A Practical Synthesis of Ammonia from Nitrogen Gas, Samarium Diiodide and Water Catalyzed by a Molybdenum-PCP Pincer Complex

被引:19
作者
Ashida, Yuya [1 ]
Kondo, Shoichi [2 ]
Arashiba, Kazuya [1 ]
Kikuchi, Takamasa [2 ]
Nakajima, Kazunari [3 ]
Kakimoto, Seizo [4 ]
Nishibayashi, Yoshiaki [1 ]
机构
[1] Univ Tokyo, Sch Engn, Dept Syst Innovat, Bunkyo Ku, Tokyo 1138656, Japan
[2] Nissan Chem Corp, Mat Res Labs, Funabashi, Chiba 2740052, Japan
[3] Univ Tokyo, Sch Engn, Frontier Res Ctr Energy & Resources, Bunkyo Ku, Tokyo 1138656, Japan
[4] Nissan Chem Corp, Adv Mat & Planning Dept, Chuo Ku, Tokyo 1036119, Japan
来源
SYNTHESIS-STUTTGART | 2019年 / 51卷 / 20期
基金
日本科学技术振兴机构; 日本学术振兴会;
关键词
ammonia; dinitrogen; molybdenum; samarium diiodide; water; N-2-TO-NH3; CONVERSION; DINITROGEN; REDUCTION; BEARING; REACTIVITY; FIXATION; LIGANDS; FE;
D O I
10.1055/s-0039-1690151
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A practical method for ammonia synthesis is described. The reaction of atmospheric pressure of nitrogen gas with samarium diiodide as a reducing reagent and water as a proton source in the presence of a catalytic amount of a molybdenum trichloride complex bearing a PCP [1,3-bis(di- tert -butylphosphinomethyl)benzimidazol-2-ylidene]-type pincer ligand occurs under ambient conditions to afford ammonium sulfate after treatment with sulfuric acid.
引用
收藏
页码:3792 / 3795
页数:4
相关论文
共 45 条
  • [1] Catalytic conversion of nitrogen to ammonia by an iron model complex
    Anderson, John S.
    Rittle, Jonathan
    Peters, Jonas C.
    [J]. NATURE, 2013, 501 (7465) : 84 - +
  • [2] Synthesis and Catalytic Reactivity of Polystyrene-supported Molybdenum Pincer Complexes toward Ammonia Formation
    Arashiba, Kazuya
    Itabashi, Takayuki
    Nakajima, Kazunari
    Nishibayashi, Yoshiaki
    [J]. CHEMISTRY LETTERS, 2019, 48 (07) : 693 - 695
  • [3] Catalytic Nitrogen Fixation via Direct Cleavage of Nitrogen-Nitrogen Triple Bond of Molecular Dinitrogen under Ambient Reaction Conditions
    Arashiba, Kazuya
    Eizawa, Aya
    Tanaka, Hiromasa
    Nakajima, Kazunari
    Yoshizawa, Kazunari
    Nishibayashi, Yoshiaki
    [J]. BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 2017, 90 (10) : 1111 - 1118
  • [4] Catalytic Reduction of Dinitrogen to Ammonia by Use of Molybdenum-Nitride Complexes Bearing a Tridentate Triphosphine as Catalysts
    Arashiba, Kazuya
    Kinoshita, Eriko
    Kuriyama, Shogo
    Eizawa, Aya
    Nakajima, Kazunari
    Tanaka, Hiromasa
    Yoshizawa, Kazunari
    Nishibayashi, Yoshiaki
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2015, 137 (17) : 5666 - 5669
  • [5] A molybdenum complex bearing PNP-type pincer ligands leads to the catalytic reduction of dinitrogen into ammonia
    Arashiba, Kazuya
    Miyake, Yoshihiro
    Nishibayashi, Yoshiaki
    [J]. NATURE CHEMISTRY, 2011, 3 (02) : 120 - 125
  • [6] Molybdenum-Catalyzed Ammonia Formation Using Simple Monodentate and Bidentate Phosphines as Auxiliary Ligands
    Ashida, Yuya
    Arashiba, Kazuya
    Tanaka, Hiromasa
    Egi, Akihito
    Nakajima, Kazunari
    Yoshizawa, Kazunari
    Nishibayashi, Yoshiaki
    [J]. INORGANIC CHEMISTRY, 2019, 58 (14) : 8927 - 8932
  • [7] Molybdenum-catalysed ammonia production with samarium diiodide and alcohols or water
    Ashida, Yuya
    Arashiba, Kazuya
    Nakajima, Kazunari
    Nishibayashi, Yoshiaki
    [J]. NATURE, 2019, 568 (7753) : 536 - +
  • [8] Examining the relationship between coordination mode and reactivity of dinitrogen
    Burford, Richard J.
    Fryzuk, Michael D.
    [J]. NATURE REVIEWS CHEMISTRY, 2017, 1 (04)
  • [9] N2-to-NH3 Conversion by a triphos-Iron Catalyst and Enhanced Turnover under Photolysis
    Buscagan, Trixia M.
    Oyala, Paul H.
    Peters, Jonas C.
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2017, 56 (24) : 6921 - 6926
  • [10] Fe-Mediated Nitrogen Fixation with a Metallocene Mediator: Exploring pKa Effects and Demonstrating Electrocatalysis
    Chalkley, Matthew J.
    Del Castillo, Trevor J.
    Matson, Benjamin D.
    Peters, Jonas C.
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2018, 140 (19) : 6122 - 6129