Thin Solid Films, Vol.284-285, 211-215, 1996
Monolayer Behavior of Chiral Compounds at the Air-Water-Interface - 4-Hexadecyloxy-Butane-1,2-Diol
Monolayers of the pure S-enantiomer (x(S) = 1) and of two mixtures x(S) = 0.75 and x(S) = 0.5 (racemate) of 4-hexadecyloxy-butane-1,2-diol (C16H33-O-CH2-CH2-CHOH-CH2OH) (HOBD) have been studied at the air-water interface by thermodynamic measurements, fluorescence microscopy and X-ray diffraction. The isotherms depend only slightly on chirality. Above the transition pressure pi(c) condensed domains with a polygonal shape are formed. In all cases the domains start to destabilize from the notch. The branches of the S-enantiomer turn only clockwise, whereas domains of the mixtures show branches which turn clockwise and counterclockwise. The number of the left- and right-handed arms depends on the mixing ratio. At lower lateral pressures S-HOBD and the mixture with x(S) = 0.75 exhibit a chiral structure. At pressures above 25 mN m(-1) a centered rectangular structure with a tilt of the molecules towards their next-nearest neighbours (NNN) is formed, At lower surface pressures the racemate is packed in a centered-rectangular lattice with a tilt towards nearest neighbours (NN). Above 14 mN m(-1) a transition to a NNN phase occurs.
Keywords:PHOSPHOLIPID MONOLAYERS;BULK PROPERTIES;ENANTIOMERS;DIFFRACTION;SEPARATION;MESOGENS;CRYSTALS;LINKAGES