Distinguishing between the Homogeneous and Heterogeneous Mechanisms of Catalysis in the Mizoroki-Heck and Suzuki-Miyaura Reactions: Problems and Prospects

被引:92
|
作者
Schmidt, A. F. [1 ]
Kurokhtina, A. A. [1 ]
机构
[1] Irkutsk State Univ, Fac Chem, Irkutsk 664033, Russia
关键词
SUPPORTED PALLADIUM CATALYSTS; CROSS-COUPLING REACTION; LIGAND-FREE PALLADIUM; PVP-PD NANOPARTICLES; RECYCLABLE CATALYST; ARYL IODIDES; NONCONVENTIONAL METHODOLOGIES; EFFICIENT CATALYSTS; AMBIENT CONDITIONS; ORGANIC-CHEMISTRY;
D O I
10.1134/S0023158412060109
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
This review presents a critical analysis of experimental methods used in distinguishing between the homogeneous and heterogeneous catalytic mechanisms in the Mizoroki-Heck and Suzuki-Miyaura reactions. The main problems arising in the interpretation of data obtained by these methods are discussed. It is demonstrated that it is necessary to take into account the dynamics of the interconversion of molecular, nanosized, and larger palladium species that is independent of the catalyst precursor type (dissolved or solid). The role of the in situ formation of colloidal palladium particles in the case of a supported catalyst precursor is considered. DOI: 10.1134/S0023158412060109
引用
收藏
页码:714 / 730
页数:17
相关论文
共 50 条
  • [1] Distinguishing between the homogeneous and heterogeneous mechanisms of catalysis in the Mizoroki-Heck and Suzuki-Miyaura reactions: Problems and prospects
    A. F. Schmidt
    A. A. Kurokhtina
    Kinetics and Catalysis, 2012, 53 : 714 - 730
  • [2] On the nature of the active species in palladium catalyzed Mizoroki-Heck and Suzuki-Miyaura couplings - Homogeneous or heterogeneous catalysis, a critical review
    Phan, NTS
    Van Der Sluys, M
    Jones, CW
    ADVANCED SYNTHESIS & CATALYSIS, 2006, 348 (06) : 609 - 679
  • [3] Oxime ligands for Pd catalysis of the Mizoroki-Heck reaction, Suzuki-Miyaura coupling & annulation reactions
    Bangar, Pronnoy G.
    Nahide, Pradip D.
    Meroliya, Heena K.
    Waghmode, Shobha A.
    Iyer, Suresh
    SYNTHETIC COMMUNICATIONS, 2021, 51 (02) : 308 - 316
  • [4] Sunlight promoted palladium catalysed Mizoroki-Heck, Suzuki-Miyaura and Sonogashira reactions
    Chaudhary, Anju R.
    Bedekar, Ashutosh V.
    TETRAHEDRON LETTERS, 2012, 53 (45) : 6100 - 6103
  • [5] Bio-supported palladium nanoparticles as a catalyst for Suzuki-Miyaura and Mizoroki-Heck reactions
    Sobjerg, Lina Sveidal
    Gauthier, Delphine
    Lindhardt, Anders Thyboe
    Bunge, Michael
    Finster, Kai
    Meyer, Rikke Louise
    Skrydstrup, Troels
    GREEN CHEMISTRY, 2009, 11 (12) : 2041 - 2046
  • [6] Palladium Nanoparticles on Graphite Oxide as Catalyst for Suzuki-Miyaura, Mizoroki-Heck, and Sonogashira Reactions
    Rumi, Luigi
    Scheuermann, Gil M.
    Muelhaupt, Rolf
    Bannwarth, Willi
    HELVETICA CHIMICA ACTA, 2011, 94 (06) : 966 - 976
  • [7] Continuous-Flow Suzuki-Miyaura and Mizoroki-Heck Reactions under Microwave Heating Conditions
    Monguchi, Yasunari
    Ichikawa, Tomohiro
    Yamada, Tsuyoshi
    Sawama, Yoshinari
    Sajiki, Hironao
    CHEMICAL RECORD, 2019, 19 (01): : 3 - 14
  • [8] A recyclable and efficient triazole ligand for the palladium-catalyzed Suzuki-Miyaura and Mizoroki-Heck reactions
    Zhu, Yi-Wei
    Yi, Wen-Bin
    Cai, Chun
    CATALYSIS COMMUNICATIONS, 2011, 15 (01) : 118 - 122
  • [9] Synthesis, characterization and application of graphene palladium porphyrin as a nanocatalyst for the coupling reactions such as: Suzuki-Miyaura and Mizoroki-Heck
    Bahrami, Kiumars
    Kamrani, Soheila Nakhjiri
    APPLIED ORGANOMETALLIC CHEMISTRY, 2018, 32 (02)
  • [10] Facile Synthesis and Characterization of Palladium@Carbon Catalyst for the Suzuki-Miyaura and Mizoroki-Heck Coupling Reactions
    Alshammari, Hamed M.
    Aldosari, Obaid F.
    Alotaibi, Mohammad Hayal
    Alotaibi, Raja L.
    Alhumaimess, Mosaed S.
    Morad, Moataz H.
    Adil, Syed Farooq
    Shaik, Mohammed Rafi
    Islam, Mohammad Shahidul
    Khan, Mujeeb
    Alwarthan, Abdulrahman
    APPLIED SCIENCES-BASEL, 2021, 11 (11):