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Hydrolytic polycondensation of bisphenol-A-bischloroformate catalyzed by phase-transfer catalysts

机译:相转移催化剂催化双酚A-双氯甲酸酯的水解缩聚

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摘要

The hydrolytic interfacial polycondensation of bisphenol-A-bischloroformate was performed with four different phase-transfer (PT) catalysts: N-butylpyridinium bromide, triethylbenzylammonium (TEBA) chloride, tetra-butylammonium hydrogen sulfate, and tetraphenylphosphonium bromide. These polycondensations were conducted at 5 or 25degreesC initial reaction temperature. The resulting poly-carbonates were characterized by viscosity and SEC measurements and by MALDI-TOF mass spectrometry. The four PT catalysts gave quite different results with respect to molecular weights (number average, (M) over bar (n) approximate to 215 kDa and weight average, (M) over bar (W) approximate to 600 kDa) were obtained with TEBA-Cl proved to be favorable for both high molecular weights and high fractions of cycles. Cyclic polycarbonates were detectable in the mass spectra up to 14 kDa (technical limit of the measurements). Low molecular weights in combination with unreacted chloroformate groups proved that the other PT-catalysts were less efficient under the given reaction conditions. [References: 22]
机译:双酚-A-双氯甲酸酯的水解界面缩聚反应使用四种不同的相转移(PT)催化剂进行:溴化N-丁基吡啶鎓,氯化三乙基苄基铵(TEBA),硫酸四丁基铵和溴化四苯基phosph。这些缩聚反应是在5或25℃的初始反应温度下进行的。通过粘度和SEC测量以及通过MALDI-TOF质谱法表征所得的聚碳酸酯。四种PT催化剂在分子量方面(通过TEBA获得的数均分子量(数均,(M)超过bar(n)约为215 kDa)和重均分子量(M)超过bar(W)约为600 kDa)给出了截然不同的结果。事实证明,-Cl对于高分子量和高循环分数都是有利的。在质谱中可检测到高达14 kDa(测量的技术极限)的环状聚碳酸酯。低分子量与未反应的氯甲酸酯基团结合证明,在给定的反应条件下,其他PT催化剂的效率较低。 [参考:22]

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