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Inserting CO.sub.2 into Terminal Alkynes via Bis--Metal Complexes
The direct interaction between CO.sub.2 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).sub.2-Ag complex showed a better catalytic performance to...
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Published in: | Catalysis letters 2017-02, Vol.147 (2), p.463 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
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Summary: | The direct interaction between CO.sub.2 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).sub.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 Cs.sub.2CO.sub.3 as additive, one atmosphere CO.sub.2 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. Graphical |
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ISSN: | 1011-372X |
DOI: | 10.1007/s10562-016-1920-5 |