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BIOCATALYSIS AND BIOTRANSFORMATION · 2021 · IF 2.181

Efficient enantiomer selective acetylation of 1-methyl-3-phenylpropylamine by Fe3O4-APTES-CS2-lipase magnetic nanoparticles in an alternating magnetic field

Hongqian Dai,Yuan Lu,Hanbing Shi,Lan Tang,Xingyuan Sun,Zhimin Ou

Fe3O4 magnetic nanoparticles were prepared by chemical co-precipitation and modified with 3-aminopropyltriethoxysilane (APTES) and CS2 to form Fe3O4-APTES-CS2 magnetic carriers. Magnetically immobilized enzymes are attractive owing to their potential applications in many biological fields. When an alternating magnetic field is applied, the magnetic nanoparticles experience a force in the direction of the field, and the magnetic moments of the magnetic nanoparticles are apt to align in the direction of the field. Thus, magnetic nanoparticles behave like microscopic stirrers. The optimal reaction conditions of the acylation reaction using Fe3O4-APTES-CS2-lipase were 200 mmol/L 1-methyl-3-amphetamine, 100 mg immobilized lipase, 200 μL ethyl acetate, 12.6 × g rotating speed, 40 °C, and 5 days in the shaker. The conversion and enantiomeric excess of R-2a reached a maximum of 36.8% and 98.5%, respectively. 1-Methyl-3-phenylpropylamine was resolved using Fe3O4-APTES-CS2-lipase in an alternating magnetic field. The optimal magnetic field frequency and magnetic field intensity were determined to be 500 Hz and 12 Gs, respectively. The conversion and enantiomeric excess of R-2a reached a maximum of 40.3% and 98.5%, respectively. The results revealed that conversion under a magnetic field was significantly higher than that without a magnetic field. Highly optically active (R)-N-acetyl-1-methyl-3-amphetamine can be obtained via an efficient resolution of racemic 1-methyl-3-phenylpropylamine with immobilized lipase magnetic nanoparticles as a catalyst and ethyl acetate as an acyl donor in organic solvents in an alternating magnetic field.

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ACS Applied Nano Materials · 2021 · IF 5.097

Rapid Wafer-Scale Growth of MoS2(1–x)Se2x Alloy Monolayers with Tunable Compositions and Optical Properties for High-Performance Photodetectors

Pengtao Tang,Haibo Shu,Mingjun Yang,Mingsong Zhang,Chuangwei Sheng,Pei Liang,Dan Cao,Xiaoshuang Chen

Monolayer transition metal dichalcogenide (TMD) alloys with tunable band gaps exhibit huge potential in nanoelectronics, optoelectronics, and photonics. The scalable production of uniform atomically thin TMD alloys is a key step for the realization of their device applications but remains a large challenge so far. Here, we report oxygen-assisted chemical vapor deposition (CVD) of uniform atomically thin MoS2(1–x)Se2x semiconductor alloys via a vertical Mo-precursor supply strategy. The growth scheme leads to the formation of highly crystalline MoS2(1–x)Se2x monolayer films within a short growth time of 8 min, which benefits from a stable and homogeneous Mo-precursor feeding environment and the synergic effect of NaBr and oxygen carrier on the growth. The high-resolution spectral characterizations and density functional theory calculations demonstrate that the chemical composition of the as-grown MoS2(1–x)Se2x monolayers can be continuously tuned from x = 0 to 1, leading to the corresponding band gap being gradually changed from 1.81 to 1.55 eV. This work provides an efficient strategy to obtain large-area uniform MoS2(1–x)Se2x monolayer alloys with tunable compositions and optical properties, which is essential for driving their applications in various functional optoelectronic devices, especially for high-performance flexible photodetectors.

