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首页> 外文期刊>Journal of Organometallic Chemistry >Syntheses and crystal structures of three cesium salts: Cesium 5-sulfosalicylate, cesium 3,5-dinitrosalicylate and cesium 2,4-dinitrophenoxide monohydrate
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Syntheses and crystal structures of three cesium salts: Cesium 5-sulfosalicylate, cesium 3,5-dinitrosalicylate and cesium 2,4-dinitrophenoxide monohydrate

机译:三种铯盐的合成和晶体结构:5-磺基水杨酸铯,3,5-二硝基水杨酸铯和2,4-二硝基苯氧基铯一水合物

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In an attempt to probe a potential template role of the large alkali-metal cation cesium in organization of biorelevant ligands, 5-sulfosalicylate, 3,5-dinitrosalicylate and 2,4-dinitrophenol complexes of cesium were prepared and structurally investigated. The structures of cesium 5-sulfosalicylate, cesium 3,5-dinitrosalicylate and cesium 2,4-dinitrophenoxide monohydrate have been determined through X-ray diffraction analysis. The 5-sulfosalicylate anion has lost the proton at the -SO3H group while the 3,5-dinitrosalicylate anion at -COOH group but both retains the usual intermolecular hydrogen bond between phenolic and carboxylic oxygen. In cesium 2,4-dinitrophenoxide monohydrate, the Cs+ cation is 12-coordinate by O atoms in anions and water molecules while the metal atoms in cesium 5-sulfosalicylate and cesium 3,5-dinitrosalicylate have coordination numbers 10 and 11, respectively, with an irregular coordination sphere made up exclusively of oxygen atoms. Even more in cesium 2,4-dinitrophenoxide monohydrate, the water molecules are in rare triply bridging positions between these cations. Both complexes have layer structures containing the cations and polar groups of the ligands in core domains sandwiched by the aromatic rings above and below. The organization of all layer structures appears to be governed mainly by steric effects and electrostatic forces with very little directional influence of the cations. (c) 2005 Elsevier B.V. All rights reserved.
机译:为了探究大碱金属阳离子铯在生物相关配体的组织中的潜在模板作用,制备了铯的5-磺基水杨酸酯,3,5-二硝基水杨酸酯和2,4-二硝基苯酚复合物并对其结构进行了研究。通过X射线衍射分析确定了5-磺基水杨酸铯,3,5-二硝基水杨酸铯和2,4-二硝基苯氧基铯一水合物的结构。 5-磺基水杨酸根阴离子在-SO3H基团上失去了质子,而3,5-二硝基水杨酸根阴离子在-COOH基团上失去了,但两者都保留了酚和羧酸氧之间通常的分子间氢键。在2,4-二硝基苯氧基铯一水合物中,Cs +阳离子在阴离子和水分子中的O原子为12配位,而5-磺基水杨酸铯和3,5-二硝基水杨酸铯中的金属原子的配位数分别为10和11,仅由氧原子组成的不规则配位球。在2,4-二硝基苯酚一水合铯中,水分子甚至处在这些阳离子之间的罕见三重桥连位置。两种络合物均具有层结构,该层结构包含在核心域中的配体的阳离子和极性基团,其被上下芳香环夹在中间。所有层结构的组织似乎主要受空间效应和静电力支配,而阳离子的方向性影响很小。 (c)2005 Elsevier B.V.保留所有权利。

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