Two mechanochemical procedures for 17O/18O-isotope labeling of fatty acids are reported: a carboxylic acid activation/hydrolysis approach and a saponification approach.
Fatty
acids are ubiquitous in biological systems and widely used
in materials science, including for the formulation of drugs and the
surface-functionalization of nanoparticles. However, important questions
regarding the structure and reactivity of these molecules are still
to be elucidated, including their mode of binding to certain metal
cations or materials surfaces. In this context, we have developed
novel, efficient, user-friendly, and cost-effective synthetic protocols
based on ball-milling, for the 17O and 18O isotopic
labeling of two key fatty acids which are widely used in (nano)materials
science, namely stearic and oleic acid. Labeled molecules were analyzed
by 1H and 13C solution NMR, IR spectroscopy,
and mass spectrometry (ESI-TOF and LC-MS), as well as 17O solid state NMR (for the 17O labeled species). In both
cases, the labeling procedures were scaled-up to produce up to gram
quantities of 17O- or 18O-enriched molecules
in just half-a-day, with very good synthetic yields (all ≥84%)
and enrichment levels (up to an average of 46% per carboxylic oxygen).
The 17O-labeled oleic acid was then used for the synthesis
of a metal soap (Zn-oleate) and the surface-functionalization of ZnO
nanoparticles (NPs), which were characterized for the first time by
high-resolution 17O NMR (at 14.1 and 35.2 T). This allowed
very detailed insight into (i) the coordination mode of the oleate
ligand in Zn-oleate to be achieved (including information on Zn···O
distances) and (ii) the mode of attachment of oleic-acid at the surface
of ZnO (including novel information on its photoreactivity upon UV-irradiation).
Overall, this work demonstrates the high interest of these fatty acid-enrichment
protocols for understanding the structure and reactivity of a variety
of functional (nano)materials systems using high resolution analyses
like 17O NMR.
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