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Synthesis and Characterization of 1,4-Diimine Complexes of 1,2,3,4,5-Pentamethylcyclopentadienylrhodium and iridium

  • Paek, Cheol-Ki (Department of Chemical Education, Korea National University of Education) ;
  • Ko, Jae-Jung (Department of Chemical Education, Korea National University of Education) ;
  • Uhm, Jae-Kook (Department of Chemsitry,College of Natural Science, Keimyung University)
  • Published : 1994.11.20

Abstract

Monomeric rhodium and iridium diimine complexes $Cp^*M(HNRNH)(Cp^*$ = 1,2,3,4,5-pentamethylcyclopentadienyl : (M=lr; R=o-$C_6H_4 (1a), 4,5-(CH_3)_2-C_6H_2-1,2 (1b), 4,5-(Cl)_2-C_6H_2-1,2$ (1c), NCC=CCN-1,2 (1d): M=Rh; R=NCC=CCN-1,2 (1e)) have been synthesized from $[CP^*MCl_2]_2$ and 2 equiv. of diamine in the presence of $NEt_3$. The Crystal structure of 1a was determined by X-ray diffraction method : 1a was crystallized in the monoclinic system, space group $P2_{1/c}$, with lattice constants a=9.543 (1) ${\AA}$, b=16.286 (1) ${\AA}$, c=10.068 (1) ${\AA}$ and ${\beta}$=99.25 (1), with Z= 4. Least-squares refinement of the structure led to R factor of 0.049. The coordination sphere of rhodium and iridium can be described as a 2-legged piano-stool. All complexes are highly colored. Electrochemical studies show that 1d and 1e display quasi-reversible reduction and 1a-1c display irreversible reductions, suggesting that the acceptor orbital might be localized on the diimine ring.

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References

  1. J. Am. Chem. Soc. v.88 Balch, A. L.;Holm, R. H.
  2. J. Chem. Soc., Chem. Commu. Buffon, R.;Leconte, M.;Choplin, A.;Basset, J.
  3. J. Chem. Soc., Dalton Trans. Espinet, P.;Bailey, P. M.;Maitlis, P. M.
  4. Inorg. Chem. v.16 Warren, L.
  5. J. Chem. Soc., Dalton Trans. Leung, W. H.;Danopoulos, A. A.;Wilkinson, G.;Hussain-Bates, B.;Hursthouse, M. B.
  6. J. Chem. Soc., Dalton Trans. Alobaidi, N.;McWhinnie, S. L. W.;Hamor, T. A.;Jones, C. J.;McCleverty, J. A.
  7. J. Chem. Soc., Dalton Trans. Redshaw, C.;Wilkinson, G,;Hussain-Bates, B.;Hursthouse, M. B.
  8. J. Chem. Soc., Dalton Trans. Anillo, A.;Barrio, C.;Garcia-Granda, S.;Obeso-Rosete, R.
  9. Bull. Kor. Chem. Soc. v.15 Paek, C.;Ko, J.;Kang, S. O.;Carrol, P. J.
  10. J. Am. Chem. Soc. v.91 Kang, J. W.
  11. Chem. Ber. v.109 Dieck, H. T.;Svoboda, M.
  12. Organometallics v.12 Michelman, R. I.;Bergman, R. C.;Andersen, R. A.
  13. Organometallics v.13 Michelman, R. I.;Ball, G. E.;Bergman, R. C.;Andersen, R. A.
  14. Inorg. Chem. v.7 Hall, G. S.;Soderberg, R. H.
  15. Organometallics v.13 Abd-El-Aziz, A. S.;Epp, K. M.;de Denus, C. R.;Fisher-Smith, G.
  16. Inorg. Chem. v.20 Belser, P.;von Zelewsky, A.;Zehnder, M.
  17. Organometallics v.1 Gross, M. E.;Ibers, J. A.;Trogler, W. C.
  18. Inorg. Chem. v.7 Heck, R. F.
  19. J. Chem. Soc., Dalton Trans. Danopoulos, A. A.;Wong, A. C. C.;Wilkinson, G.;Hursthouse, M. B.;Hussain, B.
  20. J. Am. Chem. Soc. v.106 Maroney, M. J.;Trogler, W. C.

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