4.5 Article

Inserting CO2 into Terminal Alkynes via Bis-(NHC)-Metal Complexes

期刊

CATALYSIS LETTERS
卷 147, 期 2, 页码 463-471

出版社

SPRINGER
DOI: 10.1007/s10562-016-1920-5

关键词

Carboxylation; Terminal alkyne; N-Heterocyclic carbene; Homogeneous catalysis; DFT

资金

  1. Mexican Petroleum institute [90903]
  2. Scientific Research-Foundation Flanders (FWO)
  3. Hercules foundation
  4. Flemish Government-Department EWI
  5. Natural Science Foundation of China [21172027]
  6. Fundamental Research Funds for the Central Universities [WUT: 2014-IV-099]
  7. Independent Innovation Foundation of Wuhan University of Technology [444-20510039]

向作者/读者索取更多资源

The direct interaction between CO2 and terminal alkynes in the presence of bis-(NHC)-metal catalysts at ambient conditions was studied. Two Cu and Ag-based bis-N-heterocyclic carbene Transition Metal catalysts were synthesized. The (NHC)(2)-Ag complex showed a better catalytic performance towards the carboxylation of terminal alkynes in comparison with the copper analogue even for the conversion of acetylene gas. The optimized conditions for the carboxylation are: the use of Cs2CO3 as additive, one atmosphere CO2 and room temperature using 1% mol catalyst. Mechanistic insight into the reaction mechanism is obtained by means of state-of-the-art first principles calculations. [GRAPHICS] .

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