
Journal of Organometallic Chemistry p. 173 - 182 (1984)
Update date:2022-08-11
Topics:
Seetz, J. W. F. L.
Heisteeg, B. J. J. Van De
Schat, G.
Akkerman, O. S.
Bickelhaupt, F.
The reaction of 1,3-bis(bromomagnesio)-2,2-dimethylpropane (1b) with dichlorodicyclopentadienylvanadium(IV) (5) gave 1,1-dicyclopentadienyl-3,3-dimethylvanada(IV)cyclobutane (4) in 30percent yield, contaminated with dicyclopentadienylneopentylvanadium(III) (12).Attempts to purify 4 were only partially successful due to its limited stability (t1/2 = 4 h at 25 deg C in cyclopentane).Identification of 4 is therefore based on its having sufficient thermal stability for isolation, on its reaction with bromine to give 1,3-dibromo-2,2-dimethylpropane (2b), and especially on its ESR and 1H NMR spectra.The reaction of 4 with cyclohexanone (15) gave 17 and 18 as the main products; 17 is the aldol dimer of 15, while 18 may be derived from either 4 or 12.Because methylenecyclohexane (16) is not one of the reaction products, it is concluded that 4 does not have a pronounced tendency to fragment to give a metallacarbene (20).
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