TY - JOUR
T1 - Metal nanoparticles supported on carbon nanofibers
T2 - Synthesis and application for the hydrogenation reactions
AU - Motoyama, Yukihiro
AU - Yoon, Seong Ho
AU - Nagashima, Hideo
PY - 2009/7
Y1 - 2009/7
N2 - Facile synthesis of ruthenium, palladium and platinum nanoparticles supported on three types of carbon nanofibers (platelet: CNF-P, tubular. CNF-T, herringbone: CNF-H) is accomplished by pyrolysis of ruthenium carbonyl clusters, and pyrolysis and hydrogenolysis of Pd2(dba)3-CHC1 3 and Pt(dba)2 [dba: dibenzylideneacetone). TEM studies of these M/CNFs revealed that size-controlled metal nanoparticles existed on the CNFs, and that of the location was dependent on the surface nanostructures of CNFs: On the edge of the graphite layers (CNF-P), in the tubes and on the surface (CNF-T), and between the layers and on the edge (CNF-H). Among these M/CNFs, the Ru/CNF-P showed excellent catalytic activity towards arene hydrogenation with high reusability and functional group tolerance. The present Ru system is applicable to the production of octahydro-l,l'-binaphthyls by partial hydrogenation of l,l'-binaphthyls. While the Pt/CNF-P behaves as an efficient catalyst for hydrogenation of substituted nitroarenes to the corresponding aniline derivatives with other functional groups remaining intact.
AB - Facile synthesis of ruthenium, palladium and platinum nanoparticles supported on three types of carbon nanofibers (platelet: CNF-P, tubular. CNF-T, herringbone: CNF-H) is accomplished by pyrolysis of ruthenium carbonyl clusters, and pyrolysis and hydrogenolysis of Pd2(dba)3-CHC1 3 and Pt(dba)2 [dba: dibenzylideneacetone). TEM studies of these M/CNFs revealed that size-controlled metal nanoparticles existed on the CNFs, and that of the location was dependent on the surface nanostructures of CNFs: On the edge of the graphite layers (CNF-P), in the tubes and on the surface (CNF-T), and between the layers and on the edge (CNF-H). Among these M/CNFs, the Ru/CNF-P showed excellent catalytic activity towards arene hydrogenation with high reusability and functional group tolerance. The present Ru system is applicable to the production of octahydro-l,l'-binaphthyls by partial hydrogenation of l,l'-binaphthyls. While the Pt/CNF-P behaves as an efficient catalyst for hydrogenation of substituted nitroarenes to the corresponding aniline derivatives with other functional groups remaining intact.
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U2 - 10.5059/yukigoseikyokaishi.67.724
DO - 10.5059/yukigoseikyokaishi.67.724
M3 - Review article
AN - SCOPUS:70349878599
SN - 0037-9980
VL - 67
SP - 724
EP - 734
JO - Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry
JF - Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry
IS - 7
ER -