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191.
192.
Light‐harvesting complexes (LHC) in photosynthetic organisms perform the major function of light absorption and energy transportation. Optical spectrum of LHC provides a detailed understanding of the molecular mechanisms involved in the excitation energy transfer (EET) processes, which has been widely studied. Here, we study how the geometric property of LHC in Rhodospirillum (Rs.) molischianum would affect its spectral characteristics and energy transfer process. By adopting the effective Hamiltonian and the dipole–dipole approximation, we calculate the exciton level structures for the LH2 ring and LH1 ring and the energy transfer time between different LHCs under various structural parameters and different rotational symmetries. Our numerical results show that the LHC's absorption peaks and the energy transfer time between different LHCs can be modified by changing the geometric configurations. Our study may be beneficial to the applications in designing highly efficient photovoltaic cell and other artificial photosynthetic systems. 相似文献
193.
Zichun Wang Luke A. O'Dell Xin Zeng Can Liu Shufang Zhao Wenwen Zhang Marianne Gaborieau Yijiao Jiang Jun Huang 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(50):18229-18236
Commercial bioethanol can be readily converted into ethylene by a dehydration process using solid acids, such as Brønsted acidic H‐ZSM‐5 zeolites, and thus, it is an ideal candidate to replace petroleum and coal for the sustainable production of ethylene. Now, strong Lewis acidic extra‐framework three‐coordinate Al3+ species were introduced into H‐ZSM‐5 zeolites to improve their catalytic activity. Remarkably, Al3+ species working with Brønsted acid sites can accelerate ethanol dehydration at a much lower reaction temperature and shorten the unsteady‐state period within 1–2 h, compared to >9 h for those without Al3+ species, which can significantly enhance the ethanol dehydration efficiency and reduce the cost. The reaction mechanism, studied by solid‐state NMR, shows that strong Lewis acidic EFAl‐Al3+ species can collaborate with Brønsted acid sites and promote ethanol dehydration either directly or indirectly via an aromatics‐based cycle to produce ethylene. 相似文献
194.
Jianxian Zeng Zhe Zhang Hu Zhou Guoqing Liu Yuan Liu Lingwei Zeng Jian Jian Zhengqiu Yuan 《先进技术聚合物》2019,30(7):1865-1877
While conventional approaches have been studied for removal of ruthenium(III) ions (Ru(III)), this work focuses on the applicability of ion‐imprinted poly(methyl methacrylate‐vinyl pyrrolidone)/poly(vinylidene fluoride) blending membranes (Ru(III)–ion‐imprinted membrane[IIM]) for selective removal of Ru(III) from acidic water solutions. In order to measure the effectiveness of these imprinted membranes, after fabrication, binding experiments were done with aqueous Ru(III) solutions. The results showed that Ru(III)‐IIMs were fabricated successfully at various blending ratios, and their chemical components, microstructures, hydrophilicity, and water fluxes were measured. In pH range 0.5 to 5.0, binding capacity (Qe) of Ru(III) onto Ru(III)‐IIM increases remarkably with pH and then reaches to a maximum value (53.52 mg/g) at pH 1.5. After that, Qe gradually decreases. Compared with a nonimprinted membrane, Ru(III)‐IIM demonstrates higher selectivity for Ru(III) at pH 1.5 in the presence of Ni(II) and Cu(II) ions, and its selectivity coefficients for Ru(III)/Ni(II) and Ru(III)/Cu(II) are 3.70 and 3.32, respectively. Also, Ru(III)‐IIM shows a good chemical stability and reusability. C─N and C═O bonds within poly(vinyl pyrrolidone) segments of poly(methyl methacrylate‐vinyl pyrrolidone) (P(MMA‐VP)) participate the uptake of Ru(III). Ru(III)‐IIM exhibited excellent hydrophilicity and Ru(III) selective adsorption ability and reusability and has potential to be used for Ru(III) removal from acidic water solutions. 相似文献
195.
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
196.
