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Facile Synthesis of In‐Chain, Multicomponent, Functionalized Polymers via Living Anionic Copolymerization through the Ugi Four‐Component Reaction (Ugi‐4CR)
Author(s) -
Shen Heyu,
Ma Hongwei,
Liu Pibo,
Huang Wei,
Han Li,
Li Chao,
Li Yang
Publication year - 2017
Publication title -
macromolecular rapid communications
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.348
H-Index - 154
eISSN - 1521-3927
pISSN - 1022-1336
DOI - 10.1002/marc.201700353
Subject(s) - copolymer , polystyrene , ugi reaction , polymer chemistry , polymer , surface modification , trimethylsilyl , polymerization , chemistry , anionic addition polymerization , hydrolysis , combinatorial chemistry , materials science , isocyanide , organic chemistry
By combining living anionic polymerization and the highly efficient Ugi four‐component reaction (Ugi‐4CR), in‐chain, multicomponent, functionalized polymers are facilely synthesized with efficient conversation and abundant functionality. l‐[4‐[ N , N ‐Bis(trimethylsilyl)‐amino]phenyl]‐l‐phenylethylene, which is redefined as Ugi‐DPE, is anionically copolymerized to synthesize the well‐defined in‐chain, multi‐amino functionalized polystyrene (P(St/DPE‐NH 2 )), the backbone for the Ugi‐4CR, via hydrolysis of the copolymerization (P(St/Ugi‐DPE)). Subsequently, several functionalized components are facilely clicked onto P(St/DPE‐NH 2 ) to investigate the model reactions of the in‐chain, multicomponent functionalization via the Ugi‐4CR. In contrast to conventional postpolymerization modifications, this approach proceeds under mild reaction conditions without the use of a catalyst and meanwhile an efficient conversation is obtained. Finally, the modified experimental results investigated in this research show the promising potential of the combination of well‐defined amino functionalized polymers and Ugi‐4CR in the field of multicomponent, functionalized postpolymerization modification.

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