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INORGANIC CHEMISTRY · 2022 · IF 5.436

H/F Substitution on the Spacer Cations Leads to 1D-to-2D Increment of the Pyrrolidinium-Containing Lead Iodide Hybrid Perovskites

Meng-Juan Yang,Shu-Yu Tang,Yan-Ran Weng,Feng Zhou,Yu Shi,Yong-Ju Bai,Yong Ai

Hybrid organic–inorganic perovskites (HOIPs) have emerged as multifunctional materials with remarkable optical and electronic properties. In particular, 2D-layered lead iodide-based HOIPs possess great practical application potential in the photoelectric field. In this work, we report H/F substitution-induced 1D-to-2D increment of lead iodide HOIPs. The enantiomeric HOIPs, S- and R-FPPbI3 (FP = 3-fluoropyrrolidinium), were achieved by monofluoride substitution on the spacer cations of the parent HOIP, PyPbI3 (Py = pyrrolidinium), showing mirror image structural relationship and reversible solid-state phase transition. A 2D-layered HOIP, (DFP)2PbI4 (DFP = 3,3-difluoropyrrolidinium), was achieved with a low band gap of 2.09 eV through difluoride substitution, thanks to the expansion of the Pb–I network from 1D to 2D. This work highlights the exploration of 1D chiral and 2D-layered HOIP materials with reversible phase transitions through H/F substitution strategies.

研究领域: 材料科学 · 化学
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CHEMICAL ENGINEERING JOURNAL · 2020 · IF 10.652

Rapid microwave synthesis of Fe3O4-PVP@ZIF-67 as highly effective peroxymonosulfate catalyst for degradation of bisphenol F and its mechanism analysis

Jianan Cui,Tingting Liu,Qian Zhang,Ting Wang,Xiaohong Hou

Various metal-based heterogeneous catalysts activated peroxymonosulfate for organic pollutants degradation are increasingly recognized as an environmentally important sewage treatment technology. In this study, polyvinyl pyrrolidone (PVP) modified Fe 3 O 4 loaded ZIF-67 magnetic catalyst with transition metal cobalt ion was prepared for the first time by microwave-assisted solvothermal (MS) method within 30 min to activate peroxymonosulfate. The microwave synthesis process changed the time-consuming shortcoming of conventional method. The catalytic activity of the synthesized Fe 3 O 4 -PVP@ZIF-67 was assessed on bisphenol F (BPF) removal. The result showed 99.8% BPF was removed under the conditions of catalyst content of 0.15 g·L −1 , PMS content of 0.3 mM, and pH without adjustment in 60 min. And the Fe 3 O 4 -PVP@ZIF-67/PMS system exhibited a quality catalytic performance when the solution pH of BPF varied from 3 to 11. Compared with humic acid (HA), inorganic anions (Cl − , H 2 PO 4 − , SO 4 2− , HCO 3 − , and CO 3 2− ) showed slight effect to the degradation system. The quenching experiment verified that the main active substance in this system was SO 4 − •. Based on the degradation intermediates identified by gas chromatography-mass spectrometer (GC–MS), the main degradation pathways were proposed for the degradation of BPF. Overall, Fe 3 O 4 -PVP@ZIF-67 as PMS activator is promising catalyst for sulfate radical-based wastewater treatment.

研究领域: 环境科学 · 化学工程 · 材料科学
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SEPARATION AND PURIFICATION TECHNOLOGY · 2021 · IF 7.312

Reactive distillation of tertiary olefin etherification for the purification of C8 α-olefin from F-T synthetic products

Tongtong Ren,Suli Liu,Hong Li,Angui Zhang,Xingang Li,Wei Yuan,Xin Gao

Utilization of F-T synthetic to produce value-added C 8 linear α-olefin is a promising alternative approach, however, the purification of α-olefin from F-T synthetic products is a great challenge, especially for removing 2-methyl-1-heptene (MH). This article addresses the novel method of etherification reaction to remove MH from F-T synthetic products, and develop by far the most efficiency reactive distillation (RD) method to intensified the etherification process. The scarcity of thermodynamic data was measured and regressed by the activity coefficient models, furthermore, kinetics of the etherification reaction of MH with methanol was explored using an ion exchange resin as catalyst, and then fitted by a pseudo-homogeneous model. The pilot-scale RD experimental results show that the conversion of MH reaches 91.83 % and the purity of α-olefin increases by 14.9 wt% (percentage points). Process analysis method was used to realize the optimization of design and operating parameters of etherification RD column based on the developed rigorous model. The optimization results show that the conversion of MH achieves 99.74 % and the purity of α-olefin achieves 96.87 wt%, which is also illustrated that the novel method for removing MH is proposed paving the way for purification of α-olefin from F-T synthetic products.

