SUBSTITUENT EFFECTS ON THE ZERO-FIELD SPLITTING PARAMETERS OF LOCALIZED TRIPLET 1,3-CYCLOPENTANEDIYL BIRADICALS

Citation
W. Adam et al., SUBSTITUENT EFFECTS ON THE ZERO-FIELD SPLITTING PARAMETERS OF LOCALIZED TRIPLET 1,3-CYCLOPENTANEDIYL BIRADICALS, Angewandte Chemie, International Edition in English, 32(9), 1993, pp. 1339-1340
Citations number
20
Categorie Soggetti
Chemistry
ISSN journal
05700833
Volume
32
Issue
9
Year of publication
1993
Pages
1339 - 1340
Database
ISI
SICI code
0570-0833(1993)32:9<1339:SEOTZS>2.0.ZU;2-6
Abstract
Information about the reactivity of the corresponding monoradicals is provided by the D parameters of the biradicals 1. The zero-field split ting parameter D, which can be obtained from the EPR spectrum of a loc alized triplet biradical, increases with the inverse cube of the avera ge distance between the unpaired spins. For para-substituted, bisbenzy lic triplet 1,3-cyclopentanediyls 1, the D parameter varies measurably depending on the substituents X.