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Efficient Synthesis of Long-Chain Highly Branched Polymers via One-Pot Tandem Ring-Opening Metathesis Polymerization and Acyclic Diene Metathesis Polymerization
被引:49
|作者:
Ding, Liang
[1
]
Xie, Meiran
[1
]
Yang, Dan
[1
]
Song, Chunmei
[1
]
机构:
[1] E China Normal Univ, Dept Chem, Shanghai 200062, Peoples R China
基金:
中国国家自然科学基金;
关键词:
TRANSFER RADICAL POLYMERIZATION;
ABA TRIBLOCK COPOLYMERS;
HYPERBRANCHED POLYMERS;
OLEFIN METATHESIS;
ADMET POLYMERIZATION;
RUTHENIUM CATALYSTS;
MOLECULAR-WEIGHT;
HYPERMACS;
POLYCONDENSATION;
POLYPROPYLENE;
D O I:
10.1021/ma1020903
中图分类号:
O63 [高分子化学(高聚物)];
学科分类号:
070305 ;
080501 ;
081704 ;
摘要:
A facile one-pot synthesis of long chain highly branched polymers (LCHBPs) was accomplished by a tandem ring opening metathesis polymerization (ROMP) and acyclic diene metathesis (ADMET) polymerization procedure A telechelic polymer with two terminal allyloxy groups and many pendent acrylates was first prepared through the first generation Grubbs catalyst-mediated chain transfer ROMP of 7-oxanorborn-5-ene-exo,exo-2,3-dicarboxylic acid bis(2-(acryloyloxy)ethyl) ester in the presence of a symmetrical multifunctional olefin 1,4 diallyloxy cis 2 butene as chain transfer agent (CTA), and then utilized as an A(2)B(2n) type macromonomer in subsequent ADMET polymerization between allyloxy and acrylate triggered by the most activated second generation Grubbs catalyst yielding LCHBPs as the reacton time prolonged The CTA, monomer, macromonomer, and the resulting LCHBPs were characterized by mass spectroscopy, elemental analysis, gel permeation chromatography with multiangle laser light scattering, NMR and matrix-assisted laser desorption ionization time of flight mass measurements The LCHBPs have comparatively high molecular weights and relatively moderate polydispersity indices
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页码:10336 / 10342
页数:7
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