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首页> 外文期刊>Organic & biomolecular chemistry >Halide selective anion recognition by an amide-triazolium axle containing [2]rotaxane
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Halide selective anion recognition by an amide-triazolium axle containing [2]rotaxane

机译:含[2]轮烷的酰胺-三唑鎓车轴对卤化物的选择性阴离子识别

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摘要

A new rotaxane containing the 3-amido-phenyl-triazolium group incorporated into the interlocked structure's axle component has been prepared by a chloride anion templated clipping strategy. Proton NMR titration experiments reveal that the interlocked host displays a high degree of halide anion recognition in competitive 1:1 CDCl_3-CD_3OD solvent mixture. Chloride and bromide anions are bound strongly and selectively, with negligible complexation of the larger, more basic oxoanions, acetate and dihydrogen phosphate being observed. Density functional theory calculations on the related axle motifs 3-amido-phenyl-triazolium, pyridinium bis-triazole and pyridinium bis-amide were performed, and indicate that the new rotaxane axle motif displays much weaker oxoanion binding than the pyridinium based systems.
机译:一种新的含有3-氨基-苯基-三唑鎓基团并结合到互锁结构的车轴组件中的轮烷已经通过氯离子阴离子模板化的剪切策略制备出来。质子NMR滴定实验表明,互锁主体在竞争性1:1 CDCl_3-CD_3OD溶剂混合物中显示出高度的卤化物阴离子识别能力。氯化物和溴化物的阴离子牢固且选择性地结合,观察到的较大的,更碱性的含氧阴离子,乙酸根和磷酸二氢的络合作用可忽略不计。对相关的轴基序3-酰胺基-苯基-三唑鎓,吡啶基双三唑和吡啶基双酰胺进行了密度泛函理论计算,结果表明,新的轮烷烷烃基序显示的氧代阴离子结合力比吡啶基体系弱得多。

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  • 来源
    《Organic & biomolecular chemistry》 |2014年第27期|4924-4931|共8页
  • 作者单位

    Inorganic Chemistry Laboratory, Department of Chemistry, University of Oxford, South Parks Road, Oxford, OX1 3QR, UK;

    Departamento de Quimica, CICECO and Seccao Autonoma de Ciencias da Saude, Universidade de Aveiro, 3810-193 Aveiro, Portugal;

    Departamento de Quimica, CICECO and Seccao Autonoma de Ciencias da Saude, Universidade de Aveiro, 3810-193 Aveiro, Portugal;

    Departamento de Quimica, CICECO and Seccao Autonoma de Ciencias da Saude, Universidade de Aveiro, 3810-193 Aveiro, Portugal;

    Inorganic Chemistry Laboratory, Department of Chemistry, University of Oxford, South Parks Road, Oxford, OX1 3QR, UK;

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