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the compression procedure, some disorder is induced within the mono-
layer. After stopping the compression, the molecules tend to arrange them-
selves such that an optimum order of the alkyl chains and of the head
groups is attained. This is largely the relaxation process that is also en-
countered on a slick-covered undulating water surface. With regard to the
PME films, it is well-documented >4@ that the ester head group performs a
“flip-flop”-like change in its orientation (the so-called E/Z- isomerisation).
As a consequence, the head group is prevented from hydration by the adja-
cent water layer during compression of the mono layer, and, vice
Fig. 3. Morphology of a PME-film
spread of n- hexane as determined by
BAM;
Fig. 4. Same as Fig. 3, but com-
pression status 0.24 nm 2 /molecule
compression
status
0.34
nm 2 /molecule; 1 mm = 100 Pm
Fig. 5. Same as Fig. 3, but compression
status 0.20 nm 2 / molecule
Fig. 6: Morphology of a PME-film
spread of ethanol as determined by
BAM; compression status 0.415 nm 2 /
molecule; 1 mm = 100 Pm
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