期刊
JOURNAL OF FLUORINE CHEMISTRY
卷 261, 期 -, 页码 -出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/j.jfluchem.2022.110030
关键词
Cobalt; Fluoroalkylation; Electrochemistry; Organometallic
资金
- U.S. National Science Foundation [CHE-2153730]
In this study, solvent-coordinated perfluoroethyl and n-perfluoropropyl cobalt complexes were synthesized and characterized. The electrochemical analysis revealed that [(MeCN)(4)Co(C2F5)(2)][PF6] is more easily reduced compared to [(MeCN)(3)Co (C2F5)(3)], which has significant implications for the development of redox-triggered reactions involving cobalt(II) intermediates.
Solvent-coordinated perfluoroethyl and n-perfluoropropyl cobalt complexes were prepared and characterized by a variety of analytical techniques. The new complexes reported herein include [(MeCN)(3)Co(n-C(3)F7)(3)], [fac- (H2O)(3)Co(n-C(3)F7)(3)].(6 pyridine), and [(MeCN)(4)Co(R-f)(2)][PF6] (R-f = C2F5, n-C3F7). Electrochemical analyses reveal the extent to which [(MeCN)(4)Co(C2F5)(2)][PF6] is more easily reduced compared to the known [(MeCN)(3)Co (C2F5)(3)], which has implications for the development of redox-triggered reactions involving the intermediacy of cobalt(II).
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