Studies of the Synchronous Sensing Method in the Microfluidic Cell Impedance Detection

Microfluidic impedance sensors play a significant role in point-of-care applications, clinical tests and laboratory studies. Instead of the traditional signal process method with the envelope detector, filter banks and multistage amplifier, we have reported a new implement using synchronous sampling and orthogonal detecting. By studying the intensity and phase modulation in the cell impedance sensing progress, we have calculated the SNR of the new method compare with the raw data. Base on the physical model and the calculation, we have demonstrated a simulation result which shows a capability to detect the signal of 1um cell in a noisy environment

Linear Positional Isomer Sorting in Nonporous Adaptive Crystals of a Pillar[5]arene

Here we show a new adsorptive separation approach using nonporous adaptive crystals of a pillar[5]­arene. Desolvated perethylated pillar[5]­arene crystals (<b>EtP5</b>α) with a nonporous character selectively adsorb 1-pentene (<b>1-Pe</b>) over its positional isomer 2-pentene (<b>2-Pe</b>), leading to a structural change from <b>EtP5</b>α to <b>1-Pe</b> loaded structure (<b>1-Pe</b>@<b>EtP5</b>). The purity of <b>1-Pe</b> reaches 98.7% in just one cycle and <b>EtP5</b>α can be reused without losing separation performance

Mechanochemical synthesis of pillar[5]quinone derived multi-microporous organic polymers for radioactive organic iodide capture and storage.

The incorporation of supramolecular macrocycles into porous organic polymers may endow the material with enhanced uptake of specific guests through host-guest interactions. Here we report a solvent and catalyst-free mechanochemical synthesis of pillar[5]quinone (P5Q) derived multi-microporous organic polymers with hydrophenazine linkages (MHP-P5Q), which show a unique 3-step N2 adsorption isotherm. In comparison with analogous microporous hydrophenazine-linked organic polymers (MHPs) obtained using simple twofold benzoquinones, MHP-P5Q is demonstrated to have a superior performance in radioactive iodomethane (CH3I) capture and storage. Mechanistic studies show that the rigid pillar[5]arene cavity has additional binding sites though host-guest interactions as well as the halogen bond (-I⋯N = C-) and chemical adsorption in the multi-microporous MHP-P5Q mainly account for the rapid and high-capacity adsorption and long-term storage of CH3I

Why surface hydrophobicity promotes CO2 electroreduction: a case study of hydrophobic polymer N-heterocyclic carbenes

We report the use of polymer N-heterocyclic carbenes (NHCs) to control the microenvironment surrounding metal nanocatalysts, thereby enhancing their catalytic performance in CO2 electroreduction. Three polymer NHC ligands were designed with different hydrophobicity: hydrophilic poly(ethylene oxide) (PEO–NHC), hydrophobic polystyrene (PS–NHC), and amphiphilic block copolymer (BCP) (PEO-b-PS–NHC). All three polymer NHCs exhibited enhanced reactivity of gold nanoparticles (AuNPs) during CO2 electroreduction by suppressing proton reduction. Notably, the incorporation of hydrophobic PS segments in both PS–NHC and PEO-b-PS–NHC led to a twofold increase in the partial current density for CO formation, as compared to the hydrophilic PEO–NHC. While polymer ligands did not hinder ion diffusion, their hydrophobicity altered the localized hydrogen bonding structures of water. This was confirmed experimentally and theoretically through attenuated total reflectance surface-enhanced infrared absorption spectroscopy and molecular dynamics simulation, demonstrating improved CO2 diffusion and subsequent reduction in the presence of hydrophobic polymers. Furthermore, NHCs exhibited reasonable stability under reductive conditions, preserving the structural integrity of AuNPs, unlike thiol-ended polymers. The combination of NHC binding motifs with hydrophobic polymers provides valuable insights into controlling the microenvironment of metal nanocatalysts, offering a bioinspired strategy for the design of artificial metalloenzymes

Styrene Purification by Guest-Induced Restructuring of Pillar[6]arene

The separation of styrene (St) and ethylbenzene (EB) mixtures is important in the chemical industry. Traditionally, this is done using energy-intensive vacuum distillation columns. Adsorptive separation is an alternative approach. Here, we explore the St and EB adsorption selectivity of two pillar-shaped macrocyclic pillar[n]arenes (EtP5 and EtP6; n 5 and 6). Both crystalline and amorphous EtP6 can capture St from a St-EB mixture with remarkably high selectivity. We show that EtP6 can be used to separate St from a 50:50 v/v St:EB mixture, yielding in a single adsorption cycle St with a purity of > 99 %. Single crystal structures, powder X-ray diffraction patterns and molecular simulations all suggest that this selectivity is due to a guest-induced structural change in EtP6 rather than a simple cavity/pore size effect. This restructuring means that the material ‘self-heals’ upon each recrystallization, and St separation can be carried out over multiple cycles with no loss of performance

Near-Ideal Xylene Selectivity in Adaptive Molecular Pillar[n]arene Crystals

The energy-efficient separation of alkylaromatic compounds is a major industrial sustainability challenge. The use of selectively porous extended frameworks, such as zeolites or metal–organic frameworks, is one solution to this problem. Here, we studied a flexible molecular material, perethylated pillar[n]arene crystals (n = 5, 6), which can be used to separate C8 alkylaromatic compounds. Pillar[6]arene is shown to separate para-xylene from its structural isomers, meta-xylene and ortho-xylene, with 90% specificity in the solid state. Selectivity is an intrinsic property of the pillar[6]arene host, with the flexible pillar[6]arene cavities adapting during adsorption thus enabling preferential adsorption of para-xylene in the solid state. The flexibility of pillar[6]arene as a solid sorbent is rationalized using molecular conformer searches and crystal structure prediction (CSP) combined with comprehensive characterization by X-ray diffraction and 13C solid state NMR spectroscopy. The CSP study, which takes into account the structural variability of pillar[6]arene, breaks new ground in its own right and showcases the feasibility of applying CSP methods to understand and ultimately to predict the behaviour of soft, adaptive molecular crystals

Cyclic Ether Contaminant Removal from Water Using Nonporous Adaptive Pillararene Crystals via Host-Guest Complexation at the Solid-Solution Interface

The removal of soluble cyclic ether contaminants, such as dioxane and THF, produced in industrial chemical processes from water is of great importance for environmental protection and human health. Here we report that nonporous adaptive crystals of perethylated pillar[5]arene (EtP5) and pillar[6]arene (EtP6) work as adsorbents for cyclic ether contaminant removal via host-guest complexation at the solid-solution interface. Nonporous EtP6 crystals have the ability to adsorb dioxane from water with the formation of 1:2 host-guest complex crystals, while EtP5 crystals cannot. However, both guest-free EtP5 and EtP6 crystals remove THF from water with EtP5 having a better capacity. This is because EtP5 forms a 1:2 host-guest complex with THF via host-guest complexation at the solid-solution interface while EtP6 forms a 1:1 host-guest complex with THF. EtP6 also shows the ability to selectively remove dioxane from water even in the presence of THF. Moreover, the reversible transitions between nonporous guest-free EtP5 and EtP6 structures and guest-loaded structures make them highly recyclable