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The effect of substituents on the oxidation potential for the one-electron reaction of 1,4-dimethoxybenzene was understood with a theoretical calculation based on density functional theory (DFT) at the level of B3LYP/6-311+G(d). It is found that the oxidation potential for the one-electron reaction of 1,4-dimethoxybenzene is 4.13 V (vs Li/Li(+)) and can be changed from 3.8 to 5.9 V (vs Li/Li(+)) by substituting electron-donating or electron-withdrawing groups for the hydrogen atoms on the aromatic ring. These potentials are in the range of the limited potentials for the lithium ion batteries using different cathode materials, and thus the substituted compounds can be selected as the redox shuttles for the overcharge prevention of these batteries. The oxidation potential of 1,4-dimethoxybenzene decreases when the hydrogen atoms are replaced with electron-donating groups but increases when replaced with electron-withdrawing groups. The further oxidation of these substituted compounds was also analyzed on the basis of the theoretic calculation. 相似文献
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Gang Qu Yang Li Yafeng Yu Yuxing Huang Wei Zhang Han Zhang Zhou Liu Tiantian Kong 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(32):11067-11071
Sponges, Neofibularia nolitangere, can regenerate spontaneously after being broken down into small pieces, and the regenerated structure maintains the original appearance and function. Synthetic materials with such capabilities are highly desired but hardly achieved. Presented here is a sponge‐inspired self‐regenerative powder from a double‐network (DN) tough hydrogel. Hydrogels are regenerated from their powder form, by addition of water, with preservation of the original appearance and mechanical properties. The powder‐hydrogel‐powder cycle can be repeated multiple times with little loss in mechanical properties, analogous to the regeneration of sponges. These DN hydrogels can be conveniently stored and easily shaped upon regeneration. This work may have implications in the development of regenerative materials for coatings and adhesives. 相似文献
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Jianying Dai Wenqing Zhang Tiantian Li Ling Bai Wenya He Lifei Ji Huilan Shi Xin Zhang 《Electroanalysis》2019,31(7):1381-1389
Exploration of cost‐effective, high‐performance and durable multifunctional electrocatalysts is of significant importance for renewable energy conversion and storage. In this work, a simple strategy is developed to tailor the nickel metal with the collaboration of nitrogen‐doped graphene and single‐walled carbon nanotubes. The resulted nickel catalyst exhibits superior trifunctional activities for oxygen evolution, hydrogen evolution and oxygen reduction reactions in the same electrolyte, even comparable to commercial Pt/C and RuO2 respectively, which can be attributed to the synergistic advantages between nickel, nitrogen and carbon, mainly including abundant integrated active sites achieved by the irregular charge distribution among C?N and Ni?N coupling centers. Such remarkable effects on trifunctional catalysis elicit the efficient overall water splitting, and endow the assembled zinc‐air battery with a good performance. These highlight the metallic nickel as an advanced multifunctional electrocatalysts with integrated sites developed from the collaboration of two different carbon nanomaterials. 相似文献
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Tiantian Si Lei Liu Xiaojing Liang Huixiao Duo Licheng Wang Shuai Wang 《Journal of separation science》2019,42(12):2148-2154
A zirconium(IV)‐based metal–organic framework material (MOF‐808) has been synthesized in a simple way and used for the extraction of phenoxyacetic acids in complex samples. The material has good thermal and chemical stability, large specific surface area (905.36 m²/g), and high pore size (22.18 Å). Besides, it contains a large amount of Zr‐O groups, easy‐to‐form Zr‐O‐H bond with carboxyl groups of phenoxyacetic acids, and possesses biphenyl skeleton structure, easy to interact with compounds through π‐π and hydrophobic interactions. These characteristics make the material very suitable for the extraction of certain compounds with a high extraction efficiency and excellent selectivity. The extraction conditions were optimized, and then an analytical method was successfully established and applied for analysis of actual samples. The solid‐phase extraction method based on prepared material had a wide linear range of 0.2–250 μg/L and a low detection limit of 0.1–0.5 μg/L for four phenoxyacetic acid compounds including 2,4‐dichlorophenoxyacetic acid, 2‐(2,4‐dichlorophenoxy) propionic acid, 4‐chlorophenoxyacetic acid, and dicamba. The relative standard deviations of intra‐ and interday precision were 1.8–3.8 and 4.3–6.9%, and the recoveries after spiking were between 77.1 and 109.3%. The results showed that the material is a desired substituent for the extraction of compounds with benzene ring structure containing carboxyl groups. 相似文献
