Development of Co-Rich Microwires with Graded Magnetic Anisotropy

In this paper, a gradual change in the hysteresis loop of Co-rich glass-coated microwire stress-annealed at variable temperature is observed. Such microwires annealed with a temperature gradient also present a variable squareness ratio and magnetic anisotropy field along the microwire’s length. The obtained graded anisotropy has been attributed to a gradual modification of the domain structure along the microwire originated by a counterbalance between shape, magnetoelastic, and induced magnetic anisotropies. Accordingly, we propose a rather simple route to design graded magnetic anisotropy in a magnetic microwire.

Monolayer and Bilayer Formation of Molecular 2D Networks Assembled at the Liquid/Solid Interfaces by Solution-Based Drop-Cast Method

In recent years, extending self-assembled structures from two-dimensions (2D) to three-dimensions (3D) has been a paradigm in surface supramolecular chemistry and contemporary nanotechnology. Using organic molecules of p-terphenyl-3,5,3′,5′-tetracarboxylic acid (TPTC), and scanning tunneling microscopy (STM), we present a simple route, that is the control of the solute solubility in a sample solution, to achieve the vertical growth of supramolecular self-assemblies, which would otherwise form monolayers at the organic solvent/graphite interface. Presumably, the bilayer formations were based on π-conjugated overlapped molecular dimers that worked as nuclei to induce the yielding of the second layer. We also tested other molecules, including trimesic acid (TMA) and 1,3,5-tris(4-carboxyphenyl)-benzene (BTB), as well as the further application of our methodology, demonstrating the facile preparation of layered assemblies.

Colorless-to-colorful switching of electrochromic MXene by reversible ion insertion

Electrochromic (EC) materials that change color with voltage have been widely studied for use in dynamic windows. However, colorless-to-colorful switching with high contrast ratio is generically unattainable, especially for colorless-to-black electrochromic materials with an ultrahigh contrast ratio over the entire visible region. In this work, we developed Nb1.33C MXene-based dynamic windows with colorless-to-black switching of up to 75% reversible change in transmittance from 300 to 1,500 nm. By exploring the electrochromic effects of different electrolytes through in situ optical changes and electrochemical quartz crystal microbalance (EQCM), it is found that electrochromic behavior is greatly influenced by the extent of reversible Li+ insertion/deinsertion between the two-dimensional Nb1.33C MXene nanosheets. In addition, a colorless-to-black EC device based on Nb1.33C with an overall integrated contrast ratio over 80% was successfully constructed by a solution-processable spin coating method. This work enables a simple route to fabricate MXene-based high-performance electrochromic smart windows, which is important for further expanding the application of MXenes to optoelectronic and photonic applications.

Hydroxylamine-mediated C–C amination via an aza-hock rearrangement

Despite the widespread use of anilines, synthetic challenges to these targets still exist. Selectivity is often an issue, when using the traditional nitration-reduction sequence or more modern approaches, including arene C–H aminations catalyzed by transition metals, photosensitizers, or electrodes. Accordingly, there is still a need for general methods to rapidly, directly access specific isomers of substituted anilines. Here, we report a simple route towards the synthesis of such motifs starting from benzyl alcohols, which are converted to anilines by the use of arylsulfonyl hydroxylamines, via an aza-Hock rearrangement. Good to excellent yields are observed. The method is applicable to various benzyl alcohol surrogates (such as ethers, esters, and halides) as well as simple alkylarenes. Functionalizations of pharmaceutically relevant structures are feasible under the reaction conditions. Over ten amination reagents can be used, which facilitates the rapid assembly of a vast set of compounds.

Pentamethinium Salts Nanocomposite for Electrochemical Detection of Heparin

This study presents a simple route to heparin detection and develops a voltammetric approach using supramolecular principles and nanomaterials. Nanocomposites, including gold nanoparticles (AuNPs) and γ-substituted pentamethinium salts (PMS) deposited on a glass carbon (GC) electrode surface (GC/AuNPs/PMS) and covered by a plasticized poly(vinyl chloride) (PVC) membrane, are proposed for heparin detection. The conductivity of the nonconducting PVC-plasticized membrane is guaranteed by AuNPs, and the selectivity is provided by the interaction between γ-substituted PMS and anionic analytes. In order to extend the linear range, it is necessary to apply a solvent compatible with PVC-plasticized membrane, namely tetrahydrofuran. The proposed voltammetric sensor showed a concentration dependence from 1.72 up to 45.02 IU mL−1 heparin and was used for heparin detection in saline and biological samples with recovery of 95.1–100.9%.