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hal.structure.identifierLaboratoire de physique de la matière condensée [LPMC]
dc.contributor.authorHUITOREL, Brendan
hal.structure.identifierLaboratoire de physique de la matière condensée [LPMC]
dc.contributor.authorBENITO, Quentin
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorFARGUES, Alexandre
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorGARCIA, Alain
hal.structure.identifierLaboratoire de physique de la matière condensée [LPMC]
dc.contributor.authorGACOIN, Thierry
hal.structure.identifierLaboratoire de physique de la matière condensée [LPMC]
dc.contributor.authorBOILOT, Jean-Pierre
hal.structure.identifierLaboratoire de physique de la matière condensée [LPMC]
dc.contributor.authorPERRUCHAS, Sandrine
hal.structure.identifierInstitut des Sciences Chimiques de Rennes [ISCR]
dc.contributor.authorCAMEREL, Franck
dc.date.issued2016-11-22
dc.identifier.issn0897-4756
dc.description.abstractEnMolecular copper iodide clusters with the [Cu4I4] cubane core have been functionalized by phosphine ligands carrying protomesogenic gallate-based derivatives bearing either long alkyl chains (C8, C12, and C16) or cyanobiphenyl (CBP) fragments. The mesomorphic properties of the functionalized clusters were studied by combining differential scanning calorimetry (DSC), polarized optical microscopy (POM), and small-angle X-ray scattering (SAXS) experiments. Whereas clusters functionalized solely with long alkyl chains present amorphous or crystalline states, the cluster carrying CBP fragments displays liquid crystal properties with the formation of a smectic A mesophase from room temperature up to 100 °C. Temperature-dependent photoluminescence measurements show that the CBP derivative displays an unusual luminescence thermochromism which is possibly due to a resonance energy transfer mechanism between the emissive [Cu4I4] inorganic and CBP moieties. The emission properties of this original cluster are also sensitive to variation of local order of the molecular assembly. Moreover, the liquid crystalline properties imported on the inorganic core allow for a facile deformation of its local environment, leading to mechanochromic properties related to modulation of intramolecular interactions. Indeed, mechanical constraints on the molecularly self-assembled structure induce changes at the molecular level by modification of the [Cu4I4] inorganic cluster core geometry and in particular of the strength of the cuprophilic interactions.
dc.language.isoen
dc.publisherAmerican Chemical Society
dc.subject.enCopper
dc.subject.enCrystalline materials
dc.subject.enDifferential scanning calorimetry
dc.subject.enEnergy transfer
dc.subject.enLigands
dc.subject.enLiquid crystals
dc.subject.enLiquids
dc.subject.enLuminescence
dc.subject.enPhosphorus compounds
dc.subject.enX ray scattering
dc.subject.enIntramolecular interactions
dc.subject.enLiquid crystalline properties
dc.subject.enMechanical constraints
dc.subject.enMechanochromic properties
dc.subject.enPolarized optical microscopy
dc.subject.enResonance energy transfer
dc.subject.enSelf assembled structures
dc.subject.enTemperature dependent photoluminescences
dc.subject.enCopper compounds
dc.title.enMechanochromic luminescence and liquid crystallinity of molecular copper clusters
dc.typeArticle de revue
dc.identifier.doi10.1021/acs.chemmater.6b03002
dc.subject.halChimie
bordeaux.journalChemistry of Materials
bordeaux.page8190--8200
bordeaux.volume28
bordeaux.issue22
bordeaux.peerReviewedoui
hal.identifierhal-01416449
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-01416449v1
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