Polyethylene-g-Polystyrene Copolymers by Combination of ROMP, Mn2(CO)10-Assisted TEMPO Substitution and NMRP

被引:26
作者
Ciftci, Mustafa [1 ]
Arslan, Mustafa [1 ]
Buchmeiser, Michael [2 ]
Yagci, Yusuf [1 ,3 ,4 ]
机构
[1] Istanbul Tech Univ, Dept Chem, TR-34469 Istanbul, Turkey
[2] Univ Stuttgart, Inst Polymer Chem, Pfaffenwaldring 55, D-70550 Denkendorf, Germany
[3] King Abdulaziz Univ, Ctr Excellence Adv Mat Res CEAMR, POB 80203, Jeddah 21589, Saudi Arabia
[4] King Abdulaziz Univ, Fac Sci, Dept Chem, POB 80203, Jeddah 21589, Saudi Arabia
关键词
TRANSFER RADICAL POLYMERIZATION; PROMOTED CATIONIC-POLYMERIZATION; CATALYZED CHAIN-GROWTH; METATHESIS/VINYL-INSERTION POLYMERIZATION; LIVING ANIONIC-POLYMERIZATION; BLOCK-COPOLYMERS; GRAFT-COPOLYMERS; VINYLIDENE FLUORIDE; METHYL ACRYLATE; MECHANISTIC TRANSFORMATION;
D O I
10.1021/acsmacrolett.6b00460
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The synthesis of polyethylene-graft-polystyrene copolymers by a multistep "grafting from" approach is described. In the first step, a bromo-functional polyethylene (PE-Br) was synthesized via ring opening metathesis polymerization (ROMP) of cis-cyclooctene (COE) and quantitative hydrobromination. Subsequent irradiation of PE-Br under visible light in the presence of dimanganese decacarbonyl (Mn-2(CO)(10)) and 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) resulted in the formation of TEMPO-substituted polyethylene (PE TEMPO). Polystyrene (PS) chains were then grown via nitroxide mediated radical polymerization (NMRP) from the PE-TEMPO precursor to give desired PE-g-PS copolymers in a controlled manner. The intermediates at each step and final graft copolymers were characterized by H-1 NMR, FT-IR, GPC, and DSC analyses.
引用
收藏
页码:946 / 949
页数:4
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