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Cu Catalyst System with Phosphorous Containing Bidendate Ligand for Living Radical Polymerization of MMA

机译:含双齿配体磷的铜催化剂体系对MMA的活性自由基聚合

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The polymerization of methyl methacrylate (MMA) was carried out using CuBr/bidentate phosphorus ligand catalyst systems.MMA polymerization with CuBr/phosphine-phosphinidene (PP) exhibited high conversion (approx 80%) in 5 h at 90 deg C along with a linear increase of ln([M]_0/[M]) versus time,indicating constant concentration of the propagating radicals during the polymerization.The molecular weight of the prepared PMMA tended to increase with conversion,suggesting the living polymerization characteristic of the system.On the other hand,a large difference between the measured and theoretical molecular weight and a broad molecular weight distribution were observed,implicating possible incomplete control over the polymerization.This may have been caused by the low deactivation rate constant (k_(deact)) of the system.The low k_(deact) would result in irreversible generation of radicals instead of reversible activation/deactivation process of ATRP.Polymerizations performed at different ligand to CuBr ratios and different monomer to initiator ratios did not afford better control over the polymerization,suggesting that the controllability of CuBr/phosphorus ligand system for ATRP is inherently limited.
机译:甲基丙烯酸甲酯(MMA)的聚合是使用CuBr /双齿磷配体催化剂体系进行的.MMA聚合与CuBr /膦-次膦酸酯(PP)在5个小时内在90摄氏度下表现出高转化率(约80%),并且呈线性ln([M] _0 / [M])随时间的增加而增加,表明聚合过程中自由基的浓度恒定。制得的PMMA的分子量随转化率而增加,表明该体系的活性聚合特性。另一方面,观察到的分子量与理论分子量之间存在较大差异,分子量分布范围较宽,暗示可能无法完全控制聚合反应。这可能是由于低失活速率常数(k_(deact))引起的。低k_(deact)将导致自由基的不可逆生成,而不是ATRP的可逆激活/失活过程。在不同lig进行的聚合对于CuBr比率和不同的单体与引发剂比率,不能更好地控制聚合反应,这表明CuBr /磷配体体系对ATRP的可控性固有地受到限制。

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