研究领域: 材料科学 · 纳米电子学 · 光电子学 · 光子学 · 半导体合金 · 薄膜生长
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ACS Sustainable Chemistry & Engineering · 2022 · IF 9.224

Design of a Novel La3Si6N11:Ce3+ Phosphor-in-Glass Film for High Power Laser Lighting: Luminous Efficiency toward 200 lmW–1

Li Xu,Xidong Wang,Luhan Wang,Shuyang Bao,Yu Wang,Xiaojuan Liang,Weidong Xiang

Inorganic fluorescent glass films have been widely considered in the field of high power laser lighting because of their excellent comprehensive properties as fluorescent conversion materials. Herein, we adjust the optimum sintering temperature to prepare a series of La3Si6N11:Ce3+ phosphor-in-glass films (LSN PiFs) with excellent optical properties on a single sapphire structure. The prepared LSN PiF has ultrahigh internal quantum efficiency (IQE) (98%) and excellent thermal stability. The thermal conductivity at room temperature can reach 9.8 Wm–1 K–1. When the temperature is 100 °C, the fluorescence intensity can still be maintained. The LSN:Ce phosphor particles did not react with the glass matrix and retained the original luminescence properties. Moreover, by further adjusting the concentration and thickness of LSN PiF, the luminous flux and luminous efficiency of LSN PiF under optimal conditions can reach 1071.73 and 207.58 lmW–1 under the excitation of 460 nm, which is the optimal result reported so far. In addition, the color rendering index (CRI) and low color temperature (CCT) are 64.05 and 5612.6 K, respectively, and the color coordinates are all close to the white light region. All the results show that LSN PiF has great application prospects in the high quality and high brightness laser lighting field.

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INFLAMMATION · 2023 · IF 5.1

Collagen Triple Helix Repeat Containing 1 Deficiency Protects Against Airway Remodeling and Inflammation in Asthma Models In Vivo and In Vitro

Feng Yong,Hu Jiapeng,Liu Fen,Shang Yunxiao

Asthma is a chronic inflammatory disease characterized by airway remodeling and lung inflammation. Collagen triple helix repeat containing 1 (CTHRC1), a glycoprotein, is involved in multiple pathological processes, including inflammation and fibrosis. However, the function of CTHRC1 in asthma remains unclear. In the present study, the mouse asthma model was successfully generated by sensitizing and challenging mice with ovalbumin (OVA). CTHRC1 expression at both RNA and protein levels was significantly upregulated in lung tissues of asthmatic mice. Asthmatic mice exhibited significant airway remodeling as evidenced by increased bronchial wall and smooth muscle cell layer thickness, goblet cell hyperplasia and collagen deposition, and epithelial-mesenchymal transition (EMT), but those characteristics were reversed by CTHRC1 silencing. The cell model with transforming growth factor-β1 (TGF-β1) induction in bronchial epithelial cells (BEAS-2B) was conducted to verify the effects of CTHRC1 on EMT, a classic mechanism that mediates airway remodeling. The results showed that TGF-β1 stimulation increased CTHRC1 expression, and CTHRC1 knockdown inhibited TGF-β1-induced EMT. OVA-treated mice also showed increased inflammatory cell infiltration and the production of OVA-specific immunoglobulin E (IgE), interleukin (IL)-4, IL-5, and IL-13, which were decreased by CTHRC1 downregulation. The effects of CTHRC1 on OVA-induced airway inflammation were further determined by treating BEAS-2B cells with IL-13, in which CTHRC1 knockdown reduced the IL-13-induced secretion of pro-inflammatory factors, including IL-4 and IL-5. In conclusion, these results indicate that CTHRC1 silencing attenuates asthmatic airway remodeling and inflammation in vivo and in vitro, suggesting that CTHRC1 may be a potential target for asthma treatment. Graphical Abstract

CAS / MDL: 9006-59-1 47165-04-8
✓ 已验证 产品关联 DOI PubMed 高影响因子
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CANCER LETTERS · 2023 · IF 9.7

WD repeat protein 54-mediator of ErbB2-driven cell motility 1 axis promotes bladder cancer tumorigenesis and metastasis and impairs chemosensitivity

Xiaosong Wei,Beibei Wang,Zixin Wu,Xiaoming Yang,Yufeng Guo,Yang Yang,Zhiwei Fang,Chengzhi Yi,Liuhui Zhang,Xin Fan,Lirong Zhang,Dongkui Song

