The self-association of cholesterol in dilute benzene and toluene solu
tions was investigated by conventional infrared spectroscopy. The samp
le spectra, recorded in the fundamental OH stretching range, were reso
lved into the bands of functionally different OH groups of associated
cholesterol and its predominant species identified by analysis of thei
r absorbances. The formation constants of oligomers were derived from
monomer absorbances measured as a function of cholesterol concentratio
n. In addition to the monomers A(1), open (A) over tilde(2) (Delta (H)
over tilde(2) = -11 +/- 1 kJ mol(-1)) and cyclic dimers (A) over cap(
2) (Delta (H) over cap(2) = -24 +/- 2 kJ mol(-1)) in benzene and open
dimers (A) over tilde(2) (Delta (H) over tilde(2) = -12 +/- 1 kJ mol(-
1)) and tetramers A(4) (Delta H-4 = -47 +/- 6 kJ mol(-1)) in toluene w
ere established as the prevailing species. (C) 1998 Elsevier Science B
.V. All rights reserved.