Wilk Magdalena, Janczak Jan, Videnova-Adrabinska Veneta
Department of Chemistry, Wrocław University of Technology, 27 Wybrzeże Wyspiańskiego Str., 50-370 Wrocław, Poland.
Acta Crystallogr C. 2012 Feb;68(Pt 2):m41-4. doi: 10.1107/S0108270112001461. Epub 2012 Jan 25.
The rigid organic ligand (pyridine-3,5-diyl)diphosphonic acid has been used to create the title novel three-dimensional coordination polymer, Ca(C(5)H(6)NO(6)P(2))(2)(H(2)O). The six-coordinate calcium ion is in a distorted octahedral environment, formed by five phosphonate O atoms from five different (pyridin-1-ium-3,5-diyl)diphosphonate ligands, two of which are unique, and one water O atom. Two crystallographically independent acid monoanions, L1 and L2, serve to link metal centres using two different coordination modes, viz. η(2)μ(2) and η(3)μ(3), respectively. The latter ligand, L2, forms a strongly undulated two-dimensional framework parallel to the crystallographic bc plane, whereas the former ligand, L1, is utilized in the formation of one-dimensional helical chains in the [010] direction. The two sublattices of L1 and L2 interweave at the Ca(2+) ions to form a three-dimensional framework. In addition, multiple O-H···O and N-H···O hydrogen bonds stabilize the three-dimensional coordination network. Topologically, the three-dimensional framework can be simplified as a very unusual (2,3,5)-connected three-nodal net represented by the Schläfli symbol (4·8(2))(4·8(8)·10)(8).
刚性有机配体(吡啶 - 3,5 - 二基)二膦酸已被用于合成标题新型三维配位聚合物[Ca(C₅H₆NO₆P₂)₂(H₂O)]ₙ。六配位钙离子处于扭曲的八面体环境中,由来自五个不同的(吡啶 - 1 - 鎓 - 3,5 - 二基)二膦酸酯配体的五个膦酸酯O原子形成,其中两个是独特的,还有一个水分子的O原子。两个晶体学独立的酸单阴离子L1和L2,分别使用两种不同的配位模式连接金属中心,即η₂μ₂和η₃μ₃。后一种配体L2形成一个与晶体学bc平面平行的强烈起伏的二维框架,而前一种配体L1用于在[010]方向形成一维螺旋链。L1和L2的两个子晶格在Ca²⁺离子处交织形成三维框架。此外,多个O - H···O和N - H···O氢键稳定了三维配位网络。拓扑学上,三维框架可简化为一个非常不寻常的(2,3,5)连接的三节点网络,由施莱夫利符号(4·8²)(4·8⁸·10)(8)表示。