JOURNAL OF POLYMER RESEARCH
·
2018
·Vol. 25
·期 1
·1-9
·
IF 1.434
Li Hanyuan,Wang Wei,Chen Guofei,Liu Yinfeng,Fang Xingzhong
Novel highly soluble phenylethynyl-endcapped oligoimides derived from mixed thioetherdiphthalic anhydride isomers ( m -TDPA) and 5(6)-amino-1-(4-aminophenyl)-1,3,3-trimethylindane (DAPI), 4,4′-oxydianiline (4,4’-ODA) with 4-phenylethynylphthalic anhydride (PEPA) as a reactive endcapping agent were synthesized. The calculated molecular weights of all the oligoimides were 2500 g·mol −1 .The effect of the mole ratio of DAPI/4,4’-ODA on solubility and melt viscosity of oligoimides as well as the thermal and mechanical properties of cured polyimide films was investigated. Experimental results indicated that DAPI greatly improved the solubility (>30 wt.%) of the oligoimides in low boiling points solvents when the content of DAPI was more than 10 mol% per total diamine. All the oligoimides exhibited very good processability with minimum melt viscosity lower than 60 Pa·s at about 330 °C. Tough and brown films were obtained after thermally cured at 370 °C for 1 h and dynamic mechanical analysis (DMA) showed that glass transition temperatures of the cured films increased up to 340 °C with the increasing content of DAPI. However, the thermal stability and mechanical properties decreased with the increase of DAPI content. The temperature of 5% weight loss was higher than 470 °C in both air and N 2 atmosphere obtained by thermogravimetric analysis (TGA). And the tensile strengths of the cured films were about 60 MPa.
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APPLIED CATALYSIS A-GENERAL
·
2021
·
IF 5.706
Lei Chen,Wenxia Zhuang,Jingmin Lan,Xiaoling Liu,Shi Jiang,Lei Wang,Yu Zhou,Jun Wang
Mg-bearing MTW silicalite zeolite, MgSi-ZSM-12, was straightforwardly synthesized by involving an unusual acidic pre-gelation system and engaged as the task-specific support for loading the Au nanoparticles (NPs). The resulting Au/MgSi-ZSM-12 catalyst showed stably excellent activity for the oxidation of HMF into FDCA in the presence of atmospheric dioxygen (O 2 ) without externally adding any liquid base, affording a yield of 87 % and turnover number (TON) of 331 based on the surface Au sites. Superior basicity was evidenced by embedding Mg species into the all-silica zeolitic skeleton, which enables strong, weak, and near-zero affinity towards aldehyde, alcohol, and carboxyl groups, respectively, thus, allows rapid and high-uptake adsorption of HMF, but negligible adsorption of FDCA. This unique feature of the Mg-bearing all-silica zeolite support together with its synergy with the active sites of Au NPs is revealed to accelerate the production of FDCA under the base-free mild condition.
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ChemistrySelect
·
2023
·Vol. 8
·期 9
·e202203332
·
IF 2.1
Cunwei Qian,Ying Wang,Xian Li,Changsheng Yao
Graphical A convenient, rapid and electrochemical one-pot protocol is designed for the synthesis of pyrazolo[3,4- b ]quinolines derivatives. The reaction is carried out in an undivided cell equipped with an iron cathode and a graphite anode in the presence of sodium bromide as a supporting electrolyte. Fourteen pyrazolo[3,4- b ]quinoline derivatives are obtained under a constant current of 30 mA after 0.14 F/mol of electricity passed. A convenient, rapid and electrochemical one-pot protocol was developed successfully for the preparation of pyrazolo[3,4- b ]-quinoline derivatives. The reaction is carried out in a 25 mL three neck flask equipped with graphite electrode as anode and iron electrode as cathode (electrode area of 1 cm 2 ) with sodium bromide as supporting electrolyte at room temperature in ethanol. Fourteen pyrazolo-[3,4- b ]-quinoline derivatives were synthesized by use of various aldehyde (including aryl aldehydes and aliphatic aldehydes), dimedone and 5-amino-3-methyl-1-phenylpyrazole as substrates in good yields (76–86 %) with a constant current of 30 mA after 0.14 F/mol of electricity passed. All aimed products were characterized by IR, 1 H NMR and HRMS. Notably, the presented method features ecologically sound, simple experimental procedure and good yields.
