For the preparation. of the title compound, 1,8-diiodonaphthalene was
treated with p-anisylchlorosilane and magnesium to give 1,8-bis(p-anis
ylsilyl)naphthalene (1). The reaction of compound 1 with 2 equiv. of t
riflic acid affords 8-bis[(trifluoromethyl)sulfonyl)silyl]naphthalene,
which can. be reduced to 1,8-disilylnaphthadene (2) with lithium alum
inum hydride. The crystal structures of compounds 1 and 2 have been de
termined by single crystal X-ray diffraction. The C10Si2 skeleton. in
2 is planar, but there are severe in-plane outward bendings of the two
silyl groups. In compound 1, along with a similar but smaller bending
of the silyl groups, there is also a tilting by 7 degrees of the true
benzene rings of naphthalene.