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Hydrogen-bonded clusters of methyl glycolate and methyl α-hydroxyisobutyrate are investigated by ragout-jet FTIR-spectroscopy to elucidate the influence of α-C hydrogens on the unusual aggregation of α-hydroxy esters. Highly structured OH-stretching spectra, stagnation pressure studies, and argon coating experiments show that two α-C hydrogens enable the formation of small oligomers such as trimers and tetramers, whereas the lack of α-C hydrogens stops selective aggregation beyond dimers. Methyl lactate with a single chiral α-C hydrogen is suggested to be intermediate in its clustering behavior, with a homochiral preference for trimers and a strong heterochiral preference for tetramers.
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Borho et al. (2004) studied this question.
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