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dc.contributor.authoribañez, susana
dc.contributor.authorMihály , Béla
dc.contributor.authorSanz Miguel, Pablo J.
dc.contributor.authorSteinborn, Dirk
dc.contributor.authorPretzer, Irene
dc.contributor.authorHiller, Wolf
dc.contributor.authorLippert, Bernhard
dc.date.accessioned2016-10-19T10:06:15Z
dc.date.available2016-10-19T10:06:15Z
dc.date.issued2015
dc.identifier.citationIBÁÑEZ, Susana, et al. The Challenge of Deciphering Linkage Isomers in Mixtures of Oligomeric Complexes Derived from 9‐Methyladenine and trans‐(NH3) 2PtII Units. Chemistry–A European Journal, 2015, vol. 21, no 15, p. 5794-5806.ca_CA
dc.identifier.issn0947-6539
dc.identifier.issn1521-3765
dc.identifier.urihttp://hdl.handle.net/10234/163660
dc.description.abstractMetal coordination to N9-substituted adenines, such as the model nucleobase 9-methyladenine (9MeA), under neutral or weakly acidic pH conditions in water preferably occurs at N1 and/or N7. This leads, not only to mononuclear linkage isomers with N1 or N7 binding, but also to species that involve both N1 and N7 metal binding in the form of dinuclear or oligomeric species. Application of a trans-(NH3)2PtII unit and restriction of metal coordination to the N1 and N7 sites and the size of the oligomer to four metal entities generates over 50 possible isomers, which display different feasible connectivities. Slowly interconverting rotamers are not included in this number. Based on 1H NMR spectroscopic analysis, a qualitative assessment of the spectroscopic features of N1,N7-bridged species was attempted. By studying the solution behavior of selected isolated and structurally characterized compounds, such as trans-[PtCl(9MeA-N7)(NH3)2]ClO4⋅2H2O or trans,trans-[{PtCl(NH3)2}2(9MeA-N1,N7)][ClO4]2⋅H2O, and also by application of a 9MeA complex with an (NH3)3PtII entity at N7, [Pt(9MeA-N7)(NH3)3][NO3]2, which blocks further cross-link formation at the N7 site, basic NMR spectroscopic signatures of N1,N7-bridged PtII complexes were identified. Among others, the trinuclear complex trans-[Pt(NH3)2{μ-(N1-9MeA-N7)Pt(NH3)3}2][ClO4]6⋅2H2O was crystallized and its rotational isomerism in aqueous solution was studied by NMR spectroscopy and DFT calculations. Interestingly, simultaneous PtII coordination to N1 and N7 acidifies the exocyclic amino group of the two 9MeA ligands sufficiently to permit replacement of one proton each by a bridging heterometal ion, HgII or CuII, under mild conditions in water.ca_CA
dc.description.sponsorShipThis work was supported by the Deutsche Forschungsgemeinschaft, the Spanish Ministerio de Economía y Competitividad [CTQ2011-27593, “Ramón y Cajal” program (P.J.S.M.), and a postdoctoral fellowship (S.I.)]. We are grateful to Dr. M. Bette (University of Halle) for the structural solution of complex [2][NO3].ca_CA
dc.format.extent13 p.ca_CA
dc.format.mimetypeapplication/pdfca_CA
dc.language.isoengca_CA
dc.publisherJohn Wiley & Sonsca_CA
dc.relation.isPartOfChemistry–A European Journal, 2015, vol. 21, no 15ca_CA
dc.rightsCopyright © by John Wiley & Sonsca_CA
dc.subjectadenineca_CA
dc.subjectbridging ligandsca_CA
dc.subjectlinkage isomerismca_CA
dc.subjectplatinumca_CA
dc.subjectpurinesca_CA
dc.titleThe Challenge of Deciphering Linkage Isomers in Mixtures of Oligomeric Complexes Derived from 9-Methyladenine and trans-(NH3)2PtII Unitsca_CA
dc.typeinfo:eu-repo/semantics/articleca_CA
dc.identifier.doihttp://dx.doi.org/10.1002/chem.201406378
dc.rights.accessRightsinfo:eu-repo/semantics/restrictedAccessca_CA
dc.relation.publisherVersionhttp://onlinelibrary.wiley.com/doi/10.1002/chem.201406378/fullca_CA


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