Sabine Rosenfeldt

Self-Assembly of Janus Cylinders into Hierarchical Superstructures

We present in-depth studies of the size tunability and the self-assembly behavior of Janus cylinders possessing a phase segregation into two hemicylinders. The cylinders are prepared by cross-linking the lamella-cylinder morphology of a polystyrene-block-polybutadiene-block-poly(methyl methacrylate) block terpolymer. The length of the Janus cylinders can be adjusted by both the amplitude and the duration of a sonication treatment from the micro- to the nanometer length. The corona segregation into a biphasic particle is evidenced by selective staining of the PS domains with RuO(4) and subsequent imaging. The self-assembly behavior of these facial amphiphiles on different length scales is investigated combining dynamic light scattering (DLS), small-angle neutron scattering (SANS), and imaging procedures. Cryogenic transmission electron microscopy images of the Janus cylinders in THF, which is a good solvent for both blocks, exhibit unimolecularly dissolved Janus cylinders with a core-corona structure. These results are corroborated by SANS measurements. Supramolecular aggregation takes place in acetone, which is a nonsolvent for polystyrene, leading to the observation of fiber-like aggregates. The length of these fibers depends on the concentration of the solution. A critical aggregation concentration is found, under which unimolecularly dissolved Janus cylinders exist. The fibers are composed of 2-4 Janus cylinders, shielding the inner insoluble polystyrene hemicylinder against the solvent. Herein, the SANS data reveal a core-shell structure of the aggregates. Upon deposition of the Janus cylinders from more concentrated solution, a second type of superstructure is formed on a significantly larger length scale. The Janus cylinders form fibrillar networks, in which the pore size depends on the concentration and deposition time of the sample.

Analysis of thermosensitive core–shell colloids by small-angle neutron scattering including contrast variation

We present an investigation of thermosensitive core–shell particles by small-angle neutron scattering (SANS). The particles consist of a solid poly(styrene) core and a shell of crosslinked poly(N-isopropylacrylamide) (PNIPA) chains. These latex particles are dispersed in water and have a diameter of ca. 150 nm. At ambient temperature the PNIPA-network in the shell is swollen but at higher temperature water is expelled and the shell undergoes a continuous volume transition. The radial extension of the shell is investigated as a function of temperature by use of SANS. The analysis by SANS is performed at different contrasts using appropriate mixtures of H2O and D2O. It demonstrates that the shell has a well-defined compact structure above the volume transition. The swelling of the shell upon cooling can be described in terms of an affine expansion of the network. This is followed by a slight decrease of the volume fraction with increasing distance to the surface of the cores. The analysis by SANS demonstrates that the phase behavior of the network in the shell may be undertaken in terms of average volume fractions. It thus supplements the previous analysis by SAXS in a decisive manner.

A Shielding Topology Stabilizes the Early Stage Protein–Mineral Complexes of Fetuin-A and Calcium Phosphate: A Time-Resolved Small-Angle X-ray Study

Biomineralization mechanisms: The serum protein α2‐HS glycoprotein/fetuin‐A is an important inhibitor that prevents pathological mineralization of calcium phosphate in soft tissues and in the extracellular fluid. TR‐SAXS and stopped‐flow analysis were used to monitor the growth of protein mineral particles nucleating from supersaturated salt solutions in the presence of the protein. It was found that fetuin‐A did not influence the formation of mineral nuclei, but did prevent the aggregation of nuclei and thus mineral precipitation.

