Ring-opening metathesis polymerization (ROMP) of dicyclopentadiene (DCPD) was carried out by using (ArO)6-xWClx-Et2A1C1 (ArO: 2,6-ditertiarybutyl-p-cresoxy, x=3, 4, 6) and the corresponding polymer-supported catalytic systems. Influences of different homogeneous catalysts, polymerization conditions and immobilization of the homogeneous catalytic systems on polymerization (gelation time, monomer conversion) and synthesized polydicyclopen-tadiene's (PDCPD's) mechanical properties were investigated. The experimental results show that using the polymer-supported catalytic systems can not only increase the monomer conversion of polymerization but also improve the synthesized polymer's mechanical properties to a certain extent.