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Title

Magneto-structural correlations in dinuclear Mn(III) compounds with formula [{Mn(L)(NN)}(μ-O)(μ-2-RC6H4COO)2{Mn(L′)(NN)}]n+

AuthorsGómez, Verónica; Corbella, Montserrat; Roubeau, Olivier; Teat, Simon J.
Issue Date2011
PublisherRoyal Society of Chemistry (UK)
CitationDalton Transactions 40(44): 11968-11975 (2011)
AbstractThree dinuclear Mn(iii) compounds with oxo and carboxylato bridges have been synthesized and characterized by X-ray diffraction: [{Mn(L)(NN)}(μ-2- ClC6H4COO)2(μ-O){Mn(L′)(NN)}] n+ with NN = 2,2′-bipyridine (1 and 2) or 1,10-phenanthroline (3). The counteranion is either NO3 - (1 and 3) or ClO 4 - (2) and the monodentate positions (L, L′) could be occupied by molecules of water or the counteranion. For compound 1, L = H2O and L′ = NO3 -; compound 2 shows two different dinuclear units and L and L′ could be H2O or ClO 4 -, and for compound 3 both monodentate positions are occupied by nitrate anions. The magnetic properties of the three compounds have been analyzed using the Hamiltonian H = -JS1·S2. Compound 1 exhibits a dominant ferromagnetic behavior, with J = 3.0 cm -1, DMn = 1.79 cm-1, EMn = 0.60 cm-1 with intermolecular interactions zJ′ = -0.18 cm -1. Due to the anisotropy of the Mn(iii) ions, the ground state S = 4 shows ZFS with D4 = 0.58 cm-1. Compounds 2 and 3 show antiferromagnetic couplings, with J = -10.9 and -0.3 cm-1, respectively. The magnetic interaction in this kind of compound depends on several structural factors. In the present work, the distortion around manganese ions, the torsion angle between the phenyl ring and the carboxylate group and the relative disposition of the coordination octahedra have been analyzed.
URIhttp://hdl.handle.net/10261/53109
DOI10.1039/C1DT11242B
Identifiersdoi: 10.1039/C1DT11242B
issn: 1477-9226
e-issn: 1477-9234
Appears in Collections:(ICMA) Artículos
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