Synthesis of polymers with phosphonium end groups by atom transfer radical polymerization

被引:41
作者
Coessens, V [1 ]
Matyjaszewski, K [1 ]
机构
[1] Carnegie Mellon Univ, Dept Chem, Pittsburgh, PA 15213 USA
来源
JOURNAL OF MACROMOLECULAR SCIENCE-PURE AND APPLIED CHEMISTRY | 1999年 / A36卷 / 5-6期
关键词
atom transfer radical polymerization (ATRP); end group modification; phosphines; phosphonium salts;
D O I
10.1081/MA-100101555
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 end groups of polymers prepared by atom transfer radical polymerization (ATRP), are well-defined and determined by the initiator used, at least one of them is a halogen end group. The halogen end groups can be transformed to other functionalities such as phosphonium salts as demonstrated in this paper. Kinetic studies with the compounds l-phenylethyl bromide and methyl 2-bromopropionate, models for the polystyrene and polyacrylate chain ends respectively, indicated that bromine end groups were readily transformed to phosphonium end groups upon the addition of phosphines. Stability tests with the obtained phosphonium salts showed that 1-phenylethyl trialkylphosphonium bromide was stable, even at higher temperatures and in the presence of free phosphines. The stability of the propionate analogue was limited due to the presence of the ester group in the molecule. Polystyrene and poly(methyl acrylate) phosphonium salts were synthesized and the presence of the end groups was demonstrated by H-1 NMR and ESI-MS or MALDI-TOFMS.
引用
收藏
页码:653 / 666
页数:14
相关论文
共 21 条
  • [1] APPLICATION OF FUNCTIONALIZED POLYMERS IN ORGANIC-SYNTHESIS
    AKELAH, A
    SHERRINGTON, DC
    [J]. CHEMICAL REVIEWS, 1981, 81 (06) : 557 - 587
  • [2] ARJUNAN P, 1997, CONTROLLED RADICAL P, V685, P199
  • [3] Synthesis of azido end-functionalized polyacrylates via atom transfer radical polymerization
    Coessens, V
    Nakagawa, Y
    Matyjaszewski, K
    [J]. POLYMER BULLETIN, 1998, 40 (2-3) : 135 - 142
  • [4] CORBRIDGE DEC, 1990, STUDIES INORGANIC CH, V10, P307
  • [5] Kapfenstein HM, 1998, MACROMOL CHEM PHYSIC, V199, P2403, DOI 10.1002/(SICI)1521-3935(19981101)199:11<2403::AID-MACP2403>3.0.CO
  • [6] 2-9
  • [7] POLYMERIZATION OF METHYL-METHACRYLATE WITH THE CARBON-TETRACHLORIDE DICHLOROTRIS(TRIPHENYLPHOSPHINE)RUTHENIUM(II) METHYLALUMINUM BIS(2,6-DI-TERT-BUTYLPHENOXIDE) INITIATING SYSTEM - POSSIBILITY OF LIVING RADICAL POLYMERIZATION
    KATO, M
    KAMIGAITO, M
    SAWAMOTO, M
    HIGASHIMURA, T
    [J]. MACROMOLECULES, 1995, 28 (05) : 1721 - 1723
  • [8] KIM B, 1984, J ORG CHEM, V49, P3233, DOI 10.1021/jo00191a044
  • [9] Living radical polymerization of alkyl methacrylates with ruthenium complex and synthesis of their block copolymers
    Kotani, Y
    Kato, M
    Kamigaito, M
    Sawamoto, M
    [J]. MACROMOLECULES, 1996, 29 (22) : 6979 - 6982
  • [10] Synthesis, characterization and use of reactive polymers with diisopropylphenylphosphine groups
    LiceaClaverie, A
    Rivero, IA
    Morales, MS
    Moreno, MG
    [J]. POLYMER BULLETIN, 1997, 39 (05) : 551 - 557