The catalytic activities of suspended nano-sized palladium catalysts toward
various olefin hydrogenation reactions are reported. The Pd nanoparticles
were prepared by a laser ablation method followed by careful characterizati
on. Two types of Pd nanoparticle systems were fabricated and subjected to a
series of catalytic activity measurements: (i) Pd nanoparticles stabilized
by tetraoctylammonium bromide (TC(8)ABr) ionic micelles with an average di
ameter of 2.4 +/- 0.5 nm and (ii) bare-Pd nanoparticles with an average siz
e of 12.7 +/- 5.7 nm in diameter. The catalytic activities of both TC(8)ABr
-Pd and bare-Pd nanoparticles were examined by measuring their turnover num
bers (TON) in several target olefin hydrogenation reactions, such as the tr
ansformations of styrene to ethylbenezene, 2-methyl-2-butene to 2-methylbut
ane, 1-octene to n-octane, trans-stilbene to bibenzyl, and cyclohexene to c
yclohexane. Data are compared to the hydrogenation results using a commerci
ally available Pd/C catalyst system under similar reaction conditions. An e
xclusive selectivity of the catalytic styrene hydrogenation reaction on the
C=C bond, rather than on the aromatic ring, was found among three systems,
giving ethylbenzene as the only product. The catalyst stability was found
to be on the order of TC(8)ABr-Pd > bare-Pd > 10% Pd/C. (C) 2000 Academic P
ress.