Single-mode microwave-assisted atom transfer radical polymerization catalyzed by [RuCl2(p-cymene)(PCy3)]

被引:45
作者
Delfosse, Sebastien [1 ]
Borguet, Yannick [1 ]
Delaude, Lionel [1 ]
Demonceau, Albert [1 ]
机构
[1] Univ Liege, Macromol Chem & Organ Catalysis Lab, B-4000 Liege, Belgium
关键词
atom transfer radical polymerization (ATRP); methyl methacrylate; microwave; radical polymerization; ruthenium;
D O I
10.1002/marc.200600790
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
In the atom transfer radical polymerization (ATRP) of methyl methacrylate in the presence of [RuCl2(p-cymene)(PCy3)] (p-cymene=4-isopropyltoluene, PCy3=tricyclohexylphosphine), a microwave effect is noted which strikingly depends on both the temperature and the method used (conventional microwave synthesis (CMS, i.e., without simultaneous cooling) or enhanced microwave synthesis (EMS, with simultaneous cooling)). Thus, between 85 and 120 degrees C under CMS conditions, microwave-assisted polymerizations take place in a controlled fashion, and at 120 degrees C the microwave-assisted polymerization is three times faster than the conventionally heated protocol. However, from 130 degrees C, microwave irradiation has a deleterious effect and the polymerizations are no longer controlled. Likewise, using the EMS method in the temperature range of 85-120 degrees C results in uncontrolled processes, as indicated by the unsuccessful resumption of the polymerizations. These failures might be attributed to a significantly high concentration of radical species, which results in enhanced propagation and termination - mostly disproportionation - rates.
引用
收藏
页码:492 / 503
页数:12
相关论文
共 96 条
  • [1] Microwave-assisted synthesis of N-heterocyclic carbene precursors
    Aidouni, A
    Demonceau, A
    Delaude, L
    [J]. SYNLETT, 2006, (03) : 493 - 495
  • [2] [Anonymous], J POLYM SCI A
  • [3] SUPERHEATING EFFECTS ASSOCIATED WITH MICROWAVE DIELECTRIC HEATING
    BAGHURST, DR
    MINGOS, DMP
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1992, (09) : 674 - 677
  • [4] NETWORK FORMATION .4. NATURE OF TERMINATION REACTION IN FREE-RADICAL POLYMERIZATION
    BAMFORD, CH
    DYSON, RW
    EASTMOND, GC
    [J]. POLYMER, 1969, 10 (11) : 885 - &
  • [5] Microwave accelerated synthesis of N-phenylmaleimide in a single step and polymerization in bulk
    Bezdushna, E
    Ritter, H
    [J]. MACROMOLECULAR RAPID COMMUNICATIONS, 2005, 26 (13) : 1087 - 1092
  • [6] Microwave-assisted single-step synthesis of poly(alkylene hydrogen phosphonate)s by transesterification of dimethyl hydrogen phosphonate with poly(ethylene glycol)
    Bezdushna, E
    Ritter, H
    Troev, K
    [J]. MACROMOLECULAR RAPID COMMUNICATIONS, 2005, 26 (06) : 471 - 476
  • [7] Bon SAF, 2000, J POLYM SCI POL CHEM, V38, P2678, DOI 10.1002/1099-0518(20000801)38:15<2678::AID-POLA70>3.0.CO
  • [8] 2-P
  • [9] PHOTOLYSIS OF METHYL-METHACRYLATE METHYL VINYL KETONE COPOLYMERS - A NEW ROUTE TO ACRYLIC MACROMONOMERS
    BOND, SG
    EBDON, JR
    [J]. POLYMER, 1994, 35 (03) : 451 - 460
  • [10] MICROWAVE-INDUCED ORGANIC-REACTION ENHANCEMENT CHEMISTRY .2. SIMPLIFIED TECHNIQUES
    BOSE, AK
    MANHAS, MS
    GHOSH, M
    SHAH, M
    RAJU, VS
    BARI, SS
    NEWAZ, SN
    BANIK, BK
    CHAUDHARY, AG
    BARAKAT, KJ
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 1991, 56 (25) : 6968 - 6970