JOURNAL OF ASIAN NATURAL PRODUCTS RESEARCH
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2020
·
IF 1.345
Gen-Qiang Chen,Yan-Fei Xia,Jin-Ming Yang,Zhi-Ping Che,Di Sun,Shen Li,Yue-E Tian,Sheng-Ming Liu,Jia Jiang,Xiao-Min Lin
Gramine can be intelligently and efficiently supplied with N, N-dimethylamino group and then reacted with the corresponding sulfonyl chlorides to synthesize N, N-dimethylarylsulfonamides. We herein designed and controlled synthesis of N, N-dimethylarylsulfonamide derivatives, and first reported the results of the nematicidal activity of 15 title compounds 3a-o against Meloidogyne incongnita in vitro, respectively. Among all of the title derivatives, compounds 3a, 3c, 3k, and 3o exhibited potent nematicidal activity with median lethal concentration (LC50) values ranging from 0.22 to 0.26 mg/L. Most noteworthy, N, N-dimethyl-4-methoxyphenylsulfonamide (3c) and N, N-dimethyl-8-quinolinesulfonamide (3o) showed the best promising and pronounced nematicidal activity, with LC50 values of 0.2381 and 0.2259 mg/L, respectively.
研究领域:
植物保护学
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农药化学
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有机合成化学
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产品关联
DOI
PubMed
高影响因子
CHINESE JOURNAL OF CHEMICAL ENGINEERING
·
2017
·Vol. 25
·期 10
·1435-1441
·
IF 1.174
Zhirong Chen,Weitao Yang,Hong Yin,Shenfeng Yuan
The uncatalyzed reaction of p -tolyl isocyanate ( p -TI) with water in N , N -dimethylformamide (DMF) was investigated by high performance liquid chromatography (HPLC). The reactions were carried out at different temperatures from 293 K to 323 K, using various molar ratios of water to p -TI. DMF, as a special amide , was proved to be an efficient catalyst for water–isocyanate reaction. Under the reaction conditions in this study, substituted urea was the only final product observed. An appreciable amount of intermediate p -toluidine was detected. Concentrations of the isocyanate group as well as the amine and urea were determined as a function of time. New kinetic equations were deduced for each of the substance on the basis of a multistep mechanism, instead of a simple second order reaction as usual. Kinetic constants were calculated using the software MATLAB . Furthermore, the effects of temperature and concentrations of reactants on the reaction rate and amine content were discussed. The activation energy of each step was also determined.
研究领域:
物理化学
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有机化学
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反应动力学
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高分子化学
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催化化学
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分析化学
✓ 已验证
DOI
高影响因子
JOURNAL OF CHEMICAL THERMODYNAMICS
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2022
·
IF 3.269
Hengfei Zhang,Taotao Zhan,Junshuai Chen,Xin Li,Ying Zhang,Maogang He
The speed of sound of the (n-butanol + n-heptane) mixtures was measured by the Rayleigh-Brillouin light scattering method at temperatures ranging from 298.05 to 618.29 K and pressures up to 9.0 MPa. The relative expanded uncertainty of the speed of sound experimental system is 1.2% (coverage factor k = 2). The mixing effects were analyzed from molecular interactions: the trend that speed of sound rises first and then decreases with the n-butanol concentration mainly depends on the rupture of alkanol structures and the molecular association, respectively. Lacking other thermophysical properties of mixtures at high temperature and pressure, six classical speed-of-sound mixing rules only based on pure component properties were evaluated by experimental data, including Wood, Nomoto, Van Dael, Impedance dependence relations, and Time-average model and Volume-average model. It was found that the estimates by Wood’s relation (recognized as Junjie’s relation) agree best with experimental data. The applicability of mixing rules was further evaluated by 21 mixtures of (n-alkanol + n-alkane), where Wood’s relation still obtains great accuracy (average of rRMSDs = 0.91% and maximum = 1.84%). For these (n-alkanol + n-alkane) mixtures of weak interaction, Wood’s relation is expected to give reliable estimates for the under a wide temperature and pressure range, for just insignificant volume change being ignored.
