Obtaining of highly-active catalysts of unsaturated compounds hydrogenation by using supercritical carbon dioxide

Zhang, 2006, Preparation of supported metallic nanoparticles using supercritical fluids; a review, J. Supercrit. Fluids, 38, 252, 10.1016/j.supflu.2006.03.021 Campelo, 2009, Sustainable preparation of supported metal nanoparticles and their application in catalysis, ChemSusChem, 2, 18, 10.1002/cssc.200800227 Ulusal, 2017, Supercritical carbon dioxide deposition of γ-alumina supported Pd nanocatalysts with new precursors and using on Suzuki-Miyaura reactions, J. Supercrit. Fluids, 127, 111, 10.1016/j.supflu.2017.03.024 Deal, 2017, Water gas shift reaction on alumina-supported Pt-CeOx catalysts prepared by supercritical fluid deposition, J. Supercrit. Fluids, 119, 113, 10.1016/j.supflu.2016.08.016 Morère, 2017, Supercritical fluid preparation of Pt, Ru and Ni/graphene nanocomposites and their application as selective catalysts in the partial hydrogenation of limonene, J. Supercrit. Fluids, 120, 7, 10.1016/j.supflu.2016.10.007 Matsuyamaa, 2017, Supercritical fluid-assisted immobilization of Pd nanoparticles in themesopores of hierarchical porous SiO2 for catalytic applications, J. Supercrit. Fluids, 130, 140, 10.1016/j.supflu.2017.07.032 Qiao, 2017, Preparation of SBA-15 supported Pt/Pd bimetallic catalysts using supercritical fluid reactive deposition: how do solvent effects during material synthesis affect catalytic properties?, Green Chem., 19, 977, 10.1039/C6GC02490D Tanaka, 2007, Fabrication of continuous mesoporous carbon film with face-centered orthorhombic symmetry through soft templating pathways, J. Mater. Chem., 17, 3639, 10.1039/b705692c Meng, 2005, Ordered mesoporous polymers and homologous carbon frameworks: amphiphilic surfactant templating and direct transformation, Angew. Chem. Int. Ed., 117, 7215, 10.1002/ange.200501561 Yang, 2010, Direct triblock-copolymer-templating synthesis of ordered nitrogen-containing mesoporous polymers, J. Colloid Interface Sci., 342, 579, 10.1016/j.jcis.2009.10.037 Niu, 2003, Dendrimer-encapsulated metal nanoparticles and their application to catalysis, C. R. Chim., 6, 1049, 10.1016/j.crci.2003.08.001 Karakhanov, 2009, Nanocatalysts based on dendrimers, Pure Appl. Chem., 81, 2013, 10.1351/PAC-CON-08-10-15 Karakhanov, 2012, Palladium nanoparticles on dendrimer-containing supports as catalysts for hydrogenation of unsaturated hydrocarbons, Petrol. Chem., 52, 289, 10.1134/S0965544112050052 Crooks, 2001, Dendrimer-encapsulated metal nanoparticles: synthesis, characterization, and applications to catalysis, Acc. Chem. Res., 34, 181, 10.1021/ar000110a Ooe, 2002, Dendritic nanoreactors encapsulating Pd particles for substrate-specific hydrogenation of olefins, Nano Lett., 2, 999, 10.1021/nl0202105 Karakhanov, 2010, Design of dendrimer-based nanostructured catalyst systems and their catalytic activity in hydrogenation: synthesis of ruthenium nanoparticles immobilized in dendrimer networks, Petrol. Chem., 50, 290, 10.1134/S0965544110040067 Boronoev, 2016, Palladium catalysts based on mesoporous organic materials in semihydrogenation of alkynes, Macromol. Symp., 363, 57, 10.1002/masy.201500184 Karakhanov, 2015, Alkyne hydrogenation using Pd–Ag hybrid nanocatalysts in surface-immobilized dendrimers, Appl. Organomet. Chem., 29, 777, 10.1002/aoc.3367 Karakhanov, 2017, Dendrimer-stabilized Ru nanoparticles immobilized in organo-silica materials for hydrogenation of phenols, Catalysts, 7, 86, 10.3390/catal7030086 Karakhanov, 2017, Palladium nanoparticles on dendrimer-containing supports as catalysts for hydrogenation of unsaturated hydrocarbons, Mol. Catal., 440, 107, 10.1016/j.mcat.2017.07.011 Kazarian, 2000, Polymer processing with supercritical fluids, Polym. Sci. Ser. C, 42, 78 Kikic, 2003, Supercritical impregnation of polymers, Curr. Opin. Solid State Mater. Sci., 7, 399, 10.1016/j.cossms.2003.09.001 Tomasko, 2003, A review of CO2 applications in the processing of polymers, Ind. Eng. Chem. Res., 42, 6431, 10.1021/ie030199z Morley, 2007, Synthesis and characterization of advanced UHMWPE/silver nanocomposites for biomedical applications, Eur. Polym. J., 43, 307, 10.1016/j.eurpolymj.2006.10.011 Timashev, 2014, Structure and properties of Ultra High Molecular Weight Polyethylene (UHMWPE) containing silver nanoparticles, Russ. J. Phys. Chem. B, 8, 1042, 10.1134/S1990793114080156 Miao, 2008, Highly efficient nanocatalysts supported on hollow polymer nanospheres: synthesis, characterization, and applications, J. Phys. Chem. C, 112, 774, 10.1021/jp076596v DeBrabander-van den Berg, 2003, Poly(propylene imine) dendrimers: large-scale synthesis by hetereogeneously catalyzed hydrogenations, Angew. Chem. Int. Ed., 32, 1308, 10.1002/anie.199313081 Rybakova, 2016, Synthesis of novel promising materials via impregnation of crosslinked polymeric networks with metal complexes in supercritical carbon dioxide, Russ. J. Phys. Chem. B, 10, 1163, 10.1134/S1990793116070162 Darr, 1999, New directions in inorganic and metal-organic coordination chemistry in supercritical fluids, Chem. Rev., 99, 495, 10.1021/cr970036i Duca, 1996, Selective hydrogenation of acetylene in ethylene feedstocks on Pd catalysts, Appl. Catal. A Gen., 146, 269, 10.1016/S0926-860X(96)00145-7 van Laren, 1999, Selective homogeneous palladium (0)-catalyzed hydrogenation of alkynes to (Z)-alkenes, Angew. Chem. Int. Ed., 38, 3715, 10.1002/(SICI)1521-3773(19991216)38:24<3715::AID-ANIE3715>3.0.CO;2-O Sajiki, 2008, Partial hydrogenation of alkynes to cis-olefins by using a novel Pd°–Polyethyleneimine catalyst, Chem. Eur. J., 14, 5109, 10.1002/chem.200800535 Vasil’ev, 2002, Stereospecific 1,4-cis-hydrogenation of conjugated dienes, dienynes and dienediynes catalyzed by chromium carbonyl complexes in stereocontrolled synthesis of physiologically active olefins, Russ. Chem. Bull., 51, 1341, 10.1023/A:1020990301927 Bond, 1996, Catalytic hydrogenation in the liquid phase. Part 1. hydrogenation of isoprene catalyzed by palladium, palladium−gold, and palladium−silver catalysts, J. Mol. Catal. A: Chem., 109, 261, 10.1016/1381-1169(96)00027-1 Bond, 1997, Product selectivities in isoprene hydrogenation: diagnosis of π-allylic intermediates, J. Mol. Catal. A: Chem., 118, 333, 10.1016/S1381-1169(96)00402-5