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991.
A new mixed-ligand V(IV) complex, [VO(o-Van-Val)(phen)]·CH3CN (o-Van-val = Schiff base derived from o-vanillin and l-valine, phen = 1,10-phenanthroline), was synthesized and characterized by physico-chemical methods and single-crystal X-ray diffraction. In the crystal, the V(IV) atom is six-coordinated by one oxo ligand, two oxygen atoms and one nitrogen atom from a valine Schiff base ligand, and two nitrogen atoms from 1,10-phenanthroline, giving a distorted octahedral arrangement. The DNA-binding properties of the complex were investigated by spectroscopic methods and viscosity measurements. The results suggest that the oxovanadium(IV) complex binds to DNA in an intercalation mode. 相似文献
992.
Qian Sun Xi-Ping Wang Qiao-Juan Yan Wei Chen Zheng-Qiang Jiang 《Applied biochemistry and biotechnology》2014,174(1):174-185
Purification and characterization of a chymosin from Rhizopus microsporus var. rhizopodiformis were investigated in the present study. A newly isolated R. microsporus var. rhizopodiformis F518 produced a high level of milk-clotting activity (1,001 SU/mL). A chymosin from the fungus was purified 3.66-fold with a recovery yield of 33.2 %. The enzyme appeared as a single protein band on sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) with a molecular mass of 37.0 kDa. It was optimally active at 60 °C and was stable up to 40 °C. The purified enzyme was an acid protease with an optimum pH of 5.2 and retained 80 % of residual activity within pH 2.0–8.0. The inhibition of 96 and 100 % by pepstatin A at 0.01 and 0.02 mM, respectively, revealed that the enzyme is an aspartic protease. Thus, high milk-clotting activity of the chymosin with good stability will strengthen the potential use of the chymosin as a substitute for calf rennet in cheese manufacturing. 相似文献
993.
Hongfang Wang Cong Wu Xu Liu Jing Sun Guangmei Xia Wei Huang Rui Song 《Colloid and polymer science》2014,292(11):2949-2957
Herein, a facile and noncovalent modification for multiwalled carbon nanotubes (MWNTs) is adopted by the self-polymerization of dopamine (DOPA). And, the polydopamine-coated MWNTs (D-MWNTs) were further incorporated into poly(l-lactide) (PLLA) matrix through the solvent-casting method. It is found that the D-MWNTs tend to be well dispersed in PLLA matrix than the pristine MWNTs and the D-MWNTs that can act as heterogeneous nucleators that evidently affect the morphology and crystallization behavior of PLLA. In addition, the significant improvement of dispersion and the interface interaction of PLLA/D-MWNTs, via dopamine coating between the MWNTs and PLLA matrix, results in enhanced mechanical and thermal properties and electrical conductivity. This facile methodology is believed to afford broad application potential in carbon nanotubes (CNTs)-based polymer nanocomposites. 相似文献
994.
995.
Kang-Chieh Lo Chiao-Yin Sun Yu-Ju Ding Jen-Ning Tsai Kai-Ping Chang Yi-En Wen Wan-Ling Chang Shin C. Chang Ming-Fu Chang Yun-Hsin Wang Yau-Hung Chen 《Research on Chemical Intermediates》2014,40(6):2177-2185
Benzo(a)pyrene is a chemical produced during the process of making fried, roasted, and smoked foods. It remains unclear whether benzo(a)pyrene affects the early development of human organs. In this study, we used the transgenic zebrafish line Tg(wt1b:GFP) as a model to assess benzo(a)pyrene-induced kidney malformation. By soaking zebrafish embryos in benzo(a)pyrene at various doses (2, 20, and 200 ppb), only a minor effect on the survival rate was detected (0 ppb: 97.8 ± 1.9 %; 2–200 ppb: 89.1 ± 5.8–91.5 ± 8.3 %). However, benzo(a)pyrene significantly affected the development of the kidney (malformation rates ranges from 50.0 ± 3.5 to 77.4 ± 5.3 %). Various abnormalities, such as unusual curving of pronephric tubes, swollen glomerulus, and incomplete development of pronephric ducts, were observed. This study provides a rapid and effective protocol for the evaluation of the notable effects of benzo(a)pyrene on embryonic kidney development. 相似文献
996.
Dr. Chun-Chao Hou Dr. Lianli Zou Dr. Liming Sun Dr. Kexin Zhang Dr. Zheng Liu Prof. Yinwei Li Dr. Caixia Li Prof. Ruqiang Zou Prof. Jihong Yu Prof. Qiang Xu 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(19):7454-7459
Single-atom catalysts have drawn great attention, especially in electrocatalysis. However, most of previous works focus on the enhanced catalytic properties via improving metal loading. Engineering morphologies of catalysts to facilitate mass transport through catalyst layers, thus increasing the utilization of each active site, is regarded as an appealing way for enhanced performance. Herein, we design an overhang-eave structure decorated with isolated single-atom iron sites via a silica-mediated MOF-templated approach for oxygen reduction reaction (ORR) catalysis. This catalyst demonstrates superior ORR performance in both alkaline and acidic electrolytes, comparable to the state-of-the-art Pt/C catalyst and superior to most precious-metal-free catalysts reported to date. This activity originates from its edge-rich structure, having more three-phase boundaries with enhanced mass transport of reactants to accessible single-atom iron sites (increasing the utilization of active sites), which verifies the practicability of such a synthetic approach. 相似文献
997.