Effective interaction of charged platelets in aqueous solution: Investigations of colloid laponite suspensions by static light scattering and small-angle x-ray scattering

We study dilute aqueous solutions of charged disklike mineral particles (laponite) by a combination of static light scattering (SLS) and small-angle x-ray scattering (SAXS). Laponite solutions are known to form gels above a certain critical concentration that must be described as nonequilibrium states. Here we focus on the investigation by SLS and SAXS at concentrations below gelation (c<0.016 g/L) and at low concentrations of added salt (0.001M and 0.005M). Thus, we have obtained the scattering function of single Laponite platelets as well as the structure factor describing their interaction at finite concentration. A detailed analysis of the combined sets of data proves that the solutions are in a well-defined equilibrium state. Moreover, this analysis demonstrates the internal consistency and accuracy of the scattering functions obtained at finite concentrations. We find that laponite particles interact through an effective pair potential that is attractive on short range but repulsive on longer range. This finding demonstrates that Laponite solutions exhibit only a limited stability at the concentration of added salt used herein. Raising the ionic strength to 0.005M already leads to slow flocculation as is evidenced from the enhanced scattering intensity at smallest scattering angles. All data strongly suggest that the gelation occurring at higher concentration is related to aggregation.

Softening of the stiffness of bottle-brush polymers by mutual interaction

We study bottle-brush macromolecules in a good solvent by small-angle neutron scattering (SANS), static light scattering (SLS), and dynamic light scattering (DLS). These polymers consist of a linear backbone to which long side chains are chemically grafted. The backbone contains about 1600 monomer units (weight average) and every second monomer unit carries side chains with approximately 60 monomer units. The SLS and SANS data extrapolated to infinite dilution lead to the form factor of the polymer that can be described in terms of a wormlike chain with a contour length of 380 nm and a persistence length of 17.5 nm. An analysis of the DLS data confirms these model parameters. The scattering intensities taken at finite concentration can be modeled using the polymer reference interaction site model. It reveals a softening of the bottle-brush polymers caused by their mutual interaction. We demonstrate that the persistence decreases from 17.5 nm down to 5 nm upon increasing the concentration from dilute solution to the highest concentration (40.59 gl) under consideration. The observed softening of the chains is comparable to the theoretically predicted decrease of the electrostatic persistence length of linear polyelectrolyte chains at finite concentrations.

Analysis of the correlation of counterions to rod-like macroions by anomalous small-angle X-ray scattering

We present a study of a rod-like polyelectrolyte by anomalous small-angle X-ray scattering (ASAXS). The polyelectrolyte consists of a stiff poly(p-phenylene) backbone with attached positive charged groups that are balanced by bromine counterions. The scattering data are taken far below the absorption edge (13 473.7 eV) and in its immediate neighborhood. The decrease of the measured intensity predicted by theory is directly observed. A new analysis of these ASAXS-data leads to three partial intensities in a numerically self-consistent fashion. In particular, the scattering intensity that is solely due to the cloud of the counterions could be determined and compared to the prediction of the Poisson–Boltzmann cell model. Quantitative agreement is found. ASAXS is thus shown to be a new and highly effective tool for the analysis of polyelectrolytes.

Two‐Dimensional Oligo(phenylene‐ethynylene‐butadiynylene)s: All‐Covalent Nanoscale Spoked Wheels

Round and round: Covalently bound spokes induce an efficient template-directed cyclization towards a rigid molecular wheel (see figure) and afford dramatically increased shape-persistence properties compared with non-strutted macrocycles.The synthesis and characterization of a shape-persistent two-dimensional (2D) organic compound is described in detail. In a rational modular synthesis of a dodecaacetylene precursor and its subsequent template-aided cyclization, we obtained a molecularly defined, stable, C(6)-symmetric, rigid, spoked wheel. Peripheral tert-butyl groups and alkyl chains attached to the plane of the molecule provide sufficient solubility, so that the 2D oligomer can be fully characterized by MALDI-MS, GPC, and (1)H NMR, UV/Vis absorption, and fluorescence spectroscopy. Molecular mechanics and dynamics simulations indicate that the most stable conformer of the molecule in vacuum is a shallow boat conformation with a small dihedral angle. Comparisons with the precursor as well as a ring-only structure clearly reveal the high rigidity of the title compound. Small-angle neutron scattering (SANS) experiments in [D(8)]THF and CDCl(3) affirm the rigid backbone structure in solution, that is, a radius of about 2.7 nm and a thickness of about 0.22 nm. STM investigations illustrate that the wheel molecules adsorb with their molecular plane parallel to the surface and can form hexagonal crystalline domains (unit cell parameters are a=b=6.0+/-0.2 nm and theta=60+/-2 degrees ), with the tert-butyl groups on the apexes staggered. Such staggering induces chirality in the organized domains. AFM investigations demonstrate that the wheel molecules inside overlayers organize in the same way as in the layer directly in contact with the surface. This indicates an epitaxial growth characteristic of the film.

