ven more applications.A family of high entropy oxides with the formula Mg2Ta3Ln3O14 (Ln = La, Pr, Nd, Sm, Eu, Gd) has been discovered and synthesized. Single crystals, 5 mm OD × 2.5 cm, for Ln = Nd have been grown using the laser optical floating zone technique. Crystal orientations are confirmed by Laue diffraction, and structure solutions were obtained via single crystal X-ray diffraction. The structure is found to be a partially disordered pyrochlore, space group Fd-3m, fractional chemical formula (Mg0.25Nd0.75)2(Mg0.25Ta0.75)2O7. Magnetization measurements indicate ordinary paramagnetic behavior in all compounds down to T = 2 K, except in the Eu variant which possesses Van Vleck paramagnetism. Specific heat measurements for Ln = Nd shows no phase transitions between T = 300 and 2 K. We demonstrate the ability to prepare magnetically disordered materials by substitution of Mg with Ni, Mn, and Co, demonstrating the flexibility of this family in accommodating defects. The stabilization of these compounds could be due to the entropy gain associated with defects, showcasing a “materials by design” approach by using disorder to stabilize novel magnetic and optical materials. Our work also demonstrates the feasibility of preparing high entropy oxides in single crystalline form.Hybrid metal-organic halides are an exciting class of materials that offer the opportunity to examine how fundamental aspects of chemical bonding can influence the structural topology. In this work, we describe how solvent adducts of lead halides can influence the crystallization and subsequent annealing of these hybrid phases. While the size and shape of organic molecules are known to govern the final topology of the hybrid, we show that the affinity of solvent molecules for Pb ions may also play a previously underappreciated role.The alarming growth of antibiotic resistance that is currently ongoing is a serious threat to human health. One of the most promising novel antibiotic targets is MraY (phospho-MurNAc-pentapeptide-transferase), an essential enzyme in bacterial cell wall synthesis. Through recent advances in biochemical research, there is now structural information available for MraY, and for its human homologue GPT (GlcNAc-1-P-transferase), that opens up exciting possibilities for structure-based drug design. The antibiotic compound tunicamycin is a natural product inhibitor of MraY that is also toxic to eukaryotes through its binding to GPT. In this work, we have used tunicamycin and modified versions of tunicamycin as tool compounds to explore the active site of MraY and to gain further insight into what determines inhibitor potency. We have investigated tunicamycin variants where the following motifs have been modified the length and branching of the tunicamycin fatty acyl chain, the saturation of the fatty acyl chain, the 6″-hydroxyl group of the GlcNAc ring, and the ring structure of the uracil motif. The compounds are analyzed in terms of how potently they bind to MraY, inhibit the activity of the enzyme, and affect the protein thermal stability. Finally, we rationalize these results in the context of the protein structures of MraY and GPT.Integration of amorphous structures and anion defects into ultrathin 2D materials has been identified as an effective strategy for boosting the electrocatalytic performance. selleck kinase inhibitor However, the in-depth understanding of the relationship among the amorphous structure, vacancy defect, and catalytic activity is still obscure. Herein, a facile strategy was proposed to prepare ultrathin and amorphous Mo-FeS nanosheets (NSs) with abundant sulfur defects. Benefited from the ultrathin, amorphous nanostructure, and synergy effect of Mo-doping and sulfur defect, the Mo-FeS NSs manifested excellent electrocatalytic activity toward oxygen evolution reaction (OER) in alkaline medium, as shown by an ultralow overpotential of 210 mV at 10 mA cm-2, a Tafel slope of 50 mV dec-1, and retaining such good catalytic stability over 30 h. The efficient catalytic performance for Mo-FeS NSs is superior to the commercial IrO2 and most reported top-performing electrocatalysts. Density functional theory calculations revealed that the accelerated electron/mass transfer over the oxygen-containing intermediates can be attributed to the amorphous structure and sulfur-rich defects caused by structural reconfiguration. Furthermore, the S vacancies could enhance the activity of its neighboring Fe-active sites, which was also beneficial to their OER kinetics. This work integrated both amorphous structures and sulfur vacancies into ultrathin 2D NSs and further systematically evaluated the OER performance, providing new insights for the design of amorphous-layered electrocatalysts.Understanding and controlling the driving forces for molecular alignment in optoelectronic thin-film devices is of crucial importance for improving their performance. In this context, the preferential orientation of organometallic iridium complexes is in the focus of research to benefit from their improved light-outcoupling efficiencies in organic light-emitting diodes (OLEDs). Although there has been great progress concerning the orientation behavior for heteroleptic Ir complexes, the mechanism behind the alignment of homoleptic complexes is still unclear yet. In this work, we present a sky-blue phosphorescent dye that shows variable alignment depending on systematic modifications of the ligands bound to the central iridium atom. From an optical study of the transition dipole moment orientation and the electrically accessible alignment of the permanent dipole moment, we conclude that the film morphology is related to both the aspect ratio of the dye and the local electrostatic interaction of the ligands with the film surface during growth. These results indicate a potential strategy to actively control the orientation of iridium-based emitters for the application in OLEDs.Stacked structures employing wavelength-selective organic photodiodes (OPDs) have been studied as promising alternatives to the conventional Si-based image sensors because of their color constancy. Herein, novel donor (D)-π-acceptor (A) molecules are designed, synthesized, and characterized as green-light-selective absorbers for application in organic-on-Si hybrid complementary metal-oxide-semiconductor (CMOS) color image sensors. The p-type molecules, combined with two fused-type heterocyclic donors and an electron-accepting unit, exhibit cyanine-like properties that are characterized by intense and sharp absorption. This molecular design leads to improved absorption properties, thermal stability, and higher photoelectric conversion compared to those of a molecular design based on a nonfused ring. A maximum external quantum efficiency of 66% (λmax = 550 nm) and high specific detectivity (D*) of 8 × 1013 cm Hz1/2/W are achieved in an OPD consisting of a bulk heterojunction blend with two transparent electrodes on both sides.