排序方式： 共有126条查询结果，搜索用时 15 毫秒
61.
Radim Beranek Horst Kisch 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2008,120(7):1340-1342
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Radim Knob Jan Petr Juraj Ševčík Vítězslav Maier 《Journal of separation science》2013,36(20):3426-3431
A method for the determination of tartaric acid enantiomers using CE with contactless conductivity detection has been developed. Cu(II) as a central metal ion together with l ‐hydroxyproline were used as a chiral selector, the BGE was composed of 7 mM CuCl2, 14 mM trans‐4‐hydroxy‐l ‐proline, and 100 mM ε‐aminocaproic acid; the pH was adjusted to 5 by hydrochloric acid. Separation with a resolution of 1.9 was achieved in 9 min in a polyacrylamide‐coated capillary to suppress the EOF. Various counterions of the BGE were studied, and migration order reversal was achieved when switching from ε‐aminocaproic acid to l ‐histidine. With detection limits of about 20 μM, the method was applied to the analysis of wine and grape samples; only l ‐tartaric acid was found. 相似文献
64.
The electrophoretic mobility shift assay (EMSA) is a method for the study of specific DNA–protein interactions in vitro. The pregnane X receptor (PRX) is a key xenobiotic sensor that regulates the expression of drug‐metabolizing enzymes and many other genes. Radiolabeled 32P‐DNA‐probes had been used in studies of PXR‐DNA interactions. There is an increasing need for nonradioactive assays, due to the health, safety and environmental issues. In the current study, we present a protocol for the nonradioactive electrophoretic mobility shift assay, allowing studying interactions between human PXR with promoter DNA sequences. 相似文献
65.
We investigate the optimal trade-off between information gained about an unknown coherent state and the state disturbance caused by the measurement process. We propose several optical schemes that can enable this task, and we implement one of them, a scheme that relies on only linear optics and homodyne detection. Experimentally we reach near optimal performance, limited only by detection inefficiencies. In addition, we show that such a scheme can be used to enhance the transmission fidelity of a class of noisy channels. 相似文献
66.
An algebra with fuzzy equality is a set with operations on it that is equipped with similarity , i.e. a fuzzy equivalence relation, such that each operation f is compatible with . Described verbally, compatibility says that each f yields similar results if applied to pairwise similar arguments. On the one hand, algebras with fuzzy equalities are structures for the equational fragment of fuzzy logic. On the other hand, they are the formal counterpart to the intuitive idea of having functions that are not allowed to map similar objects to dissimilar ones. In this paper, we present a generalization of the well-known Birkhoffs variety theorem: a class of algebras with fuzzy equality is the class of all models of a fuzzy set of identities iff it is closed under suitably defined morphisms, substructures, and direct products.
and Institute for Fuzzy Modeling, University of Ostrava, 30. dubna 22, 701 03 Ostrava, Czech Republic
Mathematics Subject Classification (2000):03B52, 08B05 相似文献
67.
