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Inositol derived crown ethers: effect of auxiliary protecting groups and the relative orientation of crown ether oxygen atoms on their metal ion binding ability

机译:肌醇衍生的冠醚:辅助保护基团和冠醚氧原子的相对取向对其金属离子结合能力的影响

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摘要

The binding constants of crown ethers prepared from tetra-O-substituted myo- and scyllo-inositol derivatives and 2-O-substituted myo- and scyllo-inositol-1,3,5-orthoformates, with metal picrates show that the O-substituents and the relative orientation of the crown ether oxygen atoms contribute significantly to the binding of crown ethers with metal ions. In particular, the binding efficiency of myo-inositol derived crown ethers to silver and potassium ions could be enhanced by introducing benzyl ethers in the inositol ring. Hence binding efficacy and selectivity of metal ions to inositol derived crown ethers can be tuned by varying substituents on the myo-inositol ring and/or the relative orientation of crown ether oxygen atoms. (C) 2007 Elsevier Ltd. All rights reserved.
机译:由四-O-取代的肌醇和鲨肌醇衍生物,2-O-取代的肌醇和鲨肌醇-1,3,5-原甲酸酯制得的冠醚与金属苦味酸盐的结合常数表明,O-取代基冠醚氧原子的相对取向显着地促进了冠醚与金属离子的结合。特别地,可以通过在肌醇环中引入苄基醚来提高肌醇衍生的冠醚与银和钾离子的结合效率。因此,金属离子与肌醇衍生的冠醚的结合功效和选择性可以通过改变肌醇环上的取代基和/或冠醚氧原子的相对取向来调节。 (C)2007 Elsevier Ltd.保留所有权利。

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