Dr. José I. Urgel Dr. Marco Di Giovannantonio Kristjan Eimre Thorsten G. Lohr Dr. Junzhi Liu Shantanu Mishra Dr. Qiang Sun Amogh Kinikar Dr. Roland Widmer Samuel Stolz Max Bommert Dr. Reinhard Berger Dr. Pascal Ruffieux Dr. Carlo A. Pignedoli Prof. Dr. Klaus Müllen Prof. Dr. Xinliang Feng Prof. Dr. Roman Fasel 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(32):13383-13389
Cumulene compounds are notoriously difficult to prepare and study because their reactivity increases dramatically with the increasing number of consecutive double bonds. In this respect, the emerging field of on-surface synthesis provides exceptional opportunities because it relies on reactions on clean metal substrates under well-controlled ultrahigh-vacuum conditions. Here we report the on-surface synthesis of a polymer linked by cumulene-like bonds on a Au(111) surface via sequential thermally activated dehalogenative C−C coupling of a tribenzoazulene precursor equipped with two dibromomethylene groups. The structure and electronic properties of the resulting polymer with cumulene-like pentagon–pentagon and heptagon–heptagon connections have been investigated by means of scanning probe microscopy and spectroscopy methods and X-ray photoelectron spectroscopy, complemented by density functional theory calculations. Our results provide perspectives for the on-surface synthesis of cumulene-containing compounds, as well as protocols relevant to the stepwise fabrication of carbon–carbon bonds on surfaces. 相似文献
998.
Hongyu Zhang Changlong Hao Aihua Qu Maozhong Sun Liguang Xu Chuanlai Xu Hua Kuang 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(18):7197-7204
The accumulation and deposition of β-amyloid (Aβ) plaques in the brain is considered a potential pathogenic mechanism underlying Alzheimer's disease (AD). Chiral l/d -FexCuySe nanoparticles (NPs) were fabricated that interfer with the self-assembly of Aβ42 monomers and trigger the Aβ42 fibrils in dense structures to become looser monomers under 808 nm near-infrared (NIR) illumination. d -FexCuySe NPs have a much higher affinity for Aβ42 fibrils than l -FexCuySe NPs and chiral Cu2−xSe NPs. The chiral FexCuySe NPs also generate more reactive oxygen species (ROS) than chiral Cu2−xSe NPs under NIR-light irradiation. In living MN9D cells, d -NPs attenuate the adhesion of Aβ42 to membranes and neuron loss after NIR treatment within 10 min without the photothermal effect. In-vivo experiments showed that d -FexCuySe NPs provide an efficient protection against neuronal damage induced by the deposition of Aβ42 and alleviate symptoms in a mouse model of AD, leading to the recovery of cognitive competence. 相似文献
999.
Meng Zhao Dr. Hong-Jie Peng Bo-Quan Li Dr. Xiao Chen Jin Xie Dr. Xinyan Liu Prof. Qiang Zhang Prof. Jia-Qi Huang 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(23):9096-9102
In situ evolution of electrocatalysts is of paramount importance in defining catalytic reactions. Catalysts for aprotic electrochemistry such as lithium–sulfur (Li-S) batteries are the cornerstone to enhance intrinsically sluggish reaction kinetics but the true active phases are often controversial. Herein, we reveal the electrochemical phase evolution of metal-based pre-catalysts (Co4N) in working Li-S batteries that renders highly active electrocatalysts (CoSx). Electrochemical cycling induces the transformation from single-crystalline Co4N to polycrystalline CoSx that are rich in active sites. This transformation propels all-phase polysulfide-involving reactions. Consequently, Co4N enables stable operation of high-rate (10 C, 16.7 mA cm−2) and electrolyte-starved (4.7 μL mgS−1) Li-S batteries. The general concept of electrochemically induced sulfurization is verified by thermodynamic energetics for most of low-valence metal compounds. 相似文献
1000.
Light-Driven Crawling of Molecular Crystals by Phase-Dependent Transient Elastic Lattice Deformation
Yanjun Gong Yongxian Guo Fayuan Ge Wei Xiong Jie Su Yang Sun Chuang Zhang An-Min Cao Yifan Zhang Jincai Zhao Yanke Che 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(26):10423-10428
The light-driven crawling of a molecular crystal that can form three phases, (α, β, and γ) is presented. Laser irradiation of the molecular crystal can generate phase-dependent transient elastic lattice deformation. The resulting elastic lattice deformation that follows scanning irradiation of a laser can actuate the different phases of molecular crystal to move with different velocity and direction. Because the γ phase has a large Young's modulus (ca. 26 GPa), a force of 0.1 μN can be generated under one laser spot. The generated force is sufficient to actuate the γ-formed molecular crystals in a wide dimensional range to move longitudinally at a velocity of about 60 μm min−1, which is two orders of magnitude faster than the α and β phases. 相似文献