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941.
Ming‐Liang Tong Wei Li Xiao‐Ming Chen Shao‐Liang Zheng Seik Weng Ng 《Acta Crystallographica. Section C, Structural Chemistry》2002,58(4):m232-m234
The title compound, [Cu2(C2H3O2)4(C11H9N)2] or [Cu2(MeCO2)4(phpy)2] (phpy is 4‐phenylpyridine), consists of centrosymmetric dimers in which the CuII atoms display a square‐pyramidal CuO4N coordination, with four acetate O atoms in the basal plane [Cu—O 1.975 (3)–1.987 (3) Å] and the phpy N atom in the apical position [Cu—N 2.150 (3) Å]. The Cu atoms are 2.654 (1) Å apart and are bridged by four acetate groups. The discrete dimers are extended into a three‐dimensional supramolecular array through intermolecular π–π‐stacking interactions. 相似文献
942.
In the degassing process of transformer oil with ultrasonic waves ,decompostition of the oil was observed.Light hydrocarbons,including methane,ethane,ethylene ,aceylene,propane etc,were found to be released continuously from the oil into headspace within a closed vial placed in an ultrasonic field ,The gases came from decomposition of hydrocarbon molecules under cavitation effect. 相似文献
943.
John H.T Luong Caide Xiao Š.Mircea Leabu Xiaolan Li Shashi Uniyal Bosco M.C Chan 《Analytica chimica acta》2004,501(1):61-69
Electric cell-substrate impedance sensing (ECIS) was applied to assess the structure-function of α2β1 integrin, receptor for collagen and laminin. On collagen-coated gold electrodes, expression of this integrin on human rhabdomyosarcoma (RD) cells (RDX2C2) yielded a five-fold increase in resistance when compared with mock transfected RD (RDpF) cells (34.5±5.2 versus 6.5±0.8 Ω/cell). An intermediate level of 16±2 Ω/cell was measured upon expression of an α2β1 mutant that lacked the α2 cytoplasmic domain (RDX2CO). On laminin, the resistance measured for RDX2C2 cells was also higher but only twice that of RDpF cells at 71±4 and 37±4 Ω/cell, respectively. In comparison, RDX2CO cells (38±4 Ω/cell), exhibiting no enhanced adhesive function, yielded a similar result to that of RDpF cells. On fibronectin, RDX2C2 and RDpF cells, exhibiting comparable levels of adhesion, were similar in resistance measurements at 85±5and 89±7 Ω/cell, respectively. It has been shown that deletion of α2 cytoplasmic domain results in dysregulated recruitment of the α2β1 mutant to focal adhesion complexes that mediate binding of fibronectin. RDX2CO cells on fibronectin, exhibiting reduced adhesive function, was associated with noticeably lower resistance (60±4 Ω/cell). Monitoring electroporation of the RD plasma membrane also indirectly validated cell attachment as reflected by the resistance measured. Results from this study demonstrated the potential of ECIS for study of the structure-function of βl integrin adhesion receptors. 相似文献
944.
A novel and sensitive chemiluminescence (CL) method for the determination of aminomethylbenzoic acid and aminophylline coupled with flow-injection analysis (FIA) technique is developed in this paper. It is based on the inhibition effect of the studied drugs on the chemiluminescence emission of N-bromosuccinimide-luminol (NBS-luminol) system. Under the optimum conditions, the decreased CL intensity is linear with the concentration of aminomethylbenzoic acid in the range of 2×10−8 to 1.0×10−6 g ml−1 and with the concentration of aminophylline in the range of 1×10−7 to 7.0×10−6 g ml−1, respectively. The detection limit is 7.0×10−9 g ml−1 for aminomethylbenzoic acid (3σ) and 3.4×10−8 g ml−1 for aminophylline (3σ). The relative standard deviations (R.S.D.) for 11 parallel measurements of 2.0×10−7 g ml−1 aminomethylbenzoic acid and 1.0×10−6 g ml−1 aminophylline are 2.6 and 3.0%, respectively. The proposed methods have been applied for the determination of the studied drugs in their pharmaceutical formulations with satisfactory results. The possible use of the proposed system for the determination of aminomethylbenzoic acid in plasma sample was also tested. The possible inhibition mechanism of aminomethylbenzoic acid and aminophylline on luminol-NBS system was discussed briefly. 相似文献
945.
Hua Xiao Bei Feng‐Li Wang Xin Yang Xu‐Jie Lu Lu‐De 《International journal of quantum chemistry》2006,106(5):1145-1152
A theoretical study of the polymerization reaction mechanism of maleic anhydride (MA) initiated by hydrate is presented. The reaction pathway has been studied with the density functional theory (DFT) method at the B3LYP/6‐311G** level. The geometrical parameters of transition states (TS) are optimized; intrinsic reaction coordinate (IRC) calculations have also been performed to obtain further credible features. Frequency analyses of all the stationary points are calculated at the same basis sets. The total energies of all geometries are corrected at second‐order Møller–Plesset (MP2)/6‐311G**. Calculation results reveal that the reaction mechanism is attributable to anion polymerization. © 2005 Wiley Periodicals, Inc. Int J Quantum Chem, 2006 相似文献
946.
