15min:

JAVIX THOMAS, OLEKSANDR SUKHORUKOV, WOLFGANG JÄGER, YUNJIE XU, Department of Chemistry, University of Alberta, Edmonton, AB, T6G 2G2, Canada .

The delicate competition between the inter- and intramolecular hydrogen-bonding in the complex consisting of a chiral alpha-hydroxy ester, methyl lactate, and water, has been studied using rotational spectroscopy and high level ab initio calculations. Extensive ab initio calculations have been performed to locate all possible low energy conformers of the methyl lactate-water contact pair and five lowest energy conformers have been identified. The most stable conformer forms a seven membered ring with two intermolecular hydrogen bonds: one between the alcoholic hydroxy group of methyl lactate and the oxygen of the water molecule and the other between the hydrogen of water and the oxygen of the carbonyl group. Broadband scans for the rotational spectra of these conformers have been carried out using a newly built chirped-pulse FTMW instrument and the final frequency measurements with a cavity based FTMW instrument. Spectral assignments have been made for the lowest energy conformer of methyl lactate-H₂O and D₂O. The hyperfine splitting and the source of the splitting will be discussed.