Polymeric analogs of well-known chiral Mn(III)-salen complexes were synthesized and were used as recyclable catalysts for asymmetric epoxidation of olefins. For this purpose two different monomers, 2 and 3, bearing chiral Mn(III)-salen moieties were synthesized. The monomer 3 carries a bulky substituent closer to the Schiff base moiety, while monomer 2 lacks such a substituent. These metal complexed chiral monomers were subsequently copolymerized with ethylene glycol dimethacrylate producing insoluble crosslinked functional matrices that possess macroporous morphology. Chemo- and enantioselective catalytic activities of these two polymers were evaluated for epoxidation of olefins. Both polymers catalysed the epoxidation of a variety of olefins at room temperature in the presence of iodosylbenzene (PhIO) as the terminal oxidant with yields comparable to the homogenous system. In terms of their enantioselective catalytic activity, polymer P-2 (obtained from 3) performed better than polymer P-1 (obtained from 2). Unfortunately, while the homogeneous systems are reported to offer over 80% enantioselectivity, with the present polymeric catalysts, enantioselectivity to a maximum of 30% were observed. Unlike the homogeneous system, use of an external nitrogenous donor played a very insignificant role in influencing enantioselectivity.