JOURNAL OF THE CHINESE CHEMICAL SOCIETY
·
2017
·Vol. 64
·期 4
·412-419
·
IF 0.935
Xiu-Yan Dong,Sunday Folaranmi Akogun,Wei-Min Zhou,Wen-Kui Dong
A new tetranuclear Zn(II) complex, [{Zn(L)(μ-OAc)Zn(H 2 O)} 2 ], based on an asymmetrical salamo-type bisoxime chelating ligand H 3 L (6-hydroxy-4′-chloro-2,2′-[ethylenediyldioxybis(nitrilomethylidyne)]diphenol) was synthesized and characterized by elemental analyses, differential thermal methods, single-crystal X-ray crystallography, and IR, UV–vis, and fluorescence spectra. The Zn(II) complex crystallizes in the triclinic system, space group P -1 with cell parameters a = 9.0742(6) Å, b = 11.8225(5) Å, c = 12.4182(8) Å, Z = 2, V = 1212.56(12) Å 3 , R 1 = 0.0572, and wR 2 = 0.1734. The environment of the tetranuclear Zn(II) complex is penta-coordinated having a slightly distorted trigonal bipyramidal geometry. Moreover, a 1D chain supramolecular structure is formed along the c -axis by the intermolecular C1–H1B⋯O14 hydrogen bonds; in the same manner, C2–H2C⋯Cg2 functions in the formation of supramolecular structures along the a -axis of the 1D chain. A 2D supramolecular structure along the ac plane extends infinitely under the force of intermolecular hydrogen bonds. Differential scanning calorimetry-thermogravimetry thermal analysis provides evidence of the coordination of Zn(II) atoms to the ligand H 3 L. The Zn(II) complex shows intense photoluminescence with a maximum emission at ~453 nm upon excitation at 360 nm.
研究领域:
无机化学
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配位化学
·
超分子化学
·
材料化学
·
分析化学
·
物理化学
·
晶体学
✓ 已验证
DOI
高影响因子
INDUSTRIAL CROPS AND PRODUCTS
·
2017
·
IF 3.181
Xinyan Yan,Zhaolan Zhai,Zhanqian Song,Shibin Shang,Xiaoping Rao
A series of polymeric surfactants , poly acrylic acid rosin polyethylene glycol esters (P-AAR-PEG), have been synthesized from natural diterpenic rosin. Their structures were characterized by Fourier Transform Infrared Spectrometer (FTIR) and their molecular weights were characterized by Gel Permeation Chromatography (GPC). Their critical micelle concentration (CMC), surface tension (γ CMC ), foaming property (FP), and hydrophile-lipophile balance (HLB) value were evaluated. Their thermal properties were measured by Thermal Gravimetric Analyzer (TGA) and fluid behaviors were studied by Rotational Rheometer. The influence of concentration on the properties of oil-in-water emulsions was examined and contrasted the stability of emulsion by the mean droplet size between day1 and day7. The weight-average molecular weight of P-AAR-PEG ranged from 1770 to 5071. CMC values of P-AAR-PEG were ranged from 0.33 to 0.87 g/L and the corresponding γ CMC values were ranged from 37.8 to 39.1 mN/m respectively. Their CMC and γ CMC values decreased and then increased with the increment of molecular weight of hydrophile group. Rheological measurements indicated that the P-AAR-PEG solutions changed from pseudoplastic property to Newtonian with increasing shear rate. P-AAR-PEG1000 had good emulsion ability to turpentine in water. When the concentration of P-AAR-PEG1000 was 8 wt%, the emulsion remained stable for more than 7 days.
研究领域:
高分子化学
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表面与界面化学
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材料科学
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胶体化学
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应用化学
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DOI
高影响因子
JOURNAL OF APPLIED POLYMER SCIENCE
·
2015
·Vol. 132
·期 25
·
IF 1.768
Xiao-Hui Liu,Fei-Jun Zhang,Hui-Na Li,Xiao-Hui Hu,Wen-Li Di,Shuang Zhao
A facile, safe, and inexpensive reducing agent, sodium hypophosphite (NaH 2 PO 2 ·H 2 O), has been successfully used to perform ambient temperature living radical polymerizations of methyl methacrylate (MMA) and styrene (St). The rapid radical polymerizations were readily obtained at 25°C, i.e., MMA reached a conversion of ca 90% after 2.5 h, and St reached a conversion of ca 80% after 40 h. The polymerizations of MMA and St exhibited excellent living/controlled nature, as evidenced by pseudo first-order kinetics of polymerization, linear evolution of molecular weights with increasing monomer conversions, and narrow molecular weight distributions. The various experimental parameters—ligand, solvent, and molar ratio of NaH 2 PO 2 ·H 2 O to CuSO 4 ·5H 2 O—were varied to improve the control of polymerization, molecular weight, and molecular weight distribution. 1 H NMR analyses and chain-extension reactions confirm the high chain-end functionality of the resultant poly(methyl methacrylate) and polystyrene. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132 , 42123.
