Properties of well-defined alternating and random copolymers of methacrylates and styrene prepared by controlled/living radical polymerization

被引:31
|
作者
Denizli, BK
Lutz, JF
Okrasa, L
Pakula, T
Guner, A
Matyjaszewski, K
机构
[1] Carnegie Mellon Univ, Dept Chem, Pittsburgh, PA 15213 USA
[2] Hacettepe Univ, Fac Sci, Dept Chem, TR-06532 Ankara, Turkey
[3] Fraunhofer Inst Appl Polymer Res, D-14476 Potsdam, Germany
[4] Max Planck Inst Polymer Res, D-55021 Mainz, Germany
[5] Tech Univ Lodz, Dept Mol Phys, PL-90924 Lodz, Poland
关键词
alternating copolymers; controlled/living polymerization; differential scanning calorimetry (DSC); reversible addition fragmentation chain transfer (RAFT); thermomechanical properties; WAXS;
D O I
10.1002/pola.20824
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 physical properties of well-defined alternating copolymers poly (methyl methaerylate-alt-styrene) and poly(n-butyl methacrylate-alt-styrene), prepared by reversible addition-fragmentation chain transfer polymerization in the presence of Lewis acids, were investigated with differential scanning calorimetry, wide-angle X-ray scattering, and dynamic mechanical measurements. The properties were compared with those of random copolymers of the same overall composition and the corresponding homopolymers. Wide-angle X-ray scattering data showed that the alternating copolymers possessed a more regular comonomer sequence than the random copolymers. The thermomechanical properties of alternating copolymers and random copolymers were quite similar and typical for amorphous polymers, but in one of the cases studied the glass-transition temperature for alternating copolymer was remarkably higher than for the random copolymer. (c) 2005 Wiley Periodicals, Inc.
引用
收藏
页码:3440 / 3446
页数:7
相关论文
共 50 条
  • [1] Synthesis of well-defined alternating copolymers by controlled/living radical polymerization in the presence of Lewis acids
    Lutz, JF
    Kirci, B
    Matyjaszewski, K
    MACROMOLECULES, 2003, 36 (09) : 3136 - 3145
  • [2] Well-defined random copolymers by a ''living'' free-radical polymerization process
    Hawker, CJ
    Elce, E
    Dao, JL
    Volksen, W
    Russell, TP
    Barclay, GG
    MACROMOLECULES, 1996, 29 (07) : 2686 - 2688
  • [3] Well-defined block copolymers comprising styrene acrylonitrile random copolymer sequences synthesized by ''living'' radical polymerization
    Fukuda, T
    Terauchi, T
    Goto, A
    Tsujii, Y
    Miyamoto, T
    MACROMOLECULES, 1996, 29 (08) : 3050 - 3052
  • [4] Well-defined graft copolymers of methacrylate, acrylate, and styrene via ruthenium-catalyzed living radical polymerization
    Miura, Yu
    Satoh, Kotaro
    Kamigaito, Masami
    Okamoto, Yoshio
    POLYMER JOURNAL, 2006, 38 (09) : 930 - 939
  • [5] Well-Defined Graft Copolymers of Methacrylate, Acrylate, and Styrene via Ruthenium-Catalyzed Living Radical Polymerization
    Yu Miura
    Kotaro Satoh
    Masami Kamigaito
    Yoshio Okamoto
    Polymer Journal, 2006, 38 : 930 - 939
  • [6] Synthesis and properties of a well-defined glycopolymer via living radical polymerization
    Miura, Yoshiko
    Koketsu, Daisuke
    Kobayashi, Kazukiyo
    POLYMERS FOR ADVANCED TECHNOLOGIES, 2007, 18 (08) : 647 - 651
  • [7] Nanocarbons with tunable electronic structure from well-defined copolymers containing polyacrylonitrile prepared by controlled radical polymerization
    Kowalewski, Tomasz
    McGann, John P.
    Yaron, David
    McCullough, Lynne A.
    Matyjaszewski, Krzysztof
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2008, 236
  • [8] Synthesis and Characterization of Well-Defined Block Copolymers by Combing Controlled Radical and Cationic Polymerization
    Ibrahim, Saber
    Voit, Brigitte
    MACROMOLECULAR SYMPOSIA, 2008, 275 : 59 - 66
  • [9] SYNTHESIS OF WELL-DEFINED POLYMERS BY CONTROLLED RADICAL POLYMERIZATION
    MATYJASZEWSKI, K
    GAYNOR, S
    GRESZTA, D
    MARDARE, D
    SHIGEMOTO, T
    MACROMOLECULAR SYMPOSIA, 1995, 98 : 73 - 89
  • [10] Synthesis of a well-defined polybromostyrene by living radical polymerization with a nitroxyl radical
    Kyoto Inst of Technology, Kyoto, Japan
    J Polym Sci Part A, 14 (2937-2943):