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hal.structure.identifierInstitut des Sciences Moléculaires [ISM]
dc.contributor.authorDUCROT, Aurélien
hal.structure.identifierInstitut des Sciences Moléculaires [ISM]
dc.contributor.authorVERWILST, Peter
hal.structure.identifierInstitut des Sciences Moléculaires [ISM]
dc.contributor.authorSCARPANTONIO, Luca
hal.structure.identifierInstitut des Sciences Moléculaires [ISM]
dc.contributor.authorGOUDET, Sébastien
hal.structure.identifierInstitut Européen de Chimie et Biologie [IECB]
dc.contributor.authorKAUFFMANN, Brice
hal.structure.identifierInstitut des Sciences Moléculaires [ISM]
hal.structure.identifierLaboratoire Ondes et Matière d'Aquitaine [LOMA]
dc.contributor.authorDENISOV, Sergey A.
hal.structure.identifierLaboratoire Ondes et Matière d'Aquitaine [LOMA]
dc.contributor.authorJONUSAUSKAS, Gediminas
hal.structure.identifierInstitut des Sciences Moléculaires [ISM]
dc.contributor.authorMCCLENAGHAN, Nathan
dc.date.created2012-01-30
dc.date.issued2012-07
dc.identifier.issn1061-0278
dc.description.abstractEnPhotolariat development, as an extension to the family of synthetic photochromic crown ether receptors, or photocrowns, is reported. Incorporated additional chelating groups, namely two anisoles or thioanisoles, contribute in completing the metal ion coordination sphere with different affinities and selectivities for a range of ions. Single-crystal X-ray diffraction analysis suggests that the thermally stable trans-form of the receptor is unsuitable for ion binding, consistent with spectrophotometric and NMR titration results, which is largely improved in the cis-form as the basis for the photocontrolled ion coordination/ejection. In terms of the azobenzene-containing receptor photochemistry, a photostationary state highly enriched in the cis-form (94:6, cis-/trans-) is reached, with slow thermal return (1.1-1.4 × 10− 5 s− 1) in the dark, which can undergo multiple cycles without discernable photodegradation.
dc.language.isoen
dc.publisherTaylor & Francis: STM, Behavioural Science and Public Health Titles
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/
dc.subject.enreceptor
dc.subject.enmacrocycles
dc.subject.enphotochromism
dc.subject.enphotolariat
dc.subject.enazobenzene
dc.title.enPhotolariats: synthesis, metal ion complexation and photochromism
dc.typeArticle de revue
dc.identifier.doi10.1080/10610278.2012.678851
dc.subject.halChimie/Chimie organique
dc.subject.halChimie/Chimie de coordination
dc.description.sponsorshipEuropeCommunication between Functional Molecules using Photocontrolled Ions
bordeaux.journalSupramolecular Chemistry
bordeaux.page462-472
bordeaux.volume24
bordeaux.issue4
bordeaux.peerReviewedoui
hal.identifierhal-00732071
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00732071v1
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