研究领域:
物理化学
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热力学
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产品关联
DOI
高影响因子
JOURNAL OF CHEMICAL AND ENGINEERING DATA
·
2017
·
IF 2.323
Qingsong Li,Midong Shi,Liping Wang,Gaoyin He,Fan Gan
The liquid–liquid equilibrium (LLE) experiments for n-butanol + n-hexane + ethylene glycol were carried out and LLE data were measured at 298.15, 303.15, 308.15, 313.15, and 323.15 K under atmospheric pressure. The analysis results of the effects of n-butanol content and temperature on extraction showed that high n-butanol content was not favorable for extraction, and temperature had little effect on extraction. Moreover, the NRTL and UNIQUAC models were applied to correlate the LLE data, and the correlated data indicated that the UNIQUAC model showed a better correlation performance.
研究领域:
化学工程
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物理化学
✓ 已验证
产品关联
DOI
高影响因子
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
·
2018
·
IF 3.141
Muyuan Chai,Wenbo Zhao,Genming Li,Shengchao Xu,Qingming Jia,Yuan Chen
In order to avoid the high energy consumption in SO2 capture with aqueous amine absorbents, a liquid–liquid SO2 phase-change absorbent (SPCA) was developed in the present work using N,N-dimethylaniline (DMA) as absorbent, and high-boiling liquid paraffin was used as solvent to adjust the boiling point of the solution. The homogeneous solution would form two immiscible liquid phases after SO2 bubbling, only the SO2-rich phase needed to be desorbed, which could effectively reduce the energy consumption. Different from the liquid–solid phase-change absorbents developed in our previous work, the liquid–liquid phase-change absorbent avoid their shortcomings such as difficulties in separation of absorption products. The absorption product of SPCA was proved to be a charge-transfer complex DMA·SO2 by NMR and FTIR characterization, and the phase-change mechanism was attributed to the polarity variation between DMA and DMA·SO2. The viscosities of SPCAs was lower than 11.65 mPa·s, and the viscosity of SO2-rich phase was 3.9 mPa·s at 30 °C. The mass absorption capacity was found to be 0.89 g SO2/g DMA at 1 atm and 20 °C by ignoring liquid paraffin. The SPCA exhibited extremely high mass selectivity of SO2/CO2 with the value of 351. In addition, it was found that water had no effect on the structure of the absorption product and the SO2 capacity of SPCA. SPCA could be completely regenerated in 50 min at 80 °C. All the results showed that the SPCAs composed of DMA/liquid paraffin have a good application prospect.
研究领域:
化学工程
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环境科学
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产品关联
DOI
高影响因子
JOURNAL OF CHEMICAL AND ENGINEERING DATA
·
2019
·
IF 2.298
Daofan Ma,Chunying Zhu,Taotao Fu,Xigang Yuan,Youguang Ma
The experimental values of density and viscosity for binary solutions diethylenetriamine (DETA) + H2O, DETA + N,N-diethylethanolamine (DEEA), and ternary solution DETA + DEEA + H2O over the entire concentration range were reported at atmospheric pressure and T = (293.15, 303.15, 313.15, 323.15, 333.15) K. The measured densities and viscosities were used to calculate the thermal expansion coefficient, excess molar volume, partial molar volume, apparent molar volume, partial molar volume at infinite dilution, viscosity deviation, and excess Gibbs free energy of activation for viscous flow. The molecular interactions in mixtures were discussed based on the volumetric and viscometric properties.
研究领域:
物理化学
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分子科学
✓ 已验证
DOI
高影响因子
POLYMER SCIENCE SERIES B
·
2020
·Vol. 62
·期 5
·473-482
·
IF 0.976
Henglun Cheng,Shang Mengyao,He Yuan,Shentu Baoqing,Gao Zhuyi
Abstract A phenyl-substituted terephthalamide β-nucleating agent, N,N '-diphenylterephthalamide (DPTH) was synthesized and characterized by Fourier transform infrared spectroscopy (FTIR) and 1 H nuclear magnetic resonance ( 1 H NMR). DPTH’s effect on the crystallization and melting behaviors in isotactic polypropylene (iPP) was investigated by differential scanning calorimetry (DSC), wide angle X-ray diffraction (WAXD) and polarizing optical microscope (POM). The results illustrated that DPTH was an effective β-nucleating agent for iPP. The relative content of β-crystal ( k β ) increased with the rise of the DPTH content and reached a maximum of 0.652 at 0.6% DPTH content. The Avrami and Jeziorny methods were used to describe the nonisothermal crystallization kinetics of iPP. Higher crystallization rate constant Z c and lower halftime of crystallization t 1/2 were obtained in iPP containing DPTH.
