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首页> 外文期刊>Tetrahedron >New water-soluble calix[4]arene-bis(benzocrown-6) for caesium-sodium separation by nanofiltration-complexation
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New water-soluble calix[4]arene-bis(benzocrown-6) for caesium-sodium separation by nanofiltration-complexation

机译:纳滤-络合分离铯钠的新型水溶性杯[4]芳烃双(苯并冠-6)

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摘要

Calix-bis(benzocrown-6) 6 and 7 were converted into the water-soluble receptors 9, 10, 12 and 15 by introducing hydroxy, carboxy, sulfato or diethanolamino groups at the para position of the phenolic ring and/or on the benzo-ether moieties. The complexation properties of these ionophores were studied for all alkali cations in methanolic and aqueous media. Stability constants were calculated by UV-Vis spectroscopy. All ligands showed a more or less affinity for the larger cations, depending on the nature and the position of the substituents grafted on the benzo-ether chain only or both on the calixarene ring and the benzo-ether loop. For selective Cs+/Na+ separation, the efficiency of the ligands was evaluated by means of a nanofiltration system. In comparison with the known tetrahydroxylated bis-crown-6 calix[4]arene 1, compounds 9, 12 and 15 represent the most selective ligands for the Cs+ cation in a moderate salted medium ([NaNO3]=85 g/L). (C) 2003 Elsevier Ltd. All rights reserved. [References: 48]
机译:通过在酚环的对位和/或苯并基上引入羟基,羧基,硫酸根或二乙醇氨基将杯形双(苯并冠-6)6和7转变为水溶性受体9、10、12和15。 -醚部分。研究了这些离子载体对甲醇和水性介质中所有碱金属阳离子的络合特性。通过UV-Vis光谱法计算稳定性常数。所有配体对较大的阳离子都显示出或多或少的亲和力,这取决于仅在苯并醚链上或在杯芳烃环和苯并醚环上接枝的取代基的性质和位置。对于选择性的Cs + / Na +分离,通过纳米过滤系统评估配体的效率。与已知的四羟基双皇冠6杯[4]亚芳基相比,化合物9、12和15在中等盐度介质([NaNO3] = 85 g / L)中代表Cs +阳离子的选择性最高。 (C)2003 Elsevier Ltd.保留所有权利。 [参考:48]

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