DOI QR코드

DOI QR Code

Kinetics and Stereochemistry of CO Substitution Reactions of Half-Open Chromocene Carbonyls(Ⅰ): Reactions of Cp($C_{5}H_{7}$)CrCO and Phosphines

  • Chung, Jong-Jae (Department of Chemistry, College of Natural Sciences, Kyungpook National University) ;
  • Roh, Byung-Gill (Department of Chemistry, College of Natural Sciences, Kyungpook National University) ;
  • Park, Yu-Chul (Department of Chemistry, College of Natural Sciences, Kyungpook National University)
  • 발행 : 1993.04.20

초록

The CO substitution reactions in the complex, $Cp(S-C_5H_7)CrCO$ with $PR_3(PR_3=PMePh_2,\;P(OCH_3)_3,\;PMe_2Ph)$ were investigated spectrophotometrically at various temperatures. From the reaction rates, it was suggested that the CO substitution reaction takes place by first-order (dissociative) pathway. Activation parameters in decaline are ${\Delta}H^{\neq}\;=\;24.58\;kcal\;{\cdot}\;mol^{-1},\;{\Delta}S^{\neq}\;=\;3.05 cal\;{\cdot}\;mol^{-1}{\cdot}K^{-1}$. Unusually low value of ${\Delta}S^{\neq}$ suggests an ${\eta}^5-S\;{\to}\;{\eta}^5-U$ conversion of the pentadienyl ligand. This was confirmed by the extended-Huckel molecular orbital (EHMO) calculations, which revealed that the total energy Of $Cp(S-C_5H_7)CrCO$ is about 6.84 kcal/mol more stable than that of $Cp(U-C_5H_7)CrCO$ and the energy of $[Cp(U-C_5H_7)CrCO^{\neq}$ transition state is about 4.25 kcal/mol lower than that of $[Cp(S-C_5H_7)Cr]^{\neq}$ transition state.

키워드

참고문헌

  1. Chem. Rev. v.88 R. D. Ernst
  2. Advances in Organometallic Chemistry v.26 P. Powell;R. West(ed.);F. G. A, Stone(ed.)
  3. J. Organomet. Chem. v.285 H. Yasuda;A. Nakamura
  4. J. Am. Chem. Soc. v.112 J. R. Bleeke;R. J. Wittenbrink;T. W. Clayton;M. Y. Chiang
  5. J. Am. Chem. Soc. v.104 M. C. Bohm;M. Eckert-Maksic;R. D. Ernst;D. R. Wilson;R. Gletiter
  6. J. Am. Chem. Soc. v.107 M. S. Kralik;J. P. Hutchinson;R. D. Ernst
  7. Organometallics v.6 M. S. Kralik;A. L. Rheingold;R. D. Ernst
  8. Inorg. Chem. v.22 S. J. Severson;J. H. Cymbaluk;R. D. Ernst;J. M. Higashi;R. W. Parry
  9. Organometallics v.6 J. R. Bleeke;W-J. Peng
  10. J. Am. Chem. Soc. v.108 G. T. Palmer;F. Basolo;L. B. Kool;M. D. Rausch
  11. J. Am. Chem. Soc. v.113 W. Freeman Jeffrey;C. Hallinan Noel;M. Arif Atta;W. Gedridge Robert;D. Ernst Richard;Basolo Fred
  12. J. Chem. Phys. v.39 R. Hoffmann
  13. J. Am. Chem. Soc. v.100 J. H. Ammeter;H. B. Burg;J. C. Thibeault;R. Hoffmann
  14. J. Am. Chem. Soc. v.98 R. H. Summerville;R. Hoffmann
  15. J. Am. Chem. Soc. v.107 L. Stahl;J. P. Hutchinson;D. R. Wilson
  16. J. Am. Chem. Soc. v.109 R. M. Kowaleski;W. C. Trogler;T. D. Newbound;R. D. Ernst