研究领域:
高分子化学
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聚合反应工程
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功能高分子材料
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可控/活性聚合
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绿色合成方法
✓ 已验证
DOI
高影响因子
JOURNAL OF ELECTROANALYTICAL CHEMISTRY
·
2018
·
IF 3.235
Yang Yuan,Jiaxin Wang,Xinjiong Ni,Yuhua Cao
A biosensor for determination of 3-chloro-1, 2-propandiol (3-MCPD) was developed based on the electrochemically catalytic reduction by hemoglobin (Hb). Hb was concentrated and immobilized with magnetic molecularly imprinted nanoparticles (MMIPs NPs). The MMIP NPs had a core-shell structure, with magnetic Fe 3 O 4 NPs as the core and SiO 2 as the shell. MMIPs NPs were modified on the surface of a magnetic electrode to constitute the Hb enzyme-like sensor. The biosensor could catalyze the electrochemical reduction of 3-MCPD, and a direct electrochemical determination of 3-MCPD could be achieved for the first time. The biosensor, where Hb immobilized with MMIPs NPs had high electrochemical response for 3-MCPD, increased by 37.5% compared with Hb immobilized with magnetic non-imprinted nanoparticle (MNIPs NPs). The biosensor increased the response by 19.56% again under an external magnetic field . The reduction peak current had a linear relationship with 3-MCPD concentration ranging from 1.0 mg·L −1 to 160 mg·L −1 with a detection limit (S/N = 3) of 0.25 mg·L −1 . The biosensor was applied to the determination of 3-MCPD in soy sauce samples successfully with recoveries between 97.4% and 99.6%.
研究领域:
生物传感器
·
分析化学
·
食品科学
·
电化学
·
分子生物学
·
纳米医学
✓ 已验证
DOI
高影响因子
Energy & Environmental Materials
·
2022
·Vol. 6
·期 3
·e12351
·
IF 13.443
Qiyu Wang,Xiangqun Xu,Bo Hong,Maohui Bai,Jie Li,Zhian Zhang,Yanqing Lai
Quasi-solid-state lithium metal battery is a promising candidate for next generation high energy density and high safety power supply. Despite intensive efforts on electrolytes, uncontrolled interfacial reactions on lithium with electrolyte and patchy interfacial contacts still hinder its practical process. Herein, we bring in rationally designed F contained groups into polymer skeleton via in-situ gelation for the first time to establish quasi-solid-state battery. This method achieves a capacity retention of 90% after 1000 cycles at 0.5C with LiFePO 4 cathodes. The interface constructed by polymer skeleton and reaction with –CF 3 lead to the predicted solid electrolyte interface species with high stability. Furthermore, we optimize molecular reactivity and interface stability with regulating F contained end groups in the polymer. Comparisons on different structures reveal that high performance solid stable lithium metal batteries rely on chemical modification as well as stable polymer skeleton, which is more critical to construct robust and steady SEI with uniform lithium deposition. New approach with functional groups regulation proposes a more stable cycling process with a capacity retention of 94.2% at 0.5C and 87.6% at 1C after 1000 cycles with LiFePO 4 cathodes, providing new insights for the practical development of quasi-solid-state lithium metal battery.
研究领域:
电化学
·
材料科学
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能源存储
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界面化学
·
高分子化学
✓ 已验证
DOI
高影响因子
International Journal of Electrochemical Science
·
2023
·Vol. 11
·期 8
·6466-6476
·
IF 1.5
Changling Yan,Jin Li,Tingting Meng,Xun Liu,Ruixing Zhang,Yujuan Chen,Gongke Wang
A simple and reliable method was proposed for rapid detecting ciprofloxacin, based on molecularly imprinted technology. The molecularly imprinted ciprofloxacin hydrochloride (CPX) sensor was prepared by electropolymerization of pyrrole (Py) and o-phenylenediamine (o-PD) on the pencil graphite electrode (PGE). The performance of the sensor was characterized by square wave voltammetry (SWV) using potassium ferricyanide as molecular probe. Under optimal conditions, the sensor displayed high selectivity and stability towards CPX. A linear relationship between the change in current (Δi) and the logarithm of CPX concentrations from 1×10 −9 to 1×10 −3 mol/L was obtained with a detection limit of 7.58×10 −11 mol/L (S/N=3). Furthermore, the MIP sensor was applied for the analysis of real tablet samples with high accuracies.