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高影响因子
NEW JOURNAL OF CHEMISTRY
·
2021
·Vol. 45
·期 25
·11380-11389
·
IF 3.591
Rui Yang,Yifei Liu,Zhen Dong,Haiyan Li,Zhiwen Ye
As an environmentally friendly energetic group, the azide group can not only control the melting point but also increase the energy of the compound. Therefore, the design and synthesis of energetic compounds with azido groups have long been a focus of research in the field of energetic materials. 3-R-4-(5-methyleneazide-1,2,4-oxadiazol-3-yl)furazan energetic materials were synthesized and fully characterized. Using computational chemistry methods, the interactions of some compounds were studied, and the physical and chemical properties of all of compounds were examined. The results show that 3-amino-4-(5-methyleneazide-1,2,4-oxadiazol-3-yl)furazan (2) has a melting point similar to that of TNT and can be a potential carrier for molten-cast explosives. Hydroxylamine salt (4) has an excellent detonation velocity and detonation pressure of 9090 m s−1 and 35.76 GPa, respectively, and its energy is significantly higher than that of RDX, enabling replacement of RDX as a high-energy explosive. Although the detonation performance of compound 4 is slightly lower than that of HMX, its sensitivity is better than that of HMX, which shows that compound 4 still has a high application value. Non-covalent interactions (NCIs) and Hirshfeld surface models indicate that hydrogen bonding and π–π interactions are the key factors that reduce the sensitivity of compounds. Therefore, our results for 3-R-4-(5-methyleneazide-1,2,4-oxadiazol-3-yl)furazan energetic materials suggest that it may be competitive for application in both molten-cast explosives and high-energy explosives.
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高影响因子
Inorganic and Nano-Metal Chemistry
·
2017
·
IF 0
Jiaxing Li,Meng Ni,Chaoyi Fan,Yan Li,Xiuqing Zhang
A new cobalt complex [Co3(SIP)2(4-PP)8(H2O)6]·4H2O·2(4-PP) (1) with 5-sulfoisophthalic acid sodium (NaH2SIP) and 4-phenyl pyridine (4-PP) as ligands has been synthesized in the mixed solvents of ethanol and water. It crystallized in monoclinic, space group P21/c, with a = 20.9642(9) Å, b = 15.6091(5) Å, c = 20.0126(8) Å, α = 90.00°, β = 115.493(6)°, γ = 90.00°, V = 5911.2(4) Å3, Z = 2, Dc = 1.346 g/cm−3, F(000) = 2494, the final GOOF = 1.038, Rint = 0.0258 and wR2 = 0.1793. The complex (1) was characterized by single-crystal X-ray diffraction, magnetic susceptibility and IR spectroscopy analyses. Single-crystal X-ray diffraction shows that complex (1) is trinuclear based on cobalt units. Magnetic susceptibility measurement indicates that complex (1) shows an antiferromagnetic coupling between the Co(II) ions.
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COLLOIDS AND SURFACES B-BIOINTERFACES
·
2017
·
IF 3.887
Gang Pan,Ting-ting Jia,Qian-xia Huang,Yan-yan Qiu,Jie Xu,Pei-hao Yin,Tao Liu
Novel methods to improve the anticancer performance of 5-fluorouracil (5-FU) is quite necessary for clinical medicines. In the present work, we fabricated a novel type of mesoporous silica nanoparticles (MSNs)-based inorganic/organic hybrid nanoparticles covalently attached with poly(oligo(ethylene glycol) monomethyl ether methacrylate) (POEGMA) for improved stabilization and targeting peptide (RGD) for targeted delivery with the aim of improving the anticancer performance of 5-FU. Atom transfer radical polymerization (ATRP) initiator functionalized MSN (MSN-Br) was synthesized at first, which was followed by surface-initiated ATRP of water soluble OEGMA and carboxyl-containing monomer (2-succinyloxyethyl methacrylate, SEMA). Functionalization of RGD onto the hydrophilic P(OEGMA- co -SEMA) chains afforded the final hybrid nanoparticle, MSN-P(OEGMA- co -RGD). 5-FU can be effectively loaded into the meso -pores of MSN-P(OEGMA-c o -RGD) ( [email protected] ) with drug content ∼7.5 wt%. And the dynamic diameter ( D h ) and zeta potential (ζ) of [email protected] were determined to be 199.3 ± 5.4 nm and −8.7 ± 0.5 mV, respectively. It was demonstrated that MSN-P(OEGMA-c o -RGD) exhibited improved internalization into colon cancer cells and enhanced accumulation in tumor tissues. In addition, compared with free 5-FU, [email protected] showed enhanced anticancer efficacy both in vitro and in vivo, implying promising clinical applications.
