A variety of 2,7-disubstituted derivatives of 1,8-naphthalenediol
(2) of potential value as
ligands for the complexation of transition metals can be prepared from
1,8-naphthalenediyl
bis(diethylcarbamate) (3) and
1,8-bis(methoxymethoxy)naphthalene (9) by directed
ortho-metalation and subsequent functionalization. The reaction of
TiCl4 with 1,8-naphthalenediol
(2) in the presence of diisopropyl ketone produced an adduct
of a novel chloride-bridged
dimer of
[1,8-naphthalenediolato(2-)-O,O‘]dichlorotitanium
(16; R = H). Its unusual
structure indicates that complexes derived from 1,8-naphthalenediols
can have features not
normally observed in complexes derived from simple phenols.