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Published online by Cambridge University Press: 13 February 2013
We present a combined theoretical and experimental study of the adsorption of two pairsof organic isomers, (i) acetic acid AA (CH3COOH) and methylformate MF (HCOOCH3), and (ii) ethanol EtOH(CH3CH2OH) and dimethyl ether DME (CH3OCH3),onto crystalline water ice surfaces at low temperatures. Both approaches show that, foreach pair, the most stable isomer from a thermodynamical point of view,i.e. AA and EtOH, isalso the one which is the more tightly bound to the water ice surface compared to the lessstable isomers (MF and DME). This finding, which can be explained by the ability of AA orEtOH to efficiently interact with the ice surface via hydrogen bondings, may haveimportant consequences in an astrophysical context, since it could explain why the moststable isomer is not the most abundant observed in the interstellar gas phase.