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Preparation of SNS CobaltII Pincer Model Complexes of Liver Alcohol Dehydrogenase
Published on: March 19, 2020
C(sp)-H, S-H, and Sn-H Bond Activation with a Cobalt(I) Pincer Complex
Sayantani Saha1, Jeanette A Krause1, Hairong Guan1
1Department of Chemistry, University of Cincinnati, P.O. Box 210172, Cincinnati, Ohio 45221-0172, United States.
A cobalt pincer complex effectively cleaves C-H, S-H, and Sn-H bonds. Electron-withdrawing groups promote complete reactions, enabling selective hydrostannation of alkynes.
Area of Science:
- Organometallic Chemistry
- Catalysis
- Cobalt Complexes
Background:
- Development of catalytic two-electron processes with cobalt.
- Investigation of cobalt(I) pincer complexes for bond activation.
Purpose of the Study:
- To explore stoichiometric reactions of a specific cobalt pincer complex with alkynes, thiols, and tin hydrides.
- To understand the factors influencing oxidative addition and catalytic activity.
Main Methods:
- Stoichiometric reactions of {2,6-(iPr2PO)2C6H3}Co(PMe3)2 with various substrates.
- Analysis of oxidative addition products and reaction completion.
- Evaluation of catalytic hydrostannation of terminal alkynes.
Main Results:
- The cobalt pincer complex cleaves C(sp)-H, S-H, and Sn-H bonds, forming oxidative addition products.
- Electron-withdrawing substituents on substrates enhance reaction completion.
- The complex catalyzes selective hydrostannation of terminal alkynes to yield beta-(Z)-alkenylstannanes.
Conclusions:
- The studied cobalt(I) pincer complex is a versatile reagent for activating various bonds.
- Reaction efficiency is dependent on the electronic nature of the substrate substituents.
- The complex demonstrates catalytic potential in hydrostannation reactions.
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