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981.
Peng‐Ju Xia Dan Song Zhi‐Peng Ye Yuan‐Zhuo Hu Jun‐An Xiao Hao‐Yue Xiang Xiao‐Qing Chen Hua Yang 《Angewandte Chemie (International ed. in English)》2020,59(17):6706-6710
A photoinduced SET process enables the direct B?H bond activation of NHC–boranes. In contrast to common hydrogen atom transfer (HAT) strategies, this photoinduced reaction simply takes advantage of the beneficial redox potentials of NHC–boranes, thus obviating the need for extra radical initiators. The resulting NHC–boryl radical was used for the borylation of a wide range of α‐trifluoromethylalkenes and alkenes with diverse electronic and structural features, providing facile access to highly functionalized borylated molecules. Labeling and photoquenching experiments provide insight into the mechanism of this photoinduced SET pathway. 相似文献
982.
Xiaoxiao Wang Yixin Yao Chang An Xi Li Fangtao Xiang Yangli Dong Maosen Li 《Electrophoresis》2020,41(18-19):1606-1616
Chuanxiong Rhizoma is a commonly used in traditional Chinese medicine. Chuanxiong Rhizoma is widely distributed in Sichuan province, China, including the cities of Dujiangyan, Pengzhou, Meishan, Qionglai, and Shifang. However, reports on the comparisons of quality of Chuanxiong Rhizoma of different production origins are limited. Therefore, an ultra-HPLC with triple quadrupole MS method was developed for the determination of 20 bioactive components (12 aromatic acids and eight phthalides) in 36 samples from different production origins and further assessed its quality. The contents of these 20 constituents of samples were analyzed by hierarchical cluster analysis and orthogonal partial least squares discrimination analysis; the result indicated that Chuanxiong Rhizoma of different production origins had some differences. Thirteen constituents of quality difference markers were acquired by variable importance for the project. Furthermore, the sum of the contents of these quality difference markers was different from various production origins of Chuanxiong Rhizoma. Meanwhile, Z-ligustilide and senkyunolide A as main constituents of quality difference markers, the rate of various production origins of Chuanxiong Rhizoma was different. This study provides a foundation for the quality assessment of Chuanxiong Rhizoma. 相似文献
983.
Jihua Liu Huizhu Gan Ting Li Jia Wang Guangguang Du Yang An Xiaojing Yan Cong Geng 《Biomedical chromatography : BMC》2020,34(8):e4856
Ocotillol, pseudo-ginsenoside RT5 (RT5), and pseudo-ginsenoside F11 (PF11) are ocotillol-type saponins that have the same aglycone structure but with different numbers of glucose at the C-6 position. In this study, the metabolites of ocotillol, RT5, and PF11 in rat plasma, stomach, intestine, urine, and feces after oral administration were investigated by ultra-performance liquid chromatography coupled with time-of-flight mass spectrometry. The results showed that RT5 was easily biotransformed into metabolites in vivo, whereas PF11 and RT5 were difficult to be biotransformed. Hydrogenation, dehydrogenation, dehydration, deglycosylation, deoxygenation, hydration, phosphorylation, deoxidation, glucuronidation, and reactions combining amino acid were speculated to be involved in the biotransformation of ocotillol, RT5, and PF11. Based on the structural analysis of metabolites, it was deduced that hydrogenation, dehydration, deoxidation, and reactions combining amino acid occurred on the aglycone structure, whereas deglycosylation, hydration, and phosphorylation occurred on the glycosyl chain. Further, metabolites in plasma, urine, feces, and tissues were different: First, glucuronidation products were found in urine, stomach, intestine, and feces, but not in plasma. Second, the ocotillol prototype was not identified in urine samples. Third, the RT5 prototype was found in stomach, intestine, feces, and urine, but not in plasma. 相似文献
984.
Dr. Huizeng Li Wei Fang Zhipeng Zhao An Li Dr. Zheng Li Prof. Mingzhu Li Prof. Qunyang Li Prof. Xiqiao Feng Prof. Yanlin Song 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(26):10622-10626
Precise separation and localization of microdroplets are fundamental for various fields, such as high-throughput screening, combinatorial chemistry, and the recognition of complex analytes. We have developed a droplet self-splitting strategy to divide an impacting droplet into predictable microdroplets and deposit them at preset spots for simultaneous multidetection. No matter exchange was observed between these microdroplets, so they could be manipulated independently. Droplet self-splitting was attributed to anisotropic liquid recoiling on the patterned adhesive surface, as influenced by the droplet Weber number and the width of the low-adhesive stripe. A quantitative criterion was also developed to judge the droplet self-splitting capability. The precise separation and distribution of microdroplets enabled simultaneous arrayed reactions and multiple analyte detection using one droplet of sample. 相似文献
985.
986.
Guifang Zeng Yining Liu Chunyan Gu Kai Zhang Yongling An Chuanliang Wei Jinkui Feng Jiangfeng Ni 《物理化学学报》2020,36(5):1905006-0
Lithium-ion batteries (LIBs) are widely used in cellphones, laptops, and electric cars owing to their high energy density and long operational lifetime. However, their further deployment in large-scale energy storage systems is restricted by the uneven distribution of lithium resources (~0.0017% (mass fraction, w) in the Earth's crust). Therefore, alternative energy storage systems composed of abundant elements are of urgent need. Recently, sodium-ion batteries (SIBs) have attracted significant attention and are considered to be a potential alternative for next-generation batteries owing to abundant sodium resources (~2.64% (w) of the Earth's crust), suitable potential (−2.71 V), and low cost. SIBs are similar to LIBs in terms of their physical and electrochemical properties. Previous studies have mainly focused on SIB storage materials, including hard carbon, alloys, and hexacyanoferrate, while the safety of SIBs remains largely unexplored. Similar to LIBs, the current electrolytes used in SIBs are mainly composed of flammable organic carbonate solvents (or ether solvents), sodium salts, and functional additives, which pose possible safety issues. Moreover, the chemical activity of sodium is much higher than that of lithium, leading to a higher risk of fire, thermal runaway, and explosion. To overcome this problem, herein we propose a fluorinated non-flammable electrolyte composed of 0.9 mol∙L−1 NaPF6 (sodium hexafluorophosphate) in an intermixture of di-(2, 2, 2 trifluoroethyl) carbonate (TFEC) and fluoroethylene carbonate (FEC) in a 7 : 3 ratio by volume. Its physical and electrochemical properties were studied by ionic conductivity, direct ignition, cyclic voltammetry, and charge/discharge measurements, demonstrating excellent flame-retarding ability and outstanding compatibility with sodium electrodes. The electrochemical tests showed that the Prussian blue cathode retained a capacity of 84 mAh∙g−1 over 50 cycles in the prepared electrolyte, in contrast to the rapid capacity degradation in a flammable conventional carbonate electrolyte (74 mAh∙g−1 with 57% capacity retention after 50 cycles). To test the practical application of the proposed electrolyte, a hard carbon anode was used and exhibited exceptional performance in this system. The enhancement mechanism was further verified by Fourier transform infrared (FTIR), X-ray diffraction (XRD), and scanning emission microscopy (SEM) investigations. Polycarbonate on the surface of the cathode played an important role for the studied electrolyte system. The polycarbonate may originate from FEC decomposition, which can enhance the ionic conductivity of the solid electrolyte interface (SEI) layer and reduce impedance. Hence, we believe that this proposed electrolyte may provide new opportunities for the design of robust and safe SIBs for next-generation applications. 相似文献
987.
核辐射环境中,舰船、坦克的辐射屏蔽特性关乎着核安全、防护、效应评估以及决策应对等实际应用问题。瞄准舰船的核辐射屏蔽性能开展研究。针对舰船材料及典型结构,采用中子-光子耦合输运方法,定量给出中子源、γ源同时辐照下的辐射屏蔽效能。通过借助大规模并行技术,实现了该深穿透屏蔽问题的高效模拟。该辐照屏蔽研究中考虑了入射中子和γ以及次级γ粒子的综合叠加效应。通过模拟中子和γ分别入射不同厚度、不同材料壳体后的注量、剂量、能谱演化,计算获得了屏蔽体的入射中子、入射γ射线、中子和次级γ及其综合屏蔽因子,给出腔内的屏蔽因子分布规律,材料包括Fe、Al、Pb、船体材料HSLA100钢等,辐射源包括单能中子、单能γ以及核泄漏中子谱和γ谱。研究成果将为船体、坦克等的辐射防护性能的深入分析奠定基础,为核辐射效应评估、应急处理等提供理论支撑。 相似文献
988.
依靠光压推进,太阳帆被认为是最可行的星际探测航天器,太阳帆结构总体方案主要有两类:桅杆式和旋转式,其中,帆膜被分割成窄条的条带式太阳帆在桅杆式太阳帆中具有较为理想的结构效率,如何准确计算条带式太阳帆的结构动力学特性值得研究.本文对条带式太阳帆结构的振动特性和结构稳定性进行研究,将太阳帆看作是由若干个桅杆-膜带组件依次连接而成的整体结构,桅杆-膜带组件由4根桅杆段和4条薄膜条带组成,分段轴压作用下的桅杆与薄膜条带耦合振动.考虑帆面薄膜条带与支撑桅杆之间的耦合振动,采用分布传递函数法建立了的条带式太阳帆的结构动力学模型,推导了条带式太阳帆结构自由振动和失稳载荷的求解方法.研究表明:条带式太阳帆构型有利于提高太阳帆结构的整体刚度和结构稳定性,随着帆面薄膜条带数目的增加,太阳帆结构的振动频率和失稳载荷增大;随着帆面薄膜预应力的增大,太阳帆结构振动的基频减小,稳定性变差;随着支撑桅杆刚度的提高,太阳帆结构整体的振动频率和失稳载荷增大.本文建立的解析求解方法具有求解效率快和精度高的特点,为条带式太阳帆的结构设计和姿态控制提供了有力的分析工具. 相似文献
989.
Yanyan An Liping Lu Miaoli Zhu 《Acta Crystallographica. Section C, Structural Chemistry》2019,75(9):1286-1298
Coordination polymers (CPs) with specific structures and functional luminescence have been widely designed as sensors for detecting small molecules and ions. In this study, with or without the help of an N‐donor auxiliary linker, three new ZnII CPs, namely, three‐dimensional (3D) poly[[pentaaquabis[μ3‐5‐(4‐carboxybenzyloxy)isophthalato]bis[μ6‐5‐(4‐carboxylatobenzyloxy)isophthalato]di‐μ3‐hydroxido‐hexazinc(II)] trihydrate], {[Zn6(C16H10O7)2(C16H9O7)2(OH)2(H2O)5]·3H2O}n or {[Zn6(μ3‐HL)2(μ6‐L)2(μ3‐OH)2(H2O)5]·3H2O}n, ( I ), one‐dimensional (1D) catena‐poly[[[aqua(1,10‐phenanthroline)zinc(II)]‐μ2‐5‐(4‐carboxybenzyloxy)isophthalato] dihydrate], {[Zn(C16H10O7)(C12H8N2)(H2O)]·2H2O}n or {[Zn(μ2‐HL)(phen)(H2O)]·2H2O}n (phen is 1,10‐phenanthroline), ( II ), and 3D poly[diaquatetrakis(4,4′‐bipyridine)bis[μ6‐5‐(4‐carboxylatobenzyloxy)isophthalato]di‐μ3‐formato‐di‐μ3‐hydroxido‐pentazinc(II)], [Zn5(C16H9O7)2(HCOO)2(OH)2(C10H8N2)4(H2O)2]n or [Zn5(μ4‐L)2(bpy)4(μ2‐OH)2(μ3‐HCOO)2(H2O)2]n (bpy is 4,4′‐bipyridine), ( III ), have been constructed from the semi‐rigid tricarboxylic acid 5‐(4‐carboxybenzyloxy)isophthalic acid (H3L) under hydrothermal conditions. CP ( I ) exhibits a twofold interpenetrated 3D+3D→3D skeleton with a 3 , 5 ‐conn topology constructed from triangular trinuclear [Zn3(COO)4(μ3‐OH)] clusters, in which the H3L ligand adopts three different coordination modes. CP ( II ) exhibits a 1D infinite chain and stacking that gives a 3D structure mediated by hydrogen bonds and weak interactions. CP ( III ) is an interesting 3D 3 , 4 , 8 ‐conn network including linear tetranuclear [Zn4(μ2‐OH)2(HCOO)2(COO)2] clusters with a new {4·62}2{4·64·8}{46·619·83} topological symbol. The influences of the flexible –CH2–O– linker of the H3L ligand and subtle environmental factors, such as solvent, pH value and auxiliary ligands, on the formation of the final structures are also discussed. The solid‐state fluorescence spectra of CPs ( I )–( III ) were recorded at room temperature and all show better fluorescence performances than H3L. In particular, ( II ) can act as a potential multifunctional fluorescent material for sensing hexavalent chromium ions in aqueous solution with high stability, selectivity and sensitivity. Under ultraviolet light of 365 nm from a UV lamp, a signal response of fluorescence from turning on to off can be observed with the naked eye. It was found that the detection for hexavalent chromium (i.e. Cr2O72?) by ( II ) has a high selectivity [KSV = 1.61 × 104M?1 and limit of detection (LOD) = 0.434 µM] in aqueous solution. Quenching mechanisms were also studied in detail. 相似文献
990.
Nguyen Duc Thinh Vo An Le Le Tran Trung Nghia Le Van Cuong Nguyen Thi Tra My Nguyen Thi Kim Tuyet Nguyen Thai Hoang Nguyen Huu Hieu 《Vietnam Journal of Chemistry》2019,57(4):411-417
Platinum/reduced graphene oxide (Pt/rGO) composite materials with different mass ratios were fabricated by thermal decomposition method from H2PtCl6 and reduce graphene oxide (rGO) as precursors. Pt/rGO composites were used to fabricate Pt/rGO thin film cathodes by using the screen printing technology. The electrochemical properties of the fabricated cathodes were measured using the cyclic voltammetry method. Dye‐sensitized solar cells (DSSCs) were assembled from fabricated cathodes and were measured the performances by current density‐voltage (J‐V) curves and electrochemical impedance spectroscopy (EIS). The results showed the appropriate replacement amount rGO with Pt was 40 %, with the efficiency of 4.73 %, which was higher than that of commercial Pt cathode. The characterizations of the appropriate Pt/rGO composite were investigated by Fourier‐transform infrared spectroscopy (FTIR) and Raman spectroscopy. X‐ray diffraction (XRD) patterns indicated that the interlayer distance between the rGO was 0.35 nm while the transmission electron microscopy (TEM) image showed the Pt nanoparticles with size of 10‐20 nm were evenly distributed on the rGO sheets. These results indicated that Pt/rGO could be appropriated material to replace Pt in DSSCs to reduce the produce cost and enhance the efficiency. 相似文献