<i>cis</i>–<i>trans</i>isomerizations and rearrangements during hydrothermal synthesis of metal carboxylates

dc.contributor.authorGraciela Dı́az de Delgado
dc.contributor.authorJan Contreras
dc.contributor.authorL. M. León
dc.contributor.authorMarı́a C. Gutiérrez
dc.contributor.authorJosé Miguel Delgado
dc.coverage.spatialBolivia
dc.date.accessioned2026-03-22T17:27:48Z
dc.date.available2026-03-22T17:27:48Z
dc.date.issued2008
dc.description.abstract9 1 frameworks has grown drastically over the past few years. The use of multifunctional ligands, such as organometallic complexes, permits the introduction of other functionalities within the frameworks. We have synthesized and characterized a series of metal-organometallic framework (MOMF) materials, derived from simple [CpFe-( 6 -arenecarboxylate)] bridging ligands. Depending on the reaction conditions, solid state structures ranging from simple 1D polymer chains to three dimensional square grid structures have been obtained. For example, the reaction of Ni(NO3)26H2O with [CpFe] + -metalated 1,4-benzenedicarboxylic acid (1) results in [Ni3(1-H)4(H2O)2(-H2O)2][NO3]2, a 3D framework material constructed of square grid nickel-carboxylate networks that are interconnected in the third dimension through additional nickel ions. The synthesis, structure and characterization of these materials will be presented.
dc.identifier.doi10.1107/s0108767308084742
dc.identifier.urihttps://doi.org/10.1107/s0108767308084742
dc.identifier.urihttps://andeanlibrary.org/handle/123456789/64321
dc.language.isoen
dc.publisherWiley
dc.relation.ispartofActa Crystallographica Section A Foundations of Crystallography
dc.sourceUniversidad de Los Andes
dc.subjectHydrothermal circulation
dc.subjectMetal
dc.subjectHydrothermal synthesis
dc.subjectChemistry
dc.subjectMaterials science
dc.title<i>cis</i>–<i>trans</i>isomerizations and rearrangements during hydrothermal synthesis of metal carboxylates
dc.typearticle

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