研究领域:
材料科学
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高分子化学
✓ 已验证
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2023
·
IF 15.1
Linlu Shen,Hongyi Wang,Jing Kang,Jimin Shen,Pengwei Yan,Yingxu Gong,Jiaxu Zhang,Gang Fu,Shuyu Wang,Yizhen Cheng,Shengxin Zhao,Zhonglin Chen
In this study, the ultraviolet/peroxymonosulfate (UV/PMS) process was found to be an efficient and safe strategy for simultaneously controlling NDMA during the degradation of N,N-dimethylhydrazine compounds, such as 1,1,1′,1′-Tetramethyl-4,4′-(methylene-di-p-phenylene) disemicarbazide (TMDS). The distinct roles of sulfate radicals (SO 4 − ), hydroxyl radicals (HO ), PMS, and UV in TMDS degradation as well as NDMA formation and elimination, have been elucidated, involving the kinetics and multiple-path transformation mechanisms. Moreover, to assess the feasibility of this process, a comprehensive toxicity assessment of treated water for zebrafish embryos was conducted. Mineralization analysis and an assessment of electrical energy per order (EE/O) were performed on actual water samples. The results indicate that SO 4 − , HO , PMS, and UV together degraded TMDS, but only SO 4 − and PMS led to NDMA formation. UV irradiation may coordinate SO 4 − and HO to overcome the energy barriers of NDMA elimination by providing continuous energy. The degradation of TMDS involved hydroxylation, radical addition, bond cleavage and nitrosation. Notably, NDMA formation may be closely related to the electron transfer between SO 4 − or PMS and TMDS. Subsequently, the generated NDMA was controlled through photocleavage, radical addition, and hydroxylation. Additionally, the results of toxicity evaluation and EE/O analysis suggest UV/PMS is safe and has the potential for treating N,N-dimethylhydrazine compounds-containing water.
研究领域:
环境科学
·
毒理学
·
水处理工程
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产品关联
DOI
高影响因子
ULTRASONICS SONOCHEMISTRY
·
2021
·
IF 7.491
Hanyang Gao,Kunkun Pei,Dong Lei,Guoxin Hu,Yan Chao,Aihua Meng,Hongcheng Wang,Wei Shentu
Due to the tunability in mass transfer, solvation and solubility, gas-expanded liquids show advantages over traditional organic solvents in many characteristics. Ultrasonication is a commonly used method to promote heat and mass transfer. The introduction of ultrasonic technology into the gas-expanded liquid system can promote the polymerization of polymer monomers, enhance extraction efficiency, and control the growth size of nanocrystals, etc. Although acoustic cavitation has been extensively explored in aqueous solutions, there are still few studies on cavitation in organic liquids, especially in gas-expanded liquid systems. In this article, the development of cavitation bubble cloud structure in CO 2 -expanded N, N-dimethylformamide (DMF) was observed by a high-speed camera, and the cavitation intensity was recorded using a spherical hydrophone. It was found that the magnitude of the transient cavitation energy was not only related to input power, but also closely related to CO 2 content. The combination of ultrasound (causing a rapid alternation of gas solubility) and gas-expanded liquid system (causing a decrease in viscosity and surface tension of liquids) is expected to provide a perfect platform for high-speed mass transfer.
