铜
结晶学
三斜晶系
二亚胺
化学
阳离子聚合
八面体
四面体
磁化率
配体(生物化学)
立体化学
晶体结构
高分子化学
有机化学
生物化学
受体
催化作用
作者
Svetlana Ushak,Evgenia Spodine,Diego Venegas‐Yazigi,Éric Le Fur,Jean‐Yves Pivan,O. Peña,Raúl Cardoso‐Gil,Rüdiger Kniep
摘要
The new hybrid organic-inorganic copper oxovanadium phosphates of composition Cu4(bipy)4V4O11(PO 4)2·nH2O (n ∼ 5) (1) and Cu 2(bipy)2V2P2O12 (2) (bipy = 2, 2′-bipyridine) adopting the triclinic symmetry were obtained by soft hydrothermal routes. Both structures present different oxovanadium phosphate anionic units, resulting from the vertex-sharing of PO4 and VO 4 tetrahedra, which are coordinated to copper diimine cationic groups to form a ID framework. The VPO structures are reminiscent of the known connectivity and geometry of polyphosphate anions. For the two compounds, the magnetic copper(II) centres are square pyramidally coordinated with two nitrogen atoms of the neutral diimine ligand and three oxygen atoms of the oxovanadium phosphate subunit. The CuN2O3 pyramids are linked together by oxo-bridges involving PO4 tetrahedra in Cu2(bipy) 2V2P2O12 with the closest Cu-Cu distances corresponding to 4.98 Å. Edge-sharing of the copper pyramids in Cu4(bipy)4V4O11(PO4) 2·nH2O results in
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