Over
the past decade, N-heterocyclic carbenes (NHCs) have attracted
remarkable attention as metal-coordinating ligands because of their
ability to strongly interact with transition metal complexes and surfaces.
We investigate the coordination interaction between colloidal gold
nanoparticles (AuNPs) and three sets of hydrophilic NHC-based ligands:
an amine-modified small molecule, a monomeric NHC appended with a
poly(ethylene glycol) (PEG) block, and a modified poly(isobutylene-alt-maleic anhydride), PIMA, that simultaneously presents
multiple NHC groups and several short PEG chains. In this report,
we find that all three ligands can rapidly coordinate onto AuNPs,
as characterized using a combination of NMR spectroscopy, high-resolution
transmission electron microscopy, and dynamic light scattering. These
measurements have been supplemented with colloidal stability tests
as well as competition from dithiothreitol molecules. Overall, we
find that multidentate NHC polymer coating exhibits the highest affinity
to AuNPs, which manifests in long-term colloidal stability in buffer
media, absence of any aggregation, and better resistance to competition
from reducing molecules. We further exploit these data to infer additional
insights into the interaction and coordination of NHC molecules with
Au surfaces.