Homogeneous catalytic processes often exhibit high activity and selectivity, in most cases, but the catalys-tproduct separation is generally nontrivial. In addition, the metal catalysts and ligands can be very expensive. These limit the practical application of many outstanding catalytic systems. Immobilization of analogues of homogeneous catalysts on a solid support is one of the promisingways to prepare well-defined catalytic systems, a task of great eco-nomic and environmental importance. Palladium catalysts deposited over different types of solid supports such as silica matrices, charcoal etc have been reported. However, activated charcoal and non-functionalized polymers have drawbacks such as relatively low stability or lack of active functional groups for binding Pd ions and hence the inherent restrictions for reuse. Since C and SiO2 have only a small residual charge, their affinity for metal ions will be weak. Silica is a favorable solid support, but if silica isused directly, the main problem of these catalytic systems seemsto be the metal leaching from the support during the reaction eventhough they adsorb back to the support after the completion of thereaction. Polymer supported transition metal ions have signif-icant role as catalysts in various organic reactions. Themetal ions are attached to the polymer support through a chemicalbond. This reduces the possibility of leaching of metal ions from thesolid support. Considering Pd ions as a homogeneous catalyst, theyeasily lose catalytic activity by forming Pd clusters and also theyare highly expensive. A heterogeneous catalyst is desirable in this case, especially for recycling, though it is not always as reactive ascompared to homogeneous catalysts.