Nanometre-size inorganic dots, tubes and wires exhibit a wide range of elec
trical and optical properties(1,2) that depend sensitively on both size and
shape(3,4), and are of both fundamental and technological interest. In con
trast to the syntheses of zero-dimensional systems, existing preparations o
f one-dimensional systems often yield networks of tubes or rods which are d
ifficult to separate(5-12). And, in the case of optically active II-YI and
III-V semiconductors, the resulting rod diameters are too large to exhibit
quantum confinement effects(6,8-10). Thus, except for some metal nanocrysta
ls(13), there are no methods of preparation that yield soluble and monodisp
erse particles that are quantum-confined in two of their dimensions. For se
miconductors, a benchmark preparation is the growth of nearly spherical II-
VI and III-V nanocrystals by injection of precursor molecules into a hot su
rfactant(14,15). Here we demonstrate that control of the growth kinetics of
the II-VI semiconductor cadmium selenide can be used to vary the shapes of
the resulting particles from a nearly spherical morphology to a rod-like o
ne, with aspect ratios as large as ten to one. This method should be useful
, not only for testing theories of quantum confinement, but also for obtain
ing particles with spectroscopic properties that could prove advantageous i
n biological labelling experiments(16,17) and as chromophores in light-emit
ting diodes(18,19).