JOURNAL OF APPLIED POLYMER SCIENCE
·
2017
·Vol. 134
·期 46
·45484
·
IF 1.86
Teng Xue,Erjun Tang,Jian Zhou,Ruitao Han,Shaojie Liu
A coordinating ionic liquid (IL), 1-[(diethyl amine)amine]ethyl-3-methyl imidazolium chloride ([N 3 MIM]Cl), was prepared as an alternative to a simple organic ligand to coordinate to copper(I) bromide (CuBr). We, thereby, obtained a novel catalyst for atom transfer radical polymerization (ATRP) reactions. This catalyst was applied to the ATRP of methyl methacrylate in the IL 1-allyl-3-methyl imidazolium chloride ([AMIM]Cl). The chemical structures of the ILs obtained were confirmed by Fourier transform infrared spectroscopy, mass spectrometry, and 1 H-NMR analyses. The coordination ability of [N 3 MIM]Cl was assessed by cyclic voltammetry, and the redox potential of [N 3 MIM]Cl–CuBr was −0.507 V. The [N 3 MIM]Cl–CuBr complex was expected to be a markedly more active catalyst than the amine DETA–CuBr complex. The coordination mode toward CuBr was also examined. The [N 3 MIM]Cl–CuBr catalyst system showed good controllability in the aforementioned ATRP reaction in [AMIM]Cl. The Cu catalyst was easily separated from the obtained polymer with the coordinating IL as a ligand. Consequently, the coordinating IL overcame the shortcomings of traditional organic ligands, such as poor compatibility with IL media and poor separation of the catalyst from the polymer; this makes it highly promising for applications in the ATRP field. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134 , 45484.
研究领域:
高分子化学
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催化化学
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功能材料
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绿色溶剂
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配位化学
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电化学
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DOI
高影响因子
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
·
2022
·
IF 5.895
Linhui Feng,Heping Cui,Pusen Chen,Khizar Hayat,Xiaoming Zhang,Chi-Tang Ho
An Amadori rearrangement product (ARP) derived from ribose (Rib) and glutathione (GSH) was prepared and identified as N-(1-deoxy-d-ribulos-1-yl)-glutathione by ultraperformance liquid chromatography–tandem mass spectrometry and NMR. Thermal treatment of the ARP aqueous solution was conducted, and a relatively high temperature was found to accelerate the degradation of the ARP. The concentration of furans formed at 120 °C was more than 6.39 times that at 100 °C, and especially, the high temperature favored the formation of furfural and 4-hydroxy-5-methyl-3(2H)-furanone through deoxyosone dehydration. The promoting role of extra-added GSH or its constituent amino acids was investigated in the volatile formation during thermal processing of the ARP. Both, the added GSH and its constituent amino acids, could timely capture glyoxal (GO) and methylglyoxal (MGO) to facilitate Strecker degradation, which improved pyrazine formation. Compared with glycine and glutamic acid, cysteine was the most effective extra-added amino acid to react with GO and MGO to produce pyrazine and methylpyrazine. More importantly, the cysteine degraded from extra-added GSH effectively accelerated the generation of sulfur-containing volatile compounds through the reaction of cysteine degradation products with furans and shorter-chain α-dicarbonyl compounds.
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高影响因子
FOOD CHEMISTRY
·
2025
·
IF 9.8
Han Zhang,Heping Cui,Xue Xia,Shahzad Hussain,Khizar Hayat,Xiaoming Zhang,Chi-Tang Ho
Exogenous xylose exhibited a significant temperature-dependent regulatory effect on the furans and pyrazines formation during the degradation of dual-glycated Amadori rearrangement product of lysine (Lys), N α ,N ε -di(1-deoxy- d -xylulos-1-yl)lysine ( N α ,N ε -di-Xul-Lys ARP). At 100 °C, xylose primarily enhanced the dehydration pathway of deoxypentosone. This significantly increased furans yield, while delaying lysine release by interacting with mono-glycated Lys-ARPs, thereby inhibiting the early formation of pyrazines. 120 °C accelerated the dehydration and retro-aldolization of deoxypentosone, markedly boosting furans formation and further promoting the substantial production of α -dicarbonyl compound with extra-added xylose. Additionally, xylose buffered the rapid pH decline, enhancing the α -aminoketones electrophilicity and facilitating pyrazines formation in N α ,N ε -di-Xul-Lys ARP. At 140 °C, xylose hindered furans formation but notably increased methylpyrazine levels during 30–60 min. Furthermore, increasing the xylose concentration to 60 mmol/L at 120 °C markedly enhanced glyoxal and methylglyoxal production, yielding the highest pyrazine concentration of 98.04 μg/L within 60 min.
