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961.
Two new Zn2Dy2 complexes were constructed from Zn (II) salen‐type Schiff base complex fragment and 2,6‐pyridinedimethanol (H2pdm) or its Br‐substituted analogue (4‐bromopyridine‐2,6‐diyl)dimethanol (H2Brpdm); their molecular formulas are [Zn2Dy2(L)2(pdm)2(MeOH)2](ClO4)2 [ 1 , H2L = N, N′‐ bis(3‐methoxysalicylidene)‐1,3‐diaminopropane] and [Zn2Dy2(L)2(Brpdm)2(MeOH)2](ClO4)2 [ 2 ], the Dy (III) ions of which have a NO7 triangular dodecahedral coordination sphere. The two complexes show not only ferromagnetic interaction but also field‐induced single‐molecule magnet (SMM) behavior, which are rare Dy (III)‐containing cluster complexes with the NO7 triangular dodecahedral coordination sphere that can show good magnetic relaxation. The energy barrier value of complex 2 is higher than those of complex 1 and the Dy (III) complexes with the DyNO7 triangular dodecahedral coordination configuration reported in the literature. 相似文献
962.
Zhipeng Lin Hao Zhang Guofeng Liang Yanqi Jin Hongbin Zeng Jiawang Li Jian Chen Weihong Zhang Fangyan Xie Yanshuo Jin Hui Meng 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(12):3112-3118
A composite of FeOOH nanocubes anchored on carbon ribbons has been synthesized and used as a cathode material for Li/O2 batteries. Fe2+ ion-exchanged resin serves as a precursor for both FeOOH nanocubes and carbon ribbons, which are formed simultaneously. The as-prepared FeOOH cubes are proposed to have a core–shell structure, with FeOOH as the shell and Prussian blue as the core, based on information from XPS, TEM, and EDS mapping. As a cathode material for Li/O2 batteries, FeOOH delivers a specific capacity of 14816 mA h g−1cathode with a cycling stability of 67 cycles over 400 h. The high performance is related to the low overpotential of the oxygen reduction/evolution reaction on FeOOH. The cube structure, the supporting carbon ribbons, and the -OOH moieties all contribute to the low overpotential. The discharge product Li2O2 can be efficiently decomposed in the FeOOH cathode after a charging process, leading to higher cycling stability. Its high activity and stability make FeOOH a good candidate for use in non-aqueous Li/O2 batteries. 相似文献
963.
Meng Liu Dr. Hao Fan Dr. Ou Zhuo Xiao Du Longqi Yang Prof. Peng Wang Lijun Yang Prof. Qiang Wu Prof. Xizhang Wang Prof. Zheng Hu 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(15):3843-3848
Molybdenum disulfide (MoS2) is an intensively studied anode material for lithium-ion batteries (LIBs) owing to its high theoretical capacity, but it is still confronted by severe challenges of unsatisfactory rate capability and cycle life. Herein, few-layer MoS2 nanosheets, vertically grown on hierarchical carbon nanocages (hCNC) by a facile hydrothermal method, introduce pseudocapacitive lithium storage owing to the highly exposed MoS2 basal planes, enhanced conductivity, and facilitated electrolyte access arising from good hybridization with hCNC. Thus, the optimized MoS2/hCNC exhibits reversible capacities of 1670 mAh g−1 at 0.1 A g−1 after 50 cycles, 621 mAh g−1 at 5.0 A g−1 after 500 cycles, and 196 mAh g−1 at 50 A g−1 after 2500 cycles, which are among the best for MoS2-based anode materials. The specific power and specific energy, which can reach 16.1 kW and 252.8 Wh after 3000 cycles, respectively, indicate great potential in high-power and long-life LIBs. These findings suggest a promising strategy for exploring advanced anode materials with high reversible capacity, high-rate capability, and long-term recyclability. 相似文献
964.