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PubMed
高影响因子
CRYSTENGCOMM
·
2024
·Vol. 26
·期 9
·1303-1311
·
IF 2.6
Shuyue Miao,Fangbao Jiao,Ying Wang,Qi Zhang,Suming Jing,Hongzhen Li,Xin Zhou
Compared with jagged and rod-like raw products, the spherulitic 3-nitro-1,2,4-triazol-5-one (NTO) crystalline powder is generally superior in the formulation. However, the growth mechanism and corresponding influential factors for NTO spherulites remain to be deeply explored. Herein, the morphological evolutions of NTO crystals in alcohol solvents under a range of maximum supersaturation (Smax) are systematically investigated. It was found that differences in solvent-crystal interface interactions determine the primary morphology of the growing crystals while the magnitude of Smax determines the subsequent polycrystalline evolution. The cooling rate, initial concentration and stirring rate all could affect the crystal morphology by changing the Smax. It is demonstrated that there exists a critical Smax range (1.75–1.88) above which the formation of spherulites is kinetically favorable. Face indexing tests suggest that the (0 0 1) plane of NTO is mostly prone to twinning at low supersaturation, which is because that the molecular layers on the (0 0 1) surface are prone to twisting and the energy difference before and after is only 8.77 kJ mol−1. Then, the interfacial growth theory is employed to explain how a growing crystal plane develops from smooth to rough with non-crystallographic sub-individuals as the crystallization driving force increases. The change of morphology has a positive consequence in improving the safety performance of NTO crystalline powder under drop-weight impact. These findings would forward the understanding of the spherulitic crystallization process for energetic crystals.
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高影响因子
ACS Catalysis
·
2025
·
IF 13.1
Jianghua Zhao,Yifan Wang,Huai Liu,Rui Zhang,Wenlong Jia,Junhua Zhang,Yong Sun,Lincai Peng
Defect engineering is an effective strategy to enhance the photocatalytic performance of ZnIn2S4 (ZIS), but it remains a formidable challenge to manipulate the cationic defects in the catalyst because of their high formation energies. Herein, dual Zn and In defects have been successfully created in the ZnIn2S4 (ZIS-5) with a facile cetyltrimethylammonium chloride (CTAC)-assisted hydrothermal method. The resulting ZIS-5, rich in cation vacancies, achieved a 3.6-fold higher 2,5-diformylfuran (DFF) yield (92.0%) than the pristine ZIS (25.8%) for the visible-light-driven photocatalytic air-oxidation of 5-hydroxymethylfurfural (HMF). Especially, ZIS-5 delivers a high DFF productivity of 1600 μmol g–1 h–1, significantly surpassing the previously reported catalysts (75–953 μmol g–1 h–1) for the photocatalytic oxidation of HMF to DFF in air. Density functional theory (DFT) simulations revealed that the presence of dual Zn and In defects endows the catalyst with defect states that intersect the Fermi level and lower work function. These enhance the migration and separation of photogenerated carriers in ZIS-5, significantly promoting O2 activation and resulting in the generation of more reactive oxygen species (·O2– and 1O2) for the catalytic oxidation of HMF. This study offers valuable insights for guiding the design of photoredox reaction systems through cationic-defect-engineering strategies, enabling the efficient valorization of biomass-derived platform chemicals.
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高影响因子
ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
·
2024
·Vol. 31
·期 17
·25114-25128
·
IF 0
Qi Qi,Wang Zhuang
Assessment and prediction for the ecotoxicity of engineered nanoparticles (ENPs) at the community or ecosystem levels represents a critical step toward a comprehensive understanding of the ecological risks of ENPs. Current studies on predicting the ecotoxicity of ENPs primarily focus on the cellular and individual levels, with limited exploration at the community or ecosystem levels. Herein, we present the first of the reports for the direct prediction of aquatic ecological risk for ENPs at the community level using machine learning (ML) approaches in the field of computational toxicology. Specifically, we extensively collected the threshold concentrations of twelve ENPs including metal- and carbon-based nanoparticles for aquatic species, i.e., hazardous concentrations at which 5% of species are harmed (HC 5 ), established by a species sensitivity distribution. Afterwards, we used eight supervised ML methods including Adaboost, artificial neural network, C4.5 decision tree, K-nearest neighbor, logistic regression, Naive Bayes, random forest, and support vector machine to develop nine classification models and four regression models, respectively, for the qualitative and quantitative prediction of HC 5 . The evaluation of model performance yielded the internal validation accuracy of all classification models ranging from 71.4 to 100%, and the determination coefficient of regression models ranging from 0.702 to 0.999, indicating that the developed models showed good performance. By using a cross-validation method and an application domain characterization, the selected models were further validated to have powerful predictive ability. Furthermore, the incorporation of three nanostructural descriptors (metal oxide sublimation enthalpy, zeta potential, and specific surface area) linked to toxicity mechanisms (the release of metal ions, the stability of dispersions of particles in aqueous suspensions, and the surface properties of the material) effectively enhanced the prediction power and mechanistic interpretability of the selected models. These findings would not only be beneficial in the screening of ENPs with potential high ecological risks that need to be tested as a priority but also contribute to the development of environmental regulations and standards for ENPs.
