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81.
We study the boundedness and compactness of the weighted composition followed and proceeded by differentiation operators from Qκ(p,q) space to weighted α-Bloch space and little weighted α-Bloch space.S...  相似文献   
82.
A 1-D copper(II) coordination polymer formulated as {[Cu2(bdpox)(dabt)](NO3)·H2O}n, where H3bdpox and dabt denote N-benzoate-N′-[3-(diethylamino)propyl]oxamide and 2,2′-diamino-4,4′-bithiazole, respectively, was synthesized and characterized by elemental analyses, molar conductance measurement, IR and electronic spectra studies, and single-crystal X-ray diffraction. The crystal structure analysis reveals that copper(II) ions are bridged by both cis-oxamido and carboxylato groups to form a 1-D coordination polymer with corresponding Cu···Cu separations of 5.2420(10) and 5.1551(8) Å. The endo- and exo-copper(II) ions of the cis-oxamido-bridge are located in distorted square-planar and square-pyramidal geometries, respectively. There is a 2-D hydrogen bonding network in the crystal. The in vitro anticancer activities suggest that the copper(II) complex is active against selected tumor cell lines. The reactivities toward herring sperm DNA and bovine serum albumin (BSA) reveal that the copper(II) complex can interact with DNA by intercalation and effectively quench the intrinsic fluorescence of BSA via a static mechanism. The influence of hydrophobicity of the substituents in bridging ligands on DNA and protein binding properties and the in vitro anticancer activities of such copper(II) polymers is discussed.  相似文献   
83.
We characterize the Banach spaces Y   for which certain subspaces of operators from L1(μ)L1(μ) into Y have the Bishop–Phelps–Bollobás property in terms of a geometric property of Y, namely AHSP. This characterization applies to the spaces of compact and weakly compact operators. New examples of Banach spaces Y with AHSP are provided. We also obtain that certain ideals of Asplund operators satisfy the Bishop–Phelps–Bollobás property.  相似文献   
84.
More than one century ago, Lippmann found that capillary forces can be effectively controlled by external electrostatic forces. As a simple example, by applying a voltage between a conducting liquid droplet and the surface it is sitting on we are able to adjust the wetting angle of the drop. Since Lippmann's findings, electrocapillary phenomena – or electrowetting – have developed into a series of tools for manipulating microdroplets on solid surfaces, or small amounts of liquids in capillaries for microfluidic applications. In this article, we briefly review some recent progress of fundamental understanding of electrowetting and address some still unsolved issues. Specifically, we focus on static and dynamic electrowetting. In static electrowetting, we discuss some basic phenomena found in DC and AC electrowetting, and some theories about the origin of contact angle saturation. In dynamic electrowetting, we introduce some studies about this rather recent area. At last, we address some other capillary phenomena governed by electrostatics and we give an outlook that might stimulate further investigations on electrowetting.  相似文献   
85.
In this study, diverse types of Fe3O4 nanocomposites modified by polyaniline, polypyrrole, and aniline–pyrrole copolymer were synthesized through chemical oxidative polymerization process for dispersive-μ-solid phase extraction (D-μ-SPE) in the presence of various dopants. The results showed that the nanocomposite modified by polyaniline with p-toluene sulfonic acid as a dopant demonstrated higher extraction efficiency for lorazepam (LRZ) and nitrazepam (NRZ). Also the synthesized magnetic sorbents were characterized. The nanocomposite sorbent in combination with high performance liquid chromatography–UV detection was applied for the extraction, preconcentration and determination of lorazepam and nitrazepam in urine and plasma samples. Different parameters influencing the extraction efficiency including: sample pH, amount of sorbent, sorption time, elution solvent and its volume, salt content, and elution time were optimized. The obtained optimal conditions were: sample pH, 6; amount of sorbent, 5 mg; sorption time, 5.0 min; elution solvent and its volume, 0.5 mM cethyltrimethyl ammonium bromide in acetonitrile, 150 μL; elution time, 2.0 min and without addition of NaCl. The calibration curves were linear in the concentration range of 1–2000 μg L−1. The limits of detection (LODs) were achieved in the range of 0.5–1.8 μg L−1 for NRZ and 0.2–2.0 μg L−1 for LRZ, respectively. The percent of extraction recoveries and relative standard deviations (n = 5) were in the range of 84.0–99.0, 6.1–7.8 for NRZ and 90.0–99.0, 4.1–7.0 for LRZ, respectively. Ultimately, the applicability of the method was successfully confirmed by the extraction and determination of NRZ and LRZ in human urine and plasma samples.  相似文献   
86.
