Scalable synthesis of catalysts for the Mizoroki-Heck cross coupling reaction: palladium nanoparticles assembled in a polymeric nanosphere

被引:21
作者
Zou, Jianli [1 ]
Iyer, K. Swaminathan [1 ]
Stewart, Scott G.
Raston, Colin L. [1 ]
机构
[1] Univ Western Australia, Ctr Strateg Nanofabricat, Sch Biomed Biomol & Chem Sci, Crawley, WA 6009, Australia
基金
澳大利亚研究理事会;
关键词
SUPPORTED PALLADIUM; TETRAALKYLAMMONIUM SALTS; HETEROGENEOUS CATALYSIS; ORGANIC-CHEMISTRY; PD NANOPARTICLES; SUZUKI; ARYLATION; LIGANDS; CARBON; SIZE;
D O I
10.1039/c0nj00898b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Palladium nano-spheres 160 nm in diameter, as an assembly of uniform 5 nm nanoparticles, are accessible using a facile one step method under continuous flow on a spinning disc with hydrogen gas as the reducing agent. The stable colloidal system is an effective catalyst for the Mizoroki-Heck reaction, as established for the reaction between several aryl halides and n-butyl acrylate, and can be readily recycled without a change in their catalytic activity.
引用
收藏
页码:854 / 860
页数:7
相关论文
共 56 条
  • [1] Nanoparticles as recyclable catalysts: The frontier between homogeneous and heterogeneous catalysis
    Astruc, D
    Lu, F
    Aranzaes, JR
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2005, 44 (48) : 7852 - 7872
  • [2] HETEROGENEOUS CATALYSIS IN ORGANIC-CHEMISTRY .8. THE USE OF SUPPORTED PALLADIUM CATALYSTS FOR THE HECK ARYLATION
    AUGUSTINE, RL
    OLEARY, ST
    [J]. JOURNAL OF MOLECULAR CATALYSIS, 1992, 72 (02): : 229 - 242
  • [3] HETEROGENEOUS CATALYSIS IN ORGANIC-CHEMISTRY .10. EFFECT OF THE CATALYST SUPPORT ON THE REGIOCHEMISTRY OF THE HECK ARYLATION REACTION
    AUGUSTINE, RL
    OLEARY, ST
    [J]. JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 1995, 95 (03) : 277 - 285
  • [4] A simple and efficient route to active and dispersed silica supported palladium nanoparticles
    Barau, Alexandra
    Budarin, Vitaly
    Caragheorgheopol, Agneta
    Luque, Rafael
    Macquarrie, Duncan J.
    Prelle, Ambra
    Teodorescu, Valentin S.
    Zaharescu, Maria
    [J]. CATALYSIS LETTERS, 2008, 124 (3-4) : 204 - 214
  • [5] First palladium-catalyzed Heck reactions with efficient colloidal catalyst systems
    Beller, M
    Fischer, H
    Kuhlein, K
    Reisinger, CP
    Herrmann, WA
    [J]. JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1996, 520 (1-2) : 257 - 259
  • [6] Palladium metal catalysts in Heck C-C coupling reactions
    Biffis, A
    Zecca, M
    Basato, M
    [J]. JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2001, 173 (1-2) : 249 - 274
  • [7] Measurement of liquid film thickness and the determination of spin-up radius on a rotating disc using an electrical resistance technique
    Burns, JR
    Ramshaw, C
    Jachuck, RJ
    [J]. CHEMICAL ENGINEERING SCIENCE, 2003, 58 (11) : 2245 - 2253
  • [8] PALLADIUM-CATALYZED ARYLATION OF UNSYMMETRICAL OLEFINS - BIDENTATE PHOSPHINE LIGAND CONTROLLED REGIOSELECTIVITY
    CABRI, W
    CANDIANI, I
    BEDESCHI, A
    SANTI, R
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 1992, 57 (13) : 3558 - 3563
  • [9] The role of Pd nanoparticles in ionic liquid in the Heck reaction
    Cassol, CC
    Umpierre, AP
    Machado, G
    Wolke, SI
    Dupont, J
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (10) : 3298 - 3299
  • [10] A novel tridentate NHC-Pd(II) complex and its application in the Suzuki and Heck-type cross-coupling reactions
    Chen, Tao
    Gao, Jun
    Shi, Min
    [J]. TETRAHEDRON, 2006, 62 (26) : 6289 - 6294