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981.
Back Cover: Co‐existence of Two Different α‐Synuclein Oligomers with Different Core Structures Determined by Hydrogen/Deuterium Exchange Mass Spectrometry (Angew. Chem. Int. Ed. 29/2014) 下载免费PDF全文
982.
The present article describes a capillary zone electrophoresis method which relies on a multilayered water-alkali solvent stacking with online ionization to enhance detection of mannose, arabinose, and their oligosaccharides, which are used as the migration profile standards but are also the distinctive structural components of lipoarabinomannan. Lipoarabinomannan is detected in patients having tuberculosis. The capillary electrophoresis method with ionization of the whole saccharides without degradation in alkaline solution inside the capillary is based on the structural deprotonation of the molecules under ultrahigh pH conditions. The validation of the capillary electrophoresis parameters revealed that the 15-fold electrolyte–water-injection plug allowed detection of one-third lower concentrations than detected without online concentration. For the first time, the better detectability was seen especially for highly polymerized, but otherwise poorly ionized, arabinooctaose. The applicability of the method for detecting whole large biological saccharide complexes was confirmed by the glycolipid lipoarabinomannan. For the first time also, the migration of the indestructible lipoarabinomannan was detected together with oligosaccharides used representing the capping units, namely mannose, mannobiose, and mannotriose. The myo-inositol-phosphate-lipid unit was seen to migrate separately from the arabinomannan, since it was hydrolyzed from one lipoarabinomannan product under alkaline conditions in capillary electrophoresis. 相似文献
983.
Graphene Oxide (GO)- Polyacrylamide composites prepared between 5 and 50 μl GO were performed by Fluorescence Spectroscopy. The phase transition performed on the composites was measured by calculating the critical exponents, β and γ, respectively. In addition, fractal analysis of the composites was calculated by a fluorescence intensity of 427 nm. The geometrical distribution of GO in the composites was calculated based on the power law exponent values using scaling models. While the gelation proceeded GO plates first organized themselves into a 3D percolation cluster with the fractal dimension (Df) of the composite, Df = 2.63, then After it goes to diffusion limited clusters with Df = 1.4, its dimension lines up to a Von Koch curve with a random interval of Df = 1.14. 相似文献
984.
Tapan Ghosh Srikanth Birudula Kalyan Jyoti Kalita Dr. Ratheesh K. Vijayaraghavan 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(46):10501-10509
Control over the molecular packing in the solid state is of utmost importance in regulating the bulk optical properties of organic semiconductors. The electronic coupling between the molecules makes it possible to improve the properties of the bulk materials. This work reports an example of control over the selective formation of polymorphic single crystals of donor–acceptor-type small-molecule compound 25TR by 1) kinetic or 2) thermodynamic course of crystallisation to yield slipped stack (S) and cofacial (C) dimers in the single crystals. The distinct optical characteristics of the C-dimer and S-dimer are summarised. Both forms show significant excitonic interactions in the solid state, and the S-dimeric form has strong yellowish orange fluorescence, whereas the C-dimeric form is non-fluorescent in the crystalline state. DFT calculations and differential scanning calorimetric experiments revealed that the C-dimer polymorph is the thermodynamically stable form with a free energy offset of 0.43 eV in comparison with the S-dimer. Interestingly, the thermodynamically driven non-fluorescent single crystal was found to be convertible to its fluorescent form irreversibly by thermal trigger. The charge-carrier-transport characteristics of these two polymorphs were computed by using the Marcus–Hush formalism. The computations of the charge-carrier-transport behaviour revealed that the S-dimer ( 25TR(R) ) is ambipolar, whereas the C-dimer ( 25TR(Y) ) is predominantly n-type. 相似文献
985.
