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Опубликовано 2009-05-15 Опубликовано на SciPeople2009-09-21 14:29:44

Experimental and theoretical study of the arrangement, electronic structure and properties of neutral paramagnetic binuclear nitrosyl iron complexes with azaheterocyclic thyolyls having “S-C-N type” coordination of bridging ligands
A. F. Shestakov, Yu.M. Shul’ga, N.S. Emel’yanova, N.A. Sanina, T.N. Rudneva, S.M. Aldoshin, V. N. Ikorskii, V.I. Ovcharenko / Tatiana Rudneva
Inorganica Chimica Acta, V. 362, Is. 7, 2009, pp. 2499-2504
Аннотация Geometrical and electronic structures of neutral paramagnetic binuclear nitrosyl iron complexes with azaheterocyclic thyolyls [Fe2(μ-SR)2)(NO)4] with bridging ligands: aminomercaptotriazolyl, Rdouble bond; length as m-dashC2N3H(NH2) (1), mercaptoimidazolyl, Rdouble bond; length as m-dashC3N2H3 (2), methylmercaptoimidazolyl, Rdouble bond; length as m-dashC3N2H2CH3 (3), and dihydromercaptoimidazolyl, Rdouble bond; length as m-dashC3N2H5 (4) have been calculated by the methods of density functional, B3LYP and PBE. Coordination of bridging ligands corresponds to ‘S–C–N type’, more energetically preferable than μ-S type coordination. This results in big Fecdots, three dots, centeredFe distances, with the value of intramolecular exchange interaction being inconsiderable; therefore the complexes are paramagnetic at ambient temperature, with effective magnetic moment about 2.5 Bohr magneton. The interaction of the Fe atoms spins and intermolecular exchange are antiferromagnetic, and this should be taken into account while describing the temperature dependence of magnetic susceptibility. The electronic configuration of the Fe(NO)2 unit with one unpaired electron (similar to that in binuclear diamagnetic complexes) forms due to binding of spin 3/2 of Fe+d7 center with oppositely oriented spins 1/2 of two NO groups. Theoretical approaches describe satisfactorily not only the experimental structure of the complexes but also their IR spectra.
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