dc.contributor.author | Pérez Fernández, Iñigo | |
dc.contributor.author | Serrano Larrea, Edurne | |
dc.contributor.author | Bazán Blau, Begoña del Pilar  | |
dc.contributor.author | Barandika Argoitia, Miren Gotzone  | |
dc.contributor.author | Urtiaga Greaves, Miren Karmele  | |
dc.contributor.author | Arriortua Marcaida, María Isabel  | |
dc.date.accessioned | 2020-02-04T08:34:53Z | |
dc.date.available | 2020-02-04T08:34:53Z | |
dc.date.issued | 2019-11-09 | |
dc.identifier.citation | Molecules 24(22) : (2019) // Article ID 4059 | es_ES |
dc.identifier.issn | 1420-3049 | |
dc.identifier.uri | http://hdl.handle.net/10810/40407 | |
dc.description | This article belongs to the Section Inorganic Chemistry. | es_ES |
dc.description.abstract | Ionothermal synthesis is a little used method for the preparation of coordination polymers. By this method, two cadmium compounds were synthesized, 1, with formula Cd-3(ox)F-2(Ina)(2) (Ina = isonicotinate) and 2, Cd(NO3)(2)(4,4 ' -Bpy) (4,4 ' -Bpy = 4,4 ' -Bipyridine). The modification of the reaction conditions has allowed to obtain 2 as a pure phase. The structure of both compounds was determined by a single-crystal X-ray diffraction. Compound 1 is isostructural to the previously reported Cd2Zn(ox)(OH)(2)(Ina)(2). It crystallizes in the monoclinic space group P2(1)/n and present a three-dimensional (3D) network, built-up from [Cd-3(ox)F-2](n)(2n+) layers, linked by isonicotinate ligands. Crystals of 2 are formed by twins of two components which are rotated ca. 180 degrees to each other. This compound crystallizes in the triclinic P-1 space group and its structure can be describe as a two-dimensional (2D) 4 connected 'sql' net. The layers are composed by [Cd(NO3)(2)](n) chains linked through 4,4 ' -Bpy ligands, and are pillared along the [011] direction. The thermal decomposition of 2 was studied by thermogravimetric and thermodiffractiometric techniques. The compound decomposes gradually starting from 160 degrees C, and due to heating, the structure suffers slight reversible changes in the bond distances and angles. | es_ES |
dc.description.sponsorship | This research was funded by Spanish Ministry of Economy and Competitiveness (MINECO) through projects MAT2016-76739-R (AEI/FEDER, EU) and by the University of the Basque Country (UPV/EHU) through the GIU18/197 research group funding. | es_ES |
dc.language.iso | eng | es_ES |
dc.publisher | MDPI | es_ES |
dc.relation | info:eu-repo/grantAgreement/MINECO/MAT2016-76739-R | es_ES |
dc.rights | info:eu-repo/semantics/openAccess | es_ES |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/es/ | * |
dc.subject | cadmium coordination polymers | es_ES |
dc.subject | ionothermal synthesis | es_ES |
dc.subject | crystal structure determination | es_ES |
dc.subject | metal-organic frameworks | es_ES |
dc.subject | molecular recognition | es_ES |
dc.subject | crystal-structure | es_ES |
dc.subject | symmetry | es_ES |
dc.subject | design | es_ES |
dc.subject | cation | es_ES |
dc.subject | shape | es_ES |
dc.title | Ionothermal Synthesis of Cadmium Coordination Polymers: Ionic Liquid Effects on the Synthesis, Structural, and Thermal Characterization | es_ES |
dc.type | info:eu-repo/semantics/article | es_ES |
dc.rights.holder | This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited | es_ES |
dc.rights.holder | Atribución 3.0 España | * |
dc.relation.publisherversion | https://www.mdpi.com/1420-3049/24/22/4059 | es_ES |
dc.identifier.doi | 10.3390/molecules24224059 | |
dc.departamentoes | Mineralogía y petrología | es_ES |
dc.departamentoes | Química inorgánica | es_ES |
dc.departamentoeu | Kimika ez-organikoa | es_ES |
dc.departamentoeu | Mineralogia eta petrologia | es_ES |