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An Environmentally Responsive Reciprocal Replicating Network

机译:环保型双向复制网络

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摘要

A reciprocal replication system is constructed from four building blocks, A , B , C , and D , which react in a pairwise manner through either a 1,3-dipolar cycloaddition or the condensation reaction between an amine and an aldehyde to create two templates, trans -T ~(AB ) and T ~(CD ). These templates are equipped with complementary recognition sites—two carboxylic acids (trans -T ~(AB )) or two 4,6-dimethylamidopyridines (T ~(CD ))—that enable each template to direct the formation of its complementary partner through two mutually reinforcing cross-catalytic pathways, in which the templates trans -T ~(AB ) or T ~(CD ) preorganize the appropriate building blocks within two catalytically active ternary complexes: [C •D •trans -T ~(AB )] and [A •B •T ~(CD )]. The template-directed processes within these complexes generate a heteroduplex [trans -T ~(AB )•T ~(CD )], which is shown to possess significant stability through kinetic simulations and fitting. As a consequence, the individual cross-catalytic pathways perform more efficiently in template-directed experiments when the concentration of the template being formed is below that of the template added as instruction. Comprehensive analysis of the system in which A , B , C , and D are mixed together directly, using a series of ~(1)H NMR spectroscopic kinetic experiments, demonstrates that the behavior of the reciprocal system is more than the simple sum of its parts—as part of the interconnected network, the product of each reaction clearly directs the fabrication of its reciprocal partner, facilitating both higher rates of formation for both templates and improved diastereoselectivity for trans -T ~(AB ). A simple change in experimental conditions (from dry to “wet” CDCl_(3)) demonstrates the sensitivity of the replication pathways within the network to the reaction environment, which leads to a >10-fold increase in the contribution of a new minimal self-replicator, trans -T ~(AB )*, to the replication network.
机译:相互复制系统由四个构造基元 A, B, C和 D构成,它们通过1,3-偶极环加成反应或缩合反应成对反应胺和醛之间的反应以生成两个模板,即反式-b T((b AB))和b T((b CD))。这些模板配备有互补的识别位点-两种羧酸(ans>- T〜(bAB))或两个4,6-二甲基酰胺基吡啶( T〜(bbCD)) -使每个模板都可以通过两个相互增强的交叉催化途径指导其互补伴侣的形成,其中模板 trans- T〜( AB)或 T〜(< b> CD)在两个具有催化活性的三元配合物中预组织适当的结构单元:[ C• D•反式- T〜(bbAB)]和[ A • B• T〜( CD)]。这些复合物中的模板指导过程会生成异源双链体[trans-b b T〜(b AB)•b b T〜(b CD)],通过这种方法显示具有显着的稳定性。动力学模拟和拟合。结果,当所形成的模板的浓度低于作为指示添加的模板的浓度时,在模板指导的实验中,各个交叉催化途径的执行效率更高。使用一系列〜(1)H NMR光谱动力学实验,对将 A, B, C和 D直接混合在一起的系统进行了综合分析,证明了该行为互易系统的组成部分不仅仅是其各个部分的简单总和-作为互连网络的一部分,每个反应的产物显然都指导着其互易伙伴的制造,从而促进了两种模板的较高形成速率和对 trans- T〜( AB)。实验条件的简单变化(从干到湿的CDCl_(3))证明了网络中复制路径对反应环境的敏感性,这导致新的最小自我的贡献增加了10倍以上-replicator, trans- T〜( AB)*,复制到复制网络。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2018年第22期|6832-6841|共10页
  • 作者单位

    School of Chemistry and EaStCHEM, University of St Andrews, North Haugh St Andrews, Fife KY16 9ST, United Kingdom;

    School of Chemistry and EaStCHEM, University of St Andrews, North Haugh St Andrews, Fife KY16 9ST, United Kingdom;

    School of Chemistry and EaStCHEM, University of St Andrews, North Haugh St Andrews, Fife KY16 9ST, United Kingdom;

    School of Chemistry and EaStCHEM, University of St Andrews, North Haugh St Andrews, Fife KY16 9ST, United Kingdom;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-18 03:07:20

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