Block and Hetero Ethyl Cellulose Graft Copolymers Synthe- sized via Sequent and One-pot ATRP and "Click" Reactions
Ethyl cellulose graft copolymers with block and hetero side chains, ethyl cellulose graft [polystyrene-b-poly- (ethylene glycol)] [EC-g-(PS-b-PEG)] and ethyl cellulose graft polystyrene and polyethylene glycol [EC-g-(PS-PEG )] were synthesized by atomic transfer radical polymerization (ATRP) and alk...
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Published in | 中国化学:英文版 Vol. 30; no. 9; pp. 2169 - 2175 |
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Main Author | |
Format | Journal Article |
Language | English |
Published |
2012
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Subjects | |
Online Access | Get full text |
ISSN | 1001-604X 1614-7065 |
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Summary: | Ethyl cellulose graft copolymers with block and hetero side chains, ethyl cellulose graft [polystyrene-b-poly- (ethylene glycol)] [EC-g-(PS-b-PEG)] and ethyl cellulose graft polystyrene and polyethylene glycol [EC-g-(PS-PEG )] were synthesized by atomic transfer radical polymerization (ATRP) and alkyne-azide "click" reactions and "one-pot" ATRP and "click" reactions, respectively. For the synthesis of EC-g-(PS-b-PEG), the macroinitiator for ATRP was first synthesized via the esterification of hydroxyl groups of EC with 2-bromoisobutyryl bromide to re- sult ethyl cellulose 2-bromoisobutyryl ester (EC-Br). The degree of substitution of bromide groups, which deter- mined the graft density, can be tailored by varying the feeding ratios of the hydroxyl groups to 2-bromoisobutyryl bromide. Then ATRP was carried out for preparing EC-g-PS-Br with well-defined length of PS chains. The EC-g-PS-Br copolymers were then converted to EC-g-PS-N3 and then reacted with end alkyne-functionalized PEG via click to result in EC-g-(PS-b-PEG). The EC-g-(PS-PEG) copolymers were synthesized by converting bromide groups of EC-Br to azide groups (EC-Br-N3) and then by one-pot ATRP and "click" reactions. The resultant graft copolymers were characterized by FTIR and IH NMR. The results indicate the success of the synthetic procedure of the cellulose grail copolymers with block and hetero side chains. |
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Bibliography: | ethyl cellulose, graft copolymers, atomic transfer radical polymerization (ATRP), click reaction Ethyl cellulose graft copolymers with block and hetero side chains, ethyl cellulose graft [polystyrene-b-poly- (ethylene glycol)] [EC-g-(PS-b-PEG)] and ethyl cellulose graft polystyrene and polyethylene glycol [EC-g-(PS-PEG )] were synthesized by atomic transfer radical polymerization (ATRP) and alkyne-azide "click" reactions and "one-pot" ATRP and "click" reactions, respectively. For the synthesis of EC-g-(PS-b-PEG), the macroinitiator for ATRP was first synthesized via the esterification of hydroxyl groups of EC with 2-bromoisobutyryl bromide to re- sult ethyl cellulose 2-bromoisobutyryl ester (EC-Br). The degree of substitution of bromide groups, which deter- mined the graft density, can be tailored by varying the feeding ratios of the hydroxyl groups to 2-bromoisobutyryl bromide. Then ATRP was carried out for preparing EC-g-PS-Br with well-defined length of PS chains. The EC-g-PS-Br copolymers were then converted to EC-g-PS-N3 and then reacted with end alkyne-functionalized PEG via click to result in EC-g-(PS-b-PEG). The EC-g-(PS-PEG) copolymers were synthesized by converting bromide groups of EC-Br to azide groups (EC-Br-N3) and then by one-pot ATRP and "click" reactions. The resultant graft copolymers were characterized by FTIR and IH NMR. The results indicate the success of the synthetic procedure of the cellulose grail copolymers with block and hetero side chains. 31-1547/O6 Li, Qinmei Kang, Hongliang Liu, Ruigang Huang, Yong(a Laboratory of Polymer Physics and Chemistry, Beijing National Laboratory of Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China b Graduate University, Chinese Academy of Sciences, Beijing 100039, China c National Engineering Research Center of Plastics, Technical Institute of Physics and Chemistry, Chinese Academy of Seiences, Beijing 100190, China) |
ISSN: | 1001-604X 1614-7065 |