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971.
Xiao Sun Dong Pei Wen‐Da Duan Jian‐Fei Liu Duo‐Long Di Xin‐Yi Huang 《Journal of separation science》2020,43(17):3573-3584
Elution‐extrusion counter current chromatography extrudes the most solute retained in the column with the highest possible peak resolution. It can greatly improve the hydrophobic window. In recent years, elution‐extrusion counter current chromatography has received extensive attention in the separation of complex samples. This article first reviews the development and application of elution‐extrusion counter current chromatography, including its origin, mechanism, advantages and disadvantages, and some representative applications. At the same time, this review also shared our visions and ideas on how to improve the elution‐extrusion mode. This article aims to provide certain reference for the research of this technology. 相似文献
972.
Kai Chen Gang Huang Jin‐Ling Ma Jin Wang Dong‐Yue Yang Xiao‐Yang Yang Yue Yu Xin‐Bo Zhang 《Angewandte Chemie (International ed. in English)》2020,59(38):16661-16667
The lithium (Li)–air battery has an ultrahigh theoretical specific energy, however, even in pure oxygen (O2), the vulnerability of conventional organic electrolytes and carbon cathodes towards reaction intermediates, especially O2?, and corrosive oxidation and crack/pulverization of Li metal anode lead to poor cycling stability of the Li‐air battery. Even worse, the water and/or CO2 in air bring parasitic reactions and safety issues. Therefore, applying such systems in open‐air environment is challenging. Herein, contrary to previous assertions, we have found that CO2 can improve the stability of both anode and electrolyte, and a high‐performance rechargeable Li–O2/CO2 battery is developed. The CO2 not only facilitates the in situ formation of a passivated protective Li2CO3 film on the Li anode, but also restrains side reactions involving electrolyte and cathode by capturing O2?. Moreover, the Pd/CNT catalyst in the cathode can extend the battery lifespan by effectively tuning the product morphology and catalyzing the decomposition of Li2CO3. The Li–O2/CO2 battery achieves a full discharge capacity of 6628 mAh g?1 and a long life of 715 cycles, which is even better than those of pure Li–O2 batteries. 相似文献
973.
Hai‐Dong Xia Zhong‐Liang Li Qiang‐Shuai Gu Xiao‐Yang Dong Jia‐Heng Fang Xuan‐Yi Du Li‐Lei Wang Xin‐Yuan Liu 《Angewandte Chemie (International ed. in English)》2020,59(39):16926-16932
We describe a photoinduced copper‐catalyzed asymmetric radical decarboxylative alkynylation of bench‐stable N‐hydroxyphthalimide(NHP)‐type esters of racemic alkyl carboxylic acids with terminal alkynes, which provides a flexible platform for the construction of chiral C(sp3)?C(sp) bonds. Critical to the success of this process are not only the use of the copper catalyst as a dual photo‐ and cross‐coupling catalyst but also tuning of the NHP‐type esters to inhibit the facile homodimerization of the alkyl radical and terminal alkyne, respectively. Owing to the use of stable and easily available NHP‐type esters, the reaction features a broader substrate scope compared with reactions using the alkyl halide counterparts, covering (hetero)benzyl‐, allyl‐, and aminocarbonyl‐substituted carboxylic acid derivatives, and (hetero)aryl and alkyl as well as silyl alkynes, thus providing a vital complementary approach to the previously reported method. 相似文献
974.
975.
Wenjuan Yan Mengyuan Liu Jinyao Wang Jian Shen Shuxia Zhang Xiaoqiang Xu Shuaishuai Wang Jie Ding Xin Jin 《Chemical record (New York, N.Y.)》2020,20(3):230-251
Molybdenum complexes are versatile and efficient for liquid phase olefin epoxidation reactions. Rational design of catalysts is critical to achieve high atom efficiency during epoxidation processes. Although liquid phase epoxidation has been a popular topic for decades, three key issues, (a) rational control of morphology of molybdenum nanoparticles, (b) manipulating metal‐support interaction and (c) altering electronic configuration at molybdenum center remains unsolved in this area. Therefore, in this paper, we have critically revised recent research progress on heterogeneous molybdenum catalysts for facile liquid phase olefin epoxidation in terms of catalyst synthesis, surface characterization, catalytic performance and structure‐function relationship. Furthermore, plausible reaction mechanisms will be systematically discussed with the aim to provide insights into fundamental understanding on novel epoxidation chemistry. 相似文献
976.
