Catalytic membrane reactor for Suzuki-Miyaura C-C cross-coupling: Explanation for its high efficiency via modeling

被引:14
|
作者
Gu, Yingying [1 ]
Bacchin, Patrice [1 ]
Lahitte, Jean-Francois [1 ]
Remigy, Jean-Christophe [1 ]
Favier, Isabelle [2 ]
Gomez, Montserrat [2 ]
Gin, Douglas L. [3 ,4 ]
Noble, Richard D. [3 ,4 ]
机构
[1] Univ Toulouse, CNRS, Lab Genie Chim, INPT,UPS,UMR 5503, 118 Route Narbonne, F-31062 Toulouse, France
[2] Univ Toulouse 3 Paul Sabatier, CNRS, Lab Heterochim Fondamentale & Appl, UMR 5069, 118 Route Narbonne, F-31062 Toulouse, France
[3] Univ Colorado, Dept Chem & Biol Engn, Boulder, CO 80309 USA
[4] Univ Colorado, Dept Chem & Biochem, Boulder, CO 80309 USA
关键词
polymeric catalytic membrane; palladium nanoparticles; forced flow-through; modeling; mechanism; PALLADIUM NANOPARTICLES; IONIC LIQUIDS; FLOW; DISPERSION; WATER;
D O I
10.1002/aic.15379
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
A polymeric catalytic membrane was previously prepared that showed remarkable efficiency for Suzuki-Miyaura C-C cross-coupling in a flow-through configuration. A mathematic model was developed and fitted to the experimental data to understand the significant apparent reaction rate increase exhibited by the catalytic membrane reactor compared to the catalytic system under batch reaction conditions. It appears that the high palladium nanoparticles concentration inside the membrane is mainly responsible for the high apparent reaction rate achieved. In addition, the best performance of the catalytic membrane could be achieved only in the forced flow-through configuration, that, conditions permitting to the reactants be brought to the catalytic membrane by convection. (c) 2016 American Institute of Chemical Engineers AIChE J, 63: 698-704, 2017
引用
收藏
页码:698 / 704
页数:7
相关论文
共 50 条
  • [1] Ketone C-C Bond Activation Meets the Suzuki-Miyaura Cross-coupling
    Just-Baringo, Xavier
    Larrosa, Igor
    CHEM, 2018, 4 (06): : 1203 - 1204
  • [2] Recent developments in nickel catalyzed Suzuki-Miyaura C-C cross-coupling reaction
    Datta, Sayanti
    Chandra, Anushri
    Bhattacharya, Samaresh
    INORGANICA CHIMICA ACTA, 2024, 572
  • [3] Preparation of C-arylglycals via Suzuki-Miyaura cross-coupling of dihydropyranylphosphates
    Leidy, Michelle R.
    Hoffman, J. Mason
    Pongdee, Rongson
    TETRAHEDRON LETTERS, 2013, 54 (50) : 6889 - 6891
  • [4] Organosulphur and related ligands in Suzuki-Miyaura C-C coupling
    Kumar, Arun
    Rao, Gyandshwar Kumar
    Kumar, Satyendra
    Singh, Ajai K.
    DALTON TRANSACTIONS, 2013, 42 (15) : 5200 - 5223
  • [5] Suzuki-Miyaura cross-coupling reaction in the functionalization of the C ring of morphinans
    Sipos, Attila
    Berenyi, Sandor
    LETTERS IN ORGANIC CHEMISTRY, 2007, 4 (02) : 146 - 150
  • [6] Solid-state Suzuki-Miyaura cross-coupling reactions: olefin-accelerated C-C coupling using mechanochemistry
    Seo, Tamae
    Ishiyama, Tatsuo
    Kubota, Koji
    Ito, Hajime
    CHEMICAL SCIENCE, 2019, 10 (35) : 8202 - 8210
  • [7] Palladacycles of Thioethers Catalyzing Suzuki-Miyaura C-C Coupling: Generation and Catalytic Activity of Nanoparticles
    Rao, Gyandshwar Kumar
    Kumar, Arun
    Kumar, Satyendra
    Dupare, Umesh B.
    Singh, Ajai K.
    ORGANOMETALLICS, 2013, 32 (08) : 2452 - 2458
  • [8] Scope of aminomethylations via Suzuki-Miyaura cross-coupling of organotrifluoroborates
    Molander, Gary A.
    Gormisky, Paul E.
    Sandrock, Deidre L.
    JOURNAL OF ORGANIC CHEMISTRY, 2008, 73 (06): : 2052 - 2057
  • [9] Chemoselective Suzuki-Miyaura Cross-Coupling via Kinetic Transmetallation
    Fyfe, James W. B.
    Fazakerley, Neal J.
    Watson, Allan J. B.
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2017, 56 (05) : 1249 - 1253
  • [10] Synthesis of biphenylamines via Suzuki-Miyaura cross-coupling reactions
    Maj, Anna M.
    Delaude, Lionel
    Demonceau, Albert
    Noels, Alfred F.
    TETRAHEDRON, 2007, 63 (12) : 2657 - 2663