Xz. Du et al., N-OCTADECANOYL-L-ALANINE AMPHIPHILE MONOLAYER AT THE AIR WATER INTERFACE AND LB FILM STUDIED BY FTIR SPECTROSCOPY/, Langmuir, 14(13), 1998, pp. 3631-3636
Surface pressure (pi)-molecular area (A) compression/expansion isother
ms of N-octadecanoyl-L-alanine reflect homochiral discrimination behav
ior of the enantiomeric monolayer. FTIR studies indicate that carboxyl
ic acid groups form out-of-plane ring dimers between two adjacent N-oc
tadecanoyl-L-alanine molecules in monolayer LB films and that the long
hydrocarbon chains in the film matrix take a biaxial orientation. The
enantiomeric molecules assemble regularly and twist from neighbor to
neighbor, thus giving rise to chirality of the aggregate in the two-di
mensional condensed phase. Prior to the phase transition, the transfor
mation of the triclinic subcell packing of the hydrocarbon chains into
a hexagonal packing occurs. The variable-temperature infrared spectra
of LB films provide powerful evidence for the formation of a hydrogen
-bonded structure between chiral headgroups.