研究领域: 化学工程 · 石油化学
✓ 已验证 DOI 高影响因子
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JOURNAL OF ORGANIC CHEMISTRY · 2023 · IF 3.6

Anion-Driven C–F Bond Activation of Trifluoromethyl N-Aryl Hydrazones: Application to the Synthesis of 1,3,4-Oxadiazoles

Qijie Zou,Wei Zhang,Haoyue Wang,Guangwei Yin,Yongzhi He,Fangyi Li

The CF3 group attached to N-aryl hydrazone could be activated upon treatment with a suitable base, thus serving as an excellent C1 unit for the assembly of a series of 1,3,4-oxadiazoles by reaction with hydrazides. The transformation is proposed to proceed via the intermediate formation of a gem-difluorinated azoalkene. Furthermore, this reaction features simple conditions and a broad substrate scope with respect to both trifluoromethyl N-aryl hydrazones and hydrazides.

CAS / MDL: 30516-87-1
研究领域: 有机化学 · 合成化学
✓ 已验证 产品关联 DOI PubMed 高影响因子
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INORGANIC CHEMISTRY · 2022 · IF 5.436

From Ba3Nb2O2F12(H2O)2 to Ba0.5NbO2F2(H2O): Achieving Balanced Nonlinear Optical Performance by O/F Ratio Regulation

Mei Yan,Ru-Ling Tang,Wenlong Liu,Sheng-Ping Guo

Metal oxyhalides have attracted extensive attention as fascinating nonlinear optical (NLO) materials. Here, two barium niobium oxyfluorides, Ba3Nb2O2F12(H2O)2 (1) and Ba0.5NbO2F2(H2O) (2), have been obtained by regulating the O/F ratio in Nb–O–F units (NbOF6 pyramids to NbO4F2 octahedra). The overall NLO effect is improved from 1 to 2 with larger second-harmonic generation (SHG) intensities (0.9 to 1.7 × KH2PO4 (KDP)) and maintainable large band gaps (>3.0 eV) by regulating the O/F ratio in Nb–O–F units (1:6 to 4:2).

研究领域: 材料科学 · 光学 · 化学
✓ 已验证 DOI 高影响因子
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COLLOIDS AND SURFACES B-BIOINTERFACES · 2022 · IF 5.999

Fabrication and properties of multi-functional polydopamine coated Cu/F-codoped hydroxyapatite hollow microspheres as drug carriers

Xiaodan Jiang,Xiaowei Liu,Jiayi Cai,Shibo Wei,Yanan Wang,Zhuqing Duan,Zeao Zhou,Ruixue Sun,Xiaofei Qu,Yuanzheng Tang

Due to its excellent bone conductivity and drug adsorption as well as pH-responsive drug release property, hydroxyapatite (HAp) is widely used as a drug carrier in bone repair field. Here, we report for the first time a novel multi-functional polydopamine (PDA) coated Cu/F-codoped HAp (Cu/F-HAp-PDA) hollow microspheres . Both Cu 2+ and F - were successfully doped into the lattice of HAp and uniformly distributed in the shell of hollow microspheres through a one-step hydrothermal synthesis . Then PDA was coated homogeneously on the outer layer of Cu/F-HAp hollow microspheres. Both Cu/F-HAp and Cu/F-HAp-PDA samples displayed high drug loading efficiency and pH responsive drug release behavior. Moreover, the obtained Cu/F-HAp-PDA hollow microspheres exhibited excellent photothermal conversion efficiency and photothermal stability. The molecular dynamics simulations showed that PDA and HAp can form mutual binding mainly through Ca-O bonding, while doxorubicin (DOX) is mainly bound to PDA molecules through hydrogen bonding and π-π stacking interaction.

CAS / MDL: 62-31-7
研究领域: 材料科学 · 生物医学工程
✓ 已验证 产品关联 DOI PubMed 高影响因子
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JOURNAL OF ALLOYS AND COMPOUNDS · 2025 · IF 6.3

ReS2/f-MWCNTs heterojunction for highly selective triethylamine gas sensor working at room temperature: A combined experimental and DFT study

Zhihua Zhao,Shuhan Chen,Qingsheng Shi,Chao Qiu,Lan Wu,Xinhao Zhang,Peijuan Wu,Longqi Yao

People pay more and more attention to their own health and environmental safety, which makes the monitoring and treatment of harmful amines such as triethylamine (TEA) emitted in the industrial process increasingly critical. In order to address this issue, we focus on the heterostructure construction of two-dimensional rhenium disulfide (ReS 2 ) and acid-functionalized carbon nanotubes (f-MWCNTs), using their unique electronic properties and high specific surface area for triethylamine gas detection. The findings demonstrated that, at room temperature (25°C), the ReS 2 /f-MWCNTs sensor's response to 100 ppm TEA reached 63 %. Under the same environmental conditions (25℃), the response value of the ReS 2 sensor to 100 ppm TEA is 6 %, and the sensing performance is improved by more than 10 times. In addition, the sensor has fast response recovery (73 s/46 s) and good repeatability and stability. Based on this research, we designed a simple detection device, providing a direction for the practical detection application of TEA sensors.

