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原子转移自由基聚合平衡常数的测定

Determination of equilibrium constants for atom transfer radical polymerization.

作者信息

Tang Wei, Tsarevsky Nicolay V, Matyjaszewski Krzysztof

机构信息

Center for Macromolecular Engineering, Department of Chemistry, Carnegie Mellon University, 4400 Fifth Avenue, Pittsburgh, Pennsylvania 15213, USA.

出版信息

J Am Chem Soc. 2006 Feb 8;128(5):1598-604. doi: 10.1021/ja0558591.

Abstract

Atom transfer radical polymerization (ATRP) equilibrium constants (K(ATRP)) were determined using modified Fischer's equations for the persistent radical effect. The original Fischer's equations could be used only for low conversion of Cu(I) to X-Cu(II) and consequently for relatively low values of K(ATRP). At higher conversion to X-Cu(II) (>10%) and for larger values of K(ATRP) (>10(-)(7)), modified equations that take into account the changes in catalyst and initiator concentrations should be used. The validity of new equations was confirmed by detailed kinetic simulations. UV-vis spectrometric and GC measurements were used to follow the evolution of X-Cu(II) species and the initiator concentration, respectively, and to successfully determine values of K(ATRP) for several catalysts and alkyl halides. The effect of structure on reactivities of ATRP components is presented.

摘要

使用修正的费舍尔方程来确定原子转移自由基聚合(ATRP)平衡常数(K(ATRP)),以考虑持久自由基效应。原始的费舍尔方程仅适用于Cu(I)向X-Cu(II)的低转化率,因此仅适用于相对较低的K(ATRP)值。在向X-Cu(II)的较高转化率(>10%)以及较大的K(ATRP)值(>10^(-7))时,应使用考虑催化剂和引发剂浓度变化的修正方程。详细的动力学模拟证实了新方程的有效性。紫外可见光谱法和气相色谱测量分别用于跟踪X-Cu(II)物种的演变和引发剂浓度,并成功确定了几种催化剂和卤代烷的K(ATRP)值。本文还介绍了结构对ATRP组分反应活性的影响。

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