研究领域:
化学工程
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超声技术
·
材料科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
JOURNAL OF PHYSICAL CHEMISTRY B
·
2019
·
IF 2.923
Xueqian Guan,Zhiyu Huang,Hongsheng Lu,Dejun Sun
Binary mixtures of water and organic solvents are described as the aqueous solutions of organic solvents, which are usually spatially heterogeneous on the scale of a few molecular sizes but homogeneous on longer length scales, that is, microheterogeneity. For the water–organic solvent binary mixtures with microheterogeneity, most organic solvents are miscible with water at any ratio. Interestingly, some slightly water-miscible organic solvents can also be used to prepare binary mixtures with microheterogeneity. In this study, N,N-dimethylcyclohexylamine (DMCHA) was used to prepare binary mixtures with microheterogeneity and CO2 switchability. With the help of conductivity, Fourier–transform infrared spectroscopy, ultraviolet–visible spectroscopy, and dynamic light scattering measurements, we found that water molecules are hydrogen-bonded together to form clusters over the water content range of 9 to 27 wt %, exhibiting microheterogeneity in the binary mixture. The size of the water clusters increases slightly with increasing water content. What is more, the DMCHA–water mixtures can be reversibly split into two phases by alternate bubbling of CO2 and N2, exhibiting excellent CO2 switchability. The binary mixtures can be used as reaction media for the synthesis of CaCO3 nanoparticles. Binary mixtures with microheterogeneity can also be formed under high salinity or high temperature conditions or be prepared using other slightly water-miscible organic solvents, opening up more interesting possibilities for binary mixtures with microheterogeneity.
研究领域:
化学
·
材料科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
National Science Review
·
2022
·Vol. 9
·期 10
·
IF 23.178
Ma Yilin,Zhang Qiu,Liu Luojia,Li Yixin,Li Haixia,Yan Zhenhua,Chen Jun
Rechargeable aqueous Zn batteries are considered as promising energy-storage devices because of their high capacity, environmental friendliness and low cost. However, the hydrogen evolution reaction and growth of dendritic Zn in common aqueous electrolytes severely restrict the application of Zn batteries. Here, we develop a simple strategy to suppress side reactions and boost the reversibility of the Zn electrode. By introducing 30% (volume fractions) N,N-dimethylformamide (DMF) to the 2 M Zn(CF3SO3)2–H2O electrolyte (ZHD30), the preferential hydrogen-bonding effect between DMF and H2O effectively reduces the water activity and hinders deprotonation of the electrolyte. The ZHD30 electrolyte improves the Zn plating/stripping coulombic efficiency from ∼95.3% to ∼99.4% and enhances the cycles from 65 to 300. The Zn–polyaniline full battery employing the ZHD30 electrolyte can operate over a wide temperature range from –40°C to +25°C and deliver capacities of 161.6, 127.4 and 65.8 mAh g–1 at 25, –20 and –40°C, respectively. This work provides insights into the role of tuning solvent effects in designing low-cost and effective aqueous electrolytes.
研究领域:
材料科学
·
电化学
✓ 已验证
DOI
高影响因子
Crystals
·
2020
·Vol. 10
·期 6
·528
·
IF 2.404
Chao Liu,Weiwei Zhang,Gaigai Cai
Two copper coordination compounds bearing an N,N’-dibenzylethylenediamine ligand, namely [Cu3L(CH3COO)6]n(1) and [(CuCl4)∙(C6H5CH2NH2CH2)2] (2) (L=N,N’-dibenzylethylenediamine) were synthesized by the ethanol refluxing method. Powder X-ray diffraction (PXRD), infrared spectra (IR), elemental analyses, and single crystal X-ray diffraction were used to characterize and verify their structures. Structural analyses showed that the asymmetric unit of compound (1), composed of two Cu(II) cations, three acetate anions, and half of the ligand, was bridged by one acetate to obtain an infinite 1D chain structure. The analyses further showed that the asymmetric unit of compound (2), composed of two crystallographically independent [C6H5CH2NH2CH2]+units, four chloride anions, and one central Cu(II) cation is connected into an infinite 2D network structure by the hydrogen bonding interactions. The copper compounds were used to catalyze the decomposition of H2O2,and the results showed that both of the compounds exhibited excellent catalytic activities under optimized conditions.Keywords:N,N’-dibenzylethylenediamine;crystal structure;catalyst;coordination compound
研究领域:
化学
·
材料科学
✓ 已验证
产品关联
DOI
高影响因子
危险品化学品经营许可证（带存储）