Hydrolysis and alcoholysis VOCl3 quickly hydrolyzes resulting in
vanadium pentoxide and
hydrochloric acid. An intermediate in this process is VO2Cl: :2 VOCl3 + 3 H2O → V2O5 + 6 HCl VOCl3 reacts with alcohols especially in the presence of a proton-acceptor to give
alkoxides, as illustrated by this synthesis of
vanadyl isopropoxide: :VOCl3 + 3 HOCH(CH3)2 → VO(OCH(CH3)2)3 + 3 HCl
Interconversions to other V-O-Cl compounds VOCl3 is also used in the synthesis of
vanadium oxydichloride. :V2O5 + 3 VCl3 + VOCl3 → 6 VOCl2
VO2Cl can be prepared by an unusual reaction involving
Cl2O. :VOCl3 + Cl2O → VO2Cl + 2 Cl2 At >180 °C, VO2Cl decomposes to V2O5 and VOCl3. Similarly, VOCl2 also decomposes to give VOCl3, together with VOCl.
Adduct formation VOCl3 is strongly
Lewis acidic, as demonstrated by its tendency to form
adducts with various bases such as
acetonitrile and
amines. In forming the adducts, vanadium changes from four-coordinate tetrahedral geometry to six-coordinate octahedral geometry: :VOCl3 + 2 H2NEt → VOCl3(H2NEt)2
Organic chemistry VOCl3 is a catalyst or precatalyst in production of ethylene-propylene rubbers (EPDM). In
organic synthesis, it has been used for oxidative coupling of
phenols and
anisoles. ==References==