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Helical Structures of N-Alkylated Poly(p-benzamide)s

机译:N-烷基化聚对苯甲酰胺的螺旋结构

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摘要

Poly(p-benzamide)s 1 bearing a chiral side chain on the nitrogen atom were synthesized by chain-growth polycondensation methodology.The polyamides exhibited well-defined molecular weights with narrow polydispersities.Solutions of the polyamides in several organic solvents(CH_3CN,CHCI_3,and CH3OH)showed dispersion type CD signals characteristic of coupled-oscillator and much larger as compared with the corresponding monomer.The CD signals were dependent on the temperature and molecular weight of the polyamides but independent of the solvent,as far as examined.An exciton model analysis of the absorption and CD spectra provided a clear-cut picture for the secondary structure of these polyamides in solution that the N-alkylated poly(p-benzamide)s possess a right-handed helical conformation((P)-helix).In the solid states,the results of X-ray crystallographic analysis of 4-(methylamino)benzoic acid oligomers substantiated that they have a helical conformation with three monomer units per turn.
机译:通过链增长缩聚法合成了在氮原子上带有手性侧链的聚对苯甲酰胺1,聚酰胺具有良好的分子量分布和窄的分散性,聚酰胺在几种有机溶剂(CH_3CN,CHCI_3)中的溶液(和CH3OH)表现出偶合振荡器的分散型CD信号特性,并且与相应的单体相比要大得多.CD信号取决于聚酰胺的温度和分子量,但与溶剂无关,在所研究的范围内。吸收和CD光谱的激子模型分析为溶液中这些聚酰胺的二级结构提供了清晰的图像,即N-烷基化的聚对苯甲酰胺具有右旋螺旋构型((P)-螺旋)在固态下,对4-(甲基氨基)苯甲酸低聚物的X射线晶体学分析结果证实,它们具有螺旋构型,每个构型具有三个单体单元。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2005年第23期|p.8553-8561|共9页
  • 作者单位

    Contribution from the Synthesis and Control,PRESTO,Japan Science and Technology Agency (JST),Japan,Department of Applied Chemistry,Kanagawa University,Rokkakubashi,Kanagawa-ku,Yokohama 221-8686,Japan,Faculty of Pharmaceutical Sciences at Kagawa Campu;

    Contribution from the Synthesis and Control,PRESTO,Japan Science and Technology Agency (JST),Japan,Department of Applied Chemistry,Kanagawa University,Rokkakubashi,Kanagawa-ku,Yokohama 221-8686,Japan,Faculty of Pharmaceutical Sciences at Kagawa Campu;

    Contribution from the Synthesis and Control,PRESTO,Japan Science and Technology Agency (JST),Japan,Department of Applied Chemistry,Kanagawa University,Rokkakubashi,Kanagawa-ku,Yokohama 221-8686,Japan,Faculty of Pharmaceutical Sciences at Kagawa Campu;

    Contribution from the Synthesis and Control,PRESTO,Japan Science and Technology Agency (JST),Japan,Department of Applied Chemistry,Kanagawa University,Rokkakubashi,Kanagawa-ku,Yokohama 221-8686,Japan,Faculty of Pharmaceutical Sciences at Kagawa Campu;

    Contribution from the Synthesis and Control,PRESTO,Japan Science and Technology Agency (JST),Japan,Department of Applied Chemistry,Kanagawa University,Rokkakubashi,Kanagawa-ku,Yokohama 221-8686,Japan,Faculty of Pharmaceutical Sciences at Kagawa Campu;

    Contribution from the Synthesis and Control,PRESTO,Japan Science and Technology Agency (JST),Japan,Department of Applied Chemistry,Kanagawa University,Rokkakubashi,Kanagawa-ku,Yokohama 221-8686,Japan,Faculty of Pharmaceutical Sciences at Kagawa Campu;

    Contribution from the Synthesis and Control,PRESTO,Japan Science and Technology Agency (JST),Japan,Department of Applied Chemistry,Kanagawa University,Rokkakubashi,Kanagawa-ku,Yokohama 221-8686,Japan,Faculty of Pharmaceutical Sciences at Kagawa Campu;

    Contribution from the Synthesis and Control,PRESTO,Japan Science and Technology Agency (JST),Japan,Department of Applied Chemistry,Kanagawa University,Rokkakubashi,Kanagawa-ku,Yokohama 221-8686,Japan,Faculty of Pharmaceutical Sciences at Kagawa Campu;

    Contribution from the Synthesis and Control,PRESTO,Japan Science and Technology Agency (JST),Japan,Department of Applied Chemistry,Kanagawa University,Rokkakubashi,Kanagawa-ku,Yokohama 221-8686,Japan,Faculty of Pharmaceutical Sciences at Kagawa Campu;

    Contribution from the Synthesis and Control,PRESTO,Japan Science and Technology Agency (JST),Japan,Department of Applied Chemistry,Kanagawa University,Rokkakubashi,Kanagawa-ku,Yokohama 221-8686,Japan,Faculty of Pharmaceutical Sciences at Kagawa Campu;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
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