Alkali Metal-Directed Assembly and Structural Characterization of Layered Uranyl Tetrakisphosphonates

IF 3.4 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Pius O. Adelani*, , , Jennifer E. S. Szymanowski, , , Cale B. Gaster, , and , Carmen E. Chamberlain, 
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引用次数: 0

Abstract

Two uranyl-organic hybrid compounds were self-assembled from the reaction of uranyl cations with 1,4-phenylenebis(methylidyne)tetrakis(phosphonic acid) in the presence of alkali metal cations (Rb+ and Cs+): Rb0.40{(UO2)2[(H0.90O3P)2CH–C6H4–CH(PO3H0.90)2](H2O)2} (1) and [Cs0.33(H2O)2]2{(UO2)2[(H0.67O3P)(HO3P)CH–C6H4–CH(PO3H)(PO3H0.67)](H2O)2} (2). Compound 1 consists of chains of UO7 pentagonal bipyramids linked by the tetrakisphosphonate moieties into two-dimensional layered networks. In compound 2, the –CH(PO3)2 groups chelate the uranyl centers in an exclusively bidentate mode, forming corrugated chains within a uranyl-tetrakisphosphonate framework. In both structures, the uranyl tetrakisphosphonate sheets are stabilized by weak intermolecular forces and noncovalent interactions involving water molecules and alkali metal ions.

Abstract Image

层状四磷酸铀酰盐的碱金属定向组装及结构表征
在碱金属阳离子(Rb+和Cs+)存在下,由铀酰阳离子与1,4-苯基双(甲酰基)四基(膦酸)自组装成两个铀酰有机杂化化合物:Rb0.40{(UO2)2[(H0.90O3P) 2CH-C6H4-CH (PO3H0.90)2](H2O)2}(1)和[Cs0.33(H2O)2]2{(UO2)2[(H0.67O3P)(HO3P) CH-C6H4-CH (PO3H0.67)](H2O)2}(2)。化合物1由UO7五边形双锥体链组成,由四膦酸盐部分连接成二维层状网络。在化合物2中,-CH (PO3)2基团以双齿模式螯合铀酰中心,在铀酰-四磷酸酯框架内形成波纹链。在这两种结构中,四四膦酸铀酰片被弱分子间力和涉及水分子和碱金属离子的非共价相互作用稳定。
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来源期刊
Crystal Growth & Design
Crystal Growth & Design 化学-材料科学:综合
CiteScore
6.30
自引率
10.50%
发文量
650
审稿时长
1.9 months
期刊介绍: The aim of Crystal Growth & Design is to stimulate crossfertilization of knowledge among scientists and engineers working in the fields of crystal growth, crystal engineering, and the industrial application of crystalline materials. Crystal Growth & Design publishes theoretical and experimental studies of the physical, chemical, and biological phenomena and processes related to the design, growth, and application of crystalline materials. Synergistic approaches originating from different disciplines and technologies and integrating the fields of crystal growth, crystal engineering, intermolecular interactions, and industrial application are encouraged.
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