About Solid Phase vs. Liquid Phase in Suzuki-Miyaura Reaction

被引:29
作者
Bourouina, Amine [1 ]
Meille, Valerie [1 ]
de Bellefon, Claude [1 ]
机构
[1] Univ Lyon, CNRS, UMR 5285, CPE Lyon,UCBL,Inst Chim Lyon,Lab Genie Proc Catal, F-69100 Villeurbanne, France
关键词
C-C coupling; Suzuki-Miyaura; homogeneous; heterogeneous; leaching; CROSS-COUPLING REACTIONS; HETEROGENEOUS PALLADIUM CATALYST; HIGHLY EFFICIENT CATALYST; RECYCLABLE CATALYST; ARYL CHLORIDES; C-C; PD NANOPARTICLES; MIZOROKI-HECK; CARBAPALLADACYCLE COMPLEX; LEACHING MECHANISM;
D O I
10.3390/catal9010060
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A critical review of conclusions about the putative heterogeneous mechanism in the Suzuki-Miyaura coupling by supported Pd solids is reported. In the first section, the turnover frequencies (TOF) of 20 well-established homogeneous catalysts are shown to be in the range 200 to 1,000,000,000 h(-1). The evidences used to prove a heterogeneous mechanism are discussed and another interpretation is proposed, hypothesizing that only the leached species are responsible for the catalytic reaction, even at ppb levels. Considering more than 40 published catalytic systems for which liquid phase Pd content have been reported, activities have been computed based on leached Pd concentrations and are shown to be in the range TOF 150 to 70,000,000 h(-1). Such values are compatible with those found for the well-established homogeneous catalysts which questions the validity of the conclusions raised by many papers about the heterogeneous (solid) nature of Suzuki-Miyaura catalysis. Last, a tentative methodology is proposed which involves the rational use of well-known tests (hot-filtration test, mercury test...) to help to discriminate between homogeneous and heterogeneous mechanisms.
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页数:27
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  • [1] Benzyloxycalix[8]arene: a new valuable support for NHC palladium complexes in C-C Suzuki-Miyaura couplings
    Abdellah, Ibrahim
    Kasongo, Pauline
    Labattut, Axel
    Guillot, Regis
    Schulz, Emmanuelle
    Martini, Cyril
    Huc, Vincent
    [J]. DALTON TRANSACTIONS, 2018, 47 (39) : 13843 - 13848
  • [2] Suzuki-Miyaura cross-coupling reactions using a low-leaching and highly recyclable gold-supported palladium material and two types of microwave equipments
    Al-Amin, Mohammad
    Akimoto, Masayoshi
    Tameno, Tsuyoshi
    Ohki, Yuuta
    Takahashi, Naoyuki
    Hoshiya, Naoyuki
    Shuto, Satoshi
    Arisawa, Mitsuhiro
    [J]. GREEN CHEMISTRY, 2013, 15 (05) : 1142 - 1145
  • [3] Toward the Ideal Catalyst: From Atomic Centers to a "Cocktail" of Catalysts
    Ananikov, Valentine P.
    Beletskaya, Irina P.
    [J]. ORGANOMETALLICS, 2012, 31 (05) : 1595 - 1604
  • [4] Heterogeneous suzuki reactions catalyzed by Pd(0)-Y zeolite
    Artok, L
    Bulut, H
    [J]. TETRAHEDRON LETTERS, 2004, 45 (20) : 3881 - 3884
  • [5] Automated batch scale-up of microwave-promoted Suzuki and Heck coupling reactions in water using ultra-low metal catalyst concentrations
    Arvela, RK
    Leadbeater, NE
    Collins, MJ
    [J]. TETRAHEDRON, 2005, 61 (39) : 9349 - 9355
  • [6] An oxime-carbapalladacycle complex covalently anchored to silica as an active and reusable heterogeneous catalyst for Suzuki cross-coupling in water
    Baleizao, C
    Corma, A
    García, H
    Leyva, A
    [J]. CHEMICAL COMMUNICATIONS, 2003, (05) : 606 - 607
  • [7] Solvent-free, microwave-assisted highly efficient, rapid and simple synthesis of biphenyl compounds by using silica based Pd(II) catalyst
    Baran, Talat
    [J]. JOURNAL OF MACROMOLECULAR SCIENCE PART A-PURE AND APPLIED CHEMISTRY, 2018, 55 (03): : 280 - 287
  • [8] Exceptionally high turnover frequencies recorded for a new chitosan-based palladium(II) catalyst
    Baran, Talat
    Sargin, Idris
    Mentes, Ayfer
    Kaya, Murat
    [J]. APPLIED CATALYSIS A-GENERAL, 2016, 523 : 12 - 20
  • [9] Spatial, temporal and quantitative assessment of catalyst leaching in continuous flow
    Barreiro, Elena M.
    Hao, Zhimian
    Adrio, Luis A.
    van Ommen, J. Ruud
    Hellgardt, Klaus
    Hii, King Kuok
    [J]. CATALYSIS TODAY, 2018, 308 : 64 - 70
  • [10] Extremely high activity catalysts for the Suzuki coupling of aryl chlorides: the importance of catalyst longevity
    Bedford, RB
    Hazelwood, SL
    Limmert, ME
    [J]. CHEMICAL COMMUNICATIONS, 2002, (22) : 2610 - 2611