Synthesis and characterisation of some dimeric η2-diyne compounds of cobalt

(Note: The full text of this document is currently only available in the PDF Version )

Xue-Nian Chen, Jie Zhang, Shu-Lin Wu, Yuan-Qi Yin, Wen-Ling Wang and Jie Sun


Abstract

The organometallic dimers [{Co2(CO)6}2(diyne)] [diyne = C6H4(CO2CH2C2H)2-1,2 1, HC2CH2OC6H4OCH2C2H 2 or HC2(CH2)5C2H 3] have been synthesized from reactions between [Co2(CO)8] and the appropriate diyne ligands. However, the reaction of [Co2(CO)8] with diprop-2-ynyl ether HC2CH2OCH2C2H under similar conditions gave the expected product [{Co2(CO)6}2(µ-HC2CH2OCH2C2H)] 4 and the unexpected product [Co4(CO)10(µ-CO){µ4-η∶η3-CC(CH2OCH2)CCH2}] 5. The products have been characterised by infrared, 1H NMR spectroscopy and C/H analyses, and 2, 4 and 5 also by single-crystal X-ray crystallography. In 2 and 4 both “yne” fragments of the diyne ligand are bonded to a Co2(CO)6 fragment with the C[triple bond, length half m-dash]C vector essentially perpendicular to the Co–Co vector. However, in 5 hydrogen migration and new C–C bond formation has led to novel structural features, such as µ3-CCo3 and η3-C3Co units and a “C4O” ring.


References

  1. B. Happ, T. Bartik, C. Zucchi, M. C. Rossi, F. Ghelfi, G. Palyi, G. Varadi, G. Szalontai, I. T. Horrath, A. Chiesi-Villa and C. Guastini, Organometallics, 1995, 14, 809 CrossRef CAS.
  2. A. T. Chalk and J. F. Harrod, J. Am. Chem. Soc., 1965, 87, 1133 CrossRef CAS.
  3. H. Jabic, C. C. Santini and C. Coulombean, Inorg. Chem., 1991, 30, 3088 CrossRef CAS.
  4. R. F. Heck, J. Am. Chem. Soc., 1964, 86, 2819 CrossRef CAS.
  5. J. C. Sauer, R. D. Cramer, V. A. Engelhardt, T. A. Ford, H. E. Holmquist and B. W. Howk, J. Am. Chem. Soc., 1959, 81, 3677 CrossRef CAS.
  6. M. G. Karpov, S. P. Tunik, V. R. Denisov, G. L. Starova, A. B. Nikolskii, F. M. Dolgushin, A. I. Yanovshy and Yu. T. Struchkov, J. Organomet. Chem., 1995, 485, 219 CrossRef CAS.
  7. C. E. Housecroft, B. F. G. Johnson, M. S. Khan, J. Lewis, P. R. Raithby, M. E. Robson and D. A. Wilkinson, J. Chem. Soc., Dalton Trans., 1992, 3171 RSC.
  8. P. Magnus and D. P. Becker, J. Chem. Soc., Chem. Commun., 1985, 640 RSC.
  9. D. Seyferth and H. P. Withers, Inorg. Chem., 1983, 22, 2931 CrossRef CAS.
  10. Y. Rubin, C. B. Knobler and F. Diederich, J. Am. Chem. Soc., 1990, 112, 4966 CrossRef CAS.
  11. S. Aime, A. Tiripicchio, M. Tiripicchio-Camellini and A. J. Deeming, Inorg. Chem., 1981, 20, 2027 CrossRef CAS.
  12. S. Aime and A. J. Deeming, J. Chem. Soc., Dalton Trans., 1983, 1807 RSC.
  13. G. Cetini, O. Gambino, R. Rosetti and E. Sappa, J. Organomet. Chem., 1967, 8, 149 CrossRef CAS.
  14. A. Aimi, L. Milone, R. Rosetti and P. L. Stanghellini, Inorg. Chim. Acta, 1977, 22, 135 CrossRef.
  15. R. K. Karris, Nuclear Magnetic Resonance Spectroscopy: a Physicohemical View, Pitman, London, 1983 Search PubMed.
  16. P. Brum, G. M. Dawkins, M. Green, R. M. Mills, J.-Y. Salaun, F. G. A. Stone and P. Woodward, J. Chem. Soc., Dalton Trans., 1983, 1357 RSC.
  17. J. E. Davies, M. J. Mays, P. R. Raithly, V. Sarreswaran and G. P. S. Shields, J. Chem. Soc., Dalton Trans., 1998, 775 RSC.
  18. W. Sly, J. Am. Chem. Soc., 1959, 81, 18 CrossRef CAS.
  19. D. A. Brown, J. Chem. Phys., 1960, 33, 1037 CAS.
  20. F. A. Cotton, J. D. Jamerson and B. J. Stults, J. Am. Chem. Soc., 1976, 98, 1774 CrossRef CAS.
  21. R. B. King, Organometallic Syntheses, Vol. 1, Transition-Metal Compounds, Academic Press, New York, 1965, p. 98 Search PubMed.
  22. X.-N. Chen, J. Zhang and Y.-Q. Yin, Chem. Res. (Chinese), 1998, 4, 25 Search PubMed.
  23. L. Brandsma, Preparative Acetylenic Chemistry, Elsevier, Amsterdam, 1988, 261 Search PubMed.
  24. D. T. Cromer and J. T. Waber, International Tables for Crystallography, Kynoch Press, Birmingham, 1974, vol. IV, Table 2.2 A. Search PubMed.
  25. TEXSAN, Crystal Structure Analysis Package, Molecular Structure Corporation, Houston, TX, 1985 and 1992.
Click here to see how this site uses Cookies. View our privacy policy here.