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ChemistrySelect
·
2025
·Vol. 10
·期 21
·e01335
·
IF 2
Yu-cheng Jiang,Bao-guang Zhu,Xiang-li Long
Graphical The production of 1-(4-chlorophenyl)-1H-pyrazol-3-ol from the oxidation of 1-(4-chlorophenyl)-pyrazolidin-3-one by air under the catalysis of Co(II)@AC has been enhanced by modifying the activated carbon with H₂C₂O₄ solution to increase the acidic groups and micropores on the carbon surface. The production of 1-(4-chlorophenyl)-1 H -pyrazol-3-ol by oxidizing 1-(4-chlorophenyl)- pyrazolidin-3-one with H 2 O 2 suffers from some shortcomings. The oxidation of 1-(4-chlorophenyl)-pyrazolidin-3-one to 1-(4-chlorophenyl)-1 H -pyrazol-3-ol can be realized by air catalyzed with Co(II)@AC (prepared by supporting cobalt(II) on activated carbon). Air is a good substitute for H 2 O 2 because it can minimize the cost, hazards, and pollution, which is beneficial to the improvement of the production process for pyraclostrobin. In this study, activated carbon has been modified by H 2 C 2 O 4 solution to improve the catalytic performance of Co(II)@AC. The experiments indicate that the best carbon is made by heating the carbon at 300 °C for 3 h with a heating rate of 5 °C/min in N 2 after being soaked in 0.4 mol/L H 2 C 2 O 4 solution at 50 °C for 12 h with an L/S ratio of 40/1 mL/g. The 1-(4-chlorophenyl)-1 H -pyrazol-3-ol concentration obtained by Co(II)@AC immobilized on the optimized carbon is 39.39% over that catalyzed by Co(II)@AC loaded on the original carbon. Characterization results reveal that modification with H 2 C 2 O 4 increases the specific surface area and enhances the acidity on the carbon surface. The oxidation rate of 1-(4-chlorophenyl)-pyrazolidin-3-one is primarily determined by the physical structure. The selectivity toward 1-(4-chlorophenyl)-1 H -pyrazol-3-ol is mainly influenced by the chemical characteristics.
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SEPARATION AND PURIFICATION TECHNOLOGY
·
2026
·
IF 9.1
Ruiying Xie,Feng Zhang,Guishan Hu,Mengzhen Chen,Huixian Wang,Xiaoquan Feng,Xuerui Wang,Yatao Zhang,Meixia Shan
The widespread presence of toxic nitroaromatic compounds in industrial effluents demands advanced remediation strategies. Catalytic reduction is highly effective, while the practical application of powdered catalysts is limited by challenges in recovery and reuse. To overcome this issue, macroscopic Pd@NH 2 -MIL-101/AOPIM-1 porous composite beads were fabricated via a phase inversion method, combining the high surface area of NH 2 -MIL-101 with the excellent processability of amidoxime-functionalized polymers of intrinsic microporosity (AOPIM-1). The incorporation of NH 2 -MIL-101 enriches the composite with amino functional groups, thereby enhancing the adsorption and local enrichment of reactants. Furthermore, these nitrogen-rich sites provide robust anchoring points for the uniform dispersion of Pd nanoparticles, collectively boosting catalytic activity and structural stability. The beads exhibited outstanding catalytic activity for the reduction of nitroaromatics, achieving 99% conversion of 4-nitrophenol (4-NP) within 5 min. The catalyst also maintained excellent structural stability over multiple cycles and allowed easy separation. Furthermore, the catalyst exhibited over 90% efficiency in the reduction of other common nitroaromatic pollutants, underscoring its versatility and applicability in wastewater treatment. This work provides a sustainable and practical solution for wastewater treatment by transforming hazardous contaminants into valuable aromatic amines using an easily separable catalytic system.
