INTERACTIONS BETWEEN CHOLESTEROL AND 2-METHOXYETHANOL - THE EFFECT OF2-METHOXYETHANOL AND OTHER HYDROXYLIC COMPOUNDS ON CHOLESTEROL - PROTON ACCEPTOR ASSOCIATION
P. Goralski, INTERACTIONS BETWEEN CHOLESTEROL AND 2-METHOXYETHANOL - THE EFFECT OF2-METHOXYETHANOL AND OTHER HYDROXYLIC COMPOUNDS ON CHOLESTEROL - PROTON ACCEPTOR ASSOCIATION, Physics and chemistry of liquids, 32(1), 1996, pp. 37-45
Using the 'pure base' calorimetric method, the association enthalpy (D
elta(f)H) of cholesterol and 2-methoxyethanol (MeOEtOH), triethylamine
(TEA) or tri-1-butylamine (TEA) in the presence of MeOEtOH (10% mol)
has been determined. The addition of 2-methoxyethanol to the amine bri
ngs about the same effect as the addition of other simple alcohols (me
thanol, butan-1-ol). The increase in the association enthalpy of chole
sterol and TEA in the presence of MeOEtOH can be caused by MeOEtOH hyd
roxyl group involved in the formation of mixed associates. Tn the case
of amine with a weak steric hindrance (TEA), such an effect is not ob
served. The addition of 10 mol% of water or alcohols to N,N-dimethylfo
rmamide (DMF) makes no significant change in the cholesterol-DMF assoc
iation enthalpy. This would suggest that the hydroxyl groups of added
R'OH fail to participate in the formation of cholesterol-DMF associate
s. A slight increase in Delta(f)H, taking place when water is added to
DMF, can be attributed to an increased solvation of the associates be
ing formed.