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Modest yields (<30%) of insertion products are obtained when zirconacyclopentanes or -pentenes are mixed with 1,1-dibromoalkanes or 1,1-dibromoalkenes and t-BuLi added at -100 °C. Whitby, R. J.; Vicart, N. Unpublished work
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2Zr(Cl)R and zirconacyclopentanes react well, the difference in behavior being postulated to be due to donation of the O or N lone pair into the available orbital on the formally 16 electron metal centres
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56 The calculations indicate the form 65 to be around 2.5 kcal/mol more stable than 64 , though energies from semiempirical calculations, even comparing conformers, are unreliable.
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