The highly odorous compound methanethiol, CH3SH, is commonly produced in biodegradation of biomass and industrial processes, and is classed as 2000 times more odorous than NH3. However, there is no simple analytical method for detecting low parts-per-billion in volume ratio (ppbv) levels of CH3SH. In this study, a micro gas analysis system (μGAS) was developed for continuous or near real time measurement of CH3SH at ppbv levels. In addition to a commercial fluorescence detector, a miniature high sensitivity fluorescence detector was developed using a novel micro-photomultiplier tube device. CH3SH was collected by absorption into an alkaline solution in a honeycomb-patterned microchannel scrubber and then mixed with the fluorescent reagent, 4-(N,N-dimethylaminosulfonyl)-7-fluoro-2,1,3-benzoxadiazole (DBD-F). Gaseous CH3SH was measured without serious interference from other sulfur compounds or amines. The limits of detection were 0.2 ppbv with the commercial detector and 0.3 ppbv with the miniature detector. CH3SH produced from a pulping process was monitored with the μGAS system and the data agreed well with those obtained by collection with a silica gel tube followed by thermal desorption–gas chromatography–mass spectrometry. The portable system with the miniature fluorescence detector was used to monitor CH3SH levels in near-real time in a stockyard and it was shown that the major odor component, CH3SH, presented and its concentration varied dynamically with time.  相似文献   
87.
本文研究了单位圆盘D上的μ-Bergman空间到Zygmund型空间的加权复合算子的有界性和紧性问题.利用泛函分析多复变的方法,获得了单位圆盘上μ-Bergman空间到Zygmund型空间的加权复合算子为有界算子和紧算子的充要条件.  相似文献   
88.
We report a compact and efficient LD end-pumped linearly polarized Nd:YAP laser operating at 1.34 μm. The laser system with different crystal lengths, output couplers and cavity types were compared. Based on optimizing of the pump system and laser cavity, 6.2 W laser radiation at 1341.4 nm with c-axis polarized was achieved, corresponding to an optical conversion efficiency of about 24.8% with respect to the incident pump power. The laser threshold was only about 1.3 W and the optical slope efficiency was up to 27.2%.  相似文献   
89.
90.
The trinuclear copper complex, [Cu33-OH)(CTMB)3(NO3)2(CH3CN)2]·5CH3CN·H2O (1) {CTMB = cyclohexotriazole-3-(4-methoxybenzamide)}, has been prepared by mixing Cu(NO3)2·2.5H2O and CHMBH {CHMBH = N,N′-cyclohexane-1,2-diylidene-bis(4-methoxybenzoylhydrazide)} in acetonitrile under ambient conditions. Compound 1 was characterized by IR and UV–visible spectroscopies as well as elemental analyses. X-ray crystallography shows that the cluster contains a {Cu33-OH)} core supported by three triazole-based Schiff base ligands. Each Cu is bound to the 2-N of one triazole ring and the 1-N of another. However, the coordination sphere of each Cu is different, one is five-coordinate and the other two are six-coordinate and bridged by a NO3 group. The six-coordinate sites are different, one has a terminal NO3 and the other a MeCN ligand. Magnetic measurements revealed the presence of isotropic and antisymmetric exchange between the copper(II) centers. The data were analyzed using the Hamiltonian containing isotropic exchange for an isosceles triangle together with antisymmetric exchange: H = –J1(S1S2 + S2S3)?J2S1S3 + G[S1 × S2 + S2 × S3 + S3 × S1]. Compound 1 exhibits strong antiferromagnetic coupling with J1 = ?180 and J2 = ?118 cm?1 and antisymmetric exchange with Gz = 15 cm?1. Stopped flow spectrophotometric studies show that the formation of 1 occurs in three distinct phases and the kinetics of each phase has been determined.  相似文献   
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