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首页> 外文期刊>Polyhedron: The International Journal for Inorganic and Organometallic Chemistry >Synthesis and coordination properties of functionalized beta-cyclodextrins. Thermodynamic of proton and copper(II) complexes of 3A-deoxy-3A-(2-methylaminopyridine)-2A(S),3A(R)-beta-cyclodextrin in aqueous solution
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Synthesis and coordination properties of functionalized beta-cyclodextrins. Thermodynamic of proton and copper(II) complexes of 3A-deoxy-3A-(2-methylaminopyridine)-2A(S),3A(R)-beta-cyclodextrin in aqueous solution

机译:功能化的β-环糊精的合成和配位性能。 3A-脱氧-3A-(2-甲基氨基吡啶)-2A(S),3A(R)-β-环糊精在水溶液中的质子和铜(II)配合物的热力学

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The 3A-deoxy-3A-(2-methylaminopyridine)-2A(S),3A(R)-beta-cyclodextrin (CDampy3) was synthesized and characterized by NMR spectroscopy. The proton and copper(II) complex formation and stability of this new beta-cyclodextrin derivative were determined by potentiometric and calorimetric investigations, carried out in aqueous solution at 25degreesC and I=0.1 mol dm(-3) (KNO3). The DeltaHdegrees and DeltaSdegrees values allowed to bring to light the role of the hydrogen bond between the amine and the hydroxyl groups in the basicity decrease of NH group of this 3-functionalized beta-cyclodextrin. The comparison between the log K values of copper(II) complexes with CDampy3 and those of 6-deoxy-6-(2-methylaminopyridine)-beta-cyclodextrin (CDampy6) allowed to determine the donor atoms involved in the coordination to metal ion. The high stability constant of [Cu(CDampy3)](2+) in comparison with [Cu(CDampy6)](2+) was attributed to the involvement of the OH groups in the binding to copper(II) ion. (C) 2002 Elsevier Science Ltd. All rights reserved. [References: 44]
机译:合成3A-脱氧-3A-(2-甲基氨基吡啶)-2A(S),3A(R)-β-环糊精(CDampy3),并通过NMR光谱表征。通过在水溶液中于25°C和I = 0.1 mol dm(-3)(KNO3)进行的电位和量热研究确定了这种新的β-环糊精衍生物的质子和铜(II)配合物的形成和稳定性。 DeltaHdegrees和DeltaSdegrees值使该3官能化的β-环糊精的NH基团碱性降低时,胺和羟基之间的氢键作用得以揭示。比较铜(II)与CDampy3的对数K值与6-脱氧-6-(2-甲基氨基吡啶)-β-环糊精(CDampy6)的对数K值,可以确定与金属离子配位的供体原子。与[Cu(CDampy6)](2+)相比,[Cu(CDampy3)](2+)的高稳定性常数归因于OH基团与铜(II)离子的结合。 (C)2002 Elsevier ScienceLtd。保留所有权利。 [参考:44]

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