Abstract
Catalytic hydrogenation of substituted aromatic nitrocompounds and hydrocarbons has been studied. It was established that monometallic Pd-catalysts were suitable for reduction of nitrogroups. Bifunctional catalysts such as Rh-Pt, Rh-Pd, Pd-Ru and Rh-Ru were used for hydrogenation of both aromatic ring and nitrogroup and sequence of their hydrogenation depended on support nature. Over Rh-Pt alumina supported catalysts consequent hydrogenation of NO2 and benzene ring took place, over silica supported catalysts their consecutive hydrogenation was observed. Such catalytic properties of bimetallic Rh-Pt and Rh-Pd catalysts probably connected with metal-metal interaction leading to optimal adsorption strength of uniformly adsorbed hydrogen. The optimal reaction conditions (temperature and hydrogen pressure) have been elaborated for synthesis of alicyclic amines with 95-99% yields.