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A cationic gold complex cleaves BArF24
Simone G Weber1, David Zahner, Frank Rominger
1Universität Heidelberg, INF 270, D-69120 Heidelberg, Germany.
Summary
A novel gold complex, IPr**Au-BArF(24), acts as a "soft proton" to activate C-B bonds. This sterically shielded complex enables efficient C-B bond cleavage at room temperature without solvent coordination.
Area of Science:
- Organometallic Chemistry
- Catalysis
- Inorganic Chemistry
Background:
- Sterically hindered N-heterocyclic carbene (NHC) gold complexes are valuable catalysts.
- Activation of weakly coordinating counterions is crucial for catalytic processes.
- Understanding the reactivity of monovalent transition metal electrophiles is key.
Purpose of the Study:
- To synthesize and characterize a sterically shielded cationic NHC gold complex.
- To investigate the in situ activation of a weakly coordinating counterion by the gold complex.
- To explore the potential of this complex as a "soft proton" equivalent.
Main Methods:
- In situ preparation of the gold complex IPr**Au-BArF(24) in dichloromethane.
- Spectroscopic characterization of the reaction intermediates.
- Analysis of the heterolytic C-B bond activation mechanism.
Main Results:
- The sterically shielded cationic NHC gold complex IPr**Au-BArF(24) was successfully prepared in situ.
- The complex demonstrated the ability to heterolytically activate the C-B bond of the tetrakis[3,5-bis(trifluoromethyl)phenyl]borate counterion.
- This activation occurred at room temperature without requiring solvent coordination, highlighting the complex's unique reactivity.
Conclusions:
- The synthesized gold complex functions as a "soft proton" due to its sterically shielded nature.
- Efficient C-B bond activation of weakly coordinating anions is achievable at room temperature.
- This study provides insights into the reactivity of monovalent transition metal electrophiles and their application in catalysis.
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