Integration of Metal Catalysis and Organocatalysis in a Metal Nanocluster with Anchored Proline.

Chiral metal nanoclusters have recently been attracting great attention. It is challenging to realize asymmetric catalysis via atomically precise metal nanoclusters. Herein, we report the synthesis and total structure determination of chiral clusters [Au7Ag8(dppf)3(l-/d-proline)6](BF4)2 (l-/d-Au7Ag8). Superatomic clusters l-/d-Au7Ag8 display intense and mirror-image Cotton effects in their CD spectra. Density functional theory (DFT) calculations were carried out to understand the correlation between electronic structures and the optical activity of the enantiomeric pair. Surprisingly, the incorporation of proline in a metal nanocluster can significantly promote the catalytic efficiency in asymmetric Aldol reactions. The increase of catalytic activity of Au7Ag8 in comparison with organocatalysis by proline is attributed to the cooperative effect of the metal core and prolines, showing the advantages of the integration of metal catalysis and organocatalysis in a metal nanocluster.

Chiral Crown Ethers Accessed from Catalytic Enantioselective Desymmetrization Reactions.

A diversity of unprecedented chiral aza-crown ethers were synthesized straightforwardly from readily available and inexpensive aza-crown ethers. Catalyzed by a chiral phosphoric acid, desymmetrization of an array of symmetric N-arylated aza-crown ethers through tert-amino reaction proceeded efficiently under mild conditions to produce novel tetrahydroquinoline-fused aza-crown ethers in good to excellent yields with up to 96% ee. Our strategy opens a new route to functionalized chiral crown ethers.

Wireless LC Conformal Temperature Sensor Based on Ag Film (9912-K FL) for Bearing Temperature Measurement.

As the key component of aero-engines and industrial gas turbines, a bearing's working temperature at high speed is close to 300 ℃. The measurement of an engine bearing's temperature is of great significance to ensure flight safety. In this study, we present a wireless LC conformal temperature sensor for bearing temperatures, which integrates silver on the bearing surface in situ through a screen-printing process. This process makes Ag film (9912-K FL) firmly adhere to the bearing surface and realizes wireless measurements for bearing temperatures in situ. A high-temperature holding experiment of the prepared sensor was conducted, and the results showed that the sensor can work stably for 10 h at 300 ℃. We tested the designed wireless LC conformal temperature sensor at 20−270 ℃. The results showed that the proposed temperature sensor attained as good accuracy and stability in the temperature range 20−270 ℃. The sensitivity of the temperature measurements was 20.81 KHz/℃ when the bearing rotateds, the maximum repeatability was 0.039%, the maximum uncertainty was 0.081%, and the relative error was stable within 0.08%.

Coagulation behavior of polyaluminum-titanium chloride composite coagulant with humic acid: A mechanism analysis.

The hydrolysate species of metal-based coagulants and the binding sites of humic acid (HA) are highly dependent on the pH conditions. Exploring the binding sites and modes between coagulant hydrolysates and HA molecules is critical to understanding the coagulation mechanism. In this paper, the binding behavior between HA molecules and the hydrolysates of a polyaluminum-titanium chloride composite coagulant (PATC) was investigated under different pH conditions by semi-quantitative FTIR and XPS. It was found that oligomeric and mesopolymeric hydrolysates were the dominant species under acid conditions, which could complex with the hydroxyl and carboxyl groups of HA by forming COAl/Ti coordinate bonds. However, large amounts of H+ could compete with Al3+ and weaken the removal efficiency of HA. With the increase of pH, the hydrolysis process of the PATC and the deprotonation of HA were simultaneously underway. Under weakly acid conditions, the complexation of the aluminum hydrolysates with carboxyl groups was improved due to the gradually diminishing competition of H+ and the enhanced charge neutralization of the further polymerized hydrolysates. Consequently, the maximum UV254 removal by adding PATC was observed at pH 6. Under alkaline conditions, the sweeping effect of amorphous hydroxide dominated the HA removals, which was accompanied by the surface complexation of Al/Ti nuclear with carboxyl groups as well as the hydrogen bonds between hydroxyl and hydroxide. This study provides a new clue for the interaction mechanisms between the hydrolysates of composite coagulants and the dominant functional groups of HA at various pH conditions.

Income and social support related with mental health during COVID-19 outbreak in China.