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高影响因子
Journal of Pharmaceutical Innovation
·
2026
·Vol. 21
·期 2
·172
·
IF 2.6
Wang Qilong,Gong Mingjie,Li Jiaying,Li Tingyuan,Jiang Xia,Wang Xiaowen,Hua Qinyang,Toreniyazov Elmurat,Shi Feng,Yu Jiangnan,Cao Xia,Xu Ximing,Adu-Frimpong Michael
Objective This study aimed to develop polyethylene glycol (PEG)-modified liposomes (PG-1-Ls) to overcome the poor oral bioavailability and burst release of phenolic glycoside 1 (PG-1), an anti-aging compound isolated from Moringa oleifera seeds. Methods PG-1-Ls were preparedby thin-film dispersion and optimized via a Box-Behnken design. The formulation wascharacterized for particle size, encapsulation efficiency (EE%), drug loading (DL%), andmorphology. Stability, in vitro release in four media, and safety in zebrafish were evaluated. Pharmacokinetics were studied in rats, and anti-aging efficacy was assessed in a D-galactose-induced zebrafish model by measuring β-galactosidase activity. Results The optimized PG-1-Lswere spherical and uniform (154.6 ± 3.8 nm), with high EE% (88.29%) and good stability. They successfully eliminated the initial burst release of PG-1, demonstrating sustained release profiles. In rats, PG-1-Ls increased the oral bioavailability (AUC) by 6.25-fold and the peak concentration(C~max~) by 3.9-fold compared to free PG-1. The formulation also showed improved safety in zebrafish. In the aging model, both PG-1 and PG-1-Ls significantly reduced β-galactosidaseactivity, with PG-1-Ls exhibiting superior efficacy comparable to the positive control. Conclusion PEGylated liposomes significantly enhance the sustained release, oral bioavailability, safety, and in vivo anti-aging activity of PG-1, representing a promising delivery system for its application. Graphical abstract
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JOURNAL OF POWER SOURCES
·
2017
·
IF 6.395
Haoxiang Yu,Minghe Luo,Hua Lan,Lei Yan,Shangshu Qian,Wuquan Ye,Miao Shui,Nengbing Long,Jie Shu
The preparation and characterization of Pb 1- x Ba x Li 2 Ti 6 O 14 ( x = 0, 1/4, 1/2, 3/4, 1) as anode materials for lithium ion batteries are investigated in this research. The structure, morphology and electrochemical properties are compared with each other by changing the Pb/Ba atomic ratio in Pb 1- x Ba x Li 2 Ti 6 O 14 . It can be observed that each sample shows the same orthorhombic structure with Cmca space group. Moreover, it can also be found that the working potential, conductivity, cycling and rate performances of as-received samples gradually change along with the evolution of x in Pb 1- x Ba x Li 2 Ti 6 O 14 ( x = 0, 1/4, 1/2, 3/4, 1). Electrochemical evaluation shows that the operating potential of the as-received sample gradually decreases with increasing x value in Pb 1- x Ba x Li 2 Ti 6 O 14 and its initial charge capacity increases reversely. Moreover, different Pb/Ba atomic ratio also brings different cycling stability for Pb 1- x Ba x Li 2 Ti 6 O 14 . Especially for Pb 3/4 Ba 1/4 Li 2 Ti 6 O 14 , it presents better electrochemical properties than other samples. After 120 cycles, the reversible capacity of Pb 3/4 Ba 1/4 Li 2 Ti 6 O 14 is maintained at 129.7 mAh g −1 with capacity retention of 88.3%. In addition, its electrochemical reversibility is also demonstrated by in-situ X-ray investigation.
