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Synthesis, characterization and catalytic applications of palladium nanoparticle-cored dendrimers stabilized by metal–carbon bonds

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dc.contributor.author Ratheesh Kumar, V K
dc.contributor.author Sreedevi, K
dc.contributor.author Gopidas, K R
dc.date.accessioned 2013-05-28T04:48:16Z
dc.date.available 2013-05-28T04:48:16Z
dc.date.issued 2012-06
dc.identifier.citation European journal of organic chemistry 2012(18):3447-3458;2012 en_US
dc.identifier.uri http://hdl.handle.net/123456789/418
dc.description.abstract The synthesis and characterization of four generations of palladium nanoparticle-cored Fréchet-type dendrimers (Pd-Gn)possessing direct palladium–carbon bonds are reported. These core–shell materials have been synthesized by the simultaneous reduction of different generation diazodendrons and PdII in an organic medium. The resulting organic–inorganic hybrid materials were characterized by IR, NMR and UV/Vis spectroscopic techniques. The formation of nearly spherical particles of 2–4 nm diameter was confirmed by TEM studies. The efficiency of one member of this series, Pd-G1, in catalysing important C–C bond-forming reactions such as Suzuki, Stille and Hiyama coupling reactions was investigated.The results clearly show that Pd-G1 can efficiently catalyse the cross-coupling of arylboronic acids, aryl stannanes and organosilicon compounds with differently substituted aryl halides in addition to efficiently catalysing hydrogenation reactions. The catalyst exhibited good recovery and recyclability in Suzuki coupling reactions. The study suggests that a single catalyst capable of catalysing several reactions can be designed en_US
dc.language.iso en en_US
dc.publisher Wiley en_US
dc.subject Heterogeneous catalysis en_US
dc.subject Nanocatalysis en_US
dc.subject Nanoparticles en_US
dc.subject Palladium en_US
dc.subject Dendrimers en_US
dc.subject Cross-coupling en_US
dc.title Synthesis, characterization and catalytic applications of palladium nanoparticle-cored dendrimers stabilized by metal–carbon bonds en_US
dc.type Article en_US


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