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Uranyl Coordination Compounds with Alkaline Earth Metals and Crotonate Ligands

机译:铀酰配合物与碱土金属和共齿配体配体的化合物

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Crystal structures of three new uranyl compounds were solved using single crystal X-ray diffraction and studied using FTIR spectroscopy. Although the syntheses conditions were very similar differing only in the alkaline earth metal (Mg, Ca or Sr), the resulting structures are different, containing, respectively, mono-, tri- and hexanuclear metal-containing building units. This fact proves the profound crystal-chemical role of secon- dary metal atoms on the formation of crystal structures. Parameters of alkaline earth metal cations in the three newly synthesized compounds as well as in the earlier reported Ba- containing analog are discussed in detail using Voronoi- Dirichlet polyhedra and the method of intersecting spheres. Differences in packing of building units in the four mentioned compounds, as well as inter- and intramolecular noncovalent interactions in their structures are reported. The results of analysis are consistent with the stereoatomic model of crystal structures.
机译:使用单晶X射线衍射溶解了三种新的铀酰化合物的晶体结构,并使用FTIR光谱法进行了研究。 尽管合成条件仅在碱土金属(mg,ca或sr)中非常相似,但所得的结构分别不同,分别包含含含有单,三核金属的建筑单元。 这一事实证明了乳清原子在形成晶体结构中的深刻晶体化学作用。 使用voronoi-dirichlet polyhedra和相交球的方法详细讨论了三种新合成化合物以及早期报道的包含类似物的碱性土金属阳离子的参数。 据报道,在其结构中,在提到的四种化合物以及分子内和分子内的非共价相互作用中的建筑单元堆积差异。 分析的结果与晶体结构的立体原子因模型一致。

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