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dc.rights.licenseopenen_US
dc.contributor.authorPODJED, Nina
dc.contributor.authorMODEC, Barbara
hal.structure.identifierCentre de Recherche Paul Pascal [CRPP]
dc.contributor.authorCLERAC, Rodolphe
IDREF: 103790411
hal.structure.identifierCentre de Recherche Paul Pascal [CRPP]
dc.contributor.authorROUZIERES, Mathieu
dc.contributor.authorALCAIDE, Mari­a M.
dc.contributor.authorLOPEZ-SERRANO, Joaquin
dc.date.accessioned2022-06-13T14:49:56Z
dc.date.available2022-06-13T14:49:56Z
dc.date.issued2022
dc.identifier.issn1144-0546, 1369-9261en_US
dc.identifier.otherhttps://www.rsc.org/suppdata/d2/nj/d2nj00296e/d2nj00296e1.pdfen_US
dc.identifier.otherhttps://www.rsc.org/suppdata/d2/nj/d2nj00296e/d2nj00296e2.cifen_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/140197
dc.description.abstractEnThe reactions between [Cu(quin)2(H2O)] (quin− = the anionic form of quinoline-2-carboxylic acid) and a series of aliphatic amino alcohols have yielded structurally very diverse copper(II) complexes, labelled a–g. Single-crystal X-ray structure analysis has revealed either intact amino alcohol molecules or amino alcoholate ions serving as ligands. In type a complexes, the amino alcohols are bound in a monodentate manner via NH2. Engagement of both functional groups in coordination was observed for types b and e (a bidentate chelating mode) and type c (a bidentate bridging one) complexes. In view of the strong bidentate chelating coordination of quinaldinate in [Cu(quin)2(H2O)], the formation of homoleptic amino alcohol complexes e was not anticipated. Equally surprising was the transformation of a mononuclear starting material into a one-dimensional (1D) coordination polymer, [Cu(quin)2]n (g). Spontaneous deprotonation of some amino alcohols and coordination of, thus formed, amino alcoholates via both donors also took place. Dinuclear complexes (d) contained two bridging amino alcoholates, whilst bidentate chelating mode was observed for type f. Interestingly, the dinuclear complex exists as two isomers which differ in the position of quinaldinates with respect to the Cu(μ-OR)2Cu core. DFT calculations on isolated syn- and anti-[Cu2(quin)2(3a1pO)2] (3a1pO− = anion of 3-amino-1-propanol) have shown the syn isomer to be more stable. The explanation lies in the intramolecular π⋯π stacking of quinaldinates, possible only in this isomer. Magnetic susceptibility measurements revealed antiferromagnetic interactions between S = 1/2 copper(II) spins in all the studied compounds except in [Cu(quin)2]n (g) for which weak ferromagnetic couplings are detected.
dc.language.isoENen_US
dc.rightsAttribution-NoDerivs 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nd/3.0/us/*
dc.title.enStructural diversity and magnetic properties of copper(||) quinaldinate compounds with amino alcohols
dc.title.alternativeNew J. Chem.en_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1039/D2NJ00296Een_US
dc.subject.halChimie/Matériauxen_US
bordeaux.journalNew Journal of Chemistryen_US
bordeaux.page6899-6920en_US
bordeaux.volume46en_US
bordeaux.hal.laboratoriesCentre de Recherche Paul Pascal (CRPP) - UMR 5031en_US
bordeaux.issue15en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionCNRSen_US
bordeaux.teamMatériaux moléculaires et magnétisme (M3)
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.identifierhal-03648826
hal.version1
hal.exporttrue
dc.rights.ccCC BY-NCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=New%20Journal%20of%20Chemistry&rft.date=2022&rft.volume=46&rft.issue=15&rft.spage=6899-6920&rft.epage=6899-6920&rft.eissn=1144-0546,%201369-9261&rft.issn=1144-0546,%201369-9261&rft.au=PODJED,%20Nina&MODEC,%20Barbara&CLERAC,%20Rodolphe&ROUZIERES,%20Mathieu&ALCAIDE,%20Mari%C2%ADa%20M.&rft.genre=article


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