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11.
Colloidal 5.1 wt% Ru/γ-Al2O3 catalyst was prepared by a microwave assisted, solvothermal reduction of RuCl3 in ethylene glycol in the presence of γ-Al2O3. The catalyst subjected to heat-treatment in hydrogen up to 700 °C, was characterized by BET, XRD, TEM and H2 chemisorption. As-prepared catalyst contained Ru nanoparticles with mean size of 1.5 nm and narrow size distribution uniformly distributed over the support. The nanoparticles were stable on the alumina to 500 °C, but treatment at 600–700 °C caused some sintering of Ru due to migration and coalescence of a part of smallest ruthenium nanoparticles. However, even after H2 treatment at 700 °C, large amount of Ru nanoparticles with sizes of 1–3 nm remained in the catalyst. H2 chemisorption data revealed decrease of Ru dispersion from 0.28 to 0.19 by hydrogen treatment at 700 °C and were in good correspondence with TEM results. On the contrary, mean crystallite sizes obtained from XRD were strongly overestimated. 相似文献
12.
Janina Schmitz Norbert Furtmann Moritz Ponert Dr. Maxim Frizler Dr. Reik Löser Prof. Dr. Ulrike Bartz Prof. Dr. Jürgen Bajorath Prof. Dr. Michael Gütschow 《ChemMedChem》2015,10(8):1365-1377
Cleavage of the invariant chain is the key event in the trafficking pathway of major histocompatibility complex class II. Cathepsin S is the major processing enzyme of the invariant chain, but cathepsin F acts in macrophages as its functional synergist which is as potent as cathepsin S in invariant chain cleavage. Dedicated low‐molecular‐weight inhibitors for cathepsin F have not yet been developed. An active site mapping with 52 dipeptide nitriles, reacting as covalent–reversible inhibitors, was performed to draw structure–activity relationships for the non‐primed binding region of human cathepsin F. In a stepwise process, new compounds with optimized fragment combinations were designed and synthesized. These dipeptide nitriles were evaluated on human cysteine cathepsins F, B, L, K and S. Compounds 10 (N‐(4‐phenylbenzoyl)‐leucylglycine nitrile) and 12 (N‐(4‐phenylbenzoyl)leucylmethionine nitrile) were found to be potent inhibitors of human cathepsin F, with Ki values <10 nM . With all dipeptide nitriles from our study, a 3D activity landscape was generated to visualize structure–activity relationships for this series of cathepsin F inhibitors. 相似文献
13.
Janina Kabatc Edyta Krzyżanowska Beata Jędrzejewska Marek Pietrzak Jerzy Pączkowski 《应用聚合物科学杂志》2010,118(1):165-172
Results of kinetic studies of two‐component photoinitiator systems used in the visible‐light photoinduced polymerization of 2‐ethyl‐2‐(hydroxymethyl)‐1,3‐propanediol triacrylate are presented. Nine different styrylquinolinum dyes coupled with n‐butyltriphenylborate as a coinitiator have been used as photoinitiating systems. Reactive radicals that initiate the polymerization are formed by the well‐known mechanism of photoinduced electron transfer between dye cations acting as electron acceptors and borate anions acting as electron donors. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 相似文献
14.
Leščić Ašler I Ivić N Kovačić F Schell S Knorr J Krauss U Wilhelm S Kojić-Prodić B Jaeger KE 《Chembiochem : a European journal of chemical biology》2010,11(15):2158-2167
Several hydrolases of the SGNH superfamily, including the lipase SrLip from Streptomyces rimosus (Q93MW7), the acyl-CoA thioesterase I TesA from Pseudomonas aeruginosa (Q9HZY8) and the two lipolytic enzymes EstA (from P. aeruginosa, O33407) and EstP (from Pseudomonas putida, Q88QS0), were examined for promiscuity. These enzymes were tested against four chemically different classes of a total of 34 substrates known to be hydrolysed by esterases, thioesterases, lipases, phospholipases, Tweenases and proteases. Furthermore, they were also analysed with respect to their amino acid sequences and structural homology, and their phylogenetic relationship was determined. The Pseudomonas esterases EstA and EstP each have an N-terminal domain with catalytic activity together with a C-terminal autotransporter domain, and so the hybrid enzymes EstA(N)-EstP(C) and EstP(N)-EstA(C) were constructed by swapping the corresponding N- and C-terminal domains, and their hydrolytic activities were compared. Interestingly, substrate specificity and kinetic measurements indicated a significant influence of the autotransporter domains on the catalytic activities of these enzymes in solution. TesA, EstA and EstP were shown to function as esterases with different affinities and catalytic efficacies towards p-nitrophenyl butyrate. Of all the enzymes tested, only SrLip revealed lipase, phospholipase, esterase, thioesterase and Tweenase activities. 相似文献
15.