One of the most abundant protein-protein interaction domains in the human proteome is the WD40 repeat (WDR) domain. A Gene Expression Omnibus dataset revealed 37 differentially expressed WDR domain genes in bladder cancer (BC). WD repeat domain 54 ( WDR54 ), an upregulated WDR domain gene, was selected for further investigation. Sixty pairs of frozen BC tumor and non-malignant bladder tissues and 83 paraffin-embedded BC tissue specimens were obtained. Loss-/gain-of-function experiments were carried out using BC and xenograft tumor models. WDR54 was overexpressed in BC cells, and its high expression was linked to tumor stage and lymph node metastases in patients. WDR54 contributed to the tumorigenesis and metastasis of BC and impaired its chemosensitivity. WDR54 prevented the degradation and ubiquitination of the mediator of ErbB2-driven cell motility 1 (MEMO1). WDR54 also promoted the interaction between MEMO1 and insulin receptor substrate 1 (IRS1) and activated the IRS1/AKT/β-catenin pathway in BC cells. Particularly, WDR54 depended on MEMO1 to exert its biological functions. Our study demonstrated the relevance of WDR54 in BC and provides insight into the molecular mechanism underlying BC.

✓ 已验证 产品关联 DOI PubMed 高影响因子
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MOLECULES · 2022 ·Vol. 27 ·期 22 ·7761 · IF 4.927

Ultrasensitive Determination of Natural Flavonoid Rutin Using an Electrochemical Sensor Based on Metal-Organic Framework CAU−1/Acidified Carbon Nanotubes Composites

Yuhong Li,Jianxiong Tang,Yueli Lin,Jiejun Li,Yaqi Yang,Pengcheng Zhao,Junjie Fei,Yixi Xie

Rutin, a natural flavonol glycoside, is widely present in plants and foods, such as black tea and wheat tea. The antioxidant and anti-inflammatory effects of flavonoids are well known. In this study, a new electrochemical rutin sensor was developed using multiwalled carbon nanotubes/aluminum-based metal–organic frameworks (MWCNT/CAU-1) (CAU−1, a type of Al-MOF) as the electrode modification material. The suspension of multiwalled carbon tubes was dropped on the surface of the GCE electrode to make MWCNT/GCEs, and CAU−1 was then attached to the electrode surface by electrodeposition. MWCNTs and CAU−1 were characterized using scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS). Due to the synergistic effect of CAU−1 and MWCNT-COOH, the prepared sensor showed an ultrasensitive electrochemical response to rutin. Under optimized conditions, the sensor showed a linear relationship between 1.0 × 10−9~3.0 × 10−6M with a detection limit of 6.7 × 10−10M (S/N = 3). The sensor also showed satisfactory stability and accuracy in the detection of real samples.Keywords:electroanalysis;pyrolysis;carbon materials;drug analysis;modified electrode

CAS / MDL: 7784-13-6 10312-55-7
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Frontiers in Bioengineering and Biotechnology · 2023 · IF 5.7

Cerium oxide nanoparticles protect against chondrocytes and cartilage explants from oxidative stress via Nrf2/HO-1 pathway in temporomandibular joint osteoarthritis

Xiong Liping,Bao Han,Li Size,Gu Deao,Li Yuyang,Yin Qianwen,Li Wen,Miao Leiying,Liu Chao

Oxidative stress is closely linked to the etiology of temporomandibular joint osteoarthritis. (TMJ-OA) and is an important therapeutic target. Cerium oxide nanoparticles (CNPs) have been broadly studied owing to their powerful antioxidant properties and potential preventive and therapeutic effects against chronic diseases. The current study was designed to explore the protective effects of CNPs on the progression of TMJ-OA and their potential mechanisms. We detected the ability of CNPs to eliminate reactive oxygen species (ROS) in chondrocytes. Moreover, their protective effects on chondrocytes were detected in the level of gene and protein. Furthermore, TUNEL assay, histology and safranin O-fast green staining were used to detect the beneficial effects of CNPs on cartilage explants. The mechanism of CNPs, protecting condylar cartilage by reducing inflammation, was further explored by knocking down the Nuclear factor-erythroid 2-related factor (Nrf2) gene. CNPs could reduce the ROS levels in chondrocytes and cartilage explants and reverse the IL-1β-induced imbalance of cartilage matrix metabolism and apoptosis. The protective effects of CNPs on cartilage were lost after key antioxidant factors including Nrf2 and heme-oxygenase 1(HO-1) were significantly reduced. In conclusion, this study demonstrated for the first time that activating the Nrf2/HO-1 signaling pathway by CNPs might have therapeutic potential for TMJ-OA.

