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ESR spin-trap study of the radicals present during the thermolysis of some novel alkyl peroxy esters.

Research output: Contribution to journalJournal article


<mark>Journal publication date</mark>10/2000
<mark>Journal</mark>Magnetic Resonance in Chemistry
Number of pages8
<mark>Original language</mark>English


The thermolysis of four alkylperoxy esters was undertaken at various temperatures between 300 and 353 K and the radicals generated were trapped employing DMPO, DEPMPO, PBN-d14 and TTBNB. The adducts of a range of second-generation carbon-centred radicals, formed via decarboxylation of the acyloxyl moiety, including those of the 2,4,4-trimethylpentyl and hept-3-yl radicals, were also observed. The co-generated tert-alkoxyl radicals, released during the thermolysis of tert-butylperoxy-3,3,5-trimethylhexanoate, tert-amylperoxy-2-ethylhexanoate and the bifunctional peroxide 2,5-dimethyl-2,5-bis(2-ethylhexanoylperoxy)hexane, were all successfully trapped, as were a range of second-generation carbon-centred radicals formed following -scission of these tert-alkoxyl radicals.