Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/49121

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dc.contributor.authorFontes, Andrépor
dc.contributor.authorKarimi, Shimapor
dc.contributor.authorHelm, Lotharpor
dc.contributor.authorYulikovc, Maximpor
dc.contributor.authorFerreira, Paula M. T.por
dc.contributor.authorAndré, João P.por
dc.date.accessioned2018-01-10T10:46:26Z-
dc.date.available2018-01-10T10:46:26Z-
dc.date.issued2015-03-
dc.identifier.issn1434-1948por
dc.identifier.urihttps://hdl.handle.net/1822/49121-
dc.description.abstractThe need for MRI contrast agents with improved relaxivity maintains the development of new Gd(III) chelates an intensive and demanding field of research. In this work we introduce the new dimeric chelators bis(DOTA-AHA)adipate and bis(DOTA-AHA)1,3-phenyldiacetate (L2 = bis(1,4,7,10-tetraazacyclododecane-1-((6-amino)hexanoic)-4,7,10-triacetic acid)adipate and L3 = bis(1,4,7,10-tetraazacyclododecane-1-((6-amino)hexanoic)-4,7,10-triacetic acid)1,3-phenyldiacetate, respectively), based on the bifunctional ligand DOTA-AHA (L1 = 1,4,7,10-tetraazacyclododecane-1-((6-amino)hexanoic)-4,7,10-triacetic acid). Their Gd(III) chelates were studied by variable temperature 1H NMRD and 17O NMR spectroscopy in order to measure the relaxivity and the parameters that govern it. The exchange of inner-sphere water from the monomer GdL1 and from the two binuclear chelates Gd2L2 and Gd2L3 is very similar (298kex ≈ 6.5 x106 s-1) and slightly faster than on [Gd(DOTA)H2O]- (298kex = 4.1 x 106 s-1). All three compounds form weakly bound aggregates with equilibrium constants 298K of 2.9, 15.6 and 14.6 for GdL1, Gd2L2 and Gd2L3, respectively. Even if the aggregates contain only 10 to 15% of the total amount of Gd(III) ions a marked increase in relaxivity between 30 and 100 MHz is observed. Furthermore the distance between the two Gd(III) centers in the binuclear compounds has been determined by double electron-electron resonance (DEER) experiments and by molecular modelling studies affording comparable distances. The linkers between the chelating moieties allow Gd(III)-Gd(III) distances of circa 3.0 nm for completely stretched linker conformation and ≤ 1.9 nm for the conformation with the metal centers at closer distance. These metal to metal distances by themselves cannot explain the considerably long tumbling times of chelates in solution. Only a model consistent with some level of aggregation for the binuclear chelates in aqueous solution could satisfactorily explain our results.por
dc.description.sponsorshipThe authors thank the Foundation for Science and Technology (FCT–Portugal) for financial support through the NMR Portuguese network (Bruker 400 Avance III-Univ Minho); FCT and FEDER (European Fund for Regional Development)- COMPETE/QREN/EU for financial support through the research unity PEstC/QUI/UI686/2013 and the PhD grant attributed to André Fontes (SFRH/BD/63676/2009) also financed by the POPH and FSE. SK and LH thank the Swiss National Science Foundation for financial support.por
dc.language.isoengpor
dc.publisherWileypor
dc.relationinfo:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBD%2F63676%2F2009/PTpor
dc.rightsopenAccesspor
dc.subjectDOTApor
dc.subjectGadoliniumpor
dc.subjectBinuclearpor
dc.subjectDO3Apor
dc.subjectMRIpor
dc.subjectContrast agentspor
dc.subjectChelatespor
dc.subjectImaging agentspor
dc.subjectMacrocyclespor
dc.subjectDinuclear complexespor
dc.titleBinuclear DOTA-based Gd(III) chelates: revisiting a straightforward strategy for relaxivity improvementpor
dc.typearticlepor
dc.peerreviewedyespor
oaire.citationStartPage1579por
oaire.citationEndPage1591por
oaire.citationIssue9por
oaire.citationVolume2015por
dc.identifier.doi10.1002/ejic.201403159por
dc.subject.fosCiências Naturais::Ciências Químicaspor
dc.description.publicationversioninfo:eu-repo/semantics/publishedVersionpor
dc.subject.wosScience & Technologypor
sdum.journalEuropean Journal of Inorganic Chemistrypor
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