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981.
Volodymyr Babizhetskyy Volodymyr Levytskyi Régis Jardin Josef Bauer Roland Guérin Régis Gautier Bruno Fontaine Jean-François Halet 《无机化学与普通化学杂志》2020,646(14):1168-1175
Two novel ternary borosilicides R9Si15–xB3 (R = Tb, x = 1.80, R = Yb, x = 1.17) were synthesized from the initial elements using tin flux method. Their crystal structures were determined by means of X-ray single crystal diffraction. Both refer to space group R32, Z = 1: a = 6.668(2) Å, c = 12.405(4) Å [R1 = 0.027, wR2 = 0.031 for 1832 reflections with Io > 2σ (Io)] for Tb9Si15–xB3, and a = 6.5796(3) Å, c = 12.2599(5) Å [RF = 0.052, wR = 0.090 for 1369 reflections with Io > 2σ (Io)] for Yb9Si15–xB3. The structures represent a new structure type, derived from that of AlB2, with ordering in the metalloid sublattice resulting in distorted [Si5B] hexagons. The presence or absence of boron in this ordered structure is discussed on the basis of difference Fourier syntheses, interatomic distances, structural analysis, and theoretical calculations in relation with the parent structures of the binaries AlB2 and Yb3Si5 (Th3Pd5 type of structure). Theoretical calculations show substantial covalent interactions between the metal and nonmetal elements. The small percentage of silicon atoms, which are missing in these nonstoichiometric compounds, probably allows strengthening boron-metal and boron-silicon bonding. 相似文献
982.
Zhen Zhang Ying-Lin Gu Zheng-Yang Wang Huan-Nan Wang Yan Zhao Xue-Mei Chu Chun-Yan Zhang Mao-Cai Yan 《Journal of heterocyclic chemistry》2020,57(3):1165-1172
Novel indole amide derivatives C1-C10 were successfully synthesized and characterized by 1H NMR, 13C NMR, IR, MS, and elemental analysis, and their molecular formulas were C14H10N6O, C13H10N4O, C16H13N3O2, C19H14N2O2, C16H11N3OS, C15H13N3O, C12H9N5O, C16H10ClN3OS, C15H17N3O2, and C13H14N2O3, respectively. The primary biological activities of these compounds were evaluated in vitro by the DPPH assay, H2O2-induced oxidative stress injury assay, and cytotoxicity assay. The results indicated that compounds C1, C2, C4, C7, and C9 exhibited DPPH·scavenging ability, while C3, C4, C5, and C8 showed potent growth-inhibitory activities against various human tumor cells, including MDA-MB-231, Hela, A549, and HT29. Interestingly, compound C4 showed potent scavenging effects on the DPPH radical and possessed protective effect on H2O2-induced oxidative stress injury in human neuroblastoma SH-SY5Y cells at low concentrations; however, C4 exhibited significant toxicity against four human tumor cells at a higher concentration in all treatments, and the range of IC50 value was 7.91 to 13.35 μM. 相似文献
983.
Youshan Li Dr. Zhenbang Lou Hongyun Li Dr. Haijun Yang Prof. Dr. Yufen Zhao Prof. Dr. Hua Fu 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(9):3700-3706
A bioorthogonal ligation and cleavage method via reactions of chloroquinoxalines (CQ) and ortho-dithiophenols (DT) is presented. Double nucleophilic substitutions of ortho-dithiophenols to chloroquinoxalines provide conjugates containing tetracyclic benzo[5,6][1,4]dithiino[2,3-b]quinoxaline with strong built-in fluorescence together with release of the other functional molecules. Three cleavable linkers were designed and successfully used in release of the molecules containing biotin from the protein conjugates. The CQ-DT bioorthogonal reactions can be applied for the bioorthogonal ligations, bioorthogonal cleavages, and trans-tagging of proteins, and show advantages of readily accessible unnatural orthogonal groups, appealing reaction kinetics (k2≈1.3 m −1 s−1), excellent biocompatibility of orthogonal groups, and high stability of conjugates. This complements previous bioorthogonal reactions and is a new route for protein-fishing applications and in-gel fluorescence analysis. 相似文献
984.
