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Catalysis of Organic..

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178 Hydrogenation <strong>of</strong> Dehydrolinaloolcase DiHL (3,7-dimethyl-6-octaene-3-ol, dihydrolinalool) is an unfavorablebyproduct <strong>of</strong> the reaction.OH+H 2OH+H 2OHDHLLNDiHLFigure 1. Hydrogenation <strong>of</strong> DHL to a completely saturated product DiHLLinalool is one <strong>of</strong> the most widely used fragrant substances in cosmetic andpharmaceutical industry (as a composite <strong>of</strong> many cosmetics and perfumes and as anintermediate in synthesis <strong>of</strong> vitamins (A, E)) (1). But natural resources can’t supplythe growing needs, so the necessity in synthetic LN has been increasing. Therefore thereaction <strong>of</strong> selective catalytic hydrogenation <strong>of</strong> DHL to LN is one <strong>of</strong> the mostsignificant reactions in the chemistry <strong>of</strong> fragrant substances (2), and the main problem<strong>of</strong> this research is the development <strong>of</strong> modern catalytic technology for preparation <strong>of</strong>linalool.Catalytic hydrogenation <strong>of</strong> DHL by various catalysts such as bulk metals andmetals deposited on the carbon, oxides and salts has been studied since the 70-s <strong>of</strong> thelast century (3). The disadvantages <strong>of</strong> such catalysts are the low surface area and thehigh content <strong>of</strong> the noble metals, which result in their high cost price.In contrast, modern catalysts on the base <strong>of</strong> metal nanoparticles have largesurface area-to-volume ratio <strong>of</strong> the metal, which allows effectively utilizing expensivemetals (4). However, without a suitable support the metal nanoparticles aggregatereducing the surface area and restricting the control over the particle size. Toovercome this problem, catalytic nanoparticles have been immobilized on solidsupports, e. g., carbon (5), metal oxides (6) and zeolites (7), or stabilized by cappingligands that ranged from small organic molecules to large polymers (8, 9). Theencapsulation by polymers is advantageous because in addition to stabilizing andprotecting the particles, polymers <strong>of</strong>fer unique possibilities for modifying both theenvironment around catalytic sites and access to these sites (10-12). So, the protectivepolymer not only influences particle sizes but can also have a tremendous influenceon catalytic activity and selectivity (13). Besides, polymers, which contain complexesor metal nanoparticles, combine the advantages both <strong>of</strong> homogeneous (high activityand selectivity) and heterogeneous catalysts (easy recovery from the reaction mixtureand possibility <strong>of</strong> regeneration). Catalytic properties <strong>of</strong> such systems may be changedby varying the type <strong>of</strong> polymeric matrix and characteristics <strong>of</strong> metal nanoparticles(14).

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