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双(吡咯烷酮-亚胺)钛配合物与甲基铝氧烷催化乙烯与降冰片烯的活性共聚反应。

Living copolymerization of ethylene with norbornene catalyzed by bis(pyrrolide-imine) titanium complexes with MAO.

作者信息

Yoshida Yasunori, Mohri Jun-ichi, Ishii Sei-ichi, Mitani Makoto, Saito Junji, Matsui Shigekazu, Makio Haruyuki, Nakano Takashi, Tanaka Hidetsugu, Onda Mitsuhiko, Yamamoto Yukari, Mizuno Akira, Fujita Terunori

机构信息

R & D Center, Mitsui Chemicals, Inc., 580-32 Nagaura, Sodegaura, Chiba, 299-0265, Japan.

出版信息

J Am Chem Soc. 2004 Sep 29;126(38):12023-32. doi: 10.1021/ja048357g.

Abstract

Bis(pyrrolide-imine) Ti complexes in conjunction with methylalumoxane (MAO) were found to work as efficient catalysts for the copolymerization of ethylene and norbornene to afford unique copolymers via an addition-type polymerization mechanism. The catalysts exhibited very high norbornene incorporation, superior to that obtained with Me(2)Si(Me(4)Cp)(N-tert-Bu)TiCl(2) (CGC). The sterically open and highly electrophilic nature of the catalysts is probably responsible for the excellent norbornene incorporation. The catalysts displayed a marked tendency to produce alternating copolymers, which have stereoirregular structures despite the C(2) symmetric nature of the catalysts. The norbornene/ethylene molar ratio in the polymerization medium had a profound influence on the molecular weight distribution of the resulting copolymer. At norbornene/ethylene ratios larger than ca. 1, the catalysts mediated room-temperature living copolymerization of ethylene and norbornene to form high molecular weight monodisperse copolymers (M(n) > 500,000, M(w)/M(n) < 1.20). (13)C NMR spectroscopic analysis of a copolymer, produced under conditions that gave low molecular weight, demonstrated that the copolymerization is initiated by norbornene insertion and that the catalyst mostly exists as a norbornene-last-inserted species under living conditions. Polymerization behavior coupled with DFT calculations suggested that the highly controlled living polymerization stems from the fact that the catalysts possess high affinity and high incorporation ability for norbornene as well as the characteristics of a living ethylene polymerization though under limited conditions (M(n) 225,000, M(w)/M(n) 1.15, 10-s polymerization, 25 degrees C). With the catalyst, unique block copolymers [i.e., poly(ethylene-co-norbornene)(1)-b-poly(ethylene-co-norbornene)(2), PE-b-poly(ethylene-co-norbornene)] were successfully synthesized from ethylene and norbornene. Transmission electron microscopy (TEM) indicated that the PE-b-poly(ethylene-co-norbornene) possesses high potential as a new material consisting of crystalline and amorphous segments which are chemically linked.

摘要

双(吡咯烷-亚胺)钛配合物与甲基铝氧烷(MAO)协同作用,被发现是乙烯和降冰片烯共聚的高效催化剂,通过加成型聚合机理得到独特的共聚物。这些催化剂表现出非常高的降冰片烯插入率,优于用Me(2)Si(Me(4)Cp)(N-tert-Bu)TiCl(2)(CGC)所获得的插入率。催化剂空间位阻开放且具有高亲电性,这可能是其优异的降冰片烯插入率的原因。这些催化剂显示出显著的生成交替共聚物的倾向,尽管催化剂具有C(2)对称性,但所得共聚物具有立体不规则结构。聚合介质中降冰片烯/乙烯的摩尔比对所得共聚物的分子量分布有深远影响。在降冰片烯/乙烯比大于约1时,催化剂介导乙烯和降冰片烯在室温下的活性共聚,形成高分子量单分散共聚物(M(n)>500,000,M(w)/M(n)<1.20)。对在低分子量条件下制备的共聚物进行的(13)C NMR光谱分析表明,共聚反应由降冰片烯插入引发,并且在活性条件下催化剂大多以降冰片烯最后插入的物种形式存在。聚合行为与DFT计算表明,高度可控的活性聚合源于这样一个事实,即催化剂对降冰片烯具有高亲和力和高插入能力,以及在有限条件下(M(n) 225,000,M(w)/M(n) 1.15,10-s聚合,25℃)的活性乙烯聚合特性。使用该催化剂,成功地从乙烯和降冰片烯合成了独特的嵌段共聚物[即聚(乙烯-共-降冰片烯)(1)-b-聚(乙烯-共-降冰片烯)(2),PE-b-聚(乙烯-共-降冰片烯)]。透射电子显微镜(TEM)表明,PE-b-聚(乙烯-共-降冰片烯)作为一种由化学连接的结晶段和无定形段组成的新材料具有很高的潜力。

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