The critical temperatures and the critical pressures of five polycyclic aromatic compounds, namely, acenaphthene, fluorene, anthracene, phenanthrene, and pyrene have been measured. All the compounds studied decompose at near-critical temperatures. A pulse-heating technique applicable to measuring the critical properties of thermally unstable compounds has been used. The times from the beginning of a heating pulse to the moment of reaching the critical temperature were from (0.06 to 0.85) ms. The short residence times provide little degradation of the substances in the course of the experiments. The experimental critical parameters of the polycyclic aromatic compounds have been compared with those estimated by five predictive methods. The acentric factors of polycyclic aromatic compounds studied have been calculated. 相似文献
986.
Dominique M. S. Buyens Prof. Dr. Lynne A. Pilcher Prof. Dr. Emil Roduner 《Chemphyschem》2021,22(19):2025-2033
Rare anionic forms of nucleic acids play a significant biological role and lead to spontaneous mutations and replication and translational errors. There is a lack of information surrounding the stability and reactivity of these forms. Ion pairs of mono-sodium and -potassium salts of adenine exist in DMSO solution with possible cation coordination sites at the N1, N7 and N9 atoms of the purine ring. At increasing concentrations π-π stacked dimers are the predominant species of aggregates followed by higher order aggregation governed by coordination to metal cations in which the type of counter ion present has a central role in the aggregate formation. 相似文献
987.
Carlo Mercuri Berardino Sciunzi Marco Squassina 《Journal of Mathematical Analysis and Applications》2015
We prove that the critical problem for the p-Laplacian operator admits a nontrivial solution in annular shaped domains with sufficiently small inner hole. This extends Coron's result [4] to a class of quasilinear problems. 相似文献
988.
通过实验研究了浓度对硫酸性质的影响,结果表明浓度大于等于12 mol·L-1(72%)的硫酸具有明显的吸水性、脱水性、强氧化性和能使铁、铝钝化。浓硫酸与常见指示剂作用颜色变化有各自的变色特点,和常见酸与指示剂作用的颜色变化规律不同。 相似文献
989.
《Electrophoresis》2018,39(17):2181-2187
A nanoporous poly‐(styrene sulfonate) (poly‐SS) membrane was developed for fast and selective ion transport in a microfluidic chip. The poly‐SS membrane can be photopolymerized in‐situ at arbitrary location of a microchannel, enabling integrated fluidics design in the microfluidic chip. The membrane is characterized by a low hydraulic resistance and a high surface charge to maximize the electroosmotic flow and charge selectivity. The membrane characteristics were investigated by charge‐selective electropreconcentration method. Experimental results show membranes with various percentages of poly‐SS are able to concentrate anions (fluorescein and TRITC‐labeled BSA). The anion‐selective electropreconcentration process is stable and 26‐times faster than previously reported poly‐AMPS (2‐acrylamido‐2‐methyl‐1‐propanesulfonic acid) based system. The electropreconcentration was also demonstrated to depend on the sample valency and buffer concentration. 相似文献
990.
《Acta Crystallographica. Section C, Structural Chemistry》2018,74(3):295-299
A new Cu3Au‐type ternary phase (τ phase) is found in the AuPd‐rich part of the Au–In–Pd system. It has a broad homogeneity range based on extensive (Pd,Au) and (In,Au) replacement, with the composition varying between Au17.7In25.3Pd57.0 and Au50.8In16.2Pd33.0. The occupancies of the crystallographic positions were studied by single‐crystal X‐ray diffraction for three samples of different composition. The sites with mm symmetry are occupied by atoms with a smaller scattering power than the atoms located on 4/mmm sites. Two extreme structure models were refined. Within the first, the occupation type changes from (Au,In,Pd)3(Pd,In) to (Au,Pd)3(In,Pd,Au) with an increase in the Au gross content. For the second model, the occupation type (Au,In,Pd)3(Pd,Au) remains essentially unchanged for all Au concentrations. Although the diffraction data do not allow the choice of one of these models, the latter model, where Au substitutes In on 4/mmm sites, seems to be preferable, since it agrees with the fact that the homogeneity range of the τ phase is inclined to the Au corner and provides the same occupation type for all the studied samples of different compositions. 相似文献