Electroplasticity Mechanisms in hcp Materials

Herein, the mechanisms of the electroplastic effect (EPE) in different hexagonal close-packed (hcp) metals under varying loading conditions and current densities through the analysis of flow curves and microstructural changes are investigated. The investigations show a significant change in the forming behavior of the hcp materials as a result of superimposed electric current impulses. This behavior could be attributed to two effects. On the one hand, additional dislocation types are activated; on the other hand, new characteristic twin bands are formed. This is shown for all three hcp materials under investigation: Ti, Mg, and Zn. Furthermore, the hypothesis of the existence of a critical value of the current density at which a significant change in the plastic behavior occurs is verified by the experiments. The magnitude of this critical value for the analyzed hcp materials corresponds approximately to the theoretical values reported to be in the range of 1.6 to 2.0 kA mm⁻². In addition to the current density, the duration of the pulses also has an influence on the EPE. Understanding the correlation between the individual activated deformation mechanisms during electric pulse treatment can be crucial for controlling the electroplastic forming processes in a systematic and targeted manner.     

Molecularly Imprinted Polymers as Synthetic Antibodies for Protein Recognition: The Next Generation

Molecularly imprinted polymers (MIPs) are chemical antibody mimics obtained by nanomoulding the 3D shape and chemical functionalities of a desired target in a synthetic polymer. Consequently, they possess exquisite molecular recognition cavities for binding the target molecule, often with specificity and affinity similar to those of antigen-antibody interactions. Research on MIPs targeting proteins began in the mid-90s, and this review will evaluate the progress made till now, starting from their synthesis in a monolith bulk format through surface imprinting to biocompatible soluble nanogels prepared by solid-phase synthesis. MIPs in the latter format will be discussed more in detail because of their tremendous potential of replacing antibodies in the biomedical domain like in diagnostics and therapeutics, where the workforce of antibodies is concentrated. Emphasis is also put on the development of epitope imprinting, which consists of imprinting a short surface-exposed fragment of a protein, resulting in MIPs capable of selectively recognizing the whole macromolecule, amidst others in complex biological media, on cells or tissues. Thus selecting the ‘best’ peptide antigen is crucial and in this context a rational approach, inspired from that used to predict peptide immunogens for peptide antibodies, is described for its unambiguous identification.     

Effects of enactment in virtual reality: a comparative experiment on memory for action

Virtual Reality - Virtual reality (VR) is thought of as a promising educational medium, especially for learning actions, as it enables learning by enactment. Learning by enactment is associated...     

Darstellung und selektive Komplexbildung von Bisorganylsulfiden auf [2.2.2]Paracyclophan‐Basis

The synthesis of a variety of novel functionalized bisorganyl sulfides 2 – 10 based on the [2.2.2]paracyclophane skeleton is described. The aim was to increase the endohedral silver(I) complexation of the unsubstituted [2.2.2]paracyclophane 1 by combining the cyclophane framework with a sulfur containing pendant arm bearing an additional π‐donor. The complexation behaviour of the new ligands was studied by liquid–liquid extraction from aqueous into organic solution. The new ligands reveal a higher extraction with a decreased selectivity for silver(I) compared to 1 caused by preferential interactions with the sulfur donor atoms in the molecule. Molecular modeling calculations show the different coordination patterns for the 1:1‐, 1:2‐ and 2:1‐complexes (M:L) formed in the organic phase.     

High Sensitivity Near-Infrared Imaging of Fluorescent Nanosensors

Biochemical processes are fast and occur on small-length scales, which makes them difficult to measure. Optical nanosensors based on single-wall carbon nanotubes (SWCNTs) are able to capture such dynamics. They fluoresce in the near-infrared (NIR, 850–1700 nm) tissue transparency window and the emission wavelength depends on their chirality. However, NIR imaging requires specialized indium gallium arsenide (InGaAs) cameras with a typically low resolution because the quantum yield of normal Si-based cameras rapidly decreases in the NIR. Here, an efficient one-step phase separation approach to isolate monochiral (6,4)-SWCNTs (880 nm emission) from mixed SWCNT samples is developed. It enables imaging them in the NIR with high-resolution standard Si-based cameras (>50× more pixels). (6,4)-SWCNTs modified with (GT)₁₀-ssDNA become highly sensitive to the important neurotransmitter dopamine. These sensors are 1.7× brighter and 7.5× more sensitive and allow fast imaging (<50 ms). They enable high-resolution imaging of dopamine release from cells. Thus, the assembly of biosensors from (6,4)-SWCNTs combines the advantages of nanosensors working in the NIR with the sensitivity of (Si-based) cameras and enables broad usage of these nanomaterials.     

Benchmarking and Critical Design Considerations of Zero-Excess Li-Metal Batteries

Zero-excess Li metal batteries (ZELMBs), in which a Li-anode is formed in situ during charging, have received much attention in recent years. ZELMBs bear great potential to increase energy density and facilitate battery production, thereby reducing cost as well as material and energy consumption. Practical application of ZELMBs has so far been limited by challenges related to the non-uniform deposition behavior of Li, leading to inadequate performance and safety concerns. To address these issues, promising approaches have been developed in recent years, including modifications of the current collector, electrolyte, and cycling protocols. While these approaches improve the long-term stability of ZELMB, they also reduce the energy density by introducing inactive materials into the cell. Herein, critical design criteria for the various optimization approaches in ZELMB research are established. Nominal volumetric and gravimetric energy densities are determined based on the degree of modification. Thresholds are determined for each of the strategies at which the energy density gain of ZELMB vanishes compared to other cell configurations. These findings are compared to literature results to provide guidance for the further development of ZELMB.     

Molecularly Imprinted Polymer Hydrogel Nanoparticles: Synthetic Antibodies for Cancer Diagnosis and Therapy

Cancer is a leading cause of death worldwide and according to the World Health Organization (WHO) accounted for 10 million deaths in 2020. Promising theranostic (therapy and diagnostic) agents in the treatment of cancer are nanomaterials, which have come to the forefront because of their small size approaching those of protein complexes in the human body, and of their easy functionalization giving access to nanocomposite materials with diverse functions (fluorescence, magnetic, stimuli-responsiveness, etc.), and improved biocompatibility. Among them, affinity nanoparticles, often decorated with highly specific targeting ligands such as antibodies, aptamers, lectins and peptides, have enabled enhanced binding and exquisite recognition of biomarkers overexpressed in cancer cells. In this review, we describe an emerging class of targeting ligands, molecularly imprinted polymer hydrogel nanoparticles for their application in the early detection of disease, with the aim to improve diagnosis and treatment.     

Oxidation of Hydroquinones and Hydroquinone Monomethyl Ethers to Quinones with tert‐Butyl Hydroperoxide and Catalytic Amounts of Ceric Ammonium Nitrate (CAN)

Mono‐ and bicyclic hydroquinones and hydroquinone monomethyl ethers 1, 2 are oxidized in 82—91% yield to the corresponding quinones using only 2 mol% of ceric ammonium nitrate (CAN) and 2.5 equivalents of tert‐butyl hydroperoxide.