研究领域: 材料科学 · 纳米技术 · 气体传感 · 环境监测 · 电子器件
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OPTICAL MATERIALS · 2021 · IF 3.08

Alkali-assisted synthesis of gourd flesh derived tricolor F/N co-doped carbon dots for efficient degradation of organic dyes

Congling Wang,Jun Xu,Huizhi Li,Weilin Zhao

A novel tricolor F/N co-doped CDs was synthesized by alkali-assisted control with gourd flesh as a precursor, targeting at the catalytic degradation of organic dyes with extremely high catalysis rate. The synthesized nanomaterials were characterized by X-ray diffraction, Transmission electron microscopy , Fourier transform infrared spectra and X-ray photoelectron spectroscopy techniques, indicating that the tricolor F/N-CDs have good dispersion and abundant surface defects which were gradually increasing from F/N-G-CDs, F/N-Y-CDs to F/N- O -CDs. Through the UV–visible and fluorescence spectra , the tricolor F/N-CDs all exhibited good fluorescence performance and the fluorescence lifetime was nano-scale level. The tricolor F/N-CDs displayed excellent photocatalytic activity which was evaluated by the organic dyes methylene blue (MB) and congo red (CR) as models. The important thing is that under sunlight irradiation, the degradation efficiency of using tricolor F/N-CDs for MB reaches ~100% and the degradation efficiency for CR dye reaches ~98% in a pole short time. With the red shift of the fluorescent tricolor F/N-CDs, the degradation time gradually decreased and the degradation rate gradually increased. The results explained that the prepared tricolor F/N-CDs had excellent application prospects in the natural degradation.

CAS / MDL: 1310-73-2
研究领域: 材料科学 · 环境科学
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JOURNAL OF PHYSICS D-APPLIED PHYSICS · 2023 ·Vol. 56 ·期 29 ·294003 · IF 3.4

On the dielectric properties of bisphenol A and F epoxy resins blends based on molecular dynamics

Y F Wang,B X Du,X X Kong,Fan Li,Xin Lin

Bisphenol A and F epoxy resins are often used as the primary insulation in power equipment. This paper investigates the influence of network structure on the dielectric properties of bisphenol A, bisphenol F epoxy resin and their blends. The results show that substituting isopropyl with methylene in epoxy resin enhances the molecular chain packing efficiency, thus limiting the polarization effect while reducing glass transition temperature (Tg). As the content of bisphenol F resin in the blends increases, the polarization loss of the blends continues to decrease, to even lower than that of bisphenol F resin. For the blend containing 20% bisphenol F resin, the Tg and AC breakdown strength at high temperatures are higher than that of bisphenol A resin. Furthermore, based on molecular dynamics simulation, the reason for the limited polarization effect of the blends is further discussed.

研究领域: 材料科学 · 电气工程
✓ 已验证 DOI 高影响因子
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CHEMICAL RESEARCH IN CHINESE UNIVERSITIES · 2017 ·Vol. 33 ·期 2 ·187-193 · IF 1.024

Synthesis and biological evaluation of pyrano[2,3-f]chromene-4,8-dione derivatives as potential anticancer agents

Li Hongshuang,Wu Xiaming,Zhang Ruize,Hao Liqiang,Duan Guiyun,Xiao Yuliang,Xia Chengcai,Li Furong,You Guirong,Han Junfen

Based on the hit 5-hydroxy-2-methyl-10-propyl-2,3-dihydro-4 H ,8 H -pyrano[2,3- f ]chromene-4,8-dione( 1 ), a series of pyrano[2,3- f ]chromene-4,8-dione derivatives was designed and synthesized using phloroglucinol as starting material. Meanwhile, a regioselective synthetic route was developed for 5-methoxy-2,3-dihydro-4 H ,8 H -pyrano-[2,3- f ]chromene-4,8-dione products( 11 a― 11 f), and their structures were further confirmed by nuclear Overhauser effect(NOE). The evaluation of anticancer activities of these compounds against four human cancer cell lines, including human glioma cell line (SHG-44), human lung cancer cell line(H1299), breast cancer cell line(MCF7) and human colon carcinoma cell line(HCT-116) in vitro shows that 5-methoxy-2,2-dimethyl-9-chloro-10-trifluormethyl-2,3-dihydro-4 H ,8 H -pyrano-[2,3- f ]chromene-4,8-dione( 11 e) possesses the best anticancer activities with IC 50 values of 6.68, 7.90, 5.16 and 4.82 μmol/L, respectively. Finally, the preliminary structure-activity relationships(SARs) were summarized, which could pave the way for generating more potent anticancer agents with drug-like properties.