研究领域:
材料科学
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电化学
·
能源存储
·
无机化学
·
固态化学
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DOI
高影响因子
CATALYSIS COMMUNICATIONS
·
2013
·
IF 2.915
Bin Zeng,Xiaohua Chen,Xutao Ning,Chuansheng Chen,Aiping Hu,Weina Deng
Carbon nanotubes and reduced graphene oxides (CNTs/rGO) sphere decorated with Cu 2 O, CuO nanoparticles (Cu x O–CNTs/rGO) was successfully synthesized by spray drying and post-calcinating method for the first time. Scanning electron microscopy and transmission electron microscopy observations confirmed that CNTs/rGO formed a spherical micrometer structure and Cu x O nanoparticles were decorated on their surface. The experimental results indicated that this novel architecture enhanced photocatalytic performance with 97.5% decomposition of methyl orange (MO) after 20 min in the presence of H 2 O 2 under visible light irradiation, which was much higher than that of pure Cu x O powders (31.2%).
研究领域:
材料科学
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纳米科技
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光催化
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环境功能材料
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复合材料
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DOI
高影响因子
ACS Sustainable Chemistry & Engineering
·
2026
·
IF 7.6
Yu Jiaojiao,Zuo Yi,Li Gudan,Cai Jiajun,Chen Yu,Guo Yuzhou,Xu Shutao,Li Lina,Guo Lingling,Yang Hong,Guo Xinwen
Titanium silicalite-1 (TS-1) attracts wide attention as an effective oxidative catalyst. However, the preparation of TS-1 typically requires rigorous synthesis procedures with a relatively long synthesis time and generates a substantial amount of wastewater. This study discovers that, in the presence of tetrapropylammonium hydroxide (TPAOH), Si and Ti sources can form a homogenous liquid solution that is highly stable although the two typically undergo hydrolysis at very different rates individually. With such understanding, this work develops a straightforward one-pot synthesis strategy that eliminates the cumbersome procedures aimed at suppressing the hydrolysis of the Ti source in TS-1 synthesis and demonstrates that the crystallization process of TS-1 can be accelerated by reducing the molar ratio of water to Si species ( n (H 2 O/Si)) in the synthesis solution. In propene epoxidation with H 2 O 2 , an excellent catalytic activity is obtained over the TS-1 synthesized at n (H 2 O/Si) = 3.5 and crystallized for only 6 h. This low n (H 2 O/Si) synthesis regime results in a significantly high yield per batch (12 g TS-1/100 mL batch) and, at the same time, produces almost no wastewater. The superior catalytic performance of TS-3.5-6 synthesized is attributed to its high total Ti content and the presence of catalytically active Ti(OSi) 2 (OH) 4 .
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Nature Energy
·
2026
·
IF 70.1
Chu Shiyong,Wang Liguang,Bian Jingjing,Cheng Chen,Tian Jiaming,Sheng Chuanchao,Zhuo Zengqing,Shi Tianze,Guo Jinghua,Zhang Liang,Lu Jun,Zhou Haoshen,Guo Shaohua
Lattice-oxygen redox in layered oxides can enhance energy density, but its limited reversibility causes structural instability during deep cycling. Here we develop an iron-mediated strategy to regulate lattice-oxygen redox in layered oxide cathodes. In the Na 2/3 Mn 7/12 Mg 1/4 Fe 1/6 O 2 cathode, Fe ions act as redox mediators, with Fe 4+ capturing electrons from lattice oxygen during charging and Fe 2+ donating electrons back to oxidized oxygen during discharging through chemical pathways. With the assistance of iron mediation, the reversibility of lattice-oxygen redox is dramatically improved from 75% to 99%. As a result, the lattice-oxygen-activated cathode enables a sodium-ion pouch cell to achieve an energy density of 206 Wh kg −1 and operate stably for 100 cycles at 50 mA g −1 , with a capacity retention of 87.8%.
