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hal.structure.identifierInstitut des Sciences Moléculaires [ISM]
hal.structure.identifierLaboratoire Ondes et Matière d'Aquitaine [LOMA]
dc.contributor.authorDENISOV, Sergey A.
hal.structure.identifierInstitut des Sciences Moléculaires [ISM]
dc.contributor.authorYU, Shinlin
hal.structure.identifierInstitut des Sciences Moléculaires [ISM]
dc.contributor.authorPOZZO, Jean-Luc
hal.structure.identifierLaboratoire Ondes et Matière d'Aquitaine [LOMA]
dc.contributor.authorJONUSAUSKAS, Gediminas
hal.structure.identifierInstitut des Sciences Moléculaires [ISM]
dc.contributor.authorMCCLENAGHAN, Nathan D.
dc.date.created2016-02-08
dc.date.issued2016
dc.identifier.issn1439-4235
dc.description.abstractEnReversible electronic energy transfer (REET) may be instilled in bi-/multichromophoric molecule-based systems, following photoexcitation, upon judicious structural integration of matched chromophores. This leads to a new set of photophysical properties for the ensemble, which can be fully characterized by steady-state and time-resolved spectroscopic methods. Herein, we take a comprehensive look at progress in the development of this type of supermolecule in the last five years, which has seen systems evolve from covalently tethered dyads to synthetic molecular machines, exemplified by two different pseudorotaxanes. Indeed, REET holds promise in the control of movement in molecular machines, their assembly/disassembly, as well as in charge separation.
dc.description.sponsorshipArchitectures à base de foldamères pour le transport d'electrons - ANR-12-BS08-0007
dc.language.isoen
dc.publisherWiley-VCH Verlag
dc.rights.urihttp://creativecommons.org/licenses/by-nc/
dc.subject.enFoldaxanes
dc.subject.enMolecular machines
dc.subject.enReversible electronic energy transfer
dc.subject.enTime-resolved spectroscopy
dc.subject.enTransition metal complexes
dc.title.enHarnessing Reversible Electronic Energy Transfer: From Molecular Dyads to Molecular Machines
dc.typeArticle de revue
dc.identifier.doi10.1002/cphc.201600137
dc.subject.halChimie/Chimie théorique et/ou physique
bordeaux.journalChemPhysChem
bordeaux.page1794-1804
bordeaux.volume17
bordeaux.issue12
bordeaux.peerReviewedoui
hal.identifierhal-01391653
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-01391653v1
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