Synthesis and Ring-Opening Metathesis Polymerization of Norbornene-Terminated Syndiotactic Polypropylene

被引:32
作者
Anderson-Wile, Amelia M. [1 ]
Coates, Geoffrey W. [1 ]
Auriemma, Finizia [2 ]
De Rosa, Claudio [2 ]
Silvestre, Amelia [2 ]
机构
[1] Cornell Univ, Baker Lab, Dept Chem & Chem Biol, Ithaca, NY 14853 USA
[2] Univ Naples Federico II, Dipartimento Chim Paolo Corradini, I-80126 Naples, Italy
基金
美国国家科学基金会;
关键词
COMB BLOCK-COPOLYMERS; EQUILIBRIUM MELTING TEMPERATURE; CYLINDRICAL MOLECULAR BRUSHES; BIS(PHENOXYIMINE)-BASED TITANIUM CATALYSTS; STEREOREGULAR DIBLOCK COPOLYMERS; TRANSFER RADICAL POLYMERIZATION; END FUNCTIONALIZED POLYOLEFINS; LIVING OLEFIN POLYMERIZATION; ZIEGLER-NATTA CATALYSTS; VANADIUM-BASED CATALYST;
D O I
10.1021/ma301073s
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Using nonliving bis(phenoxyimine)titanium catalysts activated by methylaluminoxane (MAO) in the presence of propylene, allyl-terminated syndiotactic polypropylene macromonomers with varying tacticity ([rrrr] = 0.80 and 0.94) and molecular weight (M-n = 3600 and 5600 g/mol) were produced. The end-functionalized polymers were converted to hydroxyl- and subsequently norbornene-terminated macromonomers. Two series of syndiotactic polypropylene comb-polymers were synthesized through metathesis polymerization of the norbornene-functionalized polypropylene. The molecular weight (M-n = 46 000-172 000 g/mol) and polydispersity (M-w/M-n = 1.21-1.89) of the comb polymers was determined by gel permeation chromatography (GPC). Using differential scanning calorimetry (DSC), melting temperature (T-m) and crystallization temperature (T-c) were determined and both were observed to decrease with increasing conversion to poly(macromonomer). To the best of our knowledge, this is the first synthesis of comb-polymers from end-functionalized syndiotactic polypropylene.
引用
收藏
页码:7863 / 7877
页数:15
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