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首页> 外文期刊>IUCrData >catena-Poly[[bis--{2-[3-(carb--oxy-meth-yl)adamantan-1-yl]acetato-κ2O,O′}cadmium(II)]-μ-N,N′-bis--(pyridine-4-carbox-amido)-piperazine-κ2N:N′]
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catena-Poly[[bis--{2-[3-(carb--oxy-meth-yl)adamantan-1-yl]acetato-κ2O,O′}cadmium(II)]-μ-N,N′-bis--(pyridine-4-carbox-amido)-piperazine-κ2N:N′]

机译:链-聚[[双-{2- [3-(碳-氧-甲基-甲基)金刚烷-1-基]乙酰-κ2O,O'}镉(II)]-μ-N,N'-双-(吡啶-4-羧酰胺基)-哌嗪-κ2N:N']

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摘要

In the title compound, [Cd(C14H19O4)2(C16H16N4O2)]n, the CdII cation is coordinated in a distorted octahedral fashion by trans pyridyl N-atom donors from two N,N0 -bis(pyridine-4-carboxamido)piperazine (bpcp) ligands, and chelating carboxylate groups from two 2-[3-(carboxymethyl)adamantan-1- yl]acetate ligands. [Cd(adaH)(bpcp)]n coordination polymer chains are oriented along [111] and aggregate into supramolecular layers parallel to (122) by O— HO hydrogen-bonding interactions. The supramolecular three-dimensional crystal structure is then constructed by interlayer C—HO non-classical interactions. The O atoms of one of the carboxylate groups were refined as disordered over two sets of sites, with occupancies 0.553 (7) and 0.447 (7).
机译:在标题化合物[Cd(C14H19O4)2(C16H16N4O2)] n中,CdII阳离子通过来自两个N,N0-双(吡啶-4-甲酰胺基)哌嗪的反式吡啶N原子供体以扭曲的八面体形式配位( bpcp)配体,并从两个2- [3-(羧甲基)金刚烷-1-基]乙酸酯配体中螯合羧酸酯基团。 [Cd(adaH)(bpcp)] n配位聚合物链沿[111]取向,并通过O-HO氢键相互作用聚集成与(122)平行的超分子层。然后通过层间C-HO非经典相互作用来构建超分子三维晶体结构。一个羧酸根基团的O原子被精炼成在两组位点上是无序的,占有率为0.553(7)和0.447(7)。

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