Assembly and alignment of conjugated polymers: materials design, processing, and applications

Conjugated polymers (CPs) are widely investigated because of their intriguing optical and semiconducting properties in various optoelectronic device applications. Because of the one-dimensional p-orbital overlap along the main chain, CPs exhibit strong anisotropy in optoelectronic characteristics. Therefore, macroscopic assembly and alignment of CPs are essential to fully utilize their potential properties in real device applications. Here we review various processing strategies and material design principles for efficient CP alignment that result in highly anisotropic optical and electronic characteristics. Furthermore, we thoroughly review the incorporation of aligned CPs layers in organic light-emitting diodes, organic thin film transistors, and organic photovoltaic devices. The achieved macroscopic CP alignment has increased the optoelectronic properties and greatly improved device performanceclos

Visible-Light-Curable Solvent-Free Acrylic Pressure-Sensitive Adhesives via Photoredox-Mediated Radical Polymerization

Owing to their excellent properties, such as transparency, resistance to oxidation, and high adhesivity, acrylic pressure-sensitive adhesives (PSAs) are widely used. Recently, solvent-free acrylic PSAs, which are typically prepared via photopolymerization, have attracted increasing attention because of the current strict environmental regulations. UV light is commonly used as an excitation source for photopolymerization, whereas visible light, which is safer for humans, is rarely utilized. In this study, we prepared solvent-free acrylic PSAs via visible light-driven photoredox-mediated radical polymerization. Three alpha-haloesters were used as additives to overcome critical shortcomings, such as the previously reported low film curing rate and poor transparency observed during additive-free photocatalytic polymerization. The film curing rate was greatly increased in the presence of alpha-haloesters, which lowered the photocatalyst loadings and, hence, improved the film transparency. These results confirmed that our method could be widely used to prepare general-purpose solvent-free PSAs-in particular, optically clear adhesives for electronics

Synthesis of solvent-free acrylic pressure-sensitive adhesives via visible-light-driven photocatalytic radical polymerization without additives

Research on solvent-free acrylic pressure-sensitive adhesives (PSAs) has tremendously grown over the last few decades due to the stringent regulations to control volatile organic compound emissions. They are mostly prepared in the presence of photoinitiators using high-energy UV light that causes several issues such as those associated with radiation safety. Herein, for the first time, solvent-free acrylic PSAs were prepared through visible-light-driven photocatalytic free radical polymerization. Importantly, we found that the use of N-vinyl-based monomers noticeably enhances the rate and conversion of polymerizations, thereby eliminating the need for additives (e.g. alpha-haloester and sacrificial electron donor) that are usually required for photoredox-mediated free radical polymerization, but concurrently needs an additional purification process to remove residues. Combined experiments and quantum chemical calculations suggest that N-vinyl-based monomers facilitate electron transfer between monomers and photocatalysts, which is responsible for the enhanced rate and converison of polymerization. Viscoelasticity, mechanical strength and adhesion performance of acrylic PSAs were well adjusted in a broad range by controlling the monomer composition, suggesting that our new method would replace the existing photoinitiated free radical polymerization

Room-Temperature-Phosphorescence-Based Dissolved Oxygen Detection by Core-Shell Polymer Nanoparticles Containing Metal-Free Organic Phosphors

The highly sensitive optical detection of oxygen including dissolved oxygen (DO) is of great interest in various applications. We devised a novel room-temperature-phosphore-scence (RTP)-based oxygen detection platform by constructing core-shell nanoparticles with water-soluble polymethyloxazoline shells and oxygen-permeable polystyrene cores crosslinked with metal-free purely organic phosphors. The resulting nanoparticles show a very high sensitivity for DO with a limit of detection (LOD) of 60 nm and can be readily used for oxygen quantification in aqueous environments as well as the gaseous phase

Visible-Light-Curable Acrylic Resins toward UV-Light-Blocking Adhesives for Foldable Displays

Current technological advances in the organic light-emitting diode panel design of foldable smartphones demand advanced adhesives with UV-blocking abilities, beyond their conventional roles of bonding objects and relieving deformation stress. However, optically clear adhesives (OCAs) with UV-blocking ability cannot be prepared using conventional UV-curing methods relying on a photoinitiator. Herein, a new acrylic resin that can be efficiently cured using visible light without oxygen removal is presented, which may be used to develop UV-blocking OCAs for use in current flexible displays. A novel photocatalyst and a specific combination of additives facilitate sufficiently rapid curing under visible light in the presence of UV-absorbers. Only a very small amount of the highly active photocatalyst is required to prepare UV-blocking OCA films with very high transparency in the visible region. Using this system, a UV-blocking OCA that nearly meets the specifications of an OCA used in commercialized foldable smartphones is realized. This technology can also be utilized in other applications that require highly efficient visible light curing, such as optically clear resins, dental resins, and 3D/4D-printable materials

Structure of papain-like protease from SARS-CoV-2 and its complexes with non-covalent inhibitors

The SARS-CoV-2 papain-like protease (PLpro) is of interest as an antiviral drug target. Here, the authors synthesize and characterise naphthalene-based inhibitors for PLpro and present the crystal structures of PLpro in its apo state and with the bound inhibitors, which is of interest for further structure-based drug design efforts

Structure of Apo- and Monometalated Forms of NDM-1—A Highly Potent Carbapenem-Hydrolyzing Metallo-β-Lactamase

The New Delhi Metallo-β-lactamase (NDM-1) gene makes multiple pathogenic microorganisms resistant to all known β-lactam antibiotics. The rapid emergence of NDM-1 has been linked to mobile plasmids that move between different strains resulting in world-wide dissemination. Biochemical studies revealed that NDM-1 is capable of efficiently hydrolyzing a wide range of β-lactams, including many carbapenems considered as “last resort” antibiotics. The crystal structures of metal-free apo- and monozinc forms of NDM-1 presented here revealed an enlarged and flexible active site of class B1 metallo-β-lactamase. This site is capable of accommodating many β-lactam substrates by having many of the catalytic residues on flexible loops, which explains the observed extended spectrum activity of this zinc dependent β-lactamase. Indeed, five loops contribute “keg” residues in the active site including side chains involved in metal binding. Loop 1 in particular, shows conformational flexibility, apparently related to the acceptance and positioning of substrates for cleavage by a zinc-activated water molecule