原子转移自由基聚合
甲基丙烯酸酯
化学
还原剂
聚合
高分子化学
胺气处理
动能
组合化学
化学工程
聚合物
物理化学
有机化学
物理
量子力学
工程类
作者
Kevin A. Payne,Dagmar D’hooge,Paul Van Steenberge,Marie‐Françoise Reyniers,Michael F. Cunningham,Robin A. Hutchinson,Guy Marin
出处
期刊:Macromolecules
[American Chemical Society]
日期:2013-05-06
卷期号:46 (10): 3828-3840
被引量:95
摘要
A comprehensive kinetic Monte Carlo (kMC) model is used to interpret and better understand the results of a systematic experimental investigation of activators regenerated by electron transfer atom transfer radical polymerization (ARGET ATRP) of butyl methacrylate (BMA) using Sn(EH)(2) as reducing agent, ethyl 2-bromoisobutyrate (EBiB) as ATRP initiator, and CuBr2/TPMA (TPMA: tris[(2-pyridyl)methyl]amine) as deactivator. The model demonstrates the importance of slow initiation, with distinct activation and deactivation rate coefficients for the initiator and polymeric species required to match the experimental data. In addition, the model incorporates a second reduction step for the reducing agent and accounts for diffusional limitations on chain-length-dependent termination. The effect of temperature on the slow ATRP initiation is limited, and a sufficiently high initial reducing agent concentration is crucial to obtain a high conversion, although achieved at the expense of decreased end-group functionality.
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