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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.
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页码:7863 / 7877
页数:15
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