Efficient One-Pot Synthesis of End-Functionalized trans-Stereoregular Polydiene Macromonomers

被引:33
作者
Georges, Sebastien [1 ]
Hashrni, Obaid Hasan [1 ]
Bria, Marc [2 ]
Zinck, Philippe [1 ]
Champouret, Yohan [1 ]
Visseaux, Marc [1 ]
机构
[1] Univ Lille, Univ Artois, ENSCL, CNRS,UMR 8181,Cent Lille,UCCS, F-59000 Lille, France
[2] Univ Lille, CCM RMN, F-59000 Lille, France
关键词
CHAIN TRANSFER POLYMERIZATION; STEREOSPECIFIC POLYMERIZATION; ISOPRENE POLYMERIZATION; MOLECULAR-WEIGHT; GROUP METAL; COPOLYMERIZATION; CATALYST; DIALKYLMAGNESIUM; 1,3-BUTADIENE; POLYOLEFINS;
D O I
10.1021/acs.macromol.8b01520
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
End-functionalized 1,4-trans-polydienes (isoprene and myrcene) were prepared by means of a neodymium-mediated continuous polymerization-functionalization process. A chain transfer stage was essential to get a high level of functionalization of the polymer. The living 1,4-trans-stereoregular polymer chain was reacted with benzophenone to afford up to 97% -CPh2OH end-group with isoprene, while in the case of myrcene, using the same strategy afforded 1,4-trans-polymyrcene with a functionalization rate of 83%. The strategy was validated with complementary functionalization experiments using benzaldehyde and styrene oxide, both affording 95% end-capped trans-stereoregular polydienes.
引用
收藏
页码:1210 / 1219
页数:10
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