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991.
Wen-Jeng?HsuehEmail author Ren-Zheng?Qiu Chang-Hung?Chen 《The European Physical Journal B - Condensed Matter and Complex Systems》2013,86(1):27
Occurrence of resonant transport due to Fabry-Perot like effect through cascade double asymmetric rings is proposed. We find that high performance reflectors with wide bands can be generated by two asymmetrical open rings with an arm ratio of 1/3. At the resonances, giant persistent currents exist in both rings of the system. The resonance energy is variant and dependent on the length of the connected wire. However, the confined space of the system at the resonance is not equal to the integral multiple of a half-wavelength of traditional Fabry-Perot etalons. 相似文献
992.
Enhancement of ultrasonically initiated emulsion polymerization rate using aliphatic alcohols as hydroxyl radical scavengers 总被引:1,自引:0,他引:1
Ultrasonically initiated emulsion polymerization of styrene was carried out in the presence of aliphatic alcohols, e.g. methanol, ethanol, n-pronanol and n-butanol, as volatile hydroxyl radical scavengers. With the addition of methanol, the polymerization rate of styrene increased, while the molecular weight and the average particle size of the produced polystyrene decreased because more radicals were produced in the presence of methanol. This is true also for the other polymerization system using other aliphatic alcohols, such as ethanol, n-pronanol and n-butanol, suggesting that the alcohols enter into cavitation bubbles and further react with hydroxyl radicals (*OH) from the sonolysis of water to produce hydroxyalkyl radicals, so as to reduce the recombination of *H and *OH radicals, therefore more radicals will be present in the systems for initiating polymerization. Obviously, it is an effective way to enhance ultrasonically initiated emulsion polymerization rate of styrene by adding volatile hydroxyl radical scavenger. 相似文献
993.
Ji‐Cheng Yin Jin‐Song Zhou Jing Sun Yi Qiu Dong‐Zhi Wei Ya‐Ling Shen 《Crystal Research and Technology》2008,43(8):888-893
This paper describes a method about the crystal shape control improving the anti‐tumor activity of tumor necrosis factor‐related apoptosis‐inducing ligand (Apo2L/TRAIL) in a batch cooling suspension crystallization by selecting pH values as a controllable variable. Three shaped TRAIL crystals could be obtained under different pH conditions, among which the hexagonal plate crystals had the highest specific activities against tumor cell line. The relationship among pH values, trimer contents and the specific activities of crystals and the purified TRAIL solutions were investigated. The results showed that different trimer contents resulted from pH altering in crystals and protein solutions is a main reason for their different specific activities. The studies may supply a new method to improve the bioactivity of TRAIL agent during its production and storage. (© 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim) 相似文献
994.
A direct synthesis of 3-(bromomethylene)isobenzofuran-1(3H)-ones from 2-alkynylbenzoic acids is developed through a regioselective 5-exo-dig bromocyclization. The reaction proceeds smoothly with a broad substrate scope. The products can be further elaborated via a palladium-catalyze cross-coupling reaction, or can convert to other heterocycles through simple operation. Preliminary mechanistic studies reveal that this transformation undergoes a radical process. 相似文献
995.
Zhenjiang Qiu Mingxiang Zhu Lu Zheng Jingya Li Dapeng Zou Yangjie Wu Yusheng Wu 《Tetrahedron letters》2019,60(19):1321-1324
An efficient protocol for the synthesis of α-benzyl azetidines starting from benzylboronic acid pinacol ester derivatives and 3-iodoazetidine was developed. A wide range of α-benzyl azetidine derivatives were obtained in moderate to good yields with high regioselectivity (>99%). 相似文献
996.
