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Complete disassembly of carbon disulfide by a ditantalum complex

机译:由二钽络合物完全分解二硫化碳

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摘要

The side-on end-on dinitrogen complex [PhP(CH_2SiMe_2NPh)_2Ta]-(μ-H)_2(μ-η~2:η~1-N_2) reacts with CS_2 with complete cleavage of both C=S double bonds and the formation of [PhP(CH_2SiMe_2NPh)_2Ta](μ-S)_2(μ-CH_2), which has two bridging sulfides and a bridging methylene unit. Further reaction with H_2 produces CH_4 and the disulfide complex. Cleavage of diatomic and triatomic molecules by transition metal complexes represents an important challenge for inorganic chemists as this is often an important step in utilization of such materials for further elaboration. For those small molecules that have multiple bonds, such processes require particularly activated precursor metal complexes capable of transferring electrons to antibonding (σ~* or π~*) orbitals of the substrate.
机译:侧向端对端二氮配合物[PhP(CH_2SiMe_2NPh)_2Ta]-(μ-H)_2(μ-η〜2:η〜1-N_2)与CS_2反应,同时完全裂解两个C = S双键,并且形成[PhP(CH_2SiMe_2NPh)_2Ta](μ-S)_2(μ-CH_2),它具有两个桥联硫化物和一个桥连亚甲基单元。与H_2的进一步反应产生CH_4和二硫化物络合物。过渡金属配合物裂解双原子和三原子分子对无机化学家而言是一个重要的挑战,因为这通常是利用此类材料进行进一步加工的重要步骤。对于具有多个键的那些小分子,这样的过程需要特别活化的前体金属络合物,该络合物能够将电子转移到衬底的反键(σ〜*或π〜*)轨道上。

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  • 来源
    《Chemical Communications》 |2010年第46期|p.8794-8796|共3页
  • 作者单位

    Department of Chemistry, The University of British Columbia,2036 Main Mall, Vancouver, BC, Canada, V6T 1Z1;

    rnDepartment of Chemistry, The University of British Columbia,2036 Main Mall, Vancouver, BC, Canada, V6T 1Z1;

    rnDepartment of Chemistry, The University of British Columbia,2036 Main Mall, Vancouver, BC, Canada, V6T 1Z1;

    rnDepartment of Chemistry, The University of British Columbia,2036 Main Mall, Vancouver, BC, Canada, V6T 1Z1;

    rnDepartment of Chemistry, The University of British Columbia,2036 Main Mall, Vancouver, BC, Canada, V6T 1Z1;

    rnDepartment of Chemistry, The University of British Columbia,2036 Main Mall, Vancouver, BC, Canada, V6T 1Z1;

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