Search results for "layer"
showing 10 items of 2667 documents
A slow process in confined polymer melts: layer exchange dynamics at a polymer solid interface
2010
Employing Molecular Dynamics simulations of a chemically realistic model of 1,4-polybutadiene between graphite walls we show that the mass exchange between layers close to the walls is a slow process already in the melt state. For the glass transition of confined polymers this process competes with the slowing down due to packing effects and intramolecular rotation barriers.
Charge dissipation in e-beam lithography with Novolak-based conducting polymer films
2008
Charging of common resist materials during electron beam (e-beam) writing leads to deflection of the electron beam path, which can result in significant pattern displacement. Here we report a new conducting polymer to eliminate charging. A common approach is to place the conducting layer underneath the e-beam resist layer. Conductivity equal or greater than 10(-4) S cm(-1) has been reported to prevent pattern displacement. Some other properties such as a flat surface layer, chemical inertness and insolubility in both the top resist solvent and the developer are also necessary. The way to achieve all these properties consisted in synthesizing a conducting polymer inside an insulating polymer…
Multilayer Thin Films by Layer-by-Layer Assembly of Hole- and Electron-Transport Polyelectrolytes: Optical and Electrochemical Properties
2006
In this paper, we pressent the synthesis of a series of p-type and n-type semicondnctring polyelectrolytes with triarylamine, oxadiazole, thiarliazole and triazine moictes. The synthesized polymeric hole and electrom iransport materials were examined optically and electrochemically using UV/Vis spectroscopy. PL spectroscopy and CV. Based on the optical and electrochemical data, each of the energy levels were calculated and all values suggested that the were promising hole-(p-type) or alectron=transprot (n-type) materials for devices. Moreover, the synthesized ionie polymers were suitable for LBL thin film deposition from ditute polymer solutions and the multilayers were fully characterized …
Weak non-covalent interactions control the relative molecular orientation in the crystals of N-pentafluorobenzyl aniline derivatives
2010
The crystal structures of N-pentafluorobenzyl aniline derivatives are controlled by versatile aromatic–aromatic interactions between the electron deficient and electron rich aromatics; the parent compound (1) possesses an L shape while protonation (2–5) induces a conformational change resulting in a planar arrangement of molecules which pack in layer type structures with different molecular orientations.
Langmuir-Blodgett Mono- and Multilayer Assemblies of Amphiphilic Liquid- Crystalline n-Alkyl-4′-n-alkoxybiphenyl-4-carboxylates. I
1991
Five n-Alkyl-4′-Alkoxy-biphenyl-4-carboxylates were investigated as Langmuir monolayers at the air/ water interface and as Langmuir-Blodgett (LB) films on solid supports. All five compounds form stable monolayers at the air/water interface and can be transferred onto solid supports yielding LB-films, whose structures and kinetic behavior strongly depend on the headgroup. The structures of the LB-films were investigated by means of optical textures and X-ray diffraction and compared with the structures of the corresponding bulk phases which were investigated by means of Differential Scanning Calorimetry and X-ray powder diffraction. The LB-films of the acid and the two methyl esters exhibit …
From Hydrophobic Matching to Interfacial Tuning: New Ideas for the Mutual Adaptation Between Membranes and Peptides
2009
It is widely accepted that membrane proteins and lipid bilayers are complementary in terms of the distribution in space of their hydrophobic and polar regions. Similarly, it is also accepted that the hydrophobic parts of the protein and the membrane must adapt to each other. Classically these ideas are rationalized under the concept of hydrophobic matching, which predicts a number of possible mechanisms by which proteins can vary their effective hydrophobic length, or membranes can change their hydrophobic thickness. Such effects have been studied in detail for simplified systems, like transmembrane peptides or protein fragments, which generally show that optimizing peptide orientation is t…
Role of hexagonal structure-forming lipids in diadinoxanthin and violaxanthin solubilization and de-epoxidation
2005
In this study, we have examined the influence of different lipids on the solubility of the xanthophyll cycle pigments diadinoxanthin (Ddx) and violaxanthin (Vx) and on the efficiency of Ddx and Vx de-epoxidation by the enzymes Vx de-epoxidase (VDE) from wheat and Ddx de-epoxidase (DDE) from the diatom Cyclotella meneghiniana, respectively. Our results show that the lipids MGDG and PE are able to solubilize both xanthophyll cycle pigments in an aqueous medium. Substrate solubilization is essential for de-epoxidase activity, because in the absence of MGDG or PE Ddx and Vx are present in an aggregated form, with limited accessibility for DDE and VDE. Our results also show that the hexagonal st…
Free-standing smectic LC elastomer films
2001
ABSTRACTWe probe the mesophase transitions and layer structures in thin ordered smectic liquid crystalline elastomer films by means of x-ray diffraction and optical microscopy. Oriented elastomer films of submicrometer thickness are produced by crosslinking freely suspended smectic polymer films. After crosslinking, the mesomorphism is similar to that of the precursor polymer. Smectic layers align parallel to the film plane. The layer spacing increases with temperature in the SmC* phase while it decays above the SmC*-SmA transition.
M�ssbauer study of the spatial distribution of the active species in Cs doped Fe2O3-V2O5 catalysts
1995
From a Cs doped Fe2O3-V2O5 (Fe:V=1.4) catalyst exhibiting an inhomogeneous composition after calcination, three different fractions have been separated by visual inspection. One fraction has been found to consist of mainly α-Fe2O3, another one of mainly FeVO4. The third fraction (S1 in the text) is the catalytically most active fraction containing besides both of the former components an amorphous phase of FexVyOz and also the dopant. By combining the results from transmission and conversion electron Mossbauer spectra it has been concluded that the amorphous component is enriched in the surface region of the crystallites of the catalyst. In addition, the formation of a thin surface layer of…
Wetting of mesoscopic soft cylinders: structure and layering transitions.
1998
The wetting of soft mesoscopic long-chain particles is studied. As a model system, a cylindrical brush with poly(vinyl)pyridine side chains on the water surface is characterized by isotherms and x-ray reflectivity. The forces from the two planar interfaces and the intra- and interparticle interactions are all of comparable magnitude. Two layering transitions occur, one from the monolayer to the double layer, the next to a homogeneous multilayer. The hard wall from which layering starts is the smooth polymer/air interface. Indeed, they particles in the top layer of both the double- and the multilayer have their cylinder axis parallel to the surface and are laterally compressed. In contrast, …