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hal.structure.identifierLaboratoire Physico-Chimie Industrielle du Médicament [LPCIM]
dc.contributor.authorESPEAU, Philippe
hal.structure.identifierLaboratoire Ondes et Matière d'Aquitaine [LOMA]
dc.contributor.authorNÉGRIER, Philippe
hal.structure.identifierLaboratoire de chimie physique, Faculté de Pharmacie
dc.contributor.authorALLOUCHI, Hassan
hal.structure.identifierLaboratoire Physico-Chimie Industrielle du Médicament [LPCIM]
dc.contributor.authorCEOLIN, René
dc.date.created2011-01-24
dc.date.issued2011
dc.identifier.issn1528-7483
dc.description.abstractEnZn(II) L- and DL-pidolates diaqua complexes dehydrate at around 407 K, leading to amorphous anhydrous complexes. Only amorphous anhydrous Zn(II) L-pidolate was found to crystallize on heating into a crystalline anhydrous phase whose crystal structure was solved from a high-resolution X-ray powder diffraction pattern. Orthorhombic anhydrous Zn(II) L-pidolate exhibits a structure in which (4 + 2)-coordinated Zn atoms (with four usual and two additional Zn-O distances of 2.53 and 2.69 Å) and L-pidolate ligands alternate so as to form a three-dimensional polymerized network. Room-temperature rehydration processes under saturating water vapor for amorphous and crystalline anhydrous complexes were found to be different from each other, although they all led back to crystalline diaqua complexes whose relative stabilities were inferred from measurements of their solubilities in water.
dc.language.isoen
dc.publisherAmerican Chemical Society
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/
dc.subject.enCRYSTAL-STRUCTURE
dc.subject.enPHASE-CHANGE
dc.subject.enDEHYDRATION
dc.subject.enKINETICS
dc.title.enSolid-State Characterization of Enantiomeric and Racemic Hydrated and Anhydrous Zinc-Pidolate Complexes
dc.typeArticle de revue
dc.identifier.doi10.1021/cg2001078
dc.subject.halChimie/Cristallographie
bordeaux.journalCrystal Growth & Design
bordeaux.page3418-3423
bordeaux.volume11
bordeaux.issue8
bordeaux.peerReviewedoui
hal.identifierhal-00617982
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00617982v1
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