Kateřina Plachká Veronika Pilařová Ondřej Horáček Taťána Gazárková Hana Kočová Vlčková Radim Kučera Lucie Nováková 《Journal of separation science》2023,46(18):2300431
Within this review, we thoroughly explored supercritical fluid chromatography (SFC) columns used across > 3000 papers published from the first study carried out under SFC conditions in 1962 to the end of 2022. We focused on the open tubular capillary, packed capillary, and packed columns, their chemistries, dimensions, and trends in used stationary phases with correlation to their specific interactions, advantages, drawbacks, used instrumentation, and application field. Since the 1990s, packed columns with liquid chromatography and SFC-dedicated stationary phases for chiral and achiral separation are predominantly used. These stationary phases are based on silica support modified with a wide range of chemical moieties. Moreover, numerous unconventional stationary phases were evaluated, including porous graphitic carbon, titania, zirconia, alumina, liquid crystals, and ionic liquids. The applications of unconventional stationary phases are described in detail as they bring essential findings required for further development of the supercritical fluid chromatography technique. 相似文献
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Chunyu Li Elisabeth Hofmeister Dr. Igor Krivtsov Dr. Dariusz Mitoraj Christiane Adler Prof. Radim Beranek Prof. Benjamin Dietzek 《ChemSusChem》2021,14(7):1728-1736
Charge accumulation in photoactive molecules and materials holds great promise in solar energy conversion as it allows for decoupling solar-driven charging from (dark) redox reactions. In this contribution, light-driven charge accumulation was investigated for a recently reported novel water-soluble carbon nitride [K,Na-poly(heptazine imide); K,Na-PHI] photocatalyst, which exhibits excellent activity and stability in highly selective photocatalytic oxidation of alcohols and concurrent reduction of dioxygen to H2O2 under quasi-homogeneous conditions. An excellent charge storage ability of the K,Na-PHI material was demonstrated, showing an optimal density of accumulated electrons (32.2 μmol of electrons per gram) in the presence of 10 vol % MeOH as a sacrificial electron donor. The long-lived electrons accumulated under anaerobic conditions as K,Na-PHI.− radical ions were utilized in interfacial electron transfer to O2 or methyl viologen in a subsequent dark reaction. Ultrafast time-resolved spectroscopy was employed to reveal the kinetics of charge-carrier recombination and methanol oxidation. Geminate recombination of electrons and holes within approximately 100 ps was followed by trap-assisted recombination. The presence of methanol as a sacrificial electron donor accelerated the decay of the transient absorption signal when a static sample was used. This behavior was ascribed to the faster charge recombination in the presence of the radical anions generated after hole extraction. The work suggests that photodriven electron storage in the water-soluble carbon nitride is enabled by localized trap states, and highlights the importance of the effective electron donor for creating long-lived photo-generated carbon nitride radicals. 相似文献
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Christiane Adler Dr. Igor Krivtsov Dr. Dariusz Mitoraj Dr. Lucía dos Santos-Gómez Prof. Santiago García-Granda Dr. Christof Neumann Julian Kund Prof. Christine Kranz Prof. Boris Mizaikoff Prof. Andrey Turchanin Prof. Radim Beranek 《ChemSusChem》2021,14(10):2170-2179
In spite of the enormous promise that polymeric carbon nitride (PCN) materials hold for various applications, the fabrication of high-quality, binder-free PCN films and electrodes has been a largely elusive goal to date. Here, we tackle this challenge by devising, for the first time, a water-based sol−gel approach that enables facile preparation of thin films based on poly(heptazine imide) (PHI), a polymer belonging to the PCN family. The sol−gel process capitalizes on the use of a water-soluble PHI precursor that allows formation of a non-covalent hydrogel. The hydrogel can be deposited on conductive substrates, resulting in formation of mechanically stable polymeric thin layers. The resulting photoanodes exhibit unprecedented photoelectrochemical (PEC) performance in alcohol reforming and highly selective (∼100 %) conversions with very high photocurrents (>0.25 mA cm−2 under 2 sun) down to <0 V vs. RHE. This enables even effective PEC operation under zero-bias conditions and represents the very first example of a ‘soft matter’-based PEC system capable of bias-free photoreforming. The robust binder-free films derived from sol−gel processing of water-soluble PCN thus constitute a new paradigm for high-performance ‘soft matter’ photoelectrocatalytic systems and pave the way for further applications in which high-quality PCN films are required. 相似文献
70.
Eliška Procházková Michal Šála Radim Nencka Martin Dračínský 《Magnetic resonance in chemistry : MRC》2012,50(3):181-186
We measured the 1H, 13 C and 15 N chemical shifts for a series of purine derivatives bearing a norbornane substituent in position 9 and various substituents in position 6. The experimental data were complemented with density functional theory (DFT) calculations. The comparison of the calculated and experimental chemical shifts provided us with information about the tautomer and conformational equilibria of the studied compounds. Copyright © 2012 John Wiley & Sons, Ltd. 相似文献