Ja. Burman et al., SYNTHESIS AND STRUCTURAL CHARACTERIZATION OF HEXA(CYCLOHEXYL)FERROCENE, [1,2,4-(C6H11)3C5H2]2FE, Journal of organometallic chemistry, 479(1-2), 1994, pp. 135-139
1,2,4-tricyclohexylcyclopentadiene can be formed from the phase-transf
er catalyzed addition of cyclohexyl bromide to cyclopentadiene. Reacti
on of two equivalents of its lithium salt with FeCl2 in THF produces t
he corresponding substituted ferrocene. Crystals of orange [1,2,4-(C6H
11)3C5H2]2Fe grown from toluene are monoclinic, space group C2/c, with
a = 16.386 (4) Angstrom, b = 12.142 (3) Angstrom, c = 21.003 (3) Angs
trom, beta = 107.38 (1), and D(calcd) = 1.131 g cm-3 for Z = 4. Least-
squares refinement based on 1291 observed reflections led to a final R
value of 0.049. The molecule possesses a classic sandwich geometry wi
th staggered rings and a crystallographically imposed two-fold rotatio
n axis passing through the metal center. Despite the presence of six c
yclohexyl rings, the cyclopentadienyl ligands can orient themselves ar
ound the iron to avoid unfavorable inter-ring steric interactions. As
a result, the average Fe-C ring distance of 2.06 (1) angstrom in hexa(
cyclohexyl)ferrocene is not significantly longer than the correspondin
g distance in ferrocene itself.