The Origin of Shape Sensitivity in Palladium-Catalyzed Suzuki-Miyaura Cross Coupling Reactions

被引:116
|
作者
Collins, Gillian [1 ,2 ,3 ]
Schmidt, Michael [1 ,2 ,3 ]
Dwyer, Colm O. [1 ,2 ,4 ]
Holmes, Justin D. [1 ,2 ,3 ]
McGlacken, Gerard P. [1 ,2 ]
机构
[1] Natl Univ Ireland Univ Coll Cork, Dept Chem Analyt & Biol Chem, Res Facil, Cork, Ireland
[2] Natl Univ Ireland Univ Coll Cork, Tyndall Natl Inst, Cork, Ireland
[3] Trinity Coll Dublin, CRANN, Dublin, Ireland
[4] Univ Limerick, MSSI, Limerick, Ireland
关键词
heterogeneous catalysis; palladium; surface facet; Suzuki-Miyaura coupling; NANOPARTICLE SHAPE; PD NANOPARTICLES; LEACHING MECHANISM; SURFACE; HECK; NANOCRYSTALS; CARBON; WATER; ACID; SIZE;
D O I
10.1002/anie.201400483
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The shape sensitivity of Pd catalysts in Suzuki-Miyaura coupling reactions is studied using nanocrystals enclosed by well-defined surface facets. The catalytic performance of Pd nanocrystals with cubic, cuboctahedral and octahedral morphologies are compared. Superior catalytic reactivity is observed for Pd NCs with {100} surface facets compared to {111} facets. The origin of the enhanced reactivity associated with a cubic morphology is related to the leaching susceptibility of the nanocrystals. Molecular oxygen plays a key role in facilitating the leaching of Pd atoms from the surface of the nanocrystals. The interaction of O-2 with Pd is itself facet-dependent, which in turn gives rise to more efficient leaching from {100} facets, compared to {111} facets under the reaction conditions.
引用
收藏
页码:4142 / 4145
页数:4
相关论文
共 50 条
  • [1] Arylcalixarenyl Phosphines in Palladium-Catalyzed Suzuki-Miyaura Cross-Coupling Reactions
    Elaieb, Fethi
    Hedhli, Ahmed
    Semeril, David
    Matt, Dominique
    EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2016, 2016 (10) : 1867 - 1873
  • [2] Palladium-Catalyzed Suzuki-Miyaura Cross-Coupling in Continuous Flow
    Len, Christophe
    Bruniaux, Sophie
    Delbecq, Frederic
    Parmar, Virinder S.
    CATALYSTS, 2017, 7 (05):
  • [3] Efficient and sustainable palladium-catalyzed Suzuki-Miyaura cross-coupling
    Marziale, Alexander N.
    Faul, Stefan H.
    Eppinger, Joerg
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2011, 241
  • [4] Palladium-catalyzed Suzuki-Miyaura coupling of thioureas or thioamides
    Shaoyu Mai
    Wendong Li
    Xue Li
    Yingwei Zhao
    Qiuling Song
    Nature Communications, 10
  • [5] Palladium-catalyzed Suzuki-Miyaura coupling of thioureas or thioamides
    Mai, Shaoyu
    Li, Wendong
    Li, Xue
    Zhao, Yingwei
    Song, Qiuling
    NATURE COMMUNICATIONS, 2019, 10 (1)
  • [6] Palladium-Catalyzed Suzuki-Miyaura Coupling of Aryl Esters
    Ben Halima, Taoufik
    Zhang, Wanying
    Yalaoui, Imane
    Hong, Xin
    Yang, Yun-Fang
    Houk, Kendall N.
    Newman, Stephen G.
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2017, 139 (03) : 1311 - 1318
  • [7] Palladium-Catalyzed Suzuki-Miyaura Cross-Coupling Reactions Employing Dialkylbiaryl Phosphine Ligands
    Martin, Ruben
    Buchwald, Stephen L.
    ACCOUNTS OF CHEMICAL RESEARCH, 2008, 41 (11) : 1461 - 1473
  • [8] Palladium-catalyzed Suzuki-Miyaura cross-coupling reactions of potassium aryl- and heteroaryltrifluoroborates
    Molander, GA
    Biolatto, B
    JOURNAL OF ORGANIC CHEMISTRY, 2003, 68 (11): : 4302 - 4314
  • [9] Mechanistic Aspects of the Palladium-Catalyzed Suzuki-Miyaura Cross-Coupling Reaction
    D'Alterio, Massimo C.
    Casals-Cruanas, Eric
    Tzouras, Nikolaos V.
    Talarico, Giovanni
    Nolan, Steven P.
    Poater, Albert
    CHEMISTRY-A EUROPEAN JOURNAL, 2021, 27 (54) : 13481 - 13493
  • [10] Cycloheptatrienyl Cyclopentadienyl Titanium Phosphane Ligands in Palladium-Catalyzed Suzuki-Miyaura Cross-Coupling Reactions
    Troendle, Sabrina
    Kuate, Alain C. Tagne
    Freytag, Matthias
    Jones, Peter G.
    Tamm, Matthias
    EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, 2017, (47) : 5588 - 5597