Issue 18, 1997

Successive insertion of tetrafluoroethylene and CO and of tetrafluoroethylene and acetylenes into aryne–nickel(0) bonds

Abstract

Aryne–nickel complexes [Ni(η 2 -C 6 H 4 )L 2 ] [L 2 = 2PEt 3 or dcpe; dcpe = (C 6 H 11 ) 2 PCH 2 CH 2 P(C 6 H 11 ) 2 ] and [Ni(η 2 -C 10 H 6 )(PEt 3 ) 2 ] reacted readily with C 2 F 4 to form the corresponding five-membered tetrafluoro-substituted nickelacycles [[upper bond 1 start]Ni(C 6 H 4 CF 2 C[upper bond 1 end]F 2 -2)L 2 ] (L 2 = dcpe or 2PEt 3 ) and [[upper bond 1 start]Ni(2-C 10 H 6 CF 2 C[upper bond 1 end]F 2 -3)(PEt 3 ) 2 ], respectively. The complex [[upper bond 1 start]Ni(C 6 H 4 CF 2 C[upper bond 1 end]F 2 -2)(dcpe)] is very stable towards air, whereas the PEt 3 analogues react readily to give µ-aryloxo dimers. The naphthalene-based dimer [upper bond 1 start][{Ni(µ-2-OC 10 H 6 CF 2 [upper bond 1 end]CF 2 -3)(PEt 3 )} 2 ] has been structurally characterized. The complexes [[upper bond 1 start]Ni(C 6 H 4 CF 2 C[upper bond 1 end]F 2 -2)L 2 ] insert CO into their aryl–nickel bonds to form six-membered acyl complexes [[upper bond 1 start]Ni{C(O)C 6 H 4 CF 2 C[upper bond 1 end] F 2 -2}L 2 ] (L 2 = dcpe or 2PEt 3 ) and, after CO-induced reductive elimination, 2,2,3,3-tetrafluoroindanone. The dcpe acyl complex has also been shown to undergo reaction with air to form the carboxylato complex [[upper bond 1 start]Ni{OC(O)C 6 H 4 CF 2 C[upper bond 1 end] F 2 -2}(dcpe)], whose structure has been confirmed by X-ray crystallography. Some insertions of acetylenes into the aryl–nickel bonds of [[upper bond 1 start]Ni(C 6 H 4 CF 2 C[upper bond 1 end]F 2 -2)L 2 ] are also reported.

Article information

Article type
Paper

J. Chem. Soc., Dalton Trans., 1997, 3105-3114

Successive insertion of tetrafluoroethylene and CO and of tetrafluoroethylene and acetylenes into aryne–nickel(0) bonds

M. A. Bennett, M. Glewis, D. C. R. Hockless and E. Wenger, J. Chem. Soc., Dalton Trans., 1997, 3105 DOI: 10.1039/A702375H

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