arXiv subjects

Ulrich W. Suter

Publications and source records attributed to Ulrich W. Suter.

4 recordsLinked to original sources

arXiv2003

Simple and Accurate Computations of Solvatochromic Shifts in pi -> pi* Transitions of Aromatic Chromophors

A new approach is introduced for calculating the spectral shifts of the most bathochromic pi -> pi* transition of an aromatic chromophore in apolar environments. As an example, perylene in solid and liquid n-alkane matrices was chosen, and all shifts are calculated relative to one well-defined solid-inclusion system. It is shown that a simple two-level treatment of the solute using Huckel theory yields spectral shifts in excellent agreement with experimental results for the most prominent inclusion sites of perylene in solid n-alkane surroundings and for the dilute solutions in liquid n-alkanes. The idea is general enough to be applied to any aromatic chromophore in a nonpolar solvent matrix. In contrast to earlier treatments, this approach is based on geometry-dependent polarizabilities, employs a r^-4 dependence for the dispersion energy, is conceptually simple and computationally efficient. Different simple models based on our general approach to compute the UV spectral shifts due to solvation indicate that the dispersive part of the van-der-Waals energy, which stabilizes the LUMO of perylene more than the HOMO, falls off with a distance dependence of r^-4 in a range up to ~1 nm and not as r^-6, as has been assumed for a long time. This finding corresponds to the interpretation of temporary dipoles as being equivalent to weak permanent dipoles with fluctuating orientation.

physics.atm-clus↗

arXiv2003

Surface Structure of Organoclays

The properties of organically modified clay minerals determine essentially the quality of polymer-clay nanocomposites. We investigate alkylammonium-micas with different alkyl chain length by molecular dynamics simulation as homogeneous mixtures and separated island structures on the mica surface (80 percent alkali exchange, 20 percent of the alkali ions remain), including a detailed model of the Si --> Al...K charge defects on the surface of phyllosilicates. By comparison with experiment, we find that long chains (C18) lead to a mixed phase of alkali ions and organic ions on the surface, while chains of a medium length (~C12) give rise to phase separation. Very short chains, by thermodynamical arguments, prefer again a homogeneously mixed surface. We explain this interesting observation with a basic free energy model and present a diagram of the phase behaviour as a function of surface saturation with alkyl chains and the chain length. Besides, an order-disorder transition of the tethered alkyl chains is found on heating when ~20 percent of the torsional angles along the hydrocarbon backbones are gauche. At higher temperature, also rearrangements of the ammonium headgroups on the surface are possible, which lead to metastable structures after quenching.

cond-mat.mtrl-sci↗

arXiv2003

Structure and Phase Transitions of Alkyl Chains on Mica

We use molecular dynamics as a tool to understand the structure and phase transitions [Osman et. al. J. Phys. Chem. B 2000, 104, 4433; 2002, 106, 653] in alkylammonium micas. The consistent force field 91 is extended for accurate simulation of mica and related minerals. We investigate mica sheets with 12 octadecyltrimethylammonium (C18) ions or 12 dioctadecyldimethylammonium (2C18) ions, respectively, as single and layered structures at different temperatures with periodicity in the xy plane by NVT dynamics. The alkylammonium ions reside preferably above the cavities in the mica surface with an aluminum-rich boundary. The nitrogen atoms are 380 to 390 pm distant to the superficial silicon-aluminum plane. With increasing temperature, rearrangements of C18 ions on the mica surface are found, while 2C18 ions remain tethered due to geometric restraints. We present basal-plane spacings in the duplicate structures, tilt angles of the alkyl chains, and gauche-trans ratios to analyze the chain conformation. Also, the individual phase transitions of the two systems on heating are explained. Where experimental data are available, the agreement is very good. We propose a geometric parameter lamba for the saturation of the surface with alkyl chains, which determines the preferred self-assembly pattern, i.e., islands, intermediate, or continuous. Lambda also determines the tilt angles in continuous layers on mica or other surfaces. The thermal decomposition appears to be a Hofmann elimination with mica as a base-template.

cond-mat.mtrl-sci↗

arXiv2003

Analysis of the Phase Transitions in Alkyl- Mica by Density and Pressure Profiles

In a previous work [H. Heinz, H. J. Castelijns, U. W. Suter, J. Am. Chem. Soc. 115, 9500 (2003)], we developed an accurate force field and simulated the phase transitions in C18-mica (octadecyltrimethylammonium-mica) as well as the absence of such transitions in 2C18-mica (dioctadecyldimethylammonium-mica) between room temperature and 100 deg C. Here we analyze (i) average z coordinates of the carbon atoms and interdigitation of the hydrocarbon bilayers, (ii) density profiles and (iii) pressure profiles of the structures along all Cartesian axes. In C18-mica, the standard deviation in the z coordinate for the chain atoms is high and more than doubles in the disordered phase. The order-disorder transition is accompanied by a change in the orientation of the ammonium headgroup, as well as decreasing tensile and shear stress in the disordered phase. In 2C18-mica, the standard deviation in the z coordinate for the chain atoms is low and does not increase remarkably on heating. The backbones display a highly regular structure, which is slightly obscured by rotations in the C18 backbones and minor headgroup displacements at 100 deg C. Close contacts between the bulky headgroups with sidearms cause significant local pressure which is in part not relieved at 100 deg C. An increase of the basal-plane spacing at higher temperature is found in both systems due to larger separation between the two hydrocarbon layers and an increased z spacing between adjacent chain atoms (=decreased tilt of the chains relative to the surface normal), and, in C18-mica only, a stronger upward orientation of the C18 chain at the ammonium headgroup. The likelihood for chain interdigitation between the two hydrocarbon layers is 0.24 to 0.30 for C18-mica,and 0.65 to 0.26 for 2C18-mica (for 20 deg C to 100 deg C).

cond-mat.soft↗