共查询到17条相似文献,搜索用时 62 毫秒
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本文介绍了质子捕技术在阳离子聚合中的应用最新研究工作进展。对质子捕捉剂在阳离子聚合反应机理研究中的应用以及质子捕捉剂在活性阳郭聚合引发体系中的作用和功能作了详尽的讨论。 相似文献
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亲核性调节剂在异丁烯活性阳离子聚合中发挥着极其重要的作用 ,其作用机理主要包括 :(1)碳阳离子稳定化作用 ,即亲核性试剂或它们与Lewis酸生成的络合物与增长链的末端结合 ,来降低活性中心阳离子的“阳离子性” ,抑制副反应 ,使聚合反应呈现活性聚合特征 ;(2 )质子捕获作用 ,即亲核性试剂捕获质子 ,抑制质子的不可控引发和链转移反应 ;(3)增长链表观稳定作用 ,即亲核试剂降低了增长速率与引发速率之比 ,提高引发效率 ,降低增长速率 ,降低分子量分布 ;(4)抑制自由离子增长作用 ,即亲核试剂与质子源和Lewis酸反应 ,生成同阴离子 ,产生同离子效应 ,抑制自由离子活性中心的引发增长作用。 相似文献
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活性阳离子聚合法合成嵌段共聚物的研究进展 总被引:2,自引:0,他引:2
在80年代,阳离子聚合研究的一个最重要突破可能就是活性阳离子聚合。目前为止,有关活性阳离子聚合的新引发体系,新单体及合成应用等方面已取得巨大进展,本综述主要介绍利用活性阳离子聚合合成二、三元嵌段和多元嵌段共聚物的研究成果。 相似文献
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本文围绕着乙烯基阳离子聚合这一核心,简要地介绍了近年来在阳离子聚合引发剂方面取得的新进展,包括活性阳离子聚合和普通阳离子聚合引发剂两个部分。 相似文献
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传统阳离子聚合只能在低温、无水、无氧和高纯惰性气体保护下进行,归因于共引发剂Lewis酸对水高度敏感,即使少量水存在也能令其失效。由于"绿色化学"概念的提出,水作为一种环境友好的绿色溶剂也一直受到工业界的青睐。近十几年来,随着耐水性引发体系的发展,使得水相体系中进行阳离子聚合成为了可能,改变了传统阳离子聚合的观念,这种新方法也备受人们的关注。本文首先介绍了水相阳离子聚合的机理,重点阐述了不同单体的水相阳离子聚合及其匹配的耐水性引发体系的研究和发展,并指出不同引发体系的优势与不足,最后总结了水相阳离子聚合中存在的问题,展望了水相阳离子聚合的研究方向和发展前景。 相似文献
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Dr. Maosheng Li Hongyu Li Dr. Xiaoyong Zhang Prof. Xianhong Wang Prof. Youhua Tao 《Angewandte Chemie (International ed. in English)》2023,62(26):e202303237
Exploiting non-covalent interactions to catalyze challenging ionic polymerizations is an ambitious goal but is in its infancy. We recently demonstrated non-covalent anion-binding catalysis as an effective methodology to enable living cationic polymerization (LCP) of vinyl ethers in an environmentally benign manner. Here, we further elucidate the structure-reactivity relationships of the elaborately designed seleno-cyclodiphosph(V)azanes catalysts and the roles of anion-binding interactions by a combined theoretical DFT study and experimental study. The investigation suggests that the distinct cis-cyclodiphosph(V)azane framework combined with “selenium effect” and electron-withdrawing 3,5-(CF3)2-Phenyl substitution pattern in catalyst enables a critical contribution to accessing excellent stability, anion affinity and solubility under polymerization conditions. Thus, the catalyst could leverage anion-binding interactions to precisely control reversible and transient dormant-active species equilibrium, allowing it to dynamically bind, recognize and pre-organize propagating ionic species and monomer, thereby facilitating efficient chain propagation and minimizing irreversible chain transfer events under mild conditions. The more in-depth understanding of the mechanism for anion-binding catalytic LCP reported herein should help to guide future catalyst design and to extend this concept to broader polymerization systems where ionic species serve as crucial intermediates. 相似文献
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<正>离子聚合是高分子科学中重要的聚合方法之一,也是制备聚异丁烯或丁基橡胶等关键材料不可或缺的聚合方法.本文总结了异丁烯、苯乙烯及其衍生物等单体可控/活性正离子聚合的新引发体系、聚合反应特征的调节与转化、水相介质中正离子聚合新方法与新工艺、微观分子混合与正离子聚合新工艺及其用于设计合成异丁烯基聚合物.这些方法与技术是发展高效节能与绿色减排先进聚合物生产技术的重要途径,部分研究成果已在产业化中得到应用与验证.发展可控/活性正离子聚合新体系、新方法与新工艺,为实现绿色低碳高分子化工过程及相关产品工程(新结构、新功能、高性能与高品质)提供了新思路与新技术. 相似文献
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Abstract Several new open-chain and cyclic enol ether monomers were prepared using simple, straightforward procedures. The reactivities of these monomers were compared using both differential scanning photocalorimetry and Fourier transform real-time infrared spectroscopy. In general, these new monomers were found to possess excellent reactivity in photoinitiated cationic polymerization using a diaryliodonium salt photoinitiator. 相似文献
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In this work, a fluorescent monomer 2-(9-carbazolyl) ethyl vinyl ether(CEVE) was synthesized in our lab, and its photo-induced living cationic copolymerization behavior with isobutyl vinyl ether(IBVE) was investigated in detail using diphenyliodonium chloride(DPICl)/2,2-dimethoxy-2-phenylacetophenone(DMPA) and zinc bromide(Zn Br2) initiating system in dichloromethane solution at 5 °C, -5 °C, and -15 °C, respectively. The living nature of this copolymerization system was confirmed by adding fresh comonomer method after the copolymerization almost finished. In addition, the obtained fluorescent copolymer poly(IBVE-co-CEVE) has a low glass transition temperature(Tg), below -10 °C. 相似文献