Two DMTCNQ (DMTCNQ = 2,5‐dimethyl‐7,7,8,8‐tetracyano‐p‐quinodimethane) and DETCNQ (DETCNQ = 2,5‐diethyl‐7,7,8,8‐tetracyano‐p‐quinodimethane) gadolinium complexes [Gd(DMTCNQ)2(CH3OH)(H2O)6][DMTCNQ] · 4H2O ( 1 ) and [Gd(DETCNQ)(H2O)7][2DETCNQ] ( 2 ) were synthesized by reactions of GdCl3 · 6H2O with Li(DMTCNQ) or Li(DETCNQ). X‐ray diffraction analysis reveals that complexes 1 and 2 are discrete complexes. The central metal atom in 1 is coordinated by two DMTCNQ ligand radicals whereas that in 2 is coordinated by just one DETCNQ ligand radical. The adjacent molecules are connected by the intermolecular hydrogen bonds to form the two‐dimensional (2D) supramolecular layer structures, which are further packed into a three‐dimensional (3D) supramolecular architecture through the π–π interactions between ligand radicals in 1 and 2 . Magnetic investigation indicates that the antiferromagnetic interactions between spin carriers exists in 1 and 2 . 相似文献
997.
998.
Xin‐Wei Zhang Alexander Oleinick Hong Jiang Quan‐Lan Liao Quan‐Fa Qiu Irina Svir Yan‐Ling Liu Christian Amatore Wei‐Hua Huang 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(23):7835-7838
The existence of a homeostatic mechanism regulating reactive oxygen/nitrogen species (ROS/RNS) amounts inside phagolysosomes has been invoked to account for the efficiency of this process but could not be unambiguously documented. Now, intracellular electrochemical analysis with platinized nanowire electrodes (Pt‐NWEs) allowed monitoring ROS/RNS effluxes with sub‐millisecond resolution from individual phagolysosomes impacting onto the electrode inserted inside a living macrophage. This shows for the first time that the consumption of ROS/RNS by their oxidation at the nanoelectrode surface stimulates the production of significant ROS/RNS amounts inside phagolysosomes. These results establish the existence of the long‐postulated ROS/RNS homeostasis and allows its kinetics and efficiency to be quantified. ROS/RNS concentrations may then be maintained at sufficiently high levels for sustaining proper pathogen digestion rates without endangering the macrophage internal structures. 相似文献
999.
Yu‐Min Liu Yu‐Qian Huang Shun‐He Liu Dandan Chen Chun Tang Zhen‐Lin Qiu Jun Zhu Yuan‐Zhi Tan 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(38):13410-13413
Bowl inversion is a unique property of buckybowls. The polarity and assembly configuration of buckybowls are reversed after bowl inversion. So far, this unique phenomenon has been studied in solution and on surface, but not in solid state due to spatial constraint. Now a series of exo‐type supramolecular assemblies of trithiasumanene and nanographene are investigated. Tuning the electron density of the nanogaphene component was found to directly affect the binding constant of the complex. Reversible bowl inversion in the solid state was then successfully achieved by subjecting the trithiasumanene–nanographene assembly with the weakest binding strength to repeated heating–cooling cycles, which was unambiguously observed by single crystal X‐ray diffraction. 相似文献
1000.
Jichuan Qiu Da Huo Jiajia Xue Guanghui Zhu Hong Liu Younan Xia 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(31):10716-10721
As a class of biocompatible and biodegradable phase‐change materials, natural fatty acids have received considerable interest in recent years for temperature‐controlled release of drugs. However, the poor dispersibility and colloidal stability of their nanoparticles under physiological conditions place a major limitation on their applications in biomedicine. Herein, we report a facile method for encapsulating a mixture of two natural fatty acids (with a eutectic melting point at 39 °C) in a biocompatible, silica‐based nanocapsule to achieve both stable dispersion and controllable release of drugs. The nanocapsules have a well‐defined hole in the wall to ensure easy loading of fatty acids, together with multiple types of functional components such as therapeutics and near‐infrared dyes. The payloads can be released through the hole when the fatty acids are melted upon photothermal heating. The release profile can be controlled by varying the size of the hole and/or the duration of laser irradiation. 相似文献