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Diaqua-2κ(2) O-bis­(μ-1-oxido-2-naphtho­ato)-1:2κ(3) O (1),O (2):O (2′);2:3κ(3) O (2):O (1),O (2′)-bis­(1-oxido-2-naphthoato)-1κ(1) O (2),O (2);3κ(2) O (1),O (2)-hexa­pyridine-1κ(2) N,2κ(2) N,3κ(2) N-trimanganese(II/III) pyridine disolvate dihydrate

The title complex, [Mn(3)(C(11)H(6)O(3))(4)(C(5)H(5)N)(6)(H(2)O)(2)]·2H(2)O·2C(5)H(5)N, is a trinuclear mixed oxidation state complex of [Image: see text] symmetry. The three Mn atoms are six-coordinated in the shape of distorted octa­hedra, each coordinated with an O(4)N(2) set of donor atoms, wher...

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Detalles Bibliográficos
Autores principales: Yang, Hua, Chen, Yuting, Li, Dacheng, Wang, Daqi
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960114/
https://www.ncbi.nlm.nih.gov/pubmed/21581213
http://dx.doi.org/10.1107/S1600536808038439
Descripción
Sumario:The title complex, [Mn(3)(C(11)H(6)O(3))(4)(C(5)H(5)N)(6)(H(2)O)(2)]·2H(2)O·2C(5)H(5)N, is a trinuclear mixed oxidation state complex of [Image: see text] symmetry. The three Mn atoms are six-coordinated in the shape of distorted octa­hedra, each coordinated with an O(4)N(2) set of donor atoms, where the ligands exhibit mono- and bidentate modes. However, the coordination of the Mn(II) ion located on the inversion centre involves water mol­ecules at two coordination sites, whereas that of the two symmetry-related Mn(III) ions involves an O(4)N(2) set of donor atoms orginating from the organic ligands. Intramolecular C—H⋯π interactions between neighbouring pyridine ligands stabilize this arrangement. A two-dimensional network parallel to (001) is formed by inter­molecular O—H⋯O hydrogen bonds.