We utilized linear and 2D infrared spectroscopy to analyze
the
carbonyl stretching modes of small esters in different solvents. Particularly
noteworthy were the distinct carbonyl spectral line shapes in aqueous
solutions, prompting our investigation of the underlying factors responsible
for these differences. Through our experimental and theoretical calculations,
we identified the presence of the hydrogen-bond-induced Fermi resonance
as the primary contributor to the varied line shapes of small esters
in aqueous solutions. Furthermore, our findings revealed that the
skeletal deformation mode plays a crucial role in the Fermi resonance
for all small esters. Specifically, the first overtone band of the
skeletal deformation mode intensifies when hydrogen bonds form with
the carbonyl group of esters, whereas such coupling is rare in aprotic
organic solvents. These spectral insights carry significant implications
for the utilization of esters as infrared probes in both biological
and chemical systems