poor stability of their generated monomeric radical cations which dimerize through C(β)-C(β) bond formation. EPR spectra of the monomeric radical cations 4(•+) , 5(•+) , and 6(•+) coincide with that of 1(•+) , suggesting that the unpaired electron in these charged species is confined in one of the pyrrolic rings. The very twisted angles between pyrrolic and phenyl planes due to steric hindrance in the X-ray analysis of the molecular structure of 4 confirm the absence of extended conjugation in the π-system
Beschreibung:Date Completed 01.08.2011
Date Revised 21.11.2013
published: Print-Electronic
Citation Status MEDLINE
ISSN:1097-458X
DOI:10.1002/mrc.2710