A coordination polymer has been formed at the water surface by reactio
n of the bifunctional ligand methylenebis(N-hexadecylsalicylidenamine)
(MBSH) with bivalent metal ions, dissolved in the subphase. Studies h
ave been carried out to elucidate the structure of this polymer in mon
olayers at the water surface as well as in Langmuir-Blodgett multilaye
rs. Results with a similar low-molecular compound are included in the
discussion. The collapse area in the monolayer at the water surface wa
s strongly dependent on the metal ion concentration. The infrared spec
trum of the copper complex Langmuir-Blodgett layer suggests complete c
onversion of MBSH, since no absorption of the free ligand could be det
ected. FTIR spectra revealed further, that complexation of copper ions
took place between the nitrogen and the oxygen atom of the ligand. (C
) 1998 Elsevier Science S.A. All rights reserved.