DOI QR코드

DOI QR Code

Iridium(Ⅲ) Complexes of η$^6$-Arenes with Olefinic and Cyclopropyl Substituents: Facile Conversion to η ³-henylallyl Complexes

  • Published : 1997.04.20

Abstract

Olefinic and cyclopropyl group substituted arenes (C6H5Y) react with [Cp*Ir(CH3COCH3)3]A2 (A=ClO4-, OTf-) to give η6-arene complexes, [Cp*Ir(η6-C6H5Y)]2+ (1a: Y=-CH=CH2 (a),-CH=CHCH3 (b),-C(CH3)=CH2 (c),-CH-CH2-CH2 (d)). Complex 1b-1d are readily converted into η3-allyl complexes, [Cp*(CH3CN)Ir(η3-CH(C6H5)CHCH2)]+ (2a) and [Cp*(CH3CN)Ir(η3-CH2(C6H5)CH2)]+ (2b), in the presence of Na2CO3 in CH3CN. The η6-styrene complex, 1a reacts with NaBH4 to give η5-cyclohexadienyl complex, [Cp*Ir(η5-C6H6-CH=CH2)]+ (3), while with H2 it gives η6-ethylbenzene complex [Cp*Ir(η6-C6H5CH2CH3)]2+ (4). Complex 1a and 1c react with HCl to give [Cp*Ir(η6-C6H5CH2CH2Cl)]2+ (5a) and [Cp*Ir(η6-C6H5CH(CH3)CH2Cl]2+ (5b), respectively.

Keywords

References

  1. J. Am. Cham. Soc. v.115 Burger, P.;Bergman, R. G.
  2. J. Am. Chem. Soc. v.110 Maghee, W. D.;Bergman, R. G.
  3. Organometallics v.9 Wake field, J. B.;Stryker, J. M.
  4. J. Chem. Soc. Dalton v.130 White, C.;Thomson, S. J.;Maitlis, P. M.
  5. J. Chem. Soc. Dalton White, C.;thomson, S. J.;Maitlis, P. M.
  6. J. Chem. Soc. (A) v.3322 White, C.;Maitlis, P. M.
  7. J. Chem. Soc. Dalton Espinet, P.;Bailey, P. M.;Downey, R. F.;Maitlis, P. M.
  8. J. Organomet. Chem. v.272 Grudy, S. L.;Maitlis, P. M.
  9. J. Am. Chem. Soc. v.108 Periana, R. A.;Bergman, R. G.
  10. Organometallics v.11 Tjaden, E. B.;Stryker, J. M.
  11. J. Organometallics v.8 Gaudet, M. V.;Hanson, A. W.;white, P. S.;Zaworoko, M.
  12. J. Am. Chem. Soc. v.113 Thompson, r. L.;Geib, S. J.;Cooper, N. J.