## Abstract During UV.‐irradiation of aliphatic carboxylic acids and esters in aqueous and nonaqueous solutions various alkyl and acyl type radicals derived from parent compounds and solvents have been observed by ESR.‐spectroscopy. The structures of the radicals point to α‐cleavage, β‐dehalogenati
Photochemical free radical formation from aliphatic dicarboxylic acids in solution as studied by electron spin resonance spectroscopy
✍ Scribed by Lotty Wymann; Tony Kaiser; Henning Paul; Hanns Fischer
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- German
- Weight
- 676 KB
- Volume
- 64
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
Various free radicals formed during UV.‐irradiation of aliphatic dicarboxylic acids in aqueous and methanolic solution are identified by ESR.‐spectroscopy. Their structures point to α‐cleavage and photoreduction as the dominant primary photochemical decay processes. The relative contributions of these reactions to the overall photodecomposition depend on solvent and degree of α‐alkylation of the acid. Emission ESR.‐spectra are found for radicals formed by C, CO‐bond cleavage of α‐dimethyl substituted acids. The polarization is referred to the triplet mechanism of CIDEP. and indicates this cleavage reaction occurs from a triplet molecular state.
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