Refine
Has Fulltext
- no (19)
Document Type
- Article (19)
Is part of the Bibliography
- yes (19)
Institute
Langmuir-Blodgett films of zinc 11,18,25-tri(tert-butyl)-4-sulfo-phthalocyanine (ZNPctSO3Na) have been deposited onto hydrophilic and hydrophobic silicon wafers. Y-type films were formed on both types of substrate, and the transfer ratio was very close to unity. The organization of the films on the molecular level was probed by X-ray specular reflectivity.
The molecular in-plane structure of uranyl arachidate Langmuir-Blodgett (LB) films formed at different subphase pH values was analysed by means of X-ray grazing-incidence diffraction. For multilayers formed at low subphase pH a reorganisation of the arachidic acid film structure is confirmed. At appropriate subphase pH values, reorganisation of the film structure, e.g. via the formation of three-dimensional crystallites, is prevented by the presence of the uranyl ions and by the subsequent introduction of conformational disorder (gauche defects) in the alkyl chains. The observation of a macroscopic flow-induced in-plane texture in these uranyl arachidate LB films has profound implications for the design of ordered, supramolecular structures by the Langmuir-Blodgett technique.
The formation of a Langmuir monolayer of an amphiphilic derivative of zinc phthalocyanine (Na[(ZnPcSO3)-S-t]) has been studied by means of surface potential technique and Brewster angle microscopy. The experiments were undertaken in order to understand the behaviour of this monolayer with a well-defined surface pressure isotherm. The floating film is described as a truly monomolecular layer formed by very rigid islands in which the phthalocyanine units tend to take on a preferential orientation with their planes perpendicular to the air-water interface, for high values of the surface pressure. (c) 2004 Elsevier B.V. All rights reserved
The complexation of highly ordered fatty acid monolayers with polyelectrolytes is expected to yield well- ordered Langmuir films suitable for the formation of Langmuir-Blodgett multilayers with improved long-term stability. Studies of the surface pressure-area isotherms and of the surface potential kinetics yield detailed information regarding the influence of these polymeric counterions on the monolayer properties. The injection of bivalent metal salts into the subphase after the complexation was used to improve the order and stability of the mono- and multilayers. The corresponding Langmuir-Blodgett films were investigated by means of X-ray reflectivity measurements and scanning force microscopy. The polyion complex multilayers show a strongly increased mechanical stability compared with films of fatty acid salts formed with bivalent metal ions. These structures are expected to be suitable as ultrathin separation layer for gas separation or ultrafiltration membranes.
Langmuir monolayers of arachidic acid have been prepared on a subphase containing uranyl ions (O-U-O)ý+. The interaction between the uranyl ions and the monolayer of arachidic acid has been studied by means of surface pressure and surface potential isotherms and Brewster angle microscopy at different pH values (ranging from 1.5 to 8). A similar systematic study has been carried out in the presence of Cdý+ ions for comparison purposes. The surface pressure and surface potential isotherms demonstrate that the acid to salt conversion of arachidic acid in the presence of uranyl ions occurs at lower bulk pH values (pH=3.5) as compared with other bivalent metal counterions such as Cdý+. Changes in the surface morphology of the monolayer induced by the interaction with uranyl- and cadmium ions are analyzed and the correlation between the surface potential change and the morphology of the films is discussed.
In this second paper we describe the comprehensive structure investigations on multilayers of uranyl arachidate formed by Langmuir-Blodgett deposition from subphases of different pH on solid substrates by means of a combination of infrared spectroscopy, X-ray specular reflection, ellipsometry, and scanning force microscopy, The structure of these multilayers and their stability are obviously influenced by the subphase pH. The pH range of the acid to salt conversion determined for the Langmuir films is confirmed by the infrared spectroscopic data of the multilayers. While arachidic acid films, deposited from an uranyl acetate subphase of low pH, are found to have strongly distorted rough surface, the films of uranyl structure, The influence of the counterions on the alkyl chain conformation, chain packing, reorganization probability, and stability of the multilayer is discussed.