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Thiacalix[4]arene-alkali metal assemblies: Crystal structures and guest-binding capabilities of supramolecular architectures supported by metal coordination and cation-π interactions

机译:硫杂杯[4]芳烃-碱金属组装体:金属配位和阳离子-π相互作用支持的超分子结构的晶体结构和客体结合能力

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摘要

To investigate alkali metal complexation with sulfur-linked calixarene analogues and their guest-binding properties for gaseous organic guest molecules, we elucidated a crystal structure of a cesium complex with p-H-thiacalix[4]arene (1·4H) ligands and guest-binding properties of the cesium complex (2) and the previously reported rubidium complex (3). In crystals of the complex 2, a 'sandwich-like' binuclear complex was formed by inter-molecular coordination of cesium cations to the thiacalixarene molecules and methanol molecules, mutually interacting by aromatic-H?S hydrogen bonding and alkali metal cation-π interactions between the alkali metal cation and thiacalixarene aromatic rings outside of the cavities. On the guest-binding behaviors both complexes 2 and 3 toward organic guest molecules, methanol, ethanol, and 1-propanol as polar molecules, the complex 2 has no methanol adsorption ability, but the complex 3 showed vapor adsorption properties for all guest molecules. In particular, both complexes exhibited a high adsorption capability toward ethanol molecule. As results of gaseous guest adsorption measurements for alcohol molecules, the guest-binding of these complexes are significantly different because the properties depend heavily on structural natures between complexes 2 and 3.
机译:为了研究碱金属与硫连接的杯芳烃类似物的络合及其对气态有机客体分子的客体结合特性,我们阐明了具有pH-噻唑杯[4]芳烃(1·4H)配体和客体结合的铯配合物的晶体结构。铯络合物(2)和先前报道的complex络合物(3)的性质。在络合物2的晶体中,铯原子与噻唑烷芳烃分子和甲醇分子的分子间配位形成“三明治”状双核络合物,并通过芳族-H 2 S氢键和碱金属阳离子-π相互作用相互作用。腔外的碱金属阳离子和噻cali芳烃芳环之间。在配合物2和3对有机客体分子,甲醇,乙醇和1-丙醇作为极性分子的客体结合行为上,配合物2没有甲醇吸附能力,但是配合物3对所有客体分子均显示出蒸气吸附性能。特别地,两种复合物均表现出对乙醇分子的高吸附能力。作为对酒精分子的气态客体吸附测量的结果,这些配合物的客体结合显着不同,因为其性质在很大程度上取决于配合物2和3之间的结构性质。

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