Multienzyme cascades analysis of α-glucosidase by oxygen deficient MoO.

Background: Recently, the enzymatic cascade reactions during the cellular process are widely used for fabricating robust biosensors and they have attracted extensive attention in analyzing various clinical biomarkers. The enzymatic cascades analysis is commonly based on the peroxidase (POD)/oxidase coupled system. However, the requirement of harsh acidic environment, poor stability and interference from the oxidase further limit their analytical practicability.

Carbon dots capped cerium oxide nanoparticles for highly efficient removal and sensitive detection of fluoride.

Since the excess exposure to F may induce serious issues to human health, the effective adsorption and sensitive detection of F is essential. Therefore, carbon dots (CDs) capped CeO (CeO@CDs) was synthesized via hydrothermal treatment of tannic acid and CeCl. Due to abundant phenolic hydroxyl are reserved and excellent hydrophilicity, CeO@CDs possess high F adsorption capacity.

Simultaneously enhancing the photocatalytic and photothermal effect of NH-MIL-125-GO-Pt ternary heterojunction for rapid therapy of bacteria-infected wounds.

Infections caused by bacteria threaten human health, so how to effectively kill bacteria is an urgent problem. We therefore synthesized a NH-MIL-125-GO-Pt ternary composite heterojunction with graphene oxide (GO) and platinum (Pt) nanoparticles co-doped with metal-organic framework (NH-MIL-125) for use in photocatalytic and photothermal synergistic disinfection under white light irradiation. Due to the good conductivity of GO and the Schottky junction between Pt and MOF, the doping of GO and Pt will effectively separate and transfer the photogenerated electron-hole pairs generated by NH-MIL-125, thereby effectively improving the photocatalytic efficiency of NH-MIL-125.

Aggregation-Induced Emission Boosting the Study of Polymer Science.

The past one hundred years have witnessed the great development of polymer science. The advancement of polymer science is closely related with the development of characterization techniques and methods, from viscometry in molecular weight determination to advanced techniques including differential scanning calorimetry, nuclear magnetic resonance, and scanning electron microscopy. However, these techniques are normally constrained to tedious sample preparation, high costs, harsh experimental conditions, or ex situ characterization.

Large π-Conjugated Porous Frameworks as Cathodes for Sodium-Ion Batteries.

Organic sodium-ion batteries (OSIBs) are promising alternatives of inorganic lithium-ion batteries. The cathodes of OSIBs still suffer from low capacity, poor rate performance, and low cyclability. For the first time, we demonstrate the large π-conjugated porous frameworks (CPFs) as cathodes for OSIBs, motivated by the speculation that the CPFs are capable of enhancing charge transport, facilitating ionic diffusion, inhibiting dissolution, as well as improving stability.

An Aggregation-Induced Emission-Active Macrocycle: Illusory Topology of the Penrose Stairs.

The facile synthesis of a tetraphenylethene-based macrocycle having aggregation-induced emission characteristics and that expresses illusory topology of the Penrose stairs is presented. As a result of the twisted chirality (P or M) of the tetraphenylethene unit and the axial chirality of the macrocyclic linkage (R or S), the macrocycle exhibits two absolute configurations whose interconversion is energetically favorable as revealed by theoretical calculations.

Aggregation-Induced-Emission-Active Macrocycle Exhibiting Analogous Triply and Singly Twisted Möbius Topologies.

Molecules with Möbius topology have drawn increasing attention from scientists in a variety of fields, such as organic chemistry, inorganic chemistry, and material science. However, synthetic difficulties and the lack of functionality impede their fundamental understanding and practical applications. Here, we report the facile synthesis of an aggregation-induced-emission (AIE)-active macrocycle (TPE-ET) and investigate its analogous triply and singly twisted Möbius topologies.

Role of redox centre in charge transport investigated by novel self-assembled conjugated polymer molecular junctions.

Molecular electronics describes a field that seeks to implement electronic components made of molecular building blocks. To date, few studies have used conjugated polymers in molecular junctions despite the fact that they potentially transport charge more efficiently than the extensively investigated small-molecular systems. Here we report a novel type of molecular tunnelling junction exploring the use of conjugated polymers, which are self-assembled into ultrathin films in a distinguishable 'planar' manner from the traditional vertically oriented small-molecule monolayers.

Structural and theoretical insights into the AIE attributes of phosphindole oxide: the balance between rigidity and flexibility.

Multiple intramolecular motions consume the excited-state energy of luminogenic molecules upon photoexcitation and lower the emission efficiency. The low frequency rotational motion of aromatic rings can be facilely restricted by steric constraint in the condensed phase, but the high frequency bond stretching motion can hardly be suppressed by aggregation. In this work, three phosphorus-containing heterocycles, 1,2,3,4,5-pentaphenylphosphole-1-oxide (PPPO), 1,2,3-triphenylphosphindole-1-oxide (TPPIO), and 1,2,3-triphenylphosphindole (TPPI), were synthesized and characterized.

A highly selective AIE fluorogen for lipid droplet imaging in live cells and green algae.

Lipid droplets (LDs) are subcellular organelles for energy storage and lipid metabolism regulation. Here we report an aggregation-induced emission-active fluorogen, TPE-AmAl, for specific LD imaging. TPE-AmAl is cell-permeable: upon entering the live cells, the dye molecules can selectively accumulate in the LDs and turn on the fluorescence.

Nanowire crystals of a rigid rod conjugated polymer.

In this paper, we show that well-defined, highly crystalline nanowires of a rigid rod conjugated polymer, a poly(para-phenylene ethynylene)s derivative with thioacetate end groups (TA-PPE), can be obtained by self-assembling from a dilute solution. Structural analyses demonstrate the nanowires with an orthorhombic crystal unit cell wherein the lattice parameters are a approximately = 13.63 A, b approximately = 7.

Molecular orientation and field-effect transistors of a rigid rod conjugated polymer thin films.

Molecular orientation in thin films of a rigid rod conjugated polymer, a derivative of poly(para-phenylene ethynylene)s with linear side chains and thioacetyl end groups, was investigated by reflection-absorption infrared spectroscopy and X-ray diffraction technique. The results indicated that TA-PPE molecules tended to align with their backbone planes perpendicular to substrates, that is, with an "edge-on" molecular orientation in the films. Such molecular orientation is favorable for the efficient carrier transport in two-dimensional direction in the polymer films (i.

Ordering rigid rod conjugated polymer molecules for high performance photoswitchers.

Molecules of a rigid rod conjugated polymer, a derivative of poly(para-phenylene ethynylene)s with thioacetyl end groups (TA-PPE), were well aligned by drop-casting the polymer solution onto the friction-transferred poly(tetrafluoroethylene) substrates. TA-PPE molecules were found to be exactly oriented with their conjugated backbones along the PTFE sliding direction. Photoresponse characteristics based on the uniaxially ordered film were significantly improved compared to those of devices with the disordered film.

Organic Single-Crystalline Ribbons of a Rigid "H"-type Anthracene Derivative and High-Performance, Short-Channel Field-Effect Transistors of Individual Micro/Nanometer-Sized Ribbons Fabricated by an "Organic Ribbon Mask" Technique.

The synthesis of a rigid, planar H-type anthracene derivative is described. Single-crystalline ribbons at micro- and nanometer sizes can be controllably produced and transistors based on an individual ribbon can be fabricated in situ through a newly developed "organic ribbon mask" method, in which the channel length of the transistors can be easily scaled down to sub-micrometer level.