Junkai Guo Cuiwen Kuang Jian Rong Dr. Lingchun Li Dr. Chuanfa Ni Prof. Dr. Jinbo Hu 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(30):7259-7264
The deoxyfluorination of alcohols is a fundamentally important approach to access alkyl fluorides, and thus the development of shelf-stable, easy-to-handle, fluorine-economical, and highly selective deoxyfluorination reagents is highly desired. This work describes the development of a crystalline compound, N-tosyl-4-chlorobenzenesulfonimidoyl fluoride (SulfoxFluor), as a novel deoxyfluorination reagent that possesses all of the aforementioned merits, which is rare in the arena of deoxyfluorination. Endowed by the multi-dimensional modulating ability of the sulfonimidoyl group, SulfoxFluor is superior to 2-pyridinesulfonyl fluoride (PyFluor) in fluorination rate, and is also superior to perfluorobutanesulfonyl fluoride (PBSF) in fluorine-economy. Its reaction with alcohols not only tolerates a wide range of functionalities including the more sterically hindered alcoholic hydroxyl groups, but also exhibits high fluorination/elimination selectivity. Because SulfoxFluor can be easily prepared from inexpensive materials and can be safely handled without special techniques, it promises to serve as a practical deoxyfluorination reagent for the synthesis of various alkyl fluorides. 相似文献
197.
Ya-Xin Li Fang-Fang Fan Jie Wang Dr. Liliana Cseh Dr. Min Xue Dr. Xiang-Bing Zeng Prof. Goran Ungar 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(60):13739-13747
Wedge-shaped molecules, such as dendrons, are among the most important building blocks for directed supramolecular self-assembly. Here we present a new approach aimed at widening the range and complexity of potential mesophases by introducing double-tapered mesogens. Two series of compounds are presented, both alkali metal salts (Li, Na, Cs) of 3,4,5-tris-alkoxybenzoic acid with a second tapered tris-alkoxyaryl group attached at the end of an alkoxy chain. The double-tapered compounds all display an unusual hexagonal columnar phase consisting of one ionic and three non-ionic columns per unit cell. The cation size has an unexpectedly drastic effect on unit cell size. Unlike most columnar phases, the current phases show unusually high dimensional stability on heating, and high stiffness in spite of being 80–85 % aliphatic, attributed to their molecular topology. The described approach may lead to co-assemblies of multifunctional materials, for example, parallel p- and n-semiconducting nanowires or parallel ionic and electronic conductors. 相似文献
198.
Zhou Jiawen Zhu Weiya Zeng Miao Yang Qingqing Li Ping Lan Linfeng Peng Junbiao Li Yuan Huang Fei Cao Yong 《中国科学:化学(英文版)》2019,62(12):1656-1665
Stable radicals are challenging to prepare due to their intrinsic high reactivity. Herein, three trisphenolamine radicals were readily synthesized and exhibited unexpected thermal/electrochemical stability and semiconductor property. These three nitroxide radicals could be considered as a class of aromatized nitro groups or HNO_3 derivatives. The closed-shell nitro-like and open-shell nitroxide resonance structure contribute to their outstanding stability. Furthermore, the tunable ground states, extremely low band gap and p-type charge transport properties were systematically investigated. More importantly, the work presents the concept of aromatic inorganic acid radical(AIAR) and aggregation-induced radical(AIR) mechanism to understand the intrinsic structureproperty relationship of these radicals. In addition, we provide a novel strategy for the design of stable and low bandgap radicals for organic electronics, magnetics, spintronics, etc. 相似文献
199.
Zhu Hong Zeng Xiangbing Han Tianli Li Xuexue Zhu Shuguang Sun Bai Zhou Ping Liu Jinyun 《Journal of Solid State Electrochemistry》2019,23(7):2173-2180
Journal of Solid State Electrochemistry - Since conventional graphite-based anode possesses a low capacity, seeking for high-capacity anode candidates becomes significant for constructing emerging... 相似文献