Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/107790
DC FieldValueLanguage
dc.contributor.authorMentel, Kamila K.-
dc.contributor.authorSerra, Arménio-
dc.contributor.authorAbreu, Paulo E.-
dc.contributor.authorArnaut, Luís G.-
dc.date.accessioned2023-08-02T08:54:23Z-
dc.date.available2023-08-02T08:54:23Z-
dc.date.issued2018-07-25-
dc.identifier.issn2041-1723pt
dc.identifier.urihttps://hdl.handle.net/10316/107790-
dc.description.abstractElectron transfer reactions are arguably the simplest chemical reactions but they have not yet ceased to intrigue chemists. Charge-separation and charge-recombination reactions are at the core of life-sustaining processes, molecular electronics and solar cells. Intramolecular electron donor-acceptor systems capture the essential features of these reactions and enable their fundamental understanding. Here, we report intramolecular electron transfers covering a range of 100 kcal mol-1 in exothermicities that show an increase, then a decrease, and finally an increase in rates with the driving force of the reactions. Concomitantly, apparent activation energies change from positive, to negative and finally to positive. Reactions with positive activation energies are found to be faster than analogous reactions with negative effective activation energies. The increase of the reorganization energy with the driving force of the reactions can explain the peculiar free-energy relationship observed in this work.pt
dc.language.isoengpt
dc.publisherSpringer Naturept
dc.relation007630UID/ QUI/00313/2013pt
dc.relationPTDC/QEQ-MED/3521/2014pt
dc.relationSFRH/BD/91209/2012pt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subject.meshKineticspt
dc.subject.meshElectron Transportpt
dc.subject.meshModels, Theoreticalpt
dc.titleHigher activation barriers can lift exothermic rate restrictions in electron transfer and enable faster reactionspt
dc.typearticle-
degois.publication.firstPage2903pt
degois.publication.issue1pt
degois.publication.titleNature Communicationspt
dc.peerreviewedyespt
dc.identifier.doi10.1038/s41467-018-05267-5pt
degois.publication.volume9pt
dc.date.embargo2018-07-25*
uc.date.periodoEmbargo0pt
item.grantfulltextopen-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.openairetypearticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextCom Texto completo-
crisitem.author.researchunitCEMMPRE - Centre for Mechanical Engineering, Materials and Processes-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.orcid0000-0001-8664-2757-
crisitem.author.orcid0000-0003-2393-0203-
crisitem.author.orcid0000-0002-3223-4819-
Appears in Collections:FCTUC Eng.Química - Artigos em Revistas Internacionais
FCTUC Química - Artigos em Revistas Internacionais
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