Colloidal quantum
dots, made of semiconductor cores and surface
coated with an organic shell, have generated much interest in areas
ranging from spectroscopy to charge and energy transfer interactions
to device design, and as probes in biology. Despite the remarkable
progress in the growth of these materials, rather limited information
about the molecular arrangements of the organic coating is available.
Here, several nuclear magnetic resonance (NMR) spectroscopic techniques
have been combined to characterize the surface ligand structure(s)
on biocompatible CdSe-ZnS quantum dots (QDs). These materials have
been prepared via a photoinduced ligand exchange method in which the
native hydrophobic coating is substituted, in situ, with a series
of polyethylene glycol-modified lipoic acid-based ligands. We first
combined diffusion ordered spectroscopy with heteronuclear single-quantum
coherence measurements to outline the conditions under which the detected
proton signals emanate from only surface-bound ligands and identify
changes in the proton shifts between free and QD-bound ligands in
the sample. Quantification of the ligand density on different size
QDs was implemented by comparing the sharp 1H signature(s)
of lateral groups in the ligands (e.g., the OCH3 group)
to an external standard. We found that both the molecular architecture
of the ligand and the surface curvature of the QDs combined play important
roles in the surface coverage. Given the non-invasive nature of NMR
as an analytical technique, the extracted information about the ligand
arrangements on the QD surfaces in hydrophilic media will be highly
valuable; it has great implications for the use of QDs in targeting
and bioconjugation, cellular imaging, and energy and charge transfer
interactions.