Highly Dispersed Pd Species Active in the Suzuki-Miyaura Reaction

被引:22
|
作者
Okumura, Kazu [1 ]
Matsui, Hirosuke [1 ]
Tomiyama, Takuya [1 ]
Sanada, Takashi [1 ]
Honma, Tetsuo [2 ]
Hirayama, Sayaka [2 ]
Niwa, Miki [1 ]
机构
[1] Tottori Univ, Grad Sch Engn, Dept Chem & Biotechnol, Minami Ku, Tottori, Japan
[2] Japan Synchroton Radiat Res Inst SPring 8, Sayo, Hyogo 6795198, Japan
基金
日本学术振兴会;
关键词
EXAFS spectroscopy; palladium; Suzuki-Miyaura reaction; X-ray absorption spectroscopy; zeolites; CROSS-COUPLING REACTIONS; N-HETEROCYCLIC CARBENES; PALLADIUM NANOPARTICLES; METAL NANOPARTICLES; ARYL CHLORIDES; HECK REACTION; USY ZEOLITE; CATALYSTS; ADSORPTION; COMPLEXES;
D O I
10.1002/cphc.200900711
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
Structures of Pd/zeolites immersed in solvents were measured by in situ X-ray absorption fine structure (XAFS). Systematic studies revealed that the selection of an appropriate support (USY-zeolite), thermal treatment temperature of USY, solvent (o-xylene), H-2 partial pressure (6%), and the use of a Pd amine complex affect the structure of Pd. As a result, we found that monomeric Pd can be obtained in the USY support with H-2 bubbling in o-xylene. The structural properties of Pd correlate well with its catalytic performance in the Suzuki-Miyaura coupling reactions; a very high TON of up to 11000 000 was obtained over the monomeric Pd.
引用
收藏
页码:3265 / 3272
页数:8
相关论文
共 50 条
  • [41] Diethyl boronobenzylphosphonates as substrates in Suzuki-Miyaura reaction
    Rydzewska, Agata
    Mangold, Anna
    Wanat, Weronika
    Kafarski, Pawel
    PHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS, 2017, 192 (06) : 758 - 762
  • [42] The Suzuki-Miyaura reaction in the chemical transformations of vindoline
    Ruszkowska, Joanna
    Chrobak, Robert
    Zero, Pawel
    Maurin, Jan K.
    Szawkalo, Joanna
    Czarnocki, Zbigniew
    ACTA BIOCHIMICA POLONICA, 2007, 54 (04) : 857 - 861
  • [43] Application of the Suzuki-Miyaura Reaction in the Synthesis of Flavonoids
    Selepe, Mamoalosi A.
    Van Heerden, Fanie R.
    MOLECULES, 2013, 18 (04) : 4739 - 4765
  • [44] Isonitriles as efficient ligands in Suzuki-Miyaura reaction
    Villemin, Didier
    Jullien, Arnaud
    Bar, Nathalie
    TETRAHEDRON LETTERS, 2007, 48 (24) : 4191 - 4193
  • [45] Highly Active Fe3O4@SBA-15@NHC-Pd Catalyst for Suzuki-Miyaura Cross-Coupling Reaction
    Akkoc, Mitat
    Bugday, Nesrin
    Altin, Serdar
    ozdemir, Ismail
    Yasar, Sedat
    CATALYSIS LETTERS, 2022, 152 (06) : 1621 - 1638
  • [46] Synthesis of β-Arylporphyrins and Oligophenylenediporphyrins by the Suzuki-Miyaura Reaction
    Cunha, Anna C.
    Gomes, Ana T. P. C.
    Ferreira, Vitor F.
    de Souza, Maria C. B. V.
    Neves, Maria G. P. M. S.
    Tome, Augusto C.
    Silva, Artur M. S.
    Cavaleiro, Jose A. S.
    SYNTHESIS-STUTTGART, 2010, (03): : 510 - 514
  • [47] Synthesis of highly functionalised dibenzylglycine derivatives via the Suzuki-Miyaura coupling reaction
    Kotha, S
    Behera, M
    Kumar, RV
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2002, 12 (01) : 105 - 108
  • [48] Atomically Dispersed Pd Sites on ZrO2 Hybridized N-Doped Carbon for Efficient Suzuki-Miyaura Reaction
    Du, Jiaqi
    Peng, Yidan
    Guo, Xu
    Zhang, Guoliang
    Zhang, Fengbao
    Fan, Xiaobin
    Peng, Wenchao
    Li, Yang
    CATALYSTS, 2023, 13 (04)
  • [49] Reusable Pd-PolyHIPE for Suzuki-Miyaura Coupling
    Ravbar, Miha
    Koler, Amadeja
    Paljevac, Muzafera
    Kolar, Mitja
    Krajnc, Peter
    Iskra, Jernej
    ACS OMEGA, 2022, 7 (15): : 12610 - 12616
  • [50] Highly efficient and reusable supported Pd catalysts for Suzuki-Miyaura reactions of aryl chlorides
    Schweizer, Stephane
    Becht, Jean-Michel
    Le Drian, Claude
    ORGANIC LETTERS, 2007, 9 (19) : 3777 - 3780