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21.
Roux P Sabra KG Kuperman WA Roux A 《The Journal of the Acoustical Society of America》2005,117(1):79-84
It has been experimentally demonstrated that the Green's function between two points could be recovered using the cross-correlation function of the ambient noise measured at these two points. This paper investigates the theory behind this result in the simple case of a homogeneous medium with attenuation. 相似文献
22.
The transverse polarization of forward Λ hyperons produced in high-energy p–A collisions is expected to display an extremum at a transverse momentum around the saturation scale. This was first observed within the context of the McLerran–Venugopalan model which has an x -independent saturation scale. The extremum arises due to the kt-odd nature of the polarization-dependent fragmentation function, which probes approximately the derivative of the dipole scattering amplitude. The amplitude changes most strongly around the saturation scale, resulting in a peak in the polarization. We find that the observation also extends to the more realistic case in which the saturation scale Qs is x-dependent. Since a range of x and therefore Qs values is probed at a given transverse momentum and rapidity, this result is a priori not expected. Moreover, the measurement of Λ polarization over a range of xF values actually provides a direct probe of the x-dependence of the saturation scale. This novel feature is demonstrated for typical LHC kinematics and for several phenomenological models of the dipole scattering amplitude. We show that although the measurement will be challenging, it may be feasible at LHC. The situation at RHIC is not favorable, because the peak will likely be at too low transverse momentum of the Λ to be a trustworthy measure of the saturation scale. 相似文献
23.
Andre Rosowsky Katherine K. N. Chen Nickolas Papathanasopoulos Edward J. Modest 《Journal of heterocyclic chemistry》1972,9(2):263-273
Eighteen new 1,3-diamino-5,6-dihydrobenzo[f] quinazolines ( 6 , R. = alkyl, Cl, MeO) were synthesized via the condensation of appropriate 2-tetralones with cyanoguanidine under fusion conditions. Methods were developed for the preparation of a number of heretofore undescribed 2-tetralones as precursors. The final products can be viewed as conformationally rigid analogs of pyrimethamine ( 2 ), and are of interest as inhibitors of dihydrofolate reductase and as potential antimalarial and antitumor agents. 相似文献
24.
7-Benz[c] acridinemethanols as tetracyclic analogs of the 2-phenyl-4-quinolinemethanol antimalarials
Andre Rosowsky Michael Chaykovsky Sandra A. Yeager Richard A. St. Amand May Lin Edward J. Modest 《Journal of heterocyclic chemistry》1971,8(5):809-820
A series of new 7-benz[c]acridinemethanols and 5,6-dihydro-7-benz[c]acridinemethanols was prepared as rigid, tetracyclic analogs of the antimalarial 2-phenyl-4-quinolinemethanols. Condensation of 5,7-dichloroisatin with 6-chloro-, 7-chloro-, and 6,7-dichloro-1-tetralone furnished halogenated 5,6-dihydro-7-benz[c]acridinecarboxylic acids, which were transformed into the corresponding acid chlorides, acyl malonates, α-bromomethyl ketones, and epoxides. Fully aromatic members of the series obtained via dehydrogenation of the 5,6-dihydro acids were likewise converted into epoxides via the acylmalonate route. Although all the epoxides studied proved to be exceptionally resistant to ring-opening by di-n-butylamine, probably on account of steric effects, they could be cleaved readily with piperidine or morpholine. Nmr spectra of the resulting amino alcohols suggest that these compounds exist in a single preferred conformation stabilized by internal O-H····N hydrogen bonding, and that free rotation about the side chain C-C bond does not occur at room temperature. 相似文献
25.
Humberto Andre Potes-Lesoinne Fernando Ramirez-Alvarez Victor H. Perez-Gonzalez Sergio O. Martinez-Chapa Roberto Carlos Gallo-Villanueva 《Electrophoresis》2022,43(1-2):249-262
The survival of living beings, including humanity, depends on a continuous supply of clean water. However, due to the development of industry, agriculture, and population growth, an increasing number of wastewaters is discarded, and the negative effects of such actions are clear. The first step in solving this situation is the collection and monitoring of pollutants in water bodies to subsequently facilitate their treatment. Nonetheless, traditional sensing techniques are typically laboratory-based, leading to potential diminishment in analysis quality. In this paper, the most recent developments in micro- and nano-electrochemical devices for pollutant detection in wastewater are reviewed. The devices reviewed are based on a variety of electrodes and the sensing of three different categories of pollutants: nutrients and phenolic compounds, heavy metals, and organic matter. From these electrodes, Cu, Co, and Bi showed promise as versatile materials to detect a grand variety of contaminants. Also, the most commonly used material is glassy carbon, present in the detection of all reviewed analytes. 相似文献
26.
Thomas Andre´s Wolcan Ezequiel Fe´liz Mario R. Capparelli Alberto L. 《Transition Metal Chemistry》1997,22(6):541-544
The kinetics of the complexation of