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首页> 外文期刊>Polymer: The International Journal for the Science and Technology of Polymers >Living/controlled radical polymerization of methyl methacrylate by reverse ATRP with DCDPS/FeCl3/PPh3 initiating system
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Living/controlled radical polymerization of methyl methacrylate by reverse ATRP with DCDPS/FeCl3/PPh3 initiating system

机译:DCDPS / FeCl3 / PPh3引发体系逆ATRP对甲基丙烯酸甲酯的活性/受控自由基聚合

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Living/controlled radical polymerization of methyl methacrylate (MMA) was investigated using a new initiating system, i.e. DCDPS/FeCl3/PPh3, in which diethyl 2,3-dicyano-2,3-diphenylsuccinate (DCDPS) is a hexa-substituted ethane thermal iniferter. The polymerization mechanism belongs to a reverse ATRP process. The polymerization was closely controlled in bull; and in solution at quite low temperature such as 75 or 60 degrees C. The molecular weights of so-obtained PMMA were high and polydispersities were quite narrow (M-w/M-n = 1.20-1.31). End group analysis result using H-1 NMR spectroscopy shows that the polymer obtained is omega-functionalized by a chlorine atom. With the Cl atom at the chain end, PMMA obtained could be used as macroinitiator to proceed chain-extension reaction with MMA and block copolymerization reaction with styrene in the presence of CuCl/bipy catalyst via a conventional ATRP process. (C) 2000 Elsevier Science Ltd. All rights reserved. [References: 33]
机译:使用新的引发系统DCDPS / FeCl3 / PPh3研究了甲基丙烯酸甲酯(MMA)的活性/受控自由基聚合,其中2,3-二氰基-2,3-二苯基琥珀酸二乙酯(DCDPS)为六取代的乙烷育种者。聚合机理属于逆ATRP过程。聚合受到严格控制。如此获得的PMMA的分子量高并且多分散性非常窄(M-w / M-n = 1.20-1.31)。使用H-1 NMR光谱的端基分析结果表明,所获得的聚合物被氯原子ω-官能化。在链末端具有Cl原子的情况下,获得的PMMA可以用作大分子引发剂,以通过常规ATRP方法在CuCl / bipy催化剂存在下与MMA进行链延长反应和与苯乙烯的嵌段共聚反应。 (C)2000 Elsevier ScienceLtd。保留所有权利。 [参考:33]

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