研究领域: 药物化学 · 肿瘤学
✓ 已验证 DOI 高影响因子
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ELECTROCHIMICA ACTA · 2019 · IF 5.383

Effect of Mg2+/F− co-doping on electrochemical performance of LiNi0.5Mn1.5O4 for 5 V lithium-ion batteries

Aijia Wei,Wen Li,Qian Chang,Xue Bai,Rui He,Lihui Zhang,Zhenfa Liu,Yanji Wang

Mg 2+ /F − co-doped LiNi 0.5 Mn 1.5 O 4 cathode material was synthesized by a facile one-step solid-state process. The effect of Mg 2+ /F − co-doping on grain morphology, phase structure, and electrochemical properties was studied by a series of characterizations. Scanning-electron-microscopy images show that Mg 2+ /F − co-doped LiNi 0.5 Mn 1.5 O 4 (denoted LNMO-MF) particles grow larger than pure LiNi 0.5 Mn 1.5 O 4 particles. X-ray diffraction, Raman spectra , Fourier transformation infrared spectroscopy , X-ray photoelectron spectroscopy, and cyclic-voltammetry tests indicate that all samples mainly display a Fd -3m space group and more Mn 3+ ions in the LNMO-MF sample after Mg 2+ /F − co-doping, which is conducive to increasing the cationic disorder degree and enhancing the electronic conductivity of electrode material. Results show that the LNMO-MF cathode material delivers an excellent rate performance with discharge capacities of 142, 144, 140 136, 132, 124, 115, and 100 mAh g −1  at 0.2, 0.5, 1, 2, 3, 5, 7, and 10C (1C = 140 mAh g −1 ), respectively. Remarkably, LNMO-MF also shows cycling stability with a capacity retention of 86.2% at 5C after 400 cycles, which is much higher than that of pure LiNi 0.5 Mn 1.5 O 4 (67.7%). The improvement of LNMO-MF's electrochemical properties could be ascribed to the Mg 2+ /F − co-doping, delivering a more stable structure, better crystallinity , the highest Li + diffusion coefficient , and the lowest charge-transfer resistance.

研究领域: 材料科学 · 电化学 · 无机非金属材料 · 能源存储 · 锂离子电池 · 固态化学 · 功能材料
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ENVIRONMENTAL POLLUTION · 2022 · IF 9.988

F–53B induces hepatotoxic effects and slows self-healing in ulcerative colitis in mice

Caihong Wang,Zihong Pan,Yuanxiang Jin

Chlorinated polyfluorinated ether sulfonate (F–53 B) is a distinct substitute for perfluorooctane sulphonate. It has been reported to be biologically toxic to mammals, causing enteric toxicity, liver toxicity and neurotoxicity. However, studies about the effects of F–53 B on patients with gastrointestinal diseases such as inflammatory bowel disease are very limited. In this study, whether the toxic impacts of F–53 B on the gut and liver can be exacerbated in mice with colitis was explored. The sensitivity of mice with acute colitis caused by dextran sulfate sodium salt (DSS) to F–53 B was compared with that of healthy mice. The mice were administered water containing F–53 B at doses of 10 and 100 μg/L sequentially for two weeks, respectively. F–53 B exposure exacerbated DSS-induced colonic inflammation, including inducing shortening of colon length, inflammatory cell infiltration and more severe histopathological symptoms. In addition, F–53 B administration significantly increased the levels of inflammatory cytokines, including interleukin (IL)-1, IL-6 and tumour necrosis factor-α, in the plasma of mice with enteritis compared with control group. F–53 B impaired intestinal integrity of mice with colitis by downregulating Claudin-1 and antimicrobial peptide-related genes while elevating serum lipopolysaccharide levels. In addition, in mice with colitis, F–53 B increased the levels of serum total cholesterol, triglyceride, low-density lipoprotein cholesterol, aspartate aminotransferase, and alanine aminotransferase, resulted in more severe liver inflammation and increased the level of genes related to the Gasdermin D-mediated pyrolysis . Conclusively, our results indicated that F–53 B delayed the self-healing of ulcerative colitis (UC) and caused liver inflammation in mice. This study provided some new insights into the health risks of F–53 B and raises concerns about the health of individuals with UC.

CAS / MDL: 9011-18-1
研究领域: 毒理学 · 胃肠病学 · 免疫学 · 肝病学
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