Yang Hua, Chen Yuting, Li Dacheng, Wang Daqi
Acta Crystallogr Sect E Struct Rep Online. 2008 Nov 26;64(Pt 12):m1622-3. doi: 10.1107/S1600536808038439.
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 symmetry. The three Mn atoms are six-coordinated in the shape of distorted octa-hedra, 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 mol-ecules 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 inter-molecular O-H⋯O hydrogen bonds.
标题配合物[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是一种具有对称结构的三核混合氧化态配合物。三个锰原子以扭曲八面体的形状六配位,每个与一组O(4)N(2)供体原子配位,其中配体呈现单齿和双齿模式。然而,位于对称中心的Mn(II)离子的配位涉及两个配位位点的水分子,而两个对称相关的Mn(III)离子的配位涉及一组源自有机配体的O(4)N(2)供体原子。相邻吡啶配体之间的分子内C-H⋯π相互作用稳定了这种排列。分子间的O-H⋯O氢键形成了一个平行于(001)的二维网络。