Abstract
We report the first isolable nickel difluorocarbene complexes (NiP2[P(OMe)3](=CF2); P2 = Ph2P(CH2)2PPh2, 2 P(OMe)3), which are also the only examples of formally d10 metal fluorocarbenes. These [Ni0]=CF2 complexes react with tetrafluoroethylene (TFE) to yield the rare perfluorometallacyclobutanes [NiP2(κ2-CF2CF2CF2-)], with potential relevance to fluoroalkene metathesis and polymerization. Preliminary kinetic experiments establish that the reactions of the new [Ni]=CF2 compounds with TFE are considerably faster than the analogous reactions of their previously reported [Co]=CF2 counterparts. Further, we show that TFE addition to 2 is a dissociative process, in contrast to [Co]=CF2, which reacts with TFE in an associative fashion. Finally, the preliminary reactivity of NiP2(κ2-CF2CF2CF2-) (P2 = Ph2P(CH2)2PPh2) is described.
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CITATION STYLE
Harrison, D. J., Daniels, A. L., Korobkov, I., & Baker, R. T. (2015). D10 Nickel Difluorocarbenes and Their Cycloaddition Reactions with Tetrafluoroethylene. Organometallics, 34(24), 5683–5686. https://doi.org/10.1021/acs.organomet.5b00808
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