应用化学 ›› 2018, Vol. 35 ›› Issue (1): 89-101.DOI: 10.11944/j.issn.1000-0518.2018.01.170031

• 研究论文 • 上一篇    下一篇

RCOO-取代的镍(Ⅱ)配合物单组分高效催化乙烯均聚和共聚反应

李威威ab,穆红亮a*(),刘靖宇a,李悦生c   

  1. a中国科学院长春应用化学研究所 高分子物理与化学国家重点实验室 长春 130022
    b中国科学院大学 北京 100049
    c天津大学材料科学与工程学院 天津 300072
  • 收稿日期:2017-02-13 接受日期:2016-03-27 出版日期:2018-01-03 发布日期:2018-01-03
  • 通讯作者: 穆红亮
  • 基金资助:
    国家自然科学基金(21304087)项目资助

Nickel(Ⅱ) Complexes Containing RCOO-Substituent as Highly Active Single-Component Catalysts for Ethylene (Co)Polymerization

LI Weiweiab,MU Honglianga*(),LIU Jingyua,LI Yueshengc   

  1. aState Key Laboratory of Polymer Physics and Chemistry,Changchun Institute of Applied Chemistry,Chinese Academy of Sciences,Changchun 130022,China
    bUniversity of Chinese Academy of Sciences,Beijing 100049,China
    cSchool of Material Science and Engineering,Tianjin University,Tianjin 300072,China
  • Received:2017-02-13 Accepted:2016-03-27 Published:2018-01-03 Online:2018-01-03
  • Contact: MU Hongliang
  • Supported by:
    Supported by the National Natural Science Foundation of China(No.21304087)

摘要:

合成并表征了含RCOO-基团的单核(Ni1~Ni2)及双核(Ni3)镍配合物[(2,6-R2-C6H3)—N=C(H)—(3-Ph-5-PhCOO-2-O-C6H2)-κ2-N,O]Ni(CH3)(pyridine)](R=iPr;3,5-tBu2C6H3),并用于催化乙烯均聚和共聚反应。 作为单组分催化剂,这些配合物可以有效地催化乙烯聚合得到中等相对分子质量的支化聚乙烯(PE)。 供电性的PhCOO—基团促进了催化剂Ni1的引发,从而在低温下比Ni0活性更高。 引入大位阻的2,6-(3,5-二叔丁基苯基)苯胺基团,催化剂Ni2在5×105 Pa下的活性高达1.8×106 g PE mol-1·Ni-1·h-1,是活性最高的水杨醛亚胺中性镍催化剂之一。 与相应的单核催化剂相比,双核催化剂Ni3对三苯基膦具有更好的耐受性。 这些催化剂可催化乙烯与1,5-己二烯、1,7-辛二烯、6-溴-1-己烯或10-十一烯酸甲酯的共聚合,制备功能化聚乙烯。

关键词: 中性镍催化剂, 电子效应, 烯烃聚合, 功能化聚烯烃

Abstract:

Mononuclear nickel complexes [(2,6-R2-C6H3)—N=C(H)—(3-Ph-5-PhCOO-2-O-C6H2)-κ2-N,O]Ni(CH3)(pyridine)](R=iPr; 3,5-tBu2C6H3)(Ni1~Ni2) and binuclear nickel complex(Ni3) were synthesized, characterized and applied in ethylene (co)polymerization. As single-component catalysts, all these complexes are capable of converting ethylene to branched polyethylenes(PE) with moderate relative molecular mass. The electron-donating group PhCOO— facilitates the initiation of catalyst Ni1, leading to better catalytic activity at low temperature compared to nickel methyl pyridine comples(Ni0). Introducing bulky 2,6-(3,5-(t-Bu)2C6H3)2C6H3N— moiety, the activities of Ni2 up to 1.8×106 g of PE mol-1·Ni-1·h-1(at 5×105 Pa ethylene) were among the highest values using phenoxyiminato neutral nickel catalysts. Binuclear catalyst Ni3 showes better tolerance toward PPh3 donor additive than its mononuclear counterpart. In the presence of comonomers 1,5-hexadiene, 1,7-octadiene, 6-bromo-1-hexene, or methyl 10-undecenoate, these catalysts effectively enchain these comonomers into the polymer chain to give functionalized polyethylenes.

Key words: neutral nickel catalysts, electronic effects, olefin polymerization, functionlized polyolefin