The Synthesis of Sequence-controlled Multiblock Copolymers by Frustrated Lewis Pair: Can the Pandora's Box be Reopened?

被引:2
|
作者
Wan, Xin-hua [1 ]
机构
[1] Peking Univ, Beijing Natl Lab Mol Sci, Dept Coll Chem & Mol Engn, Key Lab Polymer Chem & Phys,Minist Educ, Beijing 100871, Peoples R China
来源
ACTA POLYMERICA SINICA | 2020年 / 51卷 / 06期
关键词
Sequence-controlled multiblock copolymers; Frustrated Lewis pair; Living polymerization; Organophosphorus superbase; Pandora' box; LIVING POLYMERIZATION;
D O I
10.11777/j.issn1000-3304.2020.20104
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Sequence-controlled polymers have been regarded as a great challenging holy grail to be ultimately achieved in polymer science. However, its synthesis is just like a Pandora's box that is impossible to be reopened due to the lack of efficient synthetic methodologies. More recently, Yuetao Zhang's group at Jilin University has made a big breakthrough in the synthesis of sequence-controlled polymers by using living/controlled frustrated Lewis pair (FLP) polymerization system. FLP composed of organophosphorus superbase and organoaluminum Lewis acid can rapidly incoporate four methacrylic monomers into a tripentacontablock copolymers, which is by far the world's highest record for block numbers (about 2.5 times of the previous record) and the degree of polymerization is 50 per block. This synthetic strategy has several remarkable features such as room-temperature synthesis and easily scale-up to high multigram experiment over 110 grams; simple procedure: no additional initiator or catalyst but only sequential addition of monomer is required for per block copolymerization. It only took 30 min to synthesize such a tripentacontablock copolymers. All these features indicated the very promising prospects of this FLP polymerization system in industry, inspiring the polymer chemists' enthusiasm to reopen the pandora's box.
引用
收藏
页码:569 / 572
页数:4
相关论文
共 18 条
  • [1] Sequence control in polymer synthesis
    Badi, Nezha
    Lutz, Jean-Francois
    [J]. CHEMICAL SOCIETY REVIEWS, 2009, 38 (12) : 3383 - 3390
  • [2] Rapid and Scalable Access to Sequence-Controlled DHDM Multiblock Copolymers by FLP Polymerization
    Bai, Yun
    Wang, Huaiyu
    He, Jianghua
    Zhang, Yuetao
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2020, 59 (28) : 11613 - 11619
  • [3] Polymerization of Polar Vinyl Monomers Catalyzed by Lewis Pairs
    Bai, Yun
    Zhang, Yue-tao
    [J]. ACTA POLYMERICA SINICA, 2019, 50 (03): : 233 - 246
  • [4] Ultra-High-Molecular-Weight Polymers Produced by the Immortal Phosphine-Based Catalyst System
    Bai, Yun
    He, Jianghua
    Zhang, Yuetao
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2018, 57 (52) : 17230 - 17234
  • [5] Multiblock Polymers: Panacea or Pandora's Box?
    Bates, Frank S.
    Hillmyer, Marc A.
    Lodge, Timothy P.
    Bates, Christopher M.
    Delaney, Kris T.
    Fredrickson, Glenn H.
    [J]. SCIENCE, 2012, 336 (6080) : 434 - 440
  • [6] Sequence-definition from controlled polymerization: the next generation of materials
    De Neve, Jeroen
    Haven, Joris J.
    Maes, Lowie
    Junkers, Tanja
    [J]. POLYMER CHEMISTRY, 2018, 9 (38) : 4692 - 4705
  • [7] Engelis NG, 2017, NAT CHEM, V9, P171, DOI [10.1038/NCHEM.2634, 10.1038/nchem.2634]
  • [8] Rapid and quantitative one-pot synthesis of sequence-controlled polymers by radical polymerization
    Gody, Guillaume
    Maschmeyer, Thomas
    Zetterlund, Per B.
    Perrier, Sebastien
    [J]. NATURE COMMUNICATIONS, 2013, 4
  • [9] Lutz J F., 2017, MACROMOL RAPID COMM, V38
  • [10] Transition Metal-Catalyzed Living Radical Polymerization: Toward Perfection in Catalysis and Precision Polymer Synthesis
    Ouchi, Makoto
    Terashima, Takaya
    Sawamoto, Mitsuo
    [J]. CHEMICAL REVIEWS, 2009, 109 (11) : 4963 - 5050