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Volumn 15, Issue 20, 1996, Pages 4247-4257

Synthesis and reactivity of cyclic and acyclic (1-(acyloxy)pentadienyl)Fe(CO)2LX and (1-alkoxypentadienyl)Fe(CO)2LX salts (L = CO, PPh3)

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EID: 0000361282     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om960336a     Document Type: Article
Times cited : (16)

References (56)
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    • For in situ characterizations of trans cations, see: (a) Lillya, C. P.; Sahatjian, R. A. J. Organomet. Chem. 1971, 32, 371. (b) Sorensen, T. S.; Jablonski, C. R. J. Organomet. Chem. 1970, 25, C62. (c) Lillya, C. P.; Sahatjian, R. A. J. Organomet. Chem. 1970, 25, C67. (d) Brookhart, M.; Harris, D. L. J. Organomet. Chem. 1972, 42, 441.
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    • note
    • 2, the experimentally observed plots of concentration against time for 39, 38, and 40 match almost exactly those predicted by the above equations.
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    • 1 was obtained from a plot of In [A] against time for the disappearance of 44 using the integrated intensity of the H3 resonances as a measure of concentration (correlation coefficient 0.998).
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    • 1 was obtained from a plot of In [A] against time for the disappearance of 52 using the integrated intensity of the methyl resonances. Only three data points were obtained before decomposition substantially broadened the spectrum. For previous characterization of these cations, see ref 12b,c.
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    • + cation: (a) Burrows, A. L.; Parker, D. G.; Hine, K.; Johnson, B. F. G.; Lewis, J.; Poe, A.; Vichi, E. J. S. J. Chem. Soc., Dalton Trans. 1980, 1135. (b) Burrows, A. L.; Johnson, B. F. G.; Lewis, J.; Parker, D. G. J. Organomet. Chem. 1977, 127, C22.
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