Please use this identifier to cite or link to this item: http://rdu.iquimica.unam.mx/handle/20.500.12214/1266
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dc.rights.licensehttp://creativecommons.org/licenses/by-nc-nd/4.0es_MX
dc.contributorHerbert Höpfl-
dc.creatorJonathan Román Valdéz-Camacho-
dc.date.accessioned2020-06-11T17:24:21Z-
dc.date.available2020-06-11T17:24:21Z-
dc.date.issued2020-
dc.identifier.urihttp://rdu.iquimica.unam.mx/handle/20.500.12214/1266-
dc.description.abstractThe synthesis of three new mixed chelate copper (II) nitrate coordination compounds of the general formula {[Cu(phen)(L)(solv)NO3 center dot 0-0.5(solv)} is reported, where phen is 1,10-phenanthroline and L is a beta(3)-aminoacidate (beta-alaninate for 1, 3-aminobutanoate for 2 and 3-amino-3-cyclohexylpropanoate for 3), and the solvent (solv) is H2O and/or MeOH. The complexes were characterized by elemental analysis, IR and UV-Vis spectrophotometry, EPR spectroscopy, effective magnetic moment, conductometric and cyclovoltammetric measurements as well as single-crystal X-ray diffraction (SCXRD) analysis. All complexes are mononuclear Cu(II) complexes with d(9) configuration. In solution, the compounds are 1:1 electrolytes and exhibit square-based pyramidal coordination polyhedra. Meanwhile, in the solid state the coordination geometries are square-based pyramidal for compounds 1 and 2, but distorted octahedral for compound 3 due to coordination of the nitrate counterion. In vitro studies revealed that compounds 1, 2 and 3 have growth inhibition activity against MCF-7 and A549 tumor cell lines. The clustering of the experimental half-wave potential values among the three complexes could be explained by the fact of that the substitution pattern was changed on the secondary ligand, while the primary ligand remains without any structural modification.es_MX
dc.language.isoenges_MX
dc.relation.urihttps://www.sciencedirect.com/journal/inorganica-chimica-actaes_MX
dc.rightsinfo:eu-repo/semantics/closedAccesses_MX
dc.sourceInorganica Chimica Acta (ISSN 0020-1693) 506, 119542es_MX
dc.titleSynthesis, structural characterization and antiproliferative activity on MCF-7 and A549 tumor cell lines of [Cu(N-N)(beta(3)-aminoacidate)] NO3 complexes (Casiopeinas (R)es_MX
dc.typeinfo:eu-repo/semantics/articlees_MX
dc.creator.idinfo:eu-repo/dai/mx/orcid/0000-0002-3723-0753es_MX
dc.subject.ctiinfo:eu-repo/classification/cti/2es_MX
dc.subject.keywordsCopper (II) mixed chelatees_MX
dc.subject.keywordsEnantioselective synthesises_MX
dc.subject.keywordsAnticaner activityes_MX
dc.subject.keywordsInduce apoptosises_MX
dc.subject.keywordsMetal-complexeses_MX
dc.subject.keywordsDNAes_MX
dc.subject.keywordsCytotoxicityes_MX
dc.contributor.idinfo:eu-repo/dai/mx/orcid/0000-0002-4027-0131es_MX
dc.contributor.rolecolaboradores_MX
dc.type.urihttps://doi.org/10.1016/j.ica.2020.119542es_MX
dc.creator.twoAdrian Espinoza-Guillen-
dc.creator.threeVirginia Gómez-Vidales-
dc.creator.fourCarlos Alberto Tavira Montalvan-
dc.creator.fiveAngelica Meneses Acosta-
dc.creator.idtwoinfo:eu-repo/dai/mx/orcid/0000-0002-8498-8962es_MX
dc.creator.idthreeinfo:eu-repo/dai/mx/orcid/0000-0003-3070-7085es_MX
dc.creator.idfourinfo:eu-repo/dai/mx/orcid/0000-0002-0927-437Xes_MX
dc.creator.idfiveinfo:eu-repo/dai/mx/orcid/0000-0003-2677-4939es_MX
dc.contributor.oneLena Ruiz-Azuara-
dc.contributor.twoJaime Escalante-
dc.contributor.threeEusebio Juaristi-
dc.contributor.idoneinfo:eu-repo/dai/mx/orcid/0000-0003-3035-4507es_MX
dc.contributor.idtwoinfo:eu-repo/dai/mx/orcid/0000-0001-5485-0244es_MX
dc.contributor.idthreeinfo:eu-repo/dai/mx/orcid/0000-0003-0936-7020es_MX
dc.contributor.roleonecolaboradores_MX
dc.contributor.roletwocolaboradores_MX
dc.contributor.rolethreecolaboradores_MX
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