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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Cyclen based bis-macrocyclic ligands as phosphates receptors. A potentiometric and NMR study
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Cyclen based bis-macrocyclic ligands as phosphates receptors. A potentiometric and NMR study

机译:基于Cyclen的双大环配体作为磷酸盐受体。电位和NMR研究

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摘要

The host - guest interaction between orthophosphate, pyrophosphate and triphosphate anions and four cyclen based bis-macrocycles ligands possessing ortho-(BOC), meta-(BMC), para-xylenyl (BPC) or 2,6-pyridinyl (BPyC) linker was investigated by potentiometric measurements and NMR spectroscopy. Each ligand gave protonated species in aqueous solution that further formed ternary complexes after binding with anions; these complexes were analyzed as a result of hydrogen bond formation and Coulombic attraction between the organic host and the inorganic guest. The equilibrium constants for all the detected species are reported and the selectivity, illustrated with species distribution diagrams, is discussed. The results unambiguously showed the importance of the distance between the two cyclen cores and underlined, especially for the triphosphate species, the contribution of the nitrogen atom of the pyridinyl spacer as a supplementary anchoring point in acidic medium.
机译:正磷酸根,焦磷酸根和三磷酸根阴离子与具有邻-(BOC),间-(BMC),对二甲苯基(BPC)或2,6-吡啶基(BPyC)接头的四个基于周期的双大环配体之间的主体-客体相互作用为通过电位测量和NMR光谱进行了研究。每个配体在水溶液中产生质子化的物种,与阴离子结合后进一步形成三元络合物。由于有机主体和无机客体之间存在氢键形成和库仑吸引,因此对这些配合物进行了分析。报告了所有检测到的物质的平衡常数,并讨论了用物质分布图说明的选择性。结果清楚地表明了两个环芯之间的距离的重要性,并强调了下划线,特别是对于三磷酸酯类而言,吡啶基间隔基的氮原子作为酸性介质中的辅助锚定点的贡献。

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