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dc.contributor.author
Venegas-Yazigi, Diego  
dc.contributor.author
Spodine, Evgenia  
dc.contributor.author
Saldias, Marianela  
dc.contributor.author
Vega, Andrés  
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Paredes-García, Verónica  
dc.contributor.author
Calvo, Rafael  
dc.contributor.author
Santana, Ricardo C.  
dc.date.available
2019-06-21T01:47:02Z  
dc.date.issued
2015-04  
dc.identifier.citation
Venegas-Yazigi, Diego; Spodine, Evgenia; Saldias, Marianela; Vega, Andrés; Paredes-García, Verónica; et al.; 1D Magnetic Interactions in CuII Oxovanadium Phosphates, Magnetic Susceptibility, DFT and Single Crystal EPR; American Chemical Society; Inorganic Chemistry; 54; 8; 4-2015; 3805-3814  
dc.identifier.issn
0020-1669  
dc.identifier.uri
http://hdl.handle.net/11336/78614  
dc.description.abstract
We report the crystal face indexing and molecular spatial orientation, magnetic properties, electron paramagnetic resonance (EPR) spectra, and density functional theory (DFT) calculations of two previously reported oxovanadium phosphates functionalized with CuII complexes, namely, [Cu(bipy)(VO2)(PO4)]n (1) and [{Cu(phen)}2(VO2(H2O)2)(H2PO4)2 (PO4)]n (2), where bipy = 2,2′-bipyridine and phen = 1,10-phenanthroline, obtained by a new synthetic route allowing the growth of single crystals appropriate for the EPR measurements. Compounds 1 and 2 crystallize in the triclinic group P1¯and in the orthorhombic Pccn group, respectively, containing dinuclear copper units connected by two -O-P-O- bridges in 1 and by a single -O-P-O- bridge in 2, further connected through -O-P-O-V-O- bridges. We emphasize in our work the structural aspects related to the chemical paths that determine the magnetic properties. Magnetic susceptibility data indicate bulk antiferromagnetism for both compounds, allowing to calculate J = -43.0 cm-1 (dCu-Cu = 5.07 Å; J defined as Hex(i,j) = -J Si·Sj), considering dinuclear units for 1, and J = -1.44 cm-1 (dCu-Cu = 3.47 Å) using the molecular field approximation for 2. The single-crystal EPR study allows evaluation of the g matrices, which provide a better understanding of the electronic structure. The absence of structure of the EPR spectra arising from the dinuclear character of the compounds allows estimation of weak additional exchange couplings |J′| > 0.3 cm-1 for 1 (dCu-Cu = 5.54 Å) and a smaller value of |J′| 0.15 cm-1 for 2 (dCu-Cu = 6.59 Å). DFT calculations allow evaluating two different exchange couplings for each compound, specifically, J = -36.60 cm-1 (dCu-Cu = 5.07 Å) and J′ = 0.20 cm-1 (dCu-Cu =5.54 Å) for 1 and J = -1.10 cm-1 (dCu-Cu =3.47 Å) and J′ = 0.01 cm-1 (dCu-Cu = 6.59 Å) for 2, this last value being in the range of the uncertainties of the calculations. Thus, these values are in good agreement with those provided by magnetic and single-crystal EPR measurements.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
American Chemical Society  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
Materiales  
dc.subject
Magnetismo  
dc.subject
Epr  
dc.subject
Dft  
dc.title
1D Magnetic Interactions in CuII Oxovanadium Phosphates, Magnetic Susceptibility, DFT and Single Crystal EPR  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2019-06-19T16:54:06Z  
dc.journal.volume
54  
dc.journal.number
8  
dc.journal.pagination
3805-3814  
dc.journal.pais
Estados Unidos  
dc.journal.ciudad
Washington  
dc.description.fil
Fil: Venegas-Yazigi, Diego. Centro Para El Desarrollo de la Nanociencia y Nanotecnología; Chile. Universidad de Santiago de Chile; Chile  
dc.description.fil
Fil: Spodine, Evgenia. Centro Para El Desarrollo de la Nanociencia y Nanotecnología; Chile. Universidad de Chile; Chile  
dc.description.fil
Fil: Saldias, Marianela. Centro Para El Desarrollo de la Nanociencia y Nanotecnología; Chile. Universidad de Chile; Chile  
dc.description.fil
Fil: Vega, Andrés. Universidad Andrés Bello; Chile. Centro Para El Desarrollo de la Nanociencia y Nanotecnología; Chile  
dc.description.fil
Fil: Paredes-García, Verónica. Centro Para El Desarrollo de la Nanociencia y Nanotecnología; Chile. Universidad Andrés Bello; Chile  
dc.description.fil
Fil: Calvo, Rafael. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Física del Litoral. Universidad Nacional del Litoral. Instituto de Física del Litoral; Argentina  
dc.description.fil
Fil: Santana, Ricardo C.. Universidade Federal de Goiás; Brasil  
dc.journal.title
Inorganic Chemistry  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1021/ic503045d