Investigation of the chiral recognition role of cyclodextrin hydroxyl moieties high performance liquid chromatography.

Cyclodextrin (CD) is known to afford excellent enantioselectivities due to its hydrophobic cavity and external H-bonding sites from hydroxyl moieties. However, there is still a lack of direct and comprehensive evidence clearly illustrating the origin of the important H-bonding effect. Regarding this issue, herein, four allylimidazole CD derivatives by selective substitution of the primary (6-position) and/or secondary (2,3-position) CD were synthesized and clicked onto silica surfaces to afford the corresponding chiral stationary phases (CSPs).

Evaluation on the inclusion behavior of β-cyclodextrins with lycorine and its hydrochloride.

Lycorine (Lyc) and its hydrochloride (Lyc∙HCl) as effective drugs can fight against many diseases including novel coronavirus (COVID-19) based on their antiviral and antitumor mechanism. Beta-cyclodextrin (β-CD) is considered a promising carrier in improving its efficacy while minimizing cytotoxicity due to the good spatial compatibility with Lyc. However, the detailed mechanism of inclusion interaction still remains to be further evaluated.

Surface-up click access to allylimidazolium bridged cyclodextrin dimer phase for efficient enantioseparation.

In this work, a novel allylimidazolium-bridged bis(β-cyclodextrin) chiral stationary phase was fabricated via a surface-up thiol-ene click chemistry reaction between 7-SH-β-cyclodextrin and 1-allylimidazole-β-cyclodextrin bonded on a silica surface. The structure of the allylimidazolium-bridged bis(β-cyclodextrin) chiral stationary phase was characterized by Fourier transform infrared spectra, C nuclear magnetic resonance, thermogravimetric analysis, and elemental analysis. Its chiral chromatographic performances were systematically evaluated by separating 35 racemic analytes including isoxazolines, dansyl-amino acids, and flavanones under reversed-phase high-performance liquid chromatography.

[Recent advances in the research of chromatographic separation materials based on click chemistry].

Since Nobel Laureate K. B. Sharpless first introduced the concept of click chemistry in 2001, such reactions have become a powerful modular synthesis tool.

[Click preparation and application of chiral stationary phase based on intrinsic recognition ability of cyclodextrin].

Most of the studies on cyclodextrin (CD)-based chiral stationary phase (CSP) have focused on the functional derivatization of CD or the bridging arms to introduce more interaction sites and thus improve the chiral resolution ability. At present, there are only a few reports on CSP that can reflect the intrinsic recognition ability of natural CD. In this study, a mono(6-mercapto-6-deoxy)-β-CD CSP (CSP1) with a clear and controllable structure was synthesized by the "thiol-ene" click reaction.

Chiral porous organic frameworks and their application in enantioseparation.

Porous organic frameworks (POFs) are a kind of porous material with a network structure composed of repeated monomers, which have excellent physical and chemical properties, such as a high surface area, high porosity, uniform pore sizes and structural diversity, and which have aroused broad interest among researchers. With the rapid development of materials science, increasingly more porous materials have been developed and applied, especially metal organic frameworks (MOFs) and covalent organic frameworks (COFs), which have been widely applied in the fields of luminous materials, catalytic research, adsorption and drug transport. One of the most important applications for chiral porous materials is in chiral separation and these materials have become a research hotspot in the field of chromatographic separation and analysis in recent years.

Ultrafast Nonadiabatic Photoisomerization Dynamics Mechanism for the UV Photoprotection of Stilbenoids in Grape Skin.

Natural UV photoprotection plays a vital role in physiological protection. It has been reported that UVC radiation can make resveratrol (RSV) and piceatannol (PIC) accumulate in grape skin. In this work, we demonstrated that RSV and PIC could significantly absorb UVA and UVB, and confirmed their satisfactory photostability.

Anisotropic charge carrier transport of optoelectronic functional selenium-containing organic semiconductor materials.

Organic semiconductors (OSCs) materials are currently under intense investigation because of their potential applications such as organic field-effect transistors, organic photovoltaic devices, and organic light-emitting diodes. Inspired by the selenization strategy can promote anisotropic charge carrier migration, and selenium-containing compounds have been proved to be promising materials as OSCs both for hole and electron transfer. Herein, we now explore the anisotropic transport properties of the series of selenium-containing compounds.

Resiliency of Mutualistic Supplier-Manufacturer Networks.

Current Supplier-Manufacturer (SM) networks are highly complex and susceptible to local and global disruptions, due to connectivity and interdependency among suppliers and manufacturers. Resiliency of supply chains is critical for organizations to remain operational in the face of disruptive events. Existing quantitative analyses oversimplify the mutualistic nature of SM networks, in which failure of individual entities affects not only the directly connected entities but also those connected indirectly.

Excited state intramolecular proton transfer (ESIPT) luminescence mechanism for 4-N,N-diethylamino-3-hydroxyflavone in propylene carbonate, acetonitrile and the mixed solvents.

In this work, density functional theory (DFT) and time density functional theory (TDDFT) methods were employed to investigate the nature of the double fluorescence emission of DEAHF in these three solvents. We analyzed the geometric structures, vibrational frequencies, frontier molecular orbitals (MOs), molecular electrostatic potential surface (MEPS), calculated absorption and fluorescence spectra and the potential-energy curves for DEAHF. All the results show that the intramolecular hydrogen bond of DEAHF is strengthened from S to S and the electron density redistribution occurs between the proton acceptor and donor, which can facilitate ESIPT.

Present Status and Future Growth of Advanced Maintenance Technology and Strategy in US Manufacturing.

The goals of this paper are to 1) examine the current practices of diagnostics, prognostics, and maintenance employed by United States (U.S.) manufacturers to achieve productivity and quality targets and 2) to understand the present level of maintenance technologies and strategies that are being incorporated into these practices.

The present status and future growth of maintenance in US manufacturing: results from a pilot survey.

A research study was conducted (1) to examine the practices employed by US manufacturers to achieve productivity goals and (2) to understand what level of intelligent maintenance technologies and strategies are being incorporated into these practices. This study found that the effectiveness and choice of maintenance strategy were strongly correlated to the size of the manufacturing enterprise; there were large differences in adoption of advanced maintenance practices and diagnostics and prognostics technologies between small and medium-sized enterprises (SMEs). Despite their greater adoption of maintenance practices and technologies, large manufacturing organizations have had only modest success with respect to diagnostics and prognostics and preventive maintenance projects.