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   <dc:title>Quantitative estimation of ising-type magnetic anisotropy in a family of C-3-symmetric Co-II complexes</dc:title>
   <dc:creator>Mondal, Amit Kumar</dc:creator>
   <dc:creator>Jover Modrego, Jesús</dc:creator>
   <dc:creator>Ruiz Sabín, Eliseo</dc:creator>
   <dc:creator>Konar, Sanjit</dc:creator>
   <dc:subject>Imants</dc:subject>
   <dc:subject>Anisotropia</dc:subject>
   <dc:subject>Lligands</dc:subject>
   <dc:subject>Magnets</dc:subject>
   <dc:subject>Anisotropy</dc:subject>
   <dc:subject>Ligands</dc:subject>
   <dcterms:abstract>In this paper, the influence of the structural and chemical effects on the Ising-type magnetic anisotropy of pentacoordinate Co-II complexes has been investigated by using a combined experimental and theoretical approach. For this, a deliberate design and synthesis of four pentacoordinate Co-II complexes [Co(tpa)Cl]ClO4 (1), [Co(tpa)Br]ClO4 (2), [Co(tbta)Cl](ClO4)(MeCN)(2)(H2O) (3) and [Co(tbta)Br]ClO4 (4) by using the tripodal ligands tris(2-methylpyridyl)amine (tpa) and tris[(1-benzyl-1H-1,2,3-triazole-4-yl)methyl]amine) (tbta) have been carried out. Detailed dc and ac measurements show the existence of field-induced slow magnetic relaxation behavior of Co-II centers with Ising-type magnetic anisotropy. A quantitative estimation of the zero-field splitting (ZFS) parameters has been effectively achieved by using detailed ab initio theory calculations. Computational studies reveal that the wavefunction of all the studied complexes has a very strong multiconfigurational character that stabilizes the largest m(s)=+/- 3/2 components of the quartet state and hence produce a large negative contribution to the ZFS parameters. The difference in the magnitudes of the Ising-type anisotropy can be explained through ligand field theory considerations, that is, D is larger and negative in the case of weak equatorial sigma-donating and strong apical -donating ligands. To elucidate the role of intermolecular interactions in the magnetic relaxation behavior between adjacent Co-II centers, a diamagnetic isostructural Zn-II analog (5) was synthesized and the magnetic dilution experiment was performed.</dcterms:abstract>
   <dcterms:issued>2019-10-22T11:57:48Z</dcterms:issued>
   <dcterms:issued>2019-10-22T11:57:48Z</dcterms:issued>
   <dcterms:issued>2017-09-12</dcterms:issued>
   <dcterms:issued>2019-10-22T11:57:49Z</dcterms:issued>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/acceptedVersion</dc:type>
   <dc:relation>Versió postprint del document publicat a: https://doi.org/10.1002/chem.201702108</dc:relation>
   <dc:relation>Chemistry-A European Journal, 2017, vol. 23, num. 51, p. 12550-12558</dc:relation>
   <dc:relation>https://doi.org/10.1002/chem.201702108</dc:relation>
   <dc:rights>(c) Wiley-VCH, 2017</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:publisher>Wiley-VCH</dc:publisher>
   <dc:source>Articles publicats en revistes (Química Inorgànica i Orgànica)</dc:source>
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