With the rapid development of nanoscience and nanotechnology, various types of functional nanoreactors have been designed for diverse applications. Here, the recent evolution of the rational design of nanoreactors for chemical synthesis and biomedical applications are briefly summarized and discussed. The presence of nanoreactors provides constrained space isolated from the surrounding environment. Scientists are committed to studying changes in chemical reactions when the reaction system is confined to the nanosized space. Nanoreactors accelerate the reaction rate and even change mechanism of some chemical reactions. Cells and organelles as natural nanoreactors are also discussed. The development of intracellular synthesis makes it possible to realize various applications in biomedicine. The challenges on the rational design of nanoreactors and perspectives are also discussed. 相似文献
965.
Song Zhaorui Yu Lili Sun Yiyang He Hua 《Analytical and bioanalytical chemistry》2019,411(27):7293-7301
Analytical and Bioanalytical Chemistry - A simple, sensitive, and naked-eye assay of metformin (MET), based on the host–guest molecular recognition of cucurbit[6]uril (CB[6])-modified silver... 相似文献
966.
Hui‐Min Lin Jian‐Rong Li Chao Mu Ao Li Xu‐Feng Liu Pei‐Hua Zhao Yu‐Long Li Zhong‐Qing Jiang Hong‐Ke Wu 《应用有机金属化学》2019,33(11)
Five monophosphine‐substituted diiron propane‐1,2‐dithiolate complexes as the active site models of [FeFe]‐hydrogenases have been synthesized and characterized. Reactions of complex [Fe2(CO)6{μ‐SCH2CH(CH3)S}] ( 1 ) with a monophosphine ligand tris(4‐methylphenyl)phosphine, diphenyl‐2‐pyridylphosphine, tris(4‐chlorophenyl)phosphine, triphenylphosphine, or tris(4‐fluorophenyl)phosphine in the presence of the oxidative agent Me3NO·2H2O gave the monophosphine‐substituted diiron complexes [Fe2(CO)5(L){μ‐SCH2CH(CH3)S}] [L = P(4‐C6H4CH3)3, 2 ; Ph2P(2‐C5H4N), 3 ; P(4‐C6H4Cl)3, 4 ; PPh3, 5 ; P(4‐C6H4F)3, 6 ] in 81%–94% yields. Complexes 2 – 6 have been characterized by elemental analysis, spectroscopy, and X‐ray crystallography. In addition, electrochemical studies revealed that these complexes can catalyze the reduction of protons to H2 in the presence of HOAc. 相似文献
967.
968.
Two Pd(II)–NHC complexes bearing benzimidazole and pyridine groups have been successfully prepared and fully characterized by NMR and X‐ray diffraction analysis. The structure of palladium complexes are a typical square‐planar with palladium surrounded by two pairs of trans‐arranged benzimidazole and carbene ligands. The Pd–NHC complexes have been proved to be a highly efficient catalyst for the Mizoroki–Heck coupling reaction of aryl halides with various substituted acrylates under mild conditions in excellent yields. Copyright © 2013 John Wiley & Sons, Ltd. 相似文献
969.
Five novel compounds as potential phosphodiesterase type 5 (PDE‐5) inhibitors were synthesized from D‐tryptophan methyl ester via the Pictet–Spengler reaction and cyclization reaction. The structures of those compounds were confirmed by elemental analyses, IR, 1H NMR, and ESI‐MS spectra. 相似文献
970.
Qian Wang Assoc. Prof. Fuhang Song Dr. Xue Xiao Pei Huang Assoc. Prof. Li Li Prof. Aaron Monte Dr. Wael M. Abdel‐Mageed Dr. Jian Wang Hui Guo Dr. Wenni He Feng Xie Dr. Huanqin Dai Miaomiao Liu Dr. Caixia Chen Hao Xu Assoc. Prof. Mei Liu Dr. Andrew M. Piggott Assoc. Prof. Xueting Liu Prof. Robert J. Capon Prof. Lixin Zhang 《Angewandte Chemie (International ed. in English)》2013,52(4):1231-1234