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               <dc:title>Ferro- to antiferromagnetic crossover angle in diphenoxido- and carboxylato-bridged trinuclear Ni(II)2-Mn(II) complexes: experimental observations and theoretical rationalization</dc:title>
               <dc:creator>Seth, Piya</dc:creator>
               <dc:creator>Figuerola i Silvestre, Albert</dc:creator>
               <dc:creator>Jover Modrego, Jesús</dc:creator>
               <dc:creator>Ruiz Sabín, Eliseo</dc:creator>
               <dc:creator>Ghosh, Ashutosh</dc:creator>
               <dc:subject>Propietats magnètiques</dc:subject>
               <dc:subject>Oxigen</dc:subject>
               <dc:subject>Metalls de transició</dc:subject>
               <dc:subject>Lligands</dc:subject>
               <dc:subject>Magnetic properties</dc:subject>
               <dc:subject>Oxygen</dc:subject>
               <dc:subject>Transition metals</dc:subject>
               <dc:subject>Ligands</dc:subject>
               <dc:description>Three new trinuclear heterometallic NiII-MnII complexes have been synthesized using [NiL] metalloligand where H2L = N,N′- bis(salicylidene)-1,3-propanediamine. The complexes [(NiL)4Mn2(OCn)4(CH3OH)4]·2CH3OH (1), [(NiL)4Mn2(OPh)4(CH3OH)2]·H2O (2) and [(NiL)4Mn(OSal)2(CH3OH)2] (3) (where OCn = cinnamate, OPh = phenylacetate, OSal= salicylate) have been structurally characterized. In all three complexes, in addition to the double phenoxido bridge, the two terminal NiII atoms are linked to the central MnII by means of syn-syn bridging carboxylate, giving rise to a linear structure. Complexes 1 and 2 with Ni-O-Mn angle of 97.24 and 96.43° respectively exhibit ferromagnetic interactions ( JNi-Mn = +1.38 and +0.50 cm-1 respectively) whereas 3 is antiferromagnetic (JNi-Mn= -0.24 cm-1) having Ni-O-Mn angle of 98.51°. DFT calculations indicate that there is a clear magneto-structural correlation between Ni-O-Mn angle and JNi-Mn values which is in agreement with the experimental results.</dc:description>
               <dc:date>2020-04-03T10:46:26Z</dc:date>
               <dc:date>2020-04-03T10:46:26Z</dc:date>
               <dc:date>2014-09-02</dc:date>
               <dc:date>2020-04-03T10:46:27Z</dc:date>
               <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/10.1021/ic501425x</dc:relation>
               <dc:relation>Inorganic Chemistry, 2014, vol. 53, num. 17, p. 9296-9305</dc:relation>
               <dc:relation>https://doi.org/10.1021/ic501425x</dc:relation>
               <dc:rights>(c) American Chemical Society , 2014</dc:rights>
               <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
               <dc:publisher>American Chemical Society</dc:publisher>
               <dc:source>Articles publicats en revistes (Química Inorgànica i Orgànica)</dc:source>
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