N,N'-Bis(salicylidene)cyclohexane-1,2-diamine (H(2)sal-dach) reacts with oxovanadium(IV) and copper(II) exchanged zeolite-Y in refluxing methanol to yield the corresponding zeolite-Y encapsulated metal complexes, abbreviated herein as [VO(sal-dach)]-Y and [Cu(sal-dach)]-Y. Spectroscopic studies (IR, electronic and H-1 NMR), thermal analysis, scanning electron micrographs (SEM) and X-ray diffraction patterns have been used to characterise these complexes. These encapsulated complexes catalyse the oxidation, by H2O2 of styrene, cyclohexene and cyclohexane efficiently in good yield. Under the optimized conditions, the oxidation of styrene catalysed by [VO(sal-dach)]-Y and [Cu(sal-dach)]-Y gave 94.6 and 21.7 % conversion, respectively, where styreneoxide, benzaldehyde. benzoic acid, 1-phenylethane-1,2-diol and phenylacetaldehyde being the major products. Oxidation of cyclohexene catalysed by these complexes gave cyclohexeneoxide, 2-cyclohexene-1-ol, cyclohexane-1,2-diol and 2-cyclohexene-1-one as major products. Conversion of cyclohexene achieved was 86.6% with [VO(sal-dach+Y and 18.1% with [Cu(sal-dach)]-Y. A maximum of 78.1% conversion of cyclohexane catalysed by [Cu(sal-dach+Y and only 21.0% conversion by [VO(sal-dach)]-Y with major reaction products of cyclohexanone, cyclohexanol and cyclohexane-1,2-diol have been obtained. (c) 2007 Elsevier BN. All rights reserved.