CAS / MDL: 107-21-1
✓ 已验证 产品关联 DOI PubMed 高影响因子
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Aggregate · 2023 ·Vol. 4 ·期 4 ·e318 · IF 18.8

Aromatic compounds-mediated synthesis of anatase-free hierarchical TS-1 zeolite: Exploring design strategies via machine learning and enhanced catalytic performance

Chang'an Wang,Guoqing An,Jing Lin,Xiaowei Zhang,Zhiyuan Liu,Yibin Luo,Siqi Liu,Zhixiang Cheng,Tingting Guo,Hongyi Gao,Ge Wang,Xingtian Shu

Simultaneous achievement of constructing mesopores and eliminating anatase is a long-term pursuit for enhancing the catalytic performance of TS-1. Here, we developed an aromatic compounds-mediated synthesis method to prepare anatase-free and hierarchical TS-1 for olefin epoxidation. A series of hierarchical TS-1 zeolites were prepared by introducing aromatic compounds containing different functional groups via the crystallization process. The formation of intercrystalline mesopores and insertion of titanium into framework were facilitated at different extent. The synergistic coordination of carboxyl and hydroxyl in aromatic compounds with Ti(OH) 4 realizes the uniform distribution of titanium species and eliminates the generation of anatase. Noteworthily, eight machine learning models were trained to reveal the mechanism of additive functional groups and preparation conditions on anatase formation and microstructure optimization. The prediction accuracy of most models can reach more than 80%. Benefiting from the larger mesopore volumes (0.37 cm 3 ·g −1 ) and higher content of framework Ti species, TS-DHBDC-48h samples exhibit a higher catalytic performance than other zeolites, giving 1-hexene conversion of 49.3% and 1,2-epoxyhenane selectivity of 99.9%. The paper provides a facile aromatic compounds-mediated synthesis strategy and promotes the application of machine learning toward the design and optimization of new zeolites.

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MATERIALS AND CORROSION-WERKSTOFFE UND KORROSION · 2022 ·Vol. 73 ·期 7 ·1153-1162 · IF 1.832

Novel 1, 3, 5-triazine derivative is a highly efficient inhibitor of corrosion of Q235 carbon steel in an acidic medium

Cunhua Wei,Ge Xu,Jin Yu

A novel triazine derivative, 2, 4-diamino-6-dodecamido-1, 3, 5-triazine (DT), is synthesized by the dehydration condensation of melamine and lauric acid, and its inhibitive performances for the corrosion of Q235 carbon steel in 1 mol/L HCl solution is investigated by electrochemical polarization, electrochemical impedance spectroscopy, scanning electron microscopy, and atomic force microscope. The results reveal that its best inhibition efficiency reaches 96.98% at a concentration of 2.5 g/L. The calculation results of kinetic and thermodynamic parameters indicate that the adsorption of DT on carbon steel surface obeys Langmuir adsorption isotherm with both physical and chemical adsorption. It is demonstrated that long-chain amide (>8C) substituted 1, 3, 5-triazine derivative has the synergistic corrosion inhibition effect of the surface fixation on metal iron and the hydrophobic adsorption layer.

CAS / MDL: 108-78-1
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MICROPOROUS AND MESOPOROUS MATERIALS · 2022 · IF 5.876

Efficient and clean epoxidation of methyl oleate to epoxidized methyl oleate catalyzed by external surface of TS-1 supported molybdenum catalysts