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ENERGY & FUELS
·
2026
·Vol. 40
·期 33
·18043-18052
·
IF 6
Pang Bo,Pu Baian,Peng Hao,Xue Kang,Shi Chengxiang,Gao Ruijie,Ai Minhua,Huang Zhen-Feng,Zhang Xiangwen,Zou Ji-Jun,Pan Lun
Conventional
high-energy-density hydrocarbon fuels face an intrinsic
trade-off between increasing ring number and decreasing net heat of
combustion. To address this limitation, we propose a synthetic strategy
based on tandem [4 + 2]/[2 + 1] cycloaddition. Norbornadiene and methyl
dicyclopentadiene were employed as feedstocks to develop a coupled
synthetic approach that combines Diels–Alder [4 + 2] cycloaddition
for constructing a polycyclic framework with Simmons–Smith
[2 + 1] cyclopropanation for energy enhancement. By optimizing the
reaction parameters, the Diels–Alder and Simmons–Smith
reactions achieved optimal conversions of 77.89% and 90.96%, respectively,
with selectivities of 43.54% and 85.82%. The resulting fuel fraction
exhibits a high density of 1.060 g cm –3 , a volumetric
net heat of combustion of 44.85 MJ L –1 , and a freezing
point below −60 ° C. This study demonstrates an effective
strategy for simultaneously achieving high density, high volumetric
energy content, and excellent low-temperature performance, providing
useful guidance for the molecular design and synthesis of next-generation
high-energy-density fuels.
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高影响因子
Frontiers in Cell and Developmental Biology
·
2026
·
IF 5.3
Fenqian Yuan,Jingkang Yong,Xueming Liu,Yifeng Wang,Dan Zhao
Background Head and neck squamous cell carcinoma (HNSCC) is an aggressive malignancy in which epithelial–mesenchymal transition (EMT) contributes to tumor progression. Piezo1 and Galectin-1 have each been implicated in cancer progression, but their functional relationship in HNSCC remains incompletely understood. We investigated Piezo1-associated mechanosensitive signaling and its potential relationship with Galectin-1 in HNSCC. Methods Public transcriptomic and proteomic analyses were integrated with validation using 16 paired oral squamous cell carcinoma (OSCC) tumor and adjacent non-tumor specimens. Functional studies were performed in HNSCC cell lines using genetic and pharmacological modulation of PIEZO1/Piezo1 and Galectin-1-associated signaling. Two independent SCC-9 xenograft studies were conducted in separate cohorts (n = 6 per group): one comparing vehicle, Yoda1, and GsMTx4, and the other comparing vehicle, GsMTx4, OTX008, and their combination. Results Piezo1 was consistently upregulated in HNSCC datasets, OSCC tissues, and HNSCC cell lines, whereas its association with survival was modest and not uniformly reproduced across analytical platforms. Piezo1 activation was associated with increased Ca 2+ -associated signaling, nuclear YAP1 accumulation, and EMT-related phenotypes, whereas PIEZO1 silencing and pharmacological inhibition of mechanosensitive channel activity attenuated these effects. Galectin-1 emerged as a Piezo1-responsive candidate effector associated with YAP1 signaling and EMT-related phenotypes. OTX008 treatment reduced proliferation, wound closure, invasion, and EMT-related marker changes. In xenografts, combined GsMTx4 and OTX008 treatment produced greater reductions in tumor growth, Ki67 positivity, endpoint CD31 fluorescence intensity, and EMT-associated marker changes than either monotherapy at the tested doses. Conclusion These findings support an important contribution of Piezo1-associated mechanosensitive signaling to EMT-related phenotypes and tumor progression in HNSCC and support Galectin-1 as a functionally relevant, Piezo1-responsive candidate effector associated with YAP1 signaling. The greater antitumor effects observed with combined GsMTx4 and OTX008 treatment support further investigation of co-targeting mechanosensitive channel activity and Galectin-1 in HNSCC.
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PubMed
高影响因子
危险品化学品经营许可证（带存储）