研究领域:
分析化学
·
药物分析
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电化学传感
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分子印迹技术
·
药物残留检测
✓ 已验证
DOI
高影响因子
Journal of Materials Chemistry A
·
2014
·Vol. 2
·期 26
·10169-10181
·
IF 0
Shaojun Chen,Hongming Yuan,Shiguo Chen,Haipeng Yang,Zaochuan Ge,Haitao Zhuo,Jianhong Liu
Supramolecular liquid crystalline polymers and shape memory polymers are attracting increasing interest as materials. In this paper, we describe the development of a supramolecular liquid crystalline shape memory polyurethane (SLCSMPU) complex that exhibits both liquid crystalline properties and shape memory properties. The complex is formed by incorporating 4-hexadecyloxybenzoic acid (HOBA) into a pyridine-containing shape memory polyurethane (PySMPU). The HOBA is tethered to the PySMPU by strong hydrogen bonding between the pyridine rings and the COOH of the HOBA, forming a SLCSMPU complex. Heat treatment plays an important role in the formation of hydrogen-bonded supramolecular liquid crystalline structures in these SLCSMPU complexes. Thus, the SLCSMPU complex not only maintains the intrinsic liquid-crystalline properties of HOBA, but can also form a stable polymeric film for various shape memory applications. Additionally, the SLCSMPU complex forms a two-phase separated structure composed of an amorphous polyurethane matrix and a HOBA crystalline phase, which includes the hydrogen-bonded crystalline HOBA phase and the free HOBA crystalline phase. Therefore, a simple one-step programming process is developed that produces SLCSMPU complexes with excited triple-shape functionalities due to their multiple phase transitions, especially when the molar ratio of HOBA/BINA is less than 0.8.
研究领域:
高分子科学
·
材料化学
·
软物质物理
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智能材料
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功能高分子
✓ 已验证
DOI
RSC Advances
·
2016
·Vol. 6
·期 27
·22908-22916
·
IF 3.289
Jianwen Tian,Xiaohui He,Jingyin Liu,Xiaodan Deng,Defu Chen
Palladium(II) and copper(II) chloride complexes bearing bulky 9,10-dihydro-9,10-ethanoanthracene-11,12-diimine ligands were synthesized and sufficiently characterized by elemental and spectroscopic analysis along with X-ray diffraction analysis. The X-ray diffraction demonstrated that palladium(II) complexes (C1–C2) and copper(II) complexes (C3–C4) were four-coordinated. All these complexes displayed catalytic activities up to 105 gpolymer molMt−1 h−1 for norbornene vinyl-addition polymerization on treatment with excess methylaluminoxane (MAO). The parameters of the reaction conditions, the type of metals and steric effects of coordinative ligands had influences on the catalytic properties. C2 was selected as a catalyst precursor for the copolymerization of norbornene (NB) with 2-butyloxymethylene norbornene (BN), which exhibited catalytic activities up to 1.1 × 105 gpolymer molPd−1 h−1 and produced copolymers with relatively high molecular weights. The fraction of BN in the copolymer could reach up to 9.8–62.1% by controlling the monomer feed ratio range from 10–80%. The achieved vinyl-addition type poly(NB-co-BN) displayed high thermal stability and was soluble in common organic solvents, such as CHCl3 and THF.
研究领域:
高分子化学
·
配位化学
·
催化化学
·
有机金属化学
·
功能高分子材料
✓ 已验证
DOI
高影响因子
JOURNAL OF MOLECULAR LIQUIDS
·
2020
·
IF 5.065
Yu Dong,Tiantian Ping,Xiaoqin Shi,Shufeng Shen
Nonaqueous amine-based blends have great potential for energy-efficient CO 2 absorbent. In this work, densities and viscosities were measured for liquid binary mixtures of 2-(ethylamino)ethanol (EAE) and 2-(butylamino)ethanol (BAE) with 2-butoxyethanol (EGBE) at temperatures of (293.15–353.15)K over the entire concentration range and atmospheric pressure. Intermolecular interactions between EGBE and two secondary amines with different carbon chain length were discussed. The excess molar volume ( V E ), viscosity deviations ( ∆η ) and excess Gibbs free energy ( ∆G ⁎ E ) were calculated from the experimental data and also correlated with the Redlich-Kister equation to estimate the binary interaction parameters. The experimental data and the calculated from the proposed correlations for the studied binary mixtures matched well each other, with AADs within 0.01% and 1.45% for density and viscosity respectively. The variation of excess properties was also discussed in terms of intermolecular interactions. Weak interactions on mixing these binary mixtures with different mass fractions were observed from the FTIR spectra analysis.
研究领域:
化学工程
·
热力学
·
流体物理化学
·
气体吸收
·
分离科学
✓ 已验证
DOI
高影响因子
Food Analytical Methods
·
2015
·Vol. 9
·期 7
·2026-2035
·
IF 1.956
Du Jiaojiao,Gao Ruixia,Mu Hui
Phthalates represent a potential risk for humans, since they are ubiquitous environmental contaminants. Efficient extraction and purification procedures are demanded for the detection of low concentration levels of phthalates. In this work, a novel type of molecularly imprinted polymers coated onto the surface of vinyl functionalized multi-walled carbon nanotubes was synthesized and coupled with gas chromatography–mass spectrometry (GC/MS) for the selective separation and determination of dioctyl phthalate (DOP) in beverage samples. The morphology, structure property, and thermostability of the resultant polymers were characterized by transmission electron microscopy, Fourier transform infrared spectroscopy, and thermogravimetric analysis. The adsorption properties of the prepared polymers were investigated by equilibrium rebinding and competitive experiments. The resultant imprinted nanomaterials exhibited high capacity and favorable selectivity. In addition, the feasibility of the developed method using the obtained imprinted polymers as a solid-phase sorbent coupled with GC/MS for the selective isolation and determination of DOP in different beverage samples was demonstrated. Under optimal conditions, the limit of detection of the proposed method for DOP was 2.3 ng L −1 . DOP spiked at three levels of concentration in beverage samples was extracted and determined through the application of the present method, with recoveries ranging from 88.6 to 93.0 % with relative standard deviations less than 5.6 %.
研究领域:
分析化学
·
环境毒理学
·
食品安全
·
分子识别
·
材料科学
·
色谱分析
✓ 已验证
DOI
高影响因子
APPLIED SURFACE SCIENCE
·
2017
·
IF 3.387
Xiong Wang,Zhenyou Li,Xiaoyu Han,Zhengang Han,Yongxiao Bai
Porous organic Polymers (POPs) can not only exhibit high specific surface area and pore volume, but also tunable pore size distribution. Herein, copolymers of 2-hydroxyethylmethylacrylate (HEMA) and divinylbenzene (DVB) with specific pore structure were synthesized via a dispersion polymerization strategy, and then immobilized metallocene catalysts with well-defined pore structure were obtained on the produced POP supports. The nitrogen sorption and Gel permeation chromatography (GPC) results demonstrate that the pore structure of the immobilized metallocene catalyst is highly dependent on the pore structure of the POPs , and the pore structure of metallocene catalysts or the POPs has a significant influence on the molecular chain growth of the produced polyethylene. By tuning the distribution of the active species scattered in the micro- and the narrow meso-pore range (roughly ≤4 nm), the chain growth of the polyolefin can be tailored effectively during the polymerization process, although differential scanning calorimetry (DSC) and temperature rising elution fractionation (TREF) results show that the chemical composition distributions (CCDs) of produced PE from the POPs-supported metallocene catalysts are not determined by polymerization activity or molecule chain length, but mainly by the active site species scattered in the supported catalysts. Scanning electron micrograph (SEM) shows that the produced polyethylene has highly porous fabric which consists of nanofiber and spherical beads of micron dimension.
研究领域:
高分子化学
·
催化化学
·
材料科学
·
纳米材料
·
聚合物科学
·
石油化工
✓ 已验证
DOI
高影响因子
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
·
2023
·
IF 8.2
Zhanwei Yang,Jin Wang,Hualei Chen,Hecheng Meng,Xiaobing Guo,Shujuan Yu
Two low-methoxy pectins (LMPs) were obtained by local electrochemical pH modification using an H-type double-layer water bath sealed electrochemical cell at the voltage of 180 V for 3 h. The weight-average molecular weight (Mw) of citrus peel pectin (CPP) prepared in the anodic part at room temperature (CPP-A 5/RT ) and in the cathodic part at 5 °C (CPP-C 5/RT ) were 346 kDa and 328 kDa, respectively, and the degrees of methylation (DM) were 36.8 % and 11.9 %. Moreover, the second-order kinetic model was most appropriate for the degradation processes, as free radicals were generated in the anodic part and β -elimination occurred in the cathodic part. Subsequently, CPP-A 5/RT and CPP-C 5/RT were utilized to fabricate food packaging film blending with polyvinyl alcohol (PVA), bcZnO (ZnO coupled with bentonite and colophony) nanorods , and Ca 2+ ions by casting method. Then the prepared films were studied for their ability to maintain the freshness of strawberries. The addition of Ca 2+ ions and bcZnO nanorods increased the thickness, water contact angle (WCA), and mechanical properties of the composite films, while decreased water vapor permeability (WVP). Therefore, the CPP-based films, supplemented with bcZnO nanorods and crosslinked with Ca 2+ ions by “egg-box” model, can serve as an antibacterial food packaging material for food preservation.
研究领域:
食品科学
·
高分子材料
·
食品包装
·
电化学改性
·
纳米复合材料
·
农产品保鲜
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）