Langmuir monolayers were prepared using a new class of non-centrosymme
tric macrocycles, the triazolephthalocyanines, differently substituted
with aliphatic chains and/or thiophene subunits. Different monolayer
behaviour and film deposition have been observed among the different m
acrocycles. Compounds substituted with two long aliphatic chains on th
e isoindole ring opposite to the triazole unit have shown the best mon
olayer behaviour. Stable monolayers were successfully transferred onto
CaF2 substrates which had been made hydrophobic. The Langmuir-Blodget
t films were characterized by IR and UV-VIS linear dichroism. In-plane
orientation of some of the macrocycles was observed when nickel(II) a
cetate was added to the aqueous subphase.