Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/20132
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dc.contributor.authorOlivella, Santiago-
dc.contributor.authorSolé, Albert-
dc.date.accessioned2010-01-18T11:28:29Z-
dc.date.available2010-01-18T11:28:29Z-
dc.date.issued2003-08-06-
dc.identifier.citationJournal of the American Chemical Society 125(35): 10641-10650 (2004)en_US
dc.identifier.issn0002-7863-
dc.identifier.urihttp://hdl.handle.net/10261/20132-
dc.description10 pages, 8 figures, 5 tables.-- PMID: 12940748 [PubMed].-- Printed version published Sep 3, 2003.-- Supporting information available at: http://pubs.acs.org/doi/suppl/10.1021/ja030171een_US
dc.description.abstractThe three pathways postulated for 1,3-migration of the peroxyl group in the allylperoxyl radical (1a), a key reaction involved in the spontaneous autoxidation of unsaturated lipids of biological importance, have been investigated by means of quantum mechanical electronic structure calculations. According to the barrier heights calculated from RCCSD(T)/6-311+G(3df,2p) energies with optimized molecular geometries and harmonic vibrational frequencies determined at the UMP2/6-311+G(3df,2p) level, the allylperoxyl rearrangement proceeds by fragmentation of 1a through a transition structure (TS1) with a calculated ΔH(298 K) of 21.7 kcal/mol to give an allyl radical−triplet dioxygen loosely bound complex (CX). In a subsequent step, the triplet dioxygen moiety of CX recombines at either end of the allyl radical moiety to convert the complex to the rearranged peroxyl radical (1a‘) or to revert to the starting peroxyl radical 1a. CX shows an electron charge transfer of 0.026 e in the direction allyl → O2. The dominant attractive interactions holding in association the allyl radical−riplet dioxygen pair in CX are due chiefly to dispersion forces. The ΔH(298 K) for dissociation of CX in its isolated partners, allyl radical and triplet dioxygen, is predicted to be at least 1 kcal/mol. The formation of CX prevents the diffusion of its partners and maintains the stereocontrol along the fragmentation-recombination processes. The concerted 1,3-migration in allylperoxyl radical is predicted to take place through a five-membered ring peroxide transition structure (TS2) showing two long C−O bonds. The ΔH‡(298 K) calculated for this pathway is less favorable than the fragmentation−recombination pathway by 1.9 kcal/mol. The cyclization of 1a to give a dioxolanyl radical intermediate (2a) is found to proceed through a five-membered ring transition structure (TS3) with a calculated ΔH‡(298 K) of 33.9 kcal/mol. Thus, the sequence of ring closure 1a → 2a and ring opening 2a → 1a‘ is unlikely to play any significant role in allylperoxyl rearrangement 1a → 1a‘. In the three pathways investigated, the energy of the transition structure is predicted to be somewhat lower in either heptane or aqueous solution than in the gas phase. Although the energy lowering calculated for TS1 is smaller than the calculated for TS2 and TS3, it is very unlikely that the solvent effects may reverse the predicted preference of the fragmentation−recombination pathway over the concerted and stepwise ring closure-ring opening mechanisms.en_US
dc.description.sponsorshipThis research was supported by the Spanish DGICYT (Grants PB98-1240-C02-01, BQU2002-04485-C02-01, and BQU2002-04485-C02-02). Additional support came from Catalonian CIRIT (Grant 2001SGR00048).en_US
dc.format.extent22195 bytes-
dc.format.mimetypeapplication/pdf-
dc.language.isoengen_US
dc.publisherAmerican Chemical Societyen_US
dc.rightsclosedAccessen_US
dc.subjectAllylperoxyl radicalsen_US
dc.subjectPotential Energy Surface (PES)en_US
dc.subjectAllylperoxyl rearrangementen_US
dc.titleMechanism of 1,3-migration in allylperoxyl radicals: computational evidence for the formation of a loosely bound radical-dioxygen complexen_US
dc.typeartículoen_US
dc.identifier.doi10.1021/ja030171e-
dc.description.peerreviewedPeer revieweden_US
dc.relation.publisherversionhttp://dx.doi.org/10.1021/ja030171een_US
dc.identifier.e-issn1520-5126-
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
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item.cerifentitytypePublications-
item.grantfulltextnone-
item.languageiso639-1en-
item.openairetypeartículo-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
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