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Systematic evolution of ligands by exponential enrichment is a traditional approach to select aptamer, which has a great potential in biosensing field. However, chemical modifications of DNA library or targets before selection might block the real recognition and binding sites between aptamers and their targets. In this study, a label‐ and modification‐free‐based in situ selection strategy was developed to overcome this limitation. The strategy is an attempt to screen bovine serum albumin aptamers according to the principle of electrophoretic mobility shift assay, and allowed single‐stranded DNA sequence to be fully exposed to interact with bovine serum albumin which was mixed with the agarose gel beforehand. After eight rounds of selection, specific aptamer with low dissociation constant (Kd) value of 69.44 ± 7.60 nM was selected and used for subsequent establishment of fluorescence biosensor. After optimization, the optimal aptasensor exhibited a high sensitivity toward bovine serum albumin with a limit of detection of 0.24 ng/mL (linear range from 1 to 120 ng/mL). These results indicated that the label‐ and modification‐free‐based in situ selection strategy proposed in this work could effectively select specific aptamer to develop aptasensor for sensitive detection of bovine serum albumin or other targets in actual complicated samples. 相似文献
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Wang Hongda Zhang Chunxia Zuo Tiantian Li Weiwei Jia Li Wang Xiaoyan Qian Yuexin Guo Dean Yang Wenzhi 《Analytical and bioanalytical chemistry》2019,411(29):7817-7829
Analytical and Bioanalytical Chemistry - Despite Panax quinquefolius L. serving as a crucial source for food additives, healthcare products, and herbal medicines, unawareness of the metabolome... 相似文献
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Zhong Yingying Li Qing-lan Lu Minglei Wang Tiantian Yang Huiyi He Qiyi Cui Xiping Li Xiangguang Zhao Suqing 《Mikrochimica acta》2020,187(12):1-11
Microchimica Acta - Testing gluten content in food, before it reaches the consumer, becomes a major challenge where cross-contamination during processing and transportation is a very common... 相似文献
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Manman Liu Yang Zhu Tiantian Wu Dr. Junjie Cheng Prof. Yangzhong Liu 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(33):7442-7450
Ferritin is an iron-storage protein nanocage that is assembled from 24 subunits. The hollow cavity of ferritin enables its encapsulation of various therapeutic agents; therefore, ferritin has been intensively investigated for drug delivery. The use of antibody-ferritin conjugates provides an effective approach for targeted drug delivery. However, the complicated preparation and limited protein stability hamper wide applications of this system. Herein, we designed a novel nanobody-ferritin platform (Nb-Ftn) for targeted drug delivery. The site-specific conjugation between nanobody and ferritin is achieved by transglutaminase-catalyzed protein ligation. This ligation strategy allows the Nb conjugation after drug loading in ferritin, which avoids deactivation of the nanobody under the harsh pH environment required for drug encapsulation. To verify the tumor targeting of this Nb-Ftn platform, a photodynamic reagent, manganese phthalocyanine (MnPc), was loaded into the ferritin cavity, and an anti-EGFR nanobody was conjugated to the surface of the ferritin. The ferritin nanocage can encapsulate about 82 MnPc molecules. This MnPc@Nb-Ftn conjugate can be efficiently internalized by EGFR positive A431 cancer cells, but not by EGFR negative MCF-7 cells. Upon 730 nm laser irradiation, MnPc@Nb-Ftn selectively killed EGFR positive A431 cells by generating reactive oxygen species (ROS), whereas no obvious damage was observed on MCF-7 cells. Given that ferritin can be used for encapsulation of various therapeutic agents, this work provides a strategy for facile construction of nanobody-ferritin for targeted drug delivery. 相似文献