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Updated: Mar 11, 2026

The Synthesis, Characterization and Reactivity of a Series of Ruthenium N-triphosPh Complexes
Published on: April 10, 2015
Highly efficient nitrogen chelated ruthenium carbene metathesis catalysts
Yulian Duan1, Tao Wang1, Qingxiao Xie1
1Department of Chemistry, College of Science, Tianjin University, Tianjin 300350, P. R. China. wjh@tju.edu.cn and Collaborative Innovation Center of Chemical Science and Engineering, Tianjin, 300072, P. R. China.
New ruthenium carbene catalysts featuring N-heterocyclic carbene (NHC) and carbonyl groups show high activity in olefin metathesis. These catalysts, particularly those with electron-withdrawing groups, demonstrate excellent performance in ring-closing and cross metathesis reactions.
Area of Science:
- Organometallic Chemistry
- Catalysis
- Organic Synthesis
Background:
- Ruthenium carbene complexes are vital catalysts for olefin metathesis.
- Developing novel catalysts with enhanced activity and stability is an ongoing research area.
Purpose of the Study:
- To synthesize and characterize novel nitrogen-chelated ruthenium carbene complexes.
- To investigate the catalytic activity of these complexes in olefin metathesis reactions.
Main Methods:
- Synthesis of novel ruthenium carbene complexes incorporating N-heterocyclic carbene (NHC) and carbonyl functionalities.
- X-ray crystallography to determine the structural features of a representative complex.
- Evaluation of catalytic performance in ring-closing metathesis (RCM) and cross metathesis (CM) reactions.
Main Results:
- A series of nitrogen-chelated ruthenium carbene catalysts were successfully developed.
- X-ray structure revealed an octahedral coordination around the ruthenium center, with carbonyl oxygen and imine nitrogen coordinating to the metal.
- Complexes bearing electron-withdrawing groups exhibited high initiation rates.
- The catalysts demonstrated excellent performance in both RCM and CM reactions.
Conclusions:
- The developed nitrogen-chelated ruthenium carbene complexes are effective catalysts for olefin metathesis.
- Electron-withdrawing groups enhance the catalytic activity, leading to high initiation rates.
- These novel catalysts offer a promising alternative for various olefin metathesis applications.
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