ABSTRACT: To investigate psychological response of Chinese public during the regular prevention and control of Corona Virus Disease 2019 (COVID-19), and explore the relationship among income loss, social support and mental health.Five hundred twenty-six participants were randomly selected by snowball sampling method. Chinese version of Perceived Psychological Stress Scale, Perceived Social Support Scale, self-rating anxiety scale, and the PTSD Checklist for DSM-5 were used to measure the levels of psychological stress, social support, anxiety, and post-traumatic stress disorder (PTSD) symptoms. Demographic variables, income loss and income satisfaction during the outbreak period were also collected.The prevalence rate of anxiety, PTSD symptoms and stress problems were 19.8%, 23.8%, and 24.7% respectively. Multiple Regression Analysis illustrated that social support associated with stress, anxiety and PTSD after controlling demographic variables; for non-student samples, stress, anxiety, and PTSD were corelated with change in income and social support.During the regular prevention and control of COVID-19, social support might help reducing stress, anxiety, and PTSD symptoms. In addition to social support, change of income level was also an important factor for mental health. This study suggested the importance of maintaining a steady income after acute outbreak of COVID-19.

[Effect of Different Cationic Polyacrylamide Organic Dehydrating Agents on Sludge Dewatering Performance].

To study the effect of different cationic polyacrylamide organic dehydrating agents on sludge dewatering performance, eight commercially available cationic polyacrylamides of the same series with different properties were used. Based on the different cationic degree, they were named 9101, 9102, 9103, 9104, 9106, 9108, 9110, and 9112, respectively. Their properties were characterized by instruments and chemical analysis, and the indexes of sludge after treatment were also measured. The results showed that the properties of the eight organic dehydrants were different, among which the charge density, cationicity, viscosity, and Zeta potential had homologous trends, which all increased gradually from 9101 to 9112. The four indexes of 9112 were as high as 2.98 meq·L-1, 17.42%, 85.07 mPa·s, and 67.10 mV, respectively. The dewatering performance of sludge was improved by improving the specific resistance of filtration (SRF), floc properties, viscosity, Zeta potential, the bound water content, and the distribution of extracellular polymeric substances (EPS) after dosing organic dewatering agents. The results showed that the viscosity, charge density, cationic degree, and Zeta potential of the dewatering agents had a great influence on the sludge dewatering performance. The SRF of sludge was negatively correlated with the viscosity of the organic dewatering agent, and the correlation coefficient was as high as 0.92025, indicating that the sludge dewatering performance was improved mainly through the adsorption bridging effect of the organic dewatering agent in sludge dewatering.

Flocculation performance of papermaking sludge-based flocculants in different dye wastewater treatment: Comparison with commercial lignin and coagulants.

In this study, papermaking sludge-based flocculant (PSBF) and commercial lignin-based flocculant (LBF) have been synthesized by the same graft copolymerization procedures. The structures of alkaline lignin (AL), commercial lignin and the two flocculants were characterized by the modern analytical methods, also, the molecular weights and charge properties were analyzed. The effects of coagulant/flocculant dosages, pH conditions and coexistent dye auxiliaries on flocculation efficiencies were studied in the treatment of reactive turquoise blue (RTB) and disperse red (DR) dye wastewater. The flocculation experiments indicated that PSBF and LBF performed better in the removals of RTB and DR than commercial PAC and PAM. PSBF and LBF were insensitive to pH variation due to their strong charge neutralizing abilities and bridging effects even with the pH changing. In the existence of dye auxiliaries, PSBF and LBF could also exhibit superior decolorization efficiencies by slightly enlarging their dosages. Furthermore, PSBF and LBF had similar flocculation behaviors under all measured experimental conditions, suggesting that PSBF also had excellent flocculation performances even if it was prepared from papermaking sludge.

Catalytic Enantioselective Synthesis and Switchable Chiroptical Property of Inherently Chiral Macrocycles.

We report herein a strategy to construct enantiopure inherently chiral macrocycles, ABCD-type heteracalix[4]aromatics, through a catalytic enantioselective intramolecular C-N bond forming reaction. A chiral ligand-palladium complex was found to efficiently induce the inherent chirality of molecules during the macrocyclization process with ee values up to >99%. The resulting ABCD-type heteracalix[4]aromatics displayed excellent and pH-triggered switchable electronic circular dichroism and circularly polarized luminescence properties.

Organocatalytic Double Ugi Reaction with Statistical Amplification of Product Enantiopurity: A Linker Cleavage Approach To Access Highly Enantiopure Ugi Products.

Here we report an organocatalytic double Ugi reaction combining the enantioselective process and ee enhancement in a single operation to afford the chiral Ugi products with very high ee values. Both bisisocyanides and bisanilines tethered by carbonate and diester, respectively, were designed to accomplish this double multicomponent reaction that formed 10 new chemical bonds (4 C-N, 2 C-C, 2 C-O, and 2 N-H bonds). The strategy was further applied for the fast construction of an enantiomerically enriched macrocycle.