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首页> 外文期刊>Organic letters >[2]Pseudorotaxane Formation with N-Benzylanilinium Axles and 24-Crown-8 Ether Wheels
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[2]Pseudorotaxane Formation with N-Benzylanilinium Axles and 24-Crown-8 Ether Wheels

机译:[2]用N-苄基苯胺轴和24-Crown-8醚轮形成伪轮烷

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摘要

As a hybrid of the N,N-dibenzylammonium and 1,2-bis(pyridinium)ethane axles,various N-benzylanilinium cations were investigated as suitable axles for the formation of [2]pseudorotaxanes with the 24-membered crown ethers 24C8 and DB24C8.The effect of electron-donating OCH_3 and electron-withdrawing CF_3 groups on both the anilinium and benzyl aromatic rings was studied.Formation constants and structural details were compared to the [2]pseudorotaxanes formed by the two aforementioned dibenzylammonium and 1,2-bis(pyridinium)ethane axles.
机译:作为N,N-二苄基铵和1,2-双(吡啶鎓)乙烷车轴的混合体,研究了各种N-苄基苯胺阳离子作为适合与24元冠醚24C8和DB24C8形成[2]假轮烷的车轴研究了给电子的OCH_3和吸电子的CF_3基团在苯胺和苄基芳环上的作用。比较了形成常数和结构细节与上述两种二苄基铵和1,2-双形成的[2]拟轮烷(吡啶)乙烷轮轴。

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  • 来源
    《Organic letters》 |2005年第22期|p.4923-4926|共4页
  • 作者单位

    Department of Chemistry & Biochemistry,University of Windsor,Windsor,ON,Canada N9B 3P4;

    Department of Chemistry & Biochemistry,University of Windsor,Windsor,ON,Canada N9B 3P4;

    Department of Chemistry & Biochemistry,University of Windsor,Windsor,ON,Canada N9B 3P4;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 有机化学;
  • 关键词

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