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dc.rights.licenseopenen_US
dc.contributor.authorPELKA, Robert
dc.contributor.authorSTEFANCZYK, Olaf
dc.contributor.authorMAJCHER-FITAS, Anna Malgorzata
hal.structure.identifierCentre de Recherche Paul Pascal [CRPP]
dc.contributor.authorMATHONIERE, Corine
dc.contributor.authorSIEKLUCKA, Barbara
dc.date.accessioned2022-06-16T13:54:24Z
dc.date.available2022-06-16T13:54:24Z
dc.date.issued2022
dc.identifier.issn3048853en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/140245
dc.description.abstractEn[Cu(enpnen)]2[Mo(CN)8]7H2O (enpnen = N,N - bis(2- aminoethyl)- 1,3 - propane-diamine) molecular cluster compound (1) was subject to a series of irradiations with the light of 405 nm. On irradiation isothermal magnetization at 1.8 and 5 K in the field range 0–70 kOe as well as magnetic susceptibility in the temperature range of 2–300 K were subsequently detected. Both types of magnetic signals were next analyzed assuming that the irradiation triggers two independent processes: the metal to metal charge transfer (MMCT) leading to a state with the Arrhenius-type relaxation and the spin crossover (SC) transition ending in a state whose relaxation displays a threshold behavior. The first mechanism leads to an electron from the spinless Mo(IV) configuration being transferred to one of the Cu(II) ions transforming the trimer into the state Cu(II)-N-C-Mo(V)-C-N-Cu(I), with spin 1/2 on the Mo(V) ion and the spinless Cu(I) ion. The other mechanism gives rise to an excited paramagnetic Mo(IV) linked to two paramagnetic Cu(II) centers with a possible superexchange interaction. The spin of the excited Mo(IV) species is equal to 1 and associated to a disruption of the 5s-electronic pair. A reasonable result of simultaneous fitting the full series of susceptibility and magnetization data to the model taking into account both mechanisms corroborates their presence.
dc.language.isoENen_US
dc.subject.enPhotomagnetism
dc.subject.enOctacyanidometallates
dc.subject.enSusceptibility
dc.subject.enMagnetization
dc.subject.enRelaxation
dc.title.enTowards rationalizing photoswitchable behavior of Cu 2 II Mo IV cyanido-bridged molecule
dc.title.alternativeJ. Magn. Magn. Mater
dc.typeArticle de revueen_US
dc.identifier.doi10.1016/j.jmmm.2021.168697en_US
dc.subject.halChimie/Matériauxen_US
dc.identifier.arxiv2111.11822v1
bordeaux.journalJournal of Magnetism and Magnetic Materialsen_US
bordeaux.page168697en_US
bordeaux.volume544en_US
bordeaux.hal.laboratoriesCentre de Recherche Paul Pascal (CRPP) - UMR 5031en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionCNRSen_US
bordeaux.teamMatériaux moléculaires et magnétisme (M3)
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.identifierhal-03697247
hal.version1
hal.exporttrue
dc.rights.ccPas de Licence CCen_US
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