The design and synthesis of new amphiphilic ferrocene derivatives and
their capability for forming Langmuir and Langmuir-Blodgett films are
reported. The him formation at the air-water interface was followed by
surface pressure-molecular area isotherm, surface potential-molecular
area isotherm, and Brewster angle microscopy. The stability and struc
ture of the transferred films were investigated by W-vis spectroscopy
and small angle X-ray experiments. Transfer ratios near unity were obt
ained. Two hydrophobic alkyl chains combined with either one or two hy
drophilic functions gave stable and ordered films. One hydrophobic alk
yl chain associated to one hydrophilic headgroup required the presence
of an intercalant for obtaining organized molecular films. This behav
ior clearly illustrated the key role played by the three-dimensional s
tructure of the ferrocene unit which tends to decrease the intermolecu
lar interactions because of its bulkiness; this is in agreement with r
esults reported for ferrocene-containing thermotropic liquid crystals
(Deschenaux, R.; Goodby, J. W. In Ferrocenes: Homogeneous Catalysis, O
rganic Synthesis, Materials Science; Togni, A., Hayashi, T. Eds.; VCH
Verlagsgesellschaft: Weinheim, 1995; pp 471-495).