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Identity of Low-Molecular-Weight Species Formed in End-To-End Cyclization Reactions Performed in THF

机译:在THF中进行的端到端环化反应中形成的低分子量物种的身份

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摘要

Cyclic polymers were produced by end-to-end coupling of telechelic linear polymers under dilute conditions in THF, using intramolecular atom transfer radical coupling or click chemistry. In addition to the expected shift to longer elution times on gel permeation chromatography (GPC) indicative of the formation of cyclic product, lower molecular weight species were consistently observed upon analysis of the unpurified cyclization reaction mixture. By systematically removing or altering single reaction components in the highly dilute cyclization reaction, it was found that THF itself was responsible for the low-molecular-weight material, forming oligomeric chains of poly(THF) regardless of the other reaction components. When the reactions were performed at higher concentrations and for shorter time intervals, conducive to intermolecular chain-end-joining reactions, the low-molecular-weight peaks were absent. Isolation of the material and analysis by 1H NMR confirmed that poly(THF) was being formed in the highly dilute conditions required for cyclization by end-to-end coupling. When a series of mock cyclization reactions were performed with molar ratios of the reactants held constant, but concentrations changed, it was found that lower concentrations of reactants led to higher amounts of poly(THF) side product.
机译:通过分子内原子转移自由基偶联或点击化学,在稀条件下于THF中的遥螯线性聚合物端对端偶联来制备环状聚合物。除了预期在凝胶渗透色谱(GPC)上转移到更长的洗脱时间以指示形成环状产物外,在分析未纯化的环化反应混合物时,始终观察到较低分子量的物质。通过在高度稀释的环化反应中系统地除去或改变单个反应组分,发现THF本身是低分子量材料的原因,形成了聚(THF)的低聚物链,而与其他反应组分无关。当以较高的浓度和较短的时间间隔进行反应时,有利于分子间链端连接反应,低分子量峰不存在。分离材料并通过1 H NMR分析证实,聚四氢呋喃是在端对端偶联环化所需的高度稀释条件下形成的。当在使反应物的摩尔比保持恒定但浓度改变的情况下进行一系列模拟环化反应时,发现较低的反应物浓度导致较高数量的聚(THF)副产物。

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