Zbigniew Czech Agnieszka Kowalczyk Janina Kabatc Jolanta Świderska 《Polymer Bulletin》2013,70(6):1911-1918
This article discusses thermal analysis of different molecular weight poly(2-ethylhexyl acrylates) synthesized by radical polymerization of 2-ethylhexyl acrylate. The main aim of this work was to investigate the thermal properties and degradation process of synthesized acrylic homopolymers and forming of thermal degradation products during their pyrolysis. As investigated method pyrolysis combined with gas chromatography was used. Poly(2-ethylhexyl acrylates) are used as plasticizers for pressure-sensitive adhesives applied in medical area. 相似文献
16.
Errors in measurements of surface resistanceR
s
of HTS materials are due to discrepancy between a mathematical model describing physical phenomena and a real measurement environment, finite accuracy of measurements of theQ-factor, and finite accuracy of constants used for calculation ofR
s
. In this paper we analyze errors inR
s
due to uncertainties in theQ-factor, geometrical coefficients, loss tangent,R
scu, and other factors when a cylindrical copper cavity with an HTS end plate, a stripline resonator, and sapphire rod resonators are used for HTS characterization. 相似文献
17.
Daniela Drescher Ingrid Zeise Heike Traub Peter Guttmann Stephan Seifert Tina Büchner Norbert Jakubowski Gerd Schneider Janina Kneipp 《Advanced functional materials》2014,24(24):3765-3775
By adding a gold core to silica nanoparticles (BrightSilica), silica‐like nanoparticles are generated that, unlike unmodified silica nanoparticles, provide three types of complementary information to investigate the silica nano‐biointeraction inside eukaryotic cells in situ. Firstly, organic molecules in proximity of and penetrating into the silica shell in live cells are monitored by surface‐enhanced Raman scattering (SERS). The SERS data show interaction of the hybrid silica particles with tyrosine, cysteine and phenylalanine side chains of adsorbed proteins. Composition of the biomolecular corona of BrightSilica nanoparticles differs in fibroblast and macrophage cells. Secondly, quantification of the BrightSilica nanoparticles using laser ablation inductively coupled plasma mass spectrometry (LA‐ICP‐MS) micromapping indicates a different interaction of silica nanoparticles compared to gold nanoparticles under the same experimental conditions. Thirdly, the metal cores allow the investigation of particle distribution and interaction in the cellular ultrastructure by cryo nanoscale X‐ray tomography (cryo‐XT). In 3D reconstructions the assumption is confirmed that BrightSilica nanoparticles enter cells by an endocytotic mechanism. The high SERS intensities are explained by the beneficial plasmonic properties due to agglomeration of BrightSilica. The results have implications for the development of multi‐modal qualitative and quantitative characterization in comparative nanotoxicology and bionanotechnology. 相似文献
18.
Janina Rodakiewicz-Nowak Masaaki Ito 《Journal of chemical technology and biotechnology (Oxford, Oxfordshire : 1986)》2003,78(7):809-816
The effect of various water‐miscible organic solvents (ethanol, methanol, acetone, acetonitrile, N,N‐dimethylformamide (DMF) and dimethylsulfoxide (DMSO)) on the kinetics of 4‐tert‐butylcatechol (tBC) oxidation in the presence of different samples of organic solvent‐resistant tyrosinase (OSRT) has been studied. In contrast to mushroom tyrosinase the enzyme shows a high relative stability in solutions of organic solvents and increased activity toward the bulky and hydrophobic substrate, tBC, in respect to catechol. Rates of the studied OSRT‐catalyzed reactions are however reduced by the presence of organic solvents and for all studied samples of OSRT decrease exponentially with the content of an organic solvent. The effect has been satisfactorily described by the effect of organic solvents on the thermodynamic activity of tBC. The correlation of the inhibition parameters with the hydrophobicity of a particular solvent (log P), its intrinsic molar volume, Vi, and the Dimroth–Reichardt parameter, ET(30), are shown. The results allow also the prediction of OSRT activity in aqueous solutions of water‐miscible organic solvents. Copyright © 2003 Society of Chemical Industry 相似文献
19.
Nine patients were operated on in Department of Neurosurgery in Poznań throughout 1990-1993 because of the insufficient carotid blood circulation. In patients measurements of the pulsation pressure of the carotid artery were carried out with a tensometric sensor of pressure during surgery. Neurological symptoms, EEG, evoked potentials and other examinations were conducted before an after operation and correlated with results of pulsation pressure. 相似文献
20.