Magnetoresistance of one-dimensional subbands in tunnel-coupled double quantum wires

We study the low-temperature in-plane magnetoresistance of tunnel-coupled quasi-one-dimensional quantum wires. The wires are defined by two pairs of mutually aligned split gates on opposite sides of a < 1 micron thick AlGaAs/GaAs double quantum well heterostructure, allowing independent control of their widths. In the ballistic regime, when both wires are defined and the field is perpendicular to the current, a large resistance peak at ~6 Tesla is observed with a strong gate voltage dependence. The data is consistent with a counting model whereby the number of subbands crossing the Fermi level changes with field due to the formation of an anticrossing in each pair of 1D subbands

From supramolecular polymers to multi-component biomaterials

The most striking and general property of the biological fibrous architectures in the extracellular matrix (ECM) is the strong and directional interaction between biologically active protein subunits. These fibers display rich dynamic behavior without losing their architectural integrity. The complexity of the ECM taking care of many essential properties has inspired synthetic chemists to mimic these properties in artificial one-dimensional fibrous structures with the aim to arrive at multi-component biomaterials. Due to the dynamic character required for interaction with natural tissue, supramolecular biomaterials are promising candidates for regenerative medicine. Depending on the application area, and thereby the design criteria of these multi-component fibrous biomaterials, they are used as elastomeric materials or hydrogel systems. Elastomeric materials are designed to have load bearing properties whereas hydrogels are proposed to support in vitro cell culture. Although the chemical structures and systems designed and studied today are rather simple compared to the complexity of the ECM, the first examples of these functional supramolecular biomaterials reaching the clinic have been reported. The basic concept of many of these supramolecular biomaterials is based on their ability to adapt to cell behavior as a result of dynamic non-covalent interactions. In this review, we show the translation of one-dimensional supramolecular polymers into multi-component functional biomaterials for regenerative medicine applications

A systematic study of the effect of the hard end-group composition on the microphase separation, thermal and mechanical properties of supramolecular polyurethanes

This paper reports a systematic study on a series of supramolecular polyurethanes that possess microphase separated morphologies which afford elastic materials at room temperature. Combinations of urea and/or urethane linkers in addition to a phenyl spacer have been used to study the effect of the rigidity of the hard end group segments as well as the hydrogen bonding capability of the urethane-urea linker units. Small angle X-ray scattering (SAXS) experiments have revealed characteristic microphase separated morphologies. Wide angle X-ray scattering (WAXS) was used to probe the lateral packing of the urethane and/or urea within the hard segments. Differential scanning calorimetry (DSC) analysis confirmed that unsymmetrical soft/hard segment phases have been achieved by varying the urethane/urea content. Transmission electron microscopy (TEM) and atomic force microscopy (AFM) determined that a 1-D fibrillar structure was obtained when the hard segment featured ureas whereas a 3-D structure was achieved when a combination of urea and urethane groups was used, giving rise to enhanced elongation properties. Finally, we present mechanical testing data in which oscillatory rheology at a range of frequencies and temperatures has revealed the effect of the connectivity of the hard segments on the relaxation times of the supramolecular chains. Tensile tests showed that end groups with ureas or a combination of a urea and urethane yielded elastic materials with strengths of ca. 5 MPa at room temperature

Spatially resolved multicomponent gels

Multi-component supramolecular systems could be used to prepare exciting new functional materials, but it is often challenging to control the assembly across multiple length scales. Here, we report a simple approach to forming patterned, spatially resolved multi-component supramolecular hydrogels. A multi-component gel is first formed from two low-molecular-weight gelators that consists of two types of fibers, each formed by only one gelator. One type of fibres of this 'self-sorted network' is then selectively removed by a light-triggered gel-to-sol transition. We show that the remaining network has the same mechanical properties as it would if it were initially formed alone. The selective irradiation of sections of the gel through a mask leads to the formation of patterned multi-component networks, in which either one or two networks can be present at a particular position, which a high degree of spatial control

Hydrogels formed from Fmoc amino acids

A number of Fmoc amino acids can be effective low molecular weight hydrogelators. The type of gel formed depends on the amino acid used and, in the case of FmocF, the final pH of the system. The single crystal structure of two of the gelators (FmocF and FmocY) have been determined and the data compared to the fibre X-ray diffraction data. FmocF, which forms metastable gels, crystallises easily and the data for the fibre phase and crystal phase are relatively similar. For FmocF, the fibre axis in b is consistent with the hydrogen bonding repeat distances and the diffraction pattern calculated from the single crystal structure is a good match with the experimental fibre X-ray diffraction data. On the other hand, there are significant differences between the crystalline phase determined and the fibre phase for FmocY. The packing of FmocY within the crystal structure is created by interactions between the planar Fmoc groups, whilst it is clear that hydrogen bonding drives the self-assembly into fibrillar structures within the gels. This shows that understanding the packing in gel phase by analogy to isolated crystal structures has the potential to lead to erroneous conclusions