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JOURNAL OF ANALYTICAL AND APPLIED PYROLYSIS
·
2021
·
IF 5.541
Xiaohua Li,Jinlong Yan,Shanshan Shao,Shengnan Ge,Zhichao Lv,Yixi Cai
A method of template removal by direct non-thermal plasma (DNTP) system for the synthesis of HZSM-5/MCM-41 meso-micropore composite catalyst was proposed for the production of aromatic hydrocarbons by catalytic pyrolysis of rape straw. It was revealed most of the template on the catalyst was removed by oxidizing substances such as ozone produced by DNTP. During DNTP treatment, the removal effect of the template was greatly affected by the oxygen flow rate . Also, the catalyst structure was bombarded by high-energy electrons obtained by DNTP treatment, and the physicochemical property of the synthetic composite catalysts was treated quite different from that obtained by calcination method. Under the treatment condition of 22 kV-2 L/min, the BET surface area was boosted significantly by 29.91% and the amount of acid sites was boosted by 37.71%, the yield of MAHs reached 10.57 wt%. Generally, not only the template can be effectively removed by DNTP treatment, but also the physicochemical property of meso-micropore composite catalyst can be improved, and thus promoted the catalytic performance for monocyclic aromatic hydrocarbons. Therefore, DNTP is an effective technology for removing template and the catalytic performance can be efficiently improved.
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高影响因子
Food Bioscience
·
2026
·
IF 6.2
Wenhui Fu,Xuemeng Ji,Dongze Qin,Lingda Zhao,Huan Lv,Yaozhong Hu,Ruican Wang,Wentao Gu,Dongfei Tan,Shuo Wang
Chemotherapy-induced intestinal mucositis is a common and clinically important adverse effect. However, its underlying mechanisms remain poorly understood and effective interventions are limited. This study investigated the protective effects of a cell-free L. rhamnosus -fermented cereal fraction against 5-fluorouracil (5-FU) induced CIIM in a murine model. L. rhamnosus fermentation markedly enhanced the functional value of the cereal matrix by enriching soluble fermentation-derived bioactives, including TCA-soluble peptide content, total phenolic and flavonoid content, and lactic acid. Prophylactic administration of the fermented cereal fraction attenuated 5-FU-induced mucosal injury, enhanced intestinal antioxidant capacity, improved mucosal architecture and barrier-related indices, and suppressed epithelial apoptosis. Exploratory quantitative proteomic analysis identified candidate proteins whose abundance was altered following 5-FU treatment, including proteins associated with antioxidant defense, apoptosis, cytoskeletal organization, and epithelial barrier-related processes. In contrast, fermented cereal intervention restored the expression of key endogenous antioxidant and barrier-associated proteins. Notably, the final pH-matched lactic acid control indicated that low final pH and the direct presence of lactic acid were insufficient to account for the protective effects of the fermented cereal fraction, suggesting that multiple fermentation derived components contributed to the observed bioactivity. Collectively, these findings indicate that L. rhamnosus -fermented cereal mitigates CIIM through fermentation-enhanced exogenous antioxidant delivery, support of endogenous antioxidant defenses, and attenuation of mucosal and barrier-related alterations. This study supports the potential of cereal fermentation-derived bioactives as functional dietary ingredients for managing CIIM.
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高影响因子
MICROCHEMICAL JOURNAL
·
2026
·
IF 5.2
Ye Tang,Dongyan Li,Ziyin Lu,Yaxi Wang,Wenjie Liu,Guoxing Jing,Wen Liu,Jianna Yu,Wenshan Li
The severe toxicity of Pb 2+ to human health, even at trace levels, the development of highly sensitive and dependable analytical methods remains of great importance. Here, we developed a label-free and enzyme-free colorimetric method for Pb 2+ assay by integrating a GR-5 DNAzyme recognition event with a catalytic hairpin assembly (CHA)-hybridization chain reaction (HCR) cascade amplification. Upon exposure to Pb 2+ , the GR-5 DNAzyme is specifically activated, catalyzing the site-specific cleavage of hairpin H1 to release the initiator strand T. The liberated T strand subsequently drives the CHA and HCR cascade reactions, generating long DNA superstructures enriched with multiple G-rich sequences. In the presence of hemin, these G-rich sequences fold into catalytically functional G-quadruplex/hemin DNAzymes, which enable a visible colorimetric signal generation. Under optimized conditions, the proposed colorimetric method delivered a linear response over the range of 50 pM to 50 nM and achieved a limit of detection of 16.71 pM. The practical applicability of the method was further demonstrated through Pb 2+ analysis in drinking water and fish samples, where satisfactory accuracy and reliability were obtained. In addition, inductively coupled plasma mass spectrometry was employed to validate the real-sample results, and the two methods showed good consistency. Owing to its simplicity, high sensitivity, and enzyme-free design, this colorimetric method shows strong potential for practical Pb 2+ monitoring in food safety and environmental analysis.
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高影响因子
危险品化学品经营许可证（带存储）