Xing‐Cai Huang Jia‐Xin Li Yong‐Zhi Chen Wen‐Yan Wang Rui Xu Jin‐Xia Tao Dong Shao Yi‐Quan Zhang 《化学:亚洲杂志》2020,15(9):1469-1477
Tuning the magnetic anisotropy of metal ions remains highly interesting in the design of improved single‐molecule magnets (SMMs). We herein report synthetic, structural, magnetic, and computational studies of four mononuclear CoII complexes, namely [Co(hfac)2(MeCN)2] ( 1 ), [Co(hfac)2(Spy)2] ( 2 ), [Co(hfac)2(MBIm)2] ( 3 ), and [Co(hfac)2(DMF)2] ( 4 ) (MeCN=acetonitrile, hfac=hexafluoroacetylacetone, Spy=4‐styrylpyridine, MbIm=5,6‐dimethylbenzimidazole, DMF=N,N‐dimethylformamide), with distorted octahedral geometry constructed from hexafluoroacetylacetone (hfac) and various axial ligands. By a building block approach, complexes 2 – 4 were synthesized by recrystallization of the starting material of 1 from various ligands containing solution. Magnetic and theoretical studies reveal that 1 – 4 possess large positive D values and relative small E parameters, indicating easy‐plane magnetic anisotropy with significant rhombic anisotropy in 1 – 4 . Dynamic alternative current (ac) magnetic susceptibility measurements indicate that these complexes exhibit slow magnetic relaxation under external fields, suggesting field‐induced single‐ion magnets (SIMs) of 1 – 4 . These results provide a promising platform to achieve fine tuning of magnetic anisotropy through varying the axial ligands based on Co(II) bis(hexafluoroacetylacetonate) complexes. 相似文献
977.
A facile hybrid assembly between Ti3C2Tx MXene nanosheets and (3‐aminopropyl) triethoxylsilane‐modified Si nanoparticles (NH2?Si NPs) was developed to construct multilayer stacking of Ti3C2Tx nanosheets with NH2?Si NPs assembling together (NH2?Si/Ti3C2Tx). NH2?Si/Ti3C2Tx exhibits a significantly enhanced lithium storage performance compared to pristine Si, which is attributed to the robust crosslinking architecture and considerably improved electrical conductivity as well as shorter Li+ diffusion pathways. The optimized NH2?Si/Ti3C2Tx anode with Ti3C2Tx: NH2?Si mass ratio of 4 : 1 displays an enhanced capacity (864 mAh g?1 at 0.1 C) with robust capacity retention, which is significantly higher than those of NH2?Si NPs and Ti3C2Tx anodes. Furthermore, this work demonstrates the important effect of the MXene‐based electrode architecture on the electrochemical performance and can guide future work on designing high‐performance Si/MXene hybrids for energy storage applications. 相似文献
978.
In‐depth understanding of the catalytic active sites is of paramount importance for the design of efficient electrocatalysts for CO2 conversion. Here we highlight the structural evolution of SnO2 nanosheets for electrocatalytic CO2 reduction. The transformation of SnO2 into metallic Sn would occur on the surface of catalyst during the catalytic process, followed by enhanced selectivity and activity for the conversion of CO2 to HCOOH. Electrocatalytic characterization and structural analysis demonstrate that the metallic Sn derived from structural evolution plays a dominant role in the CO2 reduction to HCOOH. This work deepens the understanding of the catalytic mechanism and provides a new pathway for the rational design of advanced electrocatalysts for CO2 reduction. 相似文献
979.
Xiao‐Tong Wang Zhen‐Yi Gu Wen‐Hao Li Xin‐Xin Zhao Jin‐Zhi Guo Kai‐Di Du Xiao‐Xi Luo Xing‐Long Wu 《化学:亚洲杂志》2020,15(18):2803-2814
As the power supply of the prosperous new energy products, advanced lithium ion batteries (LIBs) are widely applied to portable energy equipment and large‐scale energy storage systems. To broaden the applicable range, considerable endeavours have been devoted towards improving the energy and power density of LIBs. However, the side reaction caused by the close contact between the electrode (particularly the cathode) and the electrolyte leads to capacity decay and structural degradation, which is a tricky problem to be solved. In order to overcome this obstacle, the researchers focused their attention on electrolyte additives. By adding additives to the electrolyte, the construction of a stable cathode‐electrolyte interphase (CEI) between the cathode and the electrolyte has been proven to competently elevate the overall electrochemical performance of LIBs. However, how to choose electrolyte additives that match different cathode systems ideally to achieve stable CEI layer construction and high‐performance LIBs is still in the stage of repeated experiments and exploration. This article specifically introduces the working mechanism of diverse electrolyte additives for forming a stable CEI layer and summarizes the latest research progress in the application of electrolyte additives for LIBs with diverse cathode materials. Finally, we tentatively set forth recommendations on the screening and customization of ideal additives required for the construction of robust CEI layer in LIBs. We believe this minireview will have a certain reference value for the design and construction of stable CEI layer to realize desirable performance of LIBs. 相似文献
980.
This paper studies the contact vibration problem of an elastic half-space coated with functionally graded materials (FGMs) subject to a rigid spherical punch. A static force superimposing a dynamic time-harmonic force acts on the rigid spherical punch. Firstly, we give the static contact problem of FGMs by a least-square fitting approach. Next, the dynamic contact pressure is solved by employing the perturbation method. Lastly, the dynamic contact stiffness with different dynamic contact displacement conditions is derived for the FGM coated half-space. The effects of the gradient index, coating thickness, internal friction, and punch radius on the dynamic contact stiffness factor are discussed in detail. 相似文献