Xiu Gao,Yingqi Zhang,Yanping Hong,Beining Luo,Xianzai Yan,Guoqiang Wu

Methyl oleate (MO) macromolecules are unable to access the microporous channel of conventional titanium silicalite-1 (TS-1) zeolite , which leads to the low catalytic activity of epoxidation of MO. Herein, the small-size TS-1 (TS-1-s) zeolite with a large surface area was synthesized successfully through steam-assisted crystallization, and then a novel blocked TS-1-s supported molybdenum (Mo/TS-1-bs) catalysts were prepared for efficient epoxidation of MO with clean H 2 O 2 to produce epoxidized methyl oleate (EMO). Various characterization results show the introduced Mo species are highly dispersed on the outer surface of TS-1-s without destroying the structure of the MFI type zeolite and the tetrahedral framework titanium (Ti 4+ ). Interestingly, a large number of Mo 6+ species exhibit certain epoxidation activity attributing to the generating of electrophilic molybdenum hydroperoxide (Mo–OOH) species via Mo species combined with H 2 O 2 , which could adsorb and react easily with MO molecules. Furthermore, the Mo species are also coordinated with Ti 4+ species through the O atom resulting in the facile attack of the Ti–O bonds by H 2 O 2 and easy to form an active intermediate. Therefore, compared with the conventional TS-1, the Mo/TS-1-bs shows higher catalytic activity in the epoxidation reaction. However, the acidity of Mo/TS-1-bs catalysts increases with increasing the Mo-loading owing to the formation of Lewis acid, which leads to the side reactions and the decrease of EMO selectivity. As a consequence, the efficient, non-corrosive and green catalytic system for epoxidation of MO was developed, and the activity improvement of Mo species and the influence of acid were also demonstrated.

CAS / MDL: 7439-98-7
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Frontiers in Chemistry · 2022 · IF 5.545

Tungsten Promoted Ni/Al2O3 as a Noble-Metal-Free Catalyst for the Conversion of 5-Hydroxymethylfurfural to 1-Hydroxy-2,5-Hexanedione

Duan Ying,Wang Rui,Liu Qihang,Qin Xuya,Li Zuhuan

The conversion of 5-hydroxymethylfurfural (HMF) to 1-hydroxy-2,5-hexanedione (HHD) represented a typical route for high-value utilization of biomass. However, this reaction was often catalyzed by the noble metal catalyst. In this manuscript, W promoted Ni/Al2O3 was prepared as a noble-metal-free catalyst for this transformation. The catalysts were characterized by XRD, XPS, NH3-TPD, TEM, and EDS-mapping to study the influence of the introduction of W. There was an interaction between Ni and W, and strong acid sites were introduced by the addition of W. The W promoted Ni/Al2O3 showed good selectivity to HHD when used as a catalyst for the hydrogenation of HMF in water. The influences of the content of W, temperature, H2 pressure, reaction time, and acetic acid (AcOH) were studied. NiWOx/Al2O3-0.5 (mole ratio of W:Ni = 0.5) was found to be the most suitable catalyst. The high selectivity to HHD was ascribed to the acid sites introduced by W. This was proved by the fact that the selectivity to HHD was increased a lot when AcOH was added just using Ni/Al2O3 as catalysts. 59% yield of HHD was achieved on NiWOx/Al2O3-0.5 at 393 K, 4 MPa H2 reacting for 6 h, which was comparable to the noble metal catalyst, showing the potential application in the production of HHD from HMF.

✓ 已验证 产品关联 DOI PubMed 高影响因子
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Small · 2022 ·Vol. 18 ·期 25 ·2202349 · IF 15.153

An Interlayer Containing Dissociated LiNO3 with Fast Release Speed for Stable Lithium Metal Batteries with 400 Wh kg−1 Energy Density

Huicong Yang,Qingyun Liu,Yaozu Wang,Zhuoting Ma,Pei Tang,Xiaoyin Zhang,Hui-Ming Cheng,Zhenhua Sun,Feng Li

Lithium metal is an ideal electrode material for future rechargeable batteries. However, dendrite formation and unstable solid electrolyte interphase film lead to safety concerns and poor Coulombic efficiency (CE). LiNO 3 significantly improves the performance of the lithium metal anode in ester electrolytes but its use is restricted by low solubility. To increase the content of LiNO 3 in the cell, a poly-(vinyl carbonate) organogel interlayer containing dissociated LiNO 3 (LNO-PVC) is placed between the cathode and anode. The dissociated LiNO 3 effectively increases the LiNO 3 -release rate and compensates for the LiNO 3 consumed in ester electrolytes during cycling. Via this interlayer, the performance of the lithium metal anode is significantly improved. The average CE of a Li-Cu cell reaches 98.6% at 0.5 mA cm −2 -1 h and 98.5% at 1 mA cm −2 -1 h for 300 cycles. Also, a Li||NCM811 pouch cell with LNO-PVC interlayer can also reach a 400 Wh kg −1 energy density with a cycling life of 65 cycles. This strategy sheds light on the effect of the state of this salt on its release/dissolution kinetics, which is determined by the interactions between the salt and host material.

CAS / MDL: 7790-69-4
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