Zhi‐Chao Jiang Yao‐Yu Xiao Lu Yin Li Han Yue Zhao 《Angewandte Chemie (International ed. in English)》2020,59(12):4925-4931
Novel main‐chain liquid crystalline Diels—Alder dynamic networks (LCDANs) were prepared that exhibit unprecedented ease for actuator programming and reprocessing compared to existing liquid crystalline network (LCN) systems. Following cooling from 125 °C, LCDANs are deformed with aligned mesogens self‐locked at room temperature by slowly formed Diels–Alder (DA) bonds, which allows for the formation of solid 3D actuators capable of reversible shape change, and strip walker and wheel‐capable light‐driven locomotion upon either thermally or optically induced order–disorder phase transition. Any actuator can readily be erased at 125 °C and reprogrammed into a new one under ambient conditions. Moreover, LCDANs can be processed directly from melt (for example, fiber drawing) and from solution (for example, casting tubular actuators), which cannot be achieved with LCNs using exchangeable covalent bonds. The combined attributes of LCDANs offer significant progress toward developing easily programmable/processable LCN actuators. 相似文献
947.
A Diffusion‐‐Reaction Competition Mechanism to Tailor Lithium Deposition for Lithium‐Metal Batteries
Xiao‐Ru Chen Yu‐Xing Yao Chong Yan Rui Zhang Xin‐Bing Cheng Qiang Zhang 《Angewandte Chemie (International ed. in English)》2020,59(20):7743-7747
Lithium metal is recognized as one of the most promising anode materials owing to its ultrahigh theoretical specific capacity and low electrochemical potential. Nonetheless, dendritic Li growth has dramatically hindered the practical applications of Li metal anodes. Realizing spherical Li deposition is an effective approach to avoid Li dendrite growth, but the mechanism of spherical deposition is unknown. Herein, a diffusion‐reaction competition mechanism is proposed to reveal the rationale of different Li deposition morphologies. By controlling the rate‐determining step (diffusion or reaction) of Li deposition, various Li deposition scenarios are realized, in which the diffusion‐controlled process tends to lead to dendritic Li deposition while the reaction‐controlled process leads to spherical Li deposition. This study sheds fresh light on the dendrite‐free Li metal anode and guides to achieve safe batteries to benefit future wireless and fossil‐fuel‐free world. 相似文献
948.
Min Zhou Yuxin Qian Jiayang Xie Wenjing Zhang Weinan Jiang Ximian Xiao Sheng Chen Chengzhi Dai Zihao Cong Zhemin Ji Ning Shao Longqiang Liu Yuequn Wu Runhui Liu 《Angewandte Chemie (International ed. in English)》2020,59(16):6412-6419
Peptides have important biological functions. However, their susceptibility to proteolysis limits their applications. We demonstrated here for the first time, that poly(2‐oxazoline) (POX) can work as a functional mimic of peptides. POX‐based glycine pseudopeptides, a host defense peptide mimic, had potent activities against methicillin‐resistant S. aureus, which causes formidable infections. The POX mimic showed potent activity against persisters that are highly resistant to antibiotics. S. aureus did not develop resistance to POX owning to the reactive oxygen species related antimicrobial mechanism. POX‐treated S. aureus is sensitive to common antibiotics, demonstrating no observable antimicrobial pressure or cross‐resistance in using antimicrobial POX. This study highlights POX as a new type of functional mimic of peptides and opens new avenues in designing and exploring peptide mimetics for biological functions and applications. 相似文献
949.
Yunqin Zhang Zixi Chen Yingying Huang Shaojun He Xingkuan Yang Zhibing Wu Xiufang Wang Guozhi Xiao 《Angewandte Chemie (International ed. in English)》2020,59(19):7576-7584
The synthesis of long, branched, and complex carbohydrate sequences remains a challenging task in chemical synthesis. Reported here is an efficient and modular one‐pot synthesis of a nona‐decasaccharide and shorter sequences from Psidium guajava polysaccharides, which have the potent α‐glucosidase inhibitory activity. The synthetic strategy features: 1) several one‐pot glycosylation reactions on the basis of N‐phenyltrifluoroacetimidate (PTFAI) and Yu glycosylation to streamline the chemical synthesis of oligosaccharides, 2) the successful and efficient assembly sequences (first O3′, second O5′, final O2′) toward the challenging 2,3,5‐branched Araf motif, 3) the stereoselective 1,2‐cis‐glucosylation by reagent control, and 4) the convergent [6+6+7] one‐pot coupling reaction for the final assembly of the target nona‐decasaccharide. This orthogonal one‐pot glycosylation strategy can streamline the chemical synthesis of long, branched, and complicated carbohydrate chains. 相似文献
950.
Jie Yang Xiao‐Ming Zhang Fu‐Min Zhang Shao‐Hua Wang Yong‐Qiang Tu Zhen Li Xi‐Chao Wang Hong Wang 《Angewandte Chemie (International ed. in English)》2020,59(22):8471-8475
An enantioselective aldehyde α‐alkylation/semipinacol rearrangement was achieved through organo‐SOMO catalysis. The catalytically generated enamine radical cation serves as a carbon radical electrophile that can stereoselectively add to the alkene of an allylic alcohol and initiate ensuing ring‐expansion of cyclopropanol or cyclobutanol. This tandem reaction enables the production of a wide range of nonracemic functionalizable α‐quaternary‐δ‐carbonyl cycloketones in high yields and excellent enantioselectivity from simple aldehydes and allylic alcohols. As a key step, the intramolecular reaction was also successfully applied in the asymmetric total synthesis of (+)‐cerapicol. 相似文献