Allyl-Terminated Polypropylene Macromonomers: A Route to Polyolefin Elastomers with Excellent Elastic Behavior

被引:71
作者
Ohtaki, Hisashi [1 ,3 ]
Deplace, Fanny [2 ]
Vo, Giang D. [1 ]
LaPointe, Anne M. [1 ]
Shimizu, Fumihiko [3 ]
Sugano, Toshihiko [4 ]
Kramer, Edward J. [2 ]
Fredrickson, Glenn H. [2 ]
Coates, Geoffrey W. [1 ]
机构
[1] Cornell Univ, Dept Chem & Chem Biol, Baker Lab, Ithaca, NY 14853 USA
[2] Univ Calif Santa Barbara, Mitsubishi Chem Ctr Adv Mat, Santa Barbara, CA 93106 USA
[3] Mitsubishi Chem Grp Sci & Technol Res Ctr Inc, Sci & Technol Res Ctr Inc, Aoba Ku, Yokohama, Kanagawa 2278502, Japan
[4] Japan Polychem Corp, Yokaichi, Mie 5100848, Japan
基金
美国国家科学基金会;
关键词
BLOCK THERMOPLASTIC ELASTOMERS; LIVING OLEFIN POLYMERIZATION; STEREOBLOCK HOMOPOLYMERS; ZIRCONOCENE CATALYSTS; COPOLYMERS; PROPYLENE; POLYMERS; STRATEGY; POLY(PROPYLENE); ARCHITECTURES;
D O I
10.1021/acs.macromol.5b01975
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
We report the design, synthesis, and physical/mechanical properties of graft copolymers containing semicrystalline polypropylene side chains and amorphous ethylene/alpha-olefin copolymer backbones. These materials, a new class of semicrystalline, polyolefin-based thermoplastic elastomers, are made in two steps. First, allyl-terminated syndiotactic or isotactic polypropylene macromonomers are synthesized with controlled microstructure and molecular weight using bis(phenoxyimine)titanium or chiral ansa-zirconocene catalysts, respectively. Second, a pyridyl-amido hafnium catalyst is used to copolymerize the macromonomer, ethylene, and an alpha-olefin with precise control of composition and side chain incorporation. With highly crystalline polypropylene side chains and amorphous backbones of low glass-transition temperatures (<-55 degrees C), the samples have strain-to-break values up to 1400% and elastic recovery above 85% at maximum strains up to 1000%. The synthetic method described herein does not require the use of a living polymerization catalyst; in addition, the mechanical properties of these graft copolymers exceed those of the best linear block polyolefins.
引用
收藏
页码:7489 / 7494
页数:6
相关论文
共 56 条
[1]  
[Anonymous], 2009, CONTROLLED LIVING PO, P445
[2]   Catalytic production of olefin block copolymers via chain shuttling polymerization [J].
Arriola, DJ ;
Carnahan, EM ;
Hustad, PD ;
Kuhlman, RL ;
Wenzel, TT .
SCIENCE, 2006, 312 (5774) :714-719
[3]   Nonconventional catalysts for isotactic propene polymerization in solution developed by using high-throughput-screening technologies [J].
Boussie, Thomas R. ;
Diamond, Gary M. ;
Goh, Christopher ;
Hall, Keith A. ;
LaPointe, Anne M. ;
Leclerc, Margarete K. ;
Murphy, Vince ;
Shoemaker, James A. W. ;
Turner, Howard ;
Rosen, Robert K. ;
Stevens, James C. ;
Alfano, Francesca ;
Busico, Vincenzo ;
Cipullo, Roberta ;
Talarico, Giovanni .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2006, 45 (20) :3278-3283
[4]  
Brobny J.G., 2007, Handbook of Thermoplastic Elastomers
[5]   A C2-symmetric, living α-diimine Ni(II) catalyst:: Regioblock copolymers from propylene [J].
Cherian, AE ;
Rose, JM ;
Lobkovsky, EB ;
Coates, GW .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (40) :13770-13771
[6]   Synthesis of allyl-terininated syndiotactic polypropylene: Macromonomers for the synthesis of branched polyolefins [J].
Cherian, AE ;
Lobkovsky, EB ;
Coates, GW .
MACROMOLECULES, 2005, 38 (15) :6259-6268
[7]  
Coates G. W., 2008, [No title captured], Patent No. [2008112133, WO 2008112133A2]
[8]  
Coates GW, 2002, ANGEW CHEM INT EDIT, V41, P2236, DOI 10.1002/1521-3773(20020703)41:13<2236::AID-ANIE2236>3.0.CO
[9]  
2-3
[10]   OSCILLATING STEREOCONTROL - A STRATEGY FOR THE SYNTHESIS OF THERMOPLASTIC ELASTOMERIC POLYPROPYLENE [J].
COATES, GW ;
WAYMOUTH, RM .
SCIENCE, 1995, 267 (5195) :217-219