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The cationic polymerization mechanism consists of three steps: initiation, propagation, and termination. In the initiation step of the polymerization process, the π bond of a monomer gets protonated by the Lewis acid catalyst, which is formed from boron trifluoride and water. The protonation of the π bond generates a carbocation stabilized by the electron‐donating group. In the propagation step, the π bond of the second monomer acts as a nucleophile and attacks the...
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The electrophilic addition of hydrogen halides such as HBr to alkenes and nonconjugated dienes gives a single product as per Markovnikov’s rule.
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Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)01:16

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Ring-opening metathesis polymerization or ROMP involves strained cycloalkenes as starting materials. The mechanism of ROMP proceeds by reacting cycloalkene with Grubbs catalyst to give metallacyclobutane intermediate which undergoes a ring-opening reaction to form new carbene. The new carbene reacts with another molecule of cycloalkene. Repetition of these steps leads to the formation of an unsaturated open-chain polymer product. All these steps are reversible, however, relieving the ring...
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Olefin Metathesis Polymerization: Overview01:13

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Recently, the development of olefin metathesis polymerization advanced the field of polymer synthesis. Simply put, the reorganization of substituents on their double bonds between two olefins in the presence of a catalyst is known as the olefin metathesis reaction. The use of metathesis reaction for polymer synthesis is called olefin metathesis polymerization.
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The Replisome

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DNA replication is carried out by a large complex of proteins that act in a coordinated matter to achieve high-fidelity DNA replication. Together this complex is known as the DNA replication machinery or the replisome.
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Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

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Step-growth or condensation polymerization is a stepwise reaction of bi or multifunctional monomers to form long-chain polymers. As all the monomers are reactive, most of the monomers are consumed at the early stages of the reaction to form small chains of reactive oligomers, which then combine to form long polymer chains in the late stages. Hence, the reaction has to proceed for a long time to achieve high molecular weight polymers.
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  2. 使用共价原料的h键模拟寡合体合成
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  2. 使用共价原料的h键模拟寡合体合成

相关实验视频

Synthesis of Information-bearing Peptoids and their Sequence-directed Dynamic Covalent Self-assembly
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Synthesis of Information-bearing Peptoids and their Sequence-directed Dynamic Covalent Self-assembly

Published on: February 6, 2020

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使用共价原料的H键模拟寡合体合成

Diego Núñez-Villanueva1, Christopher A Hunter1

  • 1Yusuf Hamied Department of Chemistry, University of Cambridge, Cambridge CB2 1EW, United Kingdom.

Journal of the American Chemical Society
|September 9, 2022

在PubMed 上查看摘要

概括
此摘要是机器生成的。

研究人员开发了一种新方法,用于模拟合成三醇寡合体,使用通过共价基对连接的原料. 这种方法可以通过结相互作用和模板再生实现高效的复制周期.

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Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives
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Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives

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Sequence-specific and Selective Recognition of Double-stranded RNAs over Single-stranded RNAs by Chemically Modified Peptide Nucleic Acids
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Sequence-specific and Selective Recognition of Double-stranded RNAs over Single-stranded RNAs by Chemically Modified Peptide Nucleic Acids

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相关实验视频

Synthesis of Information-bearing Peptoids and their Sequence-directed Dynamic Covalent Self-assembly
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Synthesis of Information-bearing Peptoids and their Sequence-directed Dynamic Covalent Self-assembly

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Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives
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Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives

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Sequence-specific and Selective Recognition of Double-stranded RNAs over Single-stranded RNAs by Chemically Modified Peptide Nucleic Acids
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Sequence-specific and Selective Recognition of Double-stranded RNAs over Single-stranded RNAs by Chemically Modified Peptide Nucleic Acids

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科学领域:

  • 化学合成
  • 超分子化学
  • 聚合物化学

背景情况:

  • 模板导向合成模仿生物核酸复制.
  • 初级扩展是聚合酶链反应 (PCR) 的关键步骤.
  • 开发高效的合成新型寡合物的方法至关重要.

研究的目的:

  • 实施初级附加模板用于三聚合物合成.
  • 研究结在模板导向反应中的作用.
  • 为了证明一个完整的复制周期与模板再生.

主要方法:

  • 共价基对形成以连接初始化器到模板.
  • 使用非共价与氧化物单体的识别单元.
  • 使用竞争反应来评估模板效应和具有约束力的亲和关系.
  • P 核磁共振光谱检测以确认产品的结构和结.

主要成果:

  • 取得了成功的三醇寡合物的模板合成.
  • 模板和氧化物单体之间的结相互作用显著加快了反应速度.
  • 氧化物单体的结合亲和力更高导致了更大的速率加速.
  • P 核磁共振检测证实产品双重中存在H键,表明共价和非共价对的兼容性.
  • 通过基对的水解完成了正式的复制周期.
  • 结论:

    • 建立了一个用于模板导向三醇寡合物的新方法.
    • 结合在提高反应速率和特异性方面起着至关重要的作用.
    • 开发的系统证明了共价和非共价结策略之间的几何兼容性.
    • 这项工作为开发人工复制系统提供了基础.