Simultaneous SAXS/WAXS/UV–Vis Study of the Nucleation and Growth of Nanoparticles: A Test of Classical Nucleation Theory

Despite the increasing interest in the applications of functional nanoparticles, a comprehensive understanding of the formation mechanism starting from the precursor reaction with subsequent nucleation and growth is still a challenge. We for the first time investigated the kinetics of gold nanoparticle formation systematically by means of a lab-based in situ small-angle X-ray scattering (SAXS)/wide-angle X-ray scattering (WAXS)/UV-vis absorption spectroscopy experiment using a stopped-flow apparatus. We thus could systematically investigate the influence of all major factors such as precursor concentration, temperature, the presence of stabilizing ligands and cosolvents on the temporal evolution of particle size, size distribution, and optical properties from the early prenucleation state to the late growth phase. We for first time formulated and numerically solved a closed nucleation and growth model including the precursor reaction. We observe that the results can be well described within the framework of classical nucleation and growth theory, including also results of previous studies by other research groups. From the analysis, we can quantitatively derive values for the rate constants of precursor reaction and growth together with their activation free enthalpies. We find the growth process to be surface-reaction limited with negligible influence of Ostwald ripening yielding narrow disperse gold nanoparticles.

Interaction of cylindrical polymer brushes in dilute and semi-dilute solution

We present a systematic study of flexible cylindrical brush-shaped macromolecules in a good solvent by small-angle neutron scattering (SANS), static light scattering (SLS), and by dynamic light scattering (DLS) in dilute and semi-dilute solution. The SLS and SANS data extrapolated to infinite dilution lead to the shape of the polymer that can be modeled in terms of a worm-like chain with a contour length of 380 nm and a persistence length of 17.5 nm. SANS data taken at higher polymer concentration were evaluated by using the polymer reference interaction site model (PRISM). We find that the persistence length reduce from 17.5 nm at infinite dilution to 5.3 nm at the highest concentration (volume fraction 0.038). This is comparable with the decrease of the persistence length in semi-dilute concentration predicted theoretically for polyelectrolytes. This finding reveals a softening of stiffness of the polymer brushes caused by their mutual interaction.

Self-assembly of smallest magnetic particles

Significance We discovered that small magnetic nanocubes spontaneously assemble into highly ordered chains, sheets, and cuboids in solution by applying a magnetic field. We elucidate how these assemblies are formed by working out the three-dimensional equilibrium arrangement of the dipoles. This classic physics problem turned out to be amazingly complex. The discovered solution self-assembly process is of high relevance in various fields reaching from high-density data storage over magnetotactic cells to medical applications. The assembly of tiny magnetic particles in external magnetic fields is important for many applications ranging from data storage to medical technologies. The development of ever smaller magnetic structures is restricted by a size limit, where the particles are just barely magnetic. For such particles we report the discovery of a kind of solution assembly hitherto unobserved, to our knowledge. The fact that the assembly occurs in solution is very relevant for applications, where magnetic nanoparticles are either solution-processed or are used in liquid biological environments. Induced by an external magnetic field, nanocubes spontaneously assemble into 1D chains, 2D monolayer sheets, and large 3D cuboids with almost perfect internal ordering. The self-assembly of the nanocubes can be elucidated considering the dipole–dipole interaction of small superparamagnetic particles. Complex 3D geometrical arrangements of the nanodipoles are obtained under the assumption that the orientation of magnetization is freely adjustable within the superlattice and tends to minimize the binding energy. On that basis the magnetic moment of the cuboids can be explained.