Prof. Shuaijun Yang Ping-An Yin Lin Li Prof. Qian Peng Prof. Xinggui Gu Prof. Ge Gao Prof. Jingsong You Prof. Ben Zhong Tang 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(25):10222-10228
Squaraines (SQs) with tunable emission in the solid state is of great importance for various demands; however a remaining challenge is emission quenching upon aggregation. Herein, a unique SQ, named as CIEE-SQ, is designed to exhibit strong emission in crystal, undergoing crystallization-induced reverse from dark 1(n+σ,π*) to bright 1(π,π*) excited states. Such an excited state of CIEE-SQ can be subtly tuned by molecular conformation changes during the unexpected temperature-triggered single-crystal to single-crystal (SCSC) reversible transformation. Furthermore, co-crystallization between CIEE-SQ and chloroform largely stabilize the 1(π,π*) state, enhancing the transition dipole moment and decreasing the reorganization energy to boost the fluorescence, which is promising in data encryption and decryption. 相似文献
985.
Arnar Guðmundsson Kim Elisabeth Schlipköter Prof. Dr. Jan-E. Bäckvall 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(13):5441-5444
We report the first FeII-catalyzed biomimetic aerobic oxidation of alcohols. The principle of this oxidation, which involves several electron-transfer steps, is reminiscent of biological oxidation in the respiratory chain. The electron transfer from the alcohol to molecular oxygen occurs with the aid of three coupled catalytic redox systems, leading to a low-energy pathway. An iron transfer-hydrogenation complex was utilized as a substrate-selective dehydrogenation catalyst, along with an electron-rich quinone and an oxygen-activating Co(salen)-type complex as electron-transfer mediators. Various primary and secondary alcohols were oxidized in air to the corresponding aldehydes or ketones with this method in good to excellent yields. 相似文献
986.
利用新的单中心Ziegler-Natta(Z-N)催化剂,通过干预分子链的生长与聚集行为,可获得低缠结的超高分子量聚乙烯(UHMWPE)初生树脂.本研究利用这类低缠结UHMWPE,通过设置不同的烧结温度(Ts)来改变熔体缠结状态,并探讨了链缠结程度对烧结制品结构与性能的影响.实验结果表明TS=220℃下,UHMWPE样品发生显著的复缠,造成高缠结度;而Ts=170℃下,初始低缠结状态能够得以充分保留,从而获得了缠结度具有明显差别的不同样品.示差扫描量热法(DSC)测试表明,在Ts=170℃下,低缠结度有利于在随后等温及冷却结晶过程中生成高熔点(最高达141℃)晶体与高的结晶度(最高达65%).力学测试表明低缠结度制品的综合力学性能显著提升,其中屈服强度提高72%,拉伸断裂强度提升139%,弹性模量提升162%以及断裂伸长率提升36%,实现了同时增强增韧.这就提供了一种从调节链缠结温度实现UHMWPE烧结制品高性能化的新思路. 相似文献
987.
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
988.
989.
Jianyang Hu Dongying Fu Chunli Xia Chi Zhang Lishuang Yao Chunlian Lu 《Liquid crystals》2020,47(4):508-515
ABSTRACTThis letter reports the optical pumped lasing behaviours of a three-layer Bragg resonance cavity consisting of dye-doped cholesteric liquid crystal (DDCLC) microdroplet, polyglycerol-2 and hollow glass microsphere. The function of PG2 is to control the parallel anchoring of the liquid crystal (LC) molecules on the surface of the LC microdroplet. The whispering-gallery mode (WGM), radial Bragg (photonic bandgap, PBG) mode and Bragg WGM (BWGM) are observed in DDCLC microspheres with different helical pitches and LC refractive indices. The formation mechanisms of six types of lasing emission conditions are analysed in detail. The study results present the prospect of controlling the output mode of the laser. Furthermore, such solid shell-based DDCLC microspheres have outstanding potential applications in miniaturised 3D Bragg lasers, sensors, and integrated and tunable optical devices. 相似文献
990.
ABSTRACTWe propose an adaptive nematic liquid crystal (LC) lens array using a dielectric layer with low dielectric constant as resistive layer. With the resistive layer and periodic-arranged iridium tin oxide (ITO) electrodes, the vertical electric field across the LC layer varies linearly over the lens aperture is obtained in the voltage-on state. As a result, a centrosymmetric gradient refractive index profile within the LC layer is generated, which causes the focusing behaviour. As a result of the optimisation, a thin cell gap which greatly reduces the switching time of the LC lens array can be achieved in our design. The main advantages of the proposed LC lens array are in the comparatively low operating voltage, the flat substrate surface, the simple electrodes, and the uniform LC cell gap. The simulation results show that the focal length of the LC lens array can be tuned continuously from infinity to 3.99 mm by changing the applied voltage. 相似文献