Nanoscale particles of metallic copper clusters have been prepared by
two methods, namely the thermal reduction and sonochemical reduction o
f copper(II) hydrazine carboxylate Cu(N2H3COO)(2) . 2H(2)O complex in
an aqueous medium. Both reduction processes-take place under an argon
atmosphere over a period of 2-3 h. The FT-IR, powder X-ray diffraction
, and UV-visible studies support the reduction products of Cu2+ ions a
s metallic copper nanocrystallites. The powder X-ray analysis of the t
hermally derived products show the formation of pure metallic copper,
while the sonochemical method yields a mixture of metallic copper and
copper oxide(Cu2O). The formation of Cu2O along with the copper nanopa
rticles in the sonochemical process can be attributed to the partial o
xidation of copper by in situ generated H2O2 under the sonochemical co
nditions. However, the presence of a mixture of ee an argon/hydrogen (
95:5) atmosphere yields pure copper metallic nanoparticles, which coul
d be due to the scavenging action of the hydrogen towards the OH. radi
cals that are produced in solution during ultrasonic irradiation. The
synthesized copper nanoparticles exhibit a distinct absorption peak in
the region of 550-650nm. The transmission electron microscopy studies
of the thermally derived copper show the presence of irregularly shap
ed particles (200-250 nm) having sharp edges and facets. On the other
hand, the sonochemically derived copper powder shows the presence of p
orous aggregates(50-70nm) that contain an irregular network of small n
anoparticles. The copper nanoparticles are catalytically active toward
an ''Ullmann reaction''-that is, the condensation of aryl halides to
an extent of 80-90% conversion. The time course of catalysis was studi
ed for condensation of iodobenzene at 200 degrees C for a period of 1-
5 h. The catalytic ability of copper nanoparticles produced by the the
rmal and sonochemical methods was compared with that of commercial cop
per powders.