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JOURNAL OF PORPHYRINS AND PHTHALOCYANINES · 2022 · IF 1.914

p-Toluenethiolate manganese(II) porphyrin complexes: Structure and spectroscopic properties

Yiwen Yuan,Jianping Zhao,Jianfeng Li

Utilizing tetraphenylporphyrin (TPP), tetratolylporphyrin (TTP), tetramesitylporphyrin (TMP), and tetra- p -chlorophenylporphyrin (T p ClPP) as ligands, several five-coordinate high-spin p -toluenethiolate Manganese(II) complexes are isolated and studied by UV-vis, single-crystal X-ray and EPR spectroscopies. The crystal structures show noteworthy features including flexible axial p -toluenethiolate ligands and intramolecular C−H ⋅ ⋅ ⋅ π and π - π interactions between ligands and porphyrin planes. All four products are further studied by X-band EPR on both solid and solution states at 4 K which confirmed the S = 2/5 high-spin states. Temperature-dependent EPR and measurements with different equivalents of ligands are also reported for comparison. The work provides new references for the study of the active center of P450s and the biochemical reaction between cysteine residues and heme.

CAS / MDL: 1310-58-3 106-45-6
研究领域: 生物化学 · 配位化学 · 结构化学
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SENSORS AND ACTUATORS B-CHEMICAL · 2016 · IF 4.758

Introducing p-n junction interface into enzyme loading matrix for enhanced glucose biosensing performance

Sisi Fan,Minggang Zhao,Longjiang Ding,Ye Ma,Jingjing Liang,Xingtao Wang,Yawen Song,Shougang Chen

Eggshell membranes were used as biotemplate to fabricate a 3D hierarchical porous Co 3 O 4 /ZnO p-n junction film. Multiple catalysis and accelerated electron transfer were achieved on the Co 3 O 4 /ZnO-GOx electrode by introducing the p-n junction interface into enzyme loading matrix. A stable and well-defined oxidation peak of glucose was obtained with a largely decreased detection potential of 0.25   V. Furthermore, an enhanced sensitivity (116.64   μA·mM −1 ·cm −2 ) was also achieved comparing with the simple biotemplate-synthesized Co 3 O 4 and ZnO film. The results demonstrated it is a novel strategy to improve the biosensing performance by introducing p-n junction interface into enzyme loading matrix.

CAS / MDL: 9012-76-4
研究领域: 生物化学 · 材料科学
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Journal of Inorganic and Organometallic Polymers and Materials · 2025 · IF 4.9

Effect of 2D-MOFs on Dielectric Properties of P(VDF-HFP) Films

Zhang Siqi,Wu Shu,Li Jinglei,Wang Qi,Yang Bowen,Guan Mengxiang,Peng Guirong,Zhao Xiaojia

The ferroelectric polymer PVDF and its copolymer have garnered significant attention in the field of dielectric energy storage due to their high permittivity and high breakdown strength. However, their high dielectric loss limits their application in the field of energy storage. Thus, reducing the dielectric loss of films while maintaining a high permittivity presents a challenge. In this paper, NiBDC and CuBDC were synthesized via solvothermal method and added into P(VDF-HFP) films, respectively. The effect of MOFs on the structure and dielectric properties of P(VDF-HFP) films were investigated. The results showed that the addition of MOFs could significantly increase the crystallization temperature while decreasing crystallinity and crystal size of the films. Tanδ decreased from 0.059 to 0.042 (10 k Hz, 18 °C) for the film with 10% CuBDC addition as coordinatively unsaturated metal centers in MOFs acted as electron traps that reduced tanδ and conductivity of the films. In addition, for the film with 1% CuBDC, the breakdown strength increased from 341.5 MV/m to 369.5 MV/m, the efficiency of the films increased from 87.7 to 93.9%.

研究领域: 材料科学 · 能源存储
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Journal of Energy Storage · 2023 · IF 9.4

P-doped S vacancy-rich NiCo2S4 hollow microspheres for high-performance supercapacitors

Xing Chen,Haijun Tao,Yinhua Jiang,Shishi Li,Yuxin Liu,Kun Xie,Yuqiao Wang

P-doped S vacancy-rich NiCo 2 S 4 hollow microspheres (P-NiCo 2 S 4-x HMSs) were prepared by hydrothermal, sulfuration, and phosphorization methods. P doping and S vacancy dual defects can be simultaneously obtained during the phosphorization process. The dual defects can modulate the electron structure and create abundant electrochemical sites, boosting electron transfer and reaction kinetics. Theoretical calculations illustrated that the dual defects could reduce the adsorption energy of OH − and Mulliken charges of Ni atoms, in favor of OH − adsorption. The hollow construction can increase the specific surface area, promote ion diffusion, and alleviate the volume variation during charge/discharge processes. The specific capacity and rate capability of the P-NiCo 2 S 4-x HMSs electrode can reach up to 1146.0 C g −1 at 1 A g −1 and 61.8 % at 30 A g −1 , respectively. The P-NiCo 2 S 4-x HMSs electrode exhibited remarkable cycling stability with a 79.5 % capacity retention after 20,000 consecutive charge/discharge cycles. The assembled P-NiCo 2 S 4-x //AC hybrid supercapacitor manifested an infusive energy density of 62.7 Wh kg −1 at 867 W kg −1 .

研究领域: 材料科学 · 能源存储与转换
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Minerals · 2021 ·Vol. 11 ·期 2 ·105 · IF 2.644

Adsorption of p-Arsanilic Acid on Iron (Hydr)oxides and Its Implications for Contamination in Soils

Yifan Yang,Shiyong Tao,Zhichun Dong,Jing Xu,Xiang Zhang,Guoyan Pan

Because of the diversification of industries in developing cities, the phenomenon of the simultaneous contamination of various kinds of pollutants is becoming common, and the environmental process of pollutants in multi-contaminated environmental mediums has attracted attention in recent years. In this study,p-arsanilic acid (ASA), a kind of organic arsenic feed additive that contains the arsenic group in a chemical structure, is used as a typical contaminant to investigate its adsorption on iron oxides and its implication for contaminated soils. The adsorption kinetics on all solids can be fitted to the pseudo-second-order kinetic model well. At the same mass dosage conditions, the adsorption amount per unit surface area on iron oxides follows the order α-FeOOH > γ-Fe2O3> α-Fe2O3, which is significantly higher than that for actual soil, because of the lower content of iron oxides in actual soil. Lower pH conditions favor ASA adsorption, while higher pH conditions inhibit its adsorption as a result of the electrostatic repulsion and weakened hydrophobic interaction. The presence of phosphate also inhibits ASA adsorption because of the competitive effect. Correlations between the amount of ASA adsorption in actual soil and the Fe2O3content, total phosphorus content, arsenic content, and organic matter content of actual soil are also investigated in this work, and a moderate positive correlation (R2= 0.630), strong negative correlation (R2= 0.734), insignificant positive correlation (R2= 0.099), and no correlation (R2= 0.006) are found, respectively. These findings would help evaluate the potential hazard of the usage of organic arsenic feed additives, as well as further the understanding of the geochemical processes of contaminants in complicated mediums.Keywords:p-arsanilic acid;iron oxides;soil contamination;adsorption

CAS / MDL: 50-78-2 1309-37-1
研究领域: 环境科学 · 化学
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CHEMICAL ENGINEERING JOURNAL · 2022 · IF 16.744

EDTA enhances the photodegradation of p-arsanilic acid in the presence of iron at near-neutral pH

Chuxuan Zhao,Zixin Liu,Yi Wu,Juntao Guo,Peng Huang,Yifei Wang,Yeheng Leng,Ivan P. Pozdnyakov,Jing Xu,Feng Wu

The widespread used organic arsenic pesticides and veterinary drugs have drawn attention for decades. Its photochemical transformation in the surface water contributes to its degradation and the formation of products. The effect of co-existent components like anthropogenic reagents (e.g. ethylenediaminetetraacetatic acid, EDTA) on the photochemical transformation has still to be investigated in depth. Fe(III)-EDTA complex is a common and abundant complex in surface water. In this work, UVA light and simulated sunlight have been used as light sources to explore the effect of Fe(III)-EDTA on the photodegradation of p -arsanilic acid (ASA), used as an organic arsenic feed additive. Whereas ASA hardly absorbs UVA light and can only be directly photolyzed by simulated sunlight, the Fe(III)-EDTA complex is photoactive under either light source. At pH 6, the presence of Fe(III)-EDTA complex enhances the photodegradation efficiency of ASA from 0% to ca. 23% after 180 min reaction under UVA light irradiation, and from 30% to ca. 58% after 45 min reaction under simulated sunlight irradiation. Appropriate amount of EDTA enhances the photodegradation efficiency, whereas excessive EDTA suppresses the initial reaction rate. Mechanistic study has revealed contributions from direct photolysis and photochemical reactions of Fe(III)-EDTA and Fe(III)–OH complexes. Generated •OH has been confirmed as the important contribution. Photodegradation products include inorganic arsenic, organic arsenic, and other organic by-products, and the proportions of these products vary in different light-induced systems due to the diverse reaction pathways. The results of this work improve our understanding of the risks of residual ASA in the environment, allow prediction of its migration and transformation, and show how organic arsenic livestock and poultry feed additives might be removed.

研究领域: 环境科学 · 化学
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APPLIED SURFACE SCIENCE · 2025 · IF 6.9

Highly Sensitive Triethylamine Sensors Enabled by Co3O4/ZnO p-n Heterojunctions

Lin Wang,Haili Huang,Dongdong Zhang,Hung-Chun Wu,Meiling Li,Huilin Hou,Weiyou Yang,Xuhui Yu,Zonghua Wang

Triethylamine (TEA) is a typically volatile organic compound that poses significant environmental and health risks, due to its high toxicity and volatility. Currently, the exploration of TEA sensors based on semiconductor ZnO is still suffered by their intrinsically low sensitivity, slow response/recovery times, and poor selectivity. Herein, we develop the highly-sensitive TEA sensors based on rationally-designed Co 3 O 4 /ZnO p-n heterojunctions, in which the clustered Co 3 O 4 are incorporated into porous ZnO nanosheets. As a result, at the given operating temperature of 260 °C, the as-constructed sensors exhibit an overall enhanced performance with an excellent response of 140.5 to 100 ppm TEA, swift response/recovery times of 6/60 s and high selectivity, representing their promise toward practical applications in advanced TEA sensors.

CAS / MDL: 121-44-8 57-13-6
研究领域: 材料科学 · 环境科学 · 化学传感器
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MATERIALS & DESIGN · 2016 · IF 3.997

Synthesis and characterization of cross-like Ni-Co-P microcomposites

Yuhua Yan,Yanping Tian,Meifeng Hao,Yuqing Miao

The cross-like crystallines of Ni-Co-P microcomposites were synthesized via a simple hydrothermal method under high pressure and temperature which is adapted from the classical electroless deposition technique for surface modification. Here hypophosphite was employed as reductant and phosphorus resource to prepare the composites of Ni, Co and P elements. The obtain Ni-Co-P microcomposites were characterized in morphology, composition and properties. They show the perfect cross-like shape with an approximate stoichiometry of Ni 12 -Co 6 -P 12 -O 70 . The high absorbance in UV area and wide absorbance in vis area are observed. They also exhibit superparamagnetic behavior and hydrogen evolution property.

研究领域: 材料科学 · 化学
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ACS Omega · 2023 · IF 4.1

Differentiated Fractionation of Various Biomass Resources by p-Toluenesulfonic Acid at Mild Conditions

Shaohua Fang,Qiuli Xia,Lin Zhang,Peng Zhan,Yan Qing,Zhiping Wu,Hui Wang,Lishu Shao,Na Liu,Jiaying He,Jin Liu

Biomass is the ideal substitute for petrochemical resources because of its renewable and abundant sources. p-Toluenesulfonic acid (p-TsOH) can effectively separate lignin from biomass under mild conditions, so it is highly expected in biomass fractionation to improve the utilization efficiency. In this study, we investigated the effect of p-TsOH differentiated fractionation of poplar sawdust, eucalyptus sawdust, and rice straw below 100 °C. According to the experimental results, upon pretreatment by p-TsOH of the three kinds of raw biomass, most of the lignin and hemicellulose of poplar sawdust and eucalyptus sawdust were removed, whereas the cellulose was retained, but most of the hemicellulose and cellulose of rice straw were kept, whereas the lignin was removed at similar conditions. The structures and compositions of pretreatment residues, lignin, and hemicellulose extracted from raw biomass were characterized by XRD, FTIR, HSQC-NMR, XPS, and SEM. The differentiated fractionation mechanism of biomass was analyzed. A better recognition and understanding of the factors affecting biomatrix opening and fractionation will allow for the identification of new pretreatment strategies that improve biomass utilization and permit the rational enzymatic hydrolysis of cellulose.

CAS / MDL: 80-41-1
研究领域: 生物化学 · 可再生能源
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MATERIALS & DESIGN · 2020 · IF 6.289

Asymmetric forward osmosis membranes from p-aramid nanofibers

Lei Miao,Tingting Jiang,Shudong Lin,Tao Jin,Jiwen Hu,Min Zhang,Yuanyuan Tu,Guojun Liu

p -Aramid is an ideal building block for forward osmosis (FO) membranes due to its extraordinary thermal resistance, chemical stability, and mechanical properties. However, existing aramid membranes have certain limitations such as large pore diameters and low salt rejection rates. In this work, we describe a facile solvent exchange-delay phase inversion strategy to prepare p -aramid nanofibrous membranes that would be suitable for FO applications. In this strategy, p -aramid nanofibers with an average diameter of 16 ± 4 nm and an average length of 382 ± 89 nm were employed as membrane matrices. Prior to the immersion of the cast film into a coagulation bath, a pre-evaporation protocol was carefully designed and introduced to provide a slower exchange rate between the good solvent and the non-solvent, which delayed the demixing process between p -aramid nanofibers and thus yielded an asymmetric membrane with a denser active layer as well as a loose substrate layer. The resultant membrane showed excellent FO water flux, NaCl rejection ratios, tensile strength, thermal properties, and solvent resistance. The membrane reported in this work may provide a promising candidate for separation applications and the results reported herein will facilitate the development of high-performance nanofibrous membranes.

CAS / MDL: 865-47-4
研究领域: 材料科学 · 环境工程 · 化学工程
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International Journal of Nanomedicine · 2023 · IF 8

Aqueous extract of Rabdosia rubescens leaves: forming nanoparticles, targeting P-selectin, and inhibiting thrombosis

Yuji Wang,Jingcheng Tang,Haimei Zhu,Xueyun Jiang,Jiawang Liu,Wenyun Xu,Haiping Ma,Qiqi Feng,Jianhui Wu,Ming Zhao,Shiqi Peng

The hot water extract of Rabdosia rubescens was traditionally used as an antithrombotic medicine. To explore its antithrombotic utility and mechanism, we carried out a series of in vitro and in vivo assays in this study. In vitro platelet aggregation assay showed that the half maximal inhibitory concentration values of aqueous extract of R. rubescens leaves (AERL) inhibiting platelet aggregation induced by thrombin, arachidonic acid, adenosine diphosphate, and platelet-activating factor ranged from 0.12 mg/mL to 1.43 mg/mL. The minimal effective oral dose of AERL inhibiting the rats from forming thrombus was 25 mg/kg. Both in vitro and in vivo actions were correlated with AERL concentration-dependently inhibiting sP-selectin release. In water, AERL formed nanoparticles, and their size depended on the concentration. Docking the five nucleotides, 21 phenolic acids, and four diterpenoids identified by high-performance liquid chromatography–photodiode array detector/(−)electrospray ionization-tandem mass spectrometry analysis into the active site of P-selectin, rosmarinic acid was predicted to be the antithrombotic ingredient of AERL. In flow cytometry analysis, 1 μM of rosmarinic acid effectively inhibited sP-selectin release in arachidonic acid-activated platelets. In a rat model, 5 mg/kg of oral rosmarinic acid effectively inhibited thrombosis.

研究领域: 药理学 · 分子生物学
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Materials · 2024 ·Vol. 17 ·期 13 ·3046 · IF 3.1

Preparation of Al@FTCS/P(VDF-HFP) Composite Energetic Materials and Their Reaction Properties

Xiang Ke,Lifang Deng,Yanping Wang,Kai Tang,Lei Xiao,Gazi Hao,Peili Li,Xiang Zhou

Strengthening the interfacial contact between the reactive components effectively boosts the energy release of energetic materials. In this study, we aimed to create a close-knit interfacial contact condition between aluminum nanoparticles (Al NPs) and Polyvinylidene fluoride-hexafluoropropylene (P(VDF-HFP)) through hydrolytic adsorption and assembling 1H, 1H, 2H, 2H-Perfluorododecyltrichlorosilane (FTCS) on the surface of Al NPs. Leveraging hydrogen bonding between –CF and –CH and the interaction between C–F⋯F–C groups, the adsorbed FTCS directly leads to the growth of the P(VDF-HFP) coating layer around the treated Al NPs, yielding Al@FTCS/P(VDF-HFP) energetic composites. In comparison with the ultrasonically processed Al/P(VDF-HFP) mixture, thermal analysis reveals that Al@FTCS/P(VDF-HFP) exhibits a 57 °C lower reaction onset temperature and a 1646 J/g increase in heat release. Associated combustion tests demonstrate a 52% shorter ignition delay, 62% shorter combustion time, and a 288% faster pressurization rate. These improvements in energetic characteristics stem from the reactivity activation of FTCS towards Al NPs by the etching effect to the surface Al2O3. Moreover, enhanced interfacial contact facilitated by the FTCS-directed growth of P(VDF-HFP) around Al NPs further accelerates the whole reaction process.

CAS / MDL: 64-17-5 109-99-9 60-29-7
研究领域: 材料科学 · 化学工程
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