Formation of Alkanes by Aerobic Carbon–Carbon Bond Coupling Reactions Catalyzed by a Phosphovanadomolybdic Acid
Abstract
The valorization of alkanes is possible via carbon–carbon coupling reactions. A series of dialkyl cobalt complexes [(RCH_2)_2Co^(III)(bpy)_2]ClO_4 (R = H, Me, Et, and Ph) were reacted with the H_5PV_2Mo_(10)O_(40) polyoxometalate as a catalyst, leading to a selective oxidative carbon–carbon bond coupling reaction. The reaction is initiated by electron transfer from [(RCH_2)_2Co^(III)(bpy)_2]^+ to H_5PV^V_2Mo_(10)O_(40) to yield an intermediate [(RCH_2)_2Co^(IV)(bpy)_2]^(2+)–H_5PV^(IV)V^VMo_(10)O_(40), as identified by a combination of EPR and X-ray photoelectron spectroscopy experiments. The reaction is catalytic with O_2 as terminal oxidant representing an aerobic C–C bond coupling reaction.
Additional Information
© 2017 American Chemical Society. ACS Editors' Choice - This is an open access article published under an ACS AuthorChoice License, which permits copying and redistribution of the article or any adaptations for non-commercial purposes. Received: February 12, 2017; Revised: March 8, 2017; Published: March 14, 2017. This research was supported by the Israel Science Foundation (grant no. 2046/14). Bidyut B. Sarma is thanked for his assistance. R.N. is the Rebecca and Israel Sieff Professor of Organic Chemistry. Author Contributions: The manuscript was written through contributions of all authors and they have given their approval to the final version of the manuscript. The authors declare no competing financial interest.Attached Files
Published - acscatal.7b00461.pdf
Supplemental Material - cs7b00461_si_001.pdf
Supplemental Material - cs7b00461_si_002.cif
Supplemental Material - cs7b00461_si_003.cif
Supplemental Material - cs7b00461_si_004.cif
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Additional details
- Eprint ID
- 77211
- Resolver ID
- CaltechAUTHORS:20170505-091159868
- Israel Science Foundation
- 2046/14
- Created
-
2017-05-05Created from EPrint's datestamp field
- Updated
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2021-11-15Created from EPrint's last_modified field