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dc.contributor.authorOrive, Joseba
dc.contributor.authorFernández De Luis, Roberto
dc.contributor.authorRodríguez Fernández, Jesús 
dc.contributor.authorLegarra, Estibaliz
dc.contributor.authorPlazaola Muguruza, Fernando
dc.contributor.authorArricortua Marcaida, María Isabel
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2017-04-28T10:06:19Z
dc.date.available2017-04-28T10:06:19Z
dc.date.issued2014-07
dc.identifier.issn1466-8033
dc.identifier.issn1466-8033
dc.identifier.urihttp://hdl.handle.net/10902/10888
dc.description.abstractThree new fluorinated mixed valence Fe(ii)-Fe(iii) phosphites were synthesized by employing mild hydrothermal conditions. (H4baepn) 0.5[FeIII 2.3FeII 1.7(H2O)2(HPO3) 4-(x+y)(HPO4)x(PO4) yF4] (x ≃ 0.13, y ≃ 0.3) (1) (baepn = N,N′-bis(2-aminoethyl)-1,3-propanediamine (C7N 4H20)) and the Co(ii)-substituted phase with the formula (H4baepn)0.5[FeIII 2.0Fe II 0.71CoII 1.29(H2O) 2(HPO3)4-x(HPO4)xF 4] (x ≃ 0.38) (2) were studied by single crystal X-ray diffraction. The phase with the major content of Co(ii), (H4baepn) 0.5[FeIII 2.0FeII 0.62CoII 1.38(H2O) 2(HPO3)4-x(HPO4)xF 4] (x ≃ 0.38) (3) was obtained as a polycrystalline powder and studied by Rietveld refinement by using the structural model of 2. These compounds were characterized by ICP-Q-MS, thermogravimetric and thermodiffractometric analyses, and XPS, IR, UV/vis and Mössbauer spectroscopy. The single crystal data indicate that phases 1 and 2 crystallize in the P21/c space group with lattice parameters a = 13.6808(4), b = 12.6340(2), c = 12.7830(3) Å and β = 116.983(4)° for 1 and a = 13.6823(4), b = 12.6063(3), c = 12.7535(4) Å and β = 116.988(4)° for 2, with Z = 4. The reciprocal space of 1 shows satellite reflections with a modulation wavevector q = 0.284(2)a* which indicate an incommensurate long-range order. The average structure of these compounds is built up by a 3D lattice constructed by inorganic layers of Fe(iii) chains and Fe(ii) and Co(ii) dimers joined by phosphite groups partially substituted by HPO4 and PO4 tetrahedral groups. These anionic layers stack along the [100] direction encapsulating linear tetramines in eight-membered open channels involving host-guest interactions. Magnetic measurements of 1 and 3 showed antiferromagnetic coupling as the major interactions, exhibiting a weak ferromagnetic component together with a spin glass transition at low temperature in the case of 1. Heat capacity measurements showed a small anomaly at 20.5 K for 1 and a sharp magnetic peak at 28 K for 3. Unexpectedly, the small anomaly observed in 1 increased with the magnetic field and became better defined.es_ES
dc.format.extent14 p.es_ES
dc.language.isoenges_ES
dc.publisherRoyal Society of Chemistry
dc.rights© The Royal Society of Chemistry 2014es_ES
dc.sourceCrystEngComm, 2014, 16(27), 6066-6079es_ES
dc.titleFluorinated mixed valence Fe(ii)-Fe(iii) phosphites with channels templated by linear tetramine chains. Structural and magnetic implications of partial replacement of Fe(ii) by Co(ii)es_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.1039/C4CE00264Des_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1039/c4ce00264d
dc.type.versionacceptedVersiones_ES


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