PREPARATION OF NEW CHIRAL DIOXOMOLYBDENUM COMPLEXES HETEROGENIZED ON MODIFIED USY-ZEOLITES - EFFICIENT CATALYSTS FOR SELECTIVE EPOXIDATION OF ALLYLIC ALCOHOLS
A. Corma et al., PREPARATION OF NEW CHIRAL DIOXOMOLYBDENUM COMPLEXES HETEROGENIZED ON MODIFIED USY-ZEOLITES - EFFICIENT CATALYSTS FOR SELECTIVE EPOXIDATION OF ALLYLIC ALCOHOLS, Journal of molecular catalysis. A, Chemical, 107(1-3), 1996, pp. 225-234
A series of dioxomolybdenum(VI) complexes were synthesised by reaction
of Mo(VI) complexes with new chiral ligands derived from (2S,4R)-4-hy
droxyproline. The complexes bearing a Si(OEt)(3) group were heterogeni
sed to a modified USY-zeolite by covalent bonding. All catalysts, homo
geneous and heterogenised, are active and regioselective in the epoxid
ation of allylic alcohols at room temperature using tert-butyl hydrope
roxide as terminal oxidant. The catalytic activity of the heterogenise
d complexes is generally comparable with the corresponding homogeneous
ones, yielding epoxyalcohols with excellent yields and selectivity an
d moderate enantioselectivity. Life time of heterogenised catalysts ha
s been examined by repeated use of the complexes leading similar rates
and yields of epoxide, whilst no appreciable loss of metal has been o
bserved over several runs.