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首页> 外文期刊>Radiochimica Acta: International Journal for Chemical Aspects of Nuclear Science and Technology >Crystal structure of 2,2'-bipyridine complexes of Np(V) and Pu(V)m-nitrobenzoates
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Crystal structure of 2,2'-bipyridine complexes of Np(V) and Pu(V)m-nitrobenzoates

机译:Np(V)和Pu(V)间硝基苯甲酸酯的2,2'-联吡啶配合物的晶体结构

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摘要

Single crystals of [AnO_2(bipy)(OOCC_6H_4NO_2)-(H_2O)]·0.5bipy (An=Np, Pu, bipy=2,2'-bipyridine) have been synthesized and their structures have been determined by X-ray analysis. The compounds are isomorphous and contain electroneutral complexes [AnO_2(bipy)(OOCC_6H_4NO_2)(H_2O)] and solvate bipy molecules. Actinide atoms in both compounds are seven coordinated. Actinide contraction results in a shortening of all bonds in the coordination spheres at the transition from Np to Pu. The structures are compared with those of other An(V) benzoate compounds. In contrast to earlier structurally characterized An(V) benzoates, cation–cation interaction in [AnO_2(bipy)(OOCC_6H_4NO_2)(H_2O)] complexes is absent. Lower complexing ability of m-nitrobenzoate is compensated by engagement of water molecule into the coordination sphere of An(V). This is accompanied by formation of strong H-bonds between AnO_2~+ cations and coordinated water molecules.
机译:合成了[AnO_2(bipy)(OOCC_6H_4NO_2)-(H_2O)]·0.5bipy(An = Np,Pu,bipy = 2,2'-联吡啶)的单晶,并通过X射线分析确定了它们的结构。这些化合物是同构的,并包含电子中性络合物[AnO_2(bipy)(OOCC_6H_4NO_2)(H_2O)]和溶剂化的Bipy分子。两种化合物中的系原子都是七个配位的。 N系元素的收缩导致从Np到Pu过渡时配位域中所有键的缩短。该结构与其他An(V)苯甲酸酯化合物的结构进行了比较。与早期结构特征的An(V)苯甲酸酯相反,[AnO_2(bipy)(OOCC_6H_4NO_2)(H_2O)]络合物中不存在阳离子-阳离子相互作用。间硝基苯甲酸酯的较低络合能力可通过水分子与An(V)的配位域结合来补偿。这伴随着在AnO_2〜+阳离子和配位的水分子之间形成强H键。

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