Phosphazene-promoted anionic polymerization

被引:50
作者
Zhao, Junpeng [1 ]
Hadjichristidis, Nikolaos [1 ]
Gnanou, Yves [2 ]
机构
[1] KAUST, Catalysis Ctr, Polymer Synth Lab, Div Phys Sci & Engn, Thuwal 23955, Saudi Arabia
[2] KAUST, Div Phys Sci & Engn, Thuwal 23955, Saudi Arabia
关键词
controlled anionic polymerization; metal-free polymerization techniques; phosphazene bases; mechanism in situ activation; RING-OPENING POLYMERIZATION; N-HETEROCYCLIC CARBENES; PROTON-TRANSFER POLYMERIZATION; OXIDE) SIDE-CHAINS; METAL-FREE; BLOCK-COPOLYMERS; ETHYLENE-OXIDE; ALKYLLITHIUM INITIATORS; (METH)ACRYLIC MONOMERS; BRUSH COPOLYMERS;
D O I
10.14314/polimery.2014.049
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
In the recent surge of metal-free polymerization techniques, phosphazene bases have shown their remarkable potential as organic promoters/catalysts for the anionic polymerization of various types of monomers. By complexation with the counterion (e.g. proton or lithium cation), phosphazene base significantly improve the nucleophilicity of the initiator/chain-end resulting in rapid and usually controlled anionic/quasi-anionic polymerization. In this review, we will introduce the general mechanism, i.e. in situ activation (of initiating sites) and polymerization, and summarize the applications of such a mechanism on macromolecular engineering toward functionalized polymers, block copolymers and complex macromolecular architectures.
引用
收藏
页码:49 / 59
页数:11
相关论文
共 70 条
[51]   NOVEL, VERY STRONG, UNCHARGED AUXILIARY BASES - DESIGN AND SYNTHESIS OF MONOMERIC AND POLYMER-BOUND TRIAMINOIMINOPHOSPHORANE BASES OF BROADLY VARIED STERIC DEMAND [J].
SCHWESINGER, R ;
WILLAREDT, J ;
SCHLEMPER, H ;
KELLER, M ;
SCHMITT, D ;
FRITZ, H .
CHEMISCHE BERICHTE-RECUEIL, 1994, 127 (12) :2435-2454
[52]   Synthesis of Well-Defined Polystyrene-Block-Polyglycidol (PS-b-PG) Block Co-polymers by Anionic Polymerization [J].
Siebert, Melanie ;
Keul, Helmut ;
Moeller, Martin .
DESIGNED MONOMERS AND POLYMERS, 2010, 13 (06) :547-563
[53]   Anionic and cationic ring-opening polymerization of 2,2,4,4,6,6-hexamethyl-8,8-divinylcyclotetrasiloxane [J].
Teng, CJ ;
Weber, WP ;
Cai, GP .
MACROMOLECULES, 2003, 36 (14) :5126-5130
[54]   One-pot synthesis of polyglycidol-containing block copolymers with alkyllithium initiators using the phosphazene base t-BuP4 [J].
Toy, Andrew Ah ;
Reinicke, Stefan ;
Mueller, Axel H. E. ;
Schmalz, Holger .
MACROMOLECULES, 2007, 40 (15) :5241-5244
[55]   Reaction kinetics for the anionic ring-opening polymerization of tetraphenyltetramethylcyclotetrasiloxane using a fast initiator system [J].
Van Dyke, ME ;
Clarson, SJ .
JOURNAL OF INORGANIC AND ORGANOMETALLIC POLYMERS, 1998, 8 (02) :111-117
[56]  
Vasilenko NG, 1998, MACROMOL CHEM PHYSIC, V199, P889
[57]   Synthesis of Poly(ε-caprolactone-co-methacrylic acid) Copolymer via Phosphazene-Catalyzed Hybrid Copolymerization [J].
Xu, Jinbao ;
Yang, Hongjun ;
Zhang, Guangzhao .
MACROMOLECULAR CHEMISTRY AND PHYSICS, 2013, 214 (03) :378-385
[58]   Synthesis and enzymatic degradation of poly(ε-caprolactone-co-ethylene carbonate-co-ethylene oxide) copolymer [J].
Yan, Manqing ;
Yang, Hongjun ;
Xing, Xinming .
POLYMER BULLETIN, 2013, 70 (02) :467-478
[59]   Hybrid copolymerization of cyclic and vinyl monomers [J].
Yang HongJun ;
Xu Jinbao ;
Zhang GuangZhao .
SCIENCE CHINA-CHEMISTRY, 2013, 56 (08) :1101-1104
[60]   Hybrid Copolymerization of ε-Caprolactone and Methyl Methacrylate [J].
Yang, Hongjun ;
Xu, Jinbao ;
Pispas, Stergios ;
Zhang, Guangzhao .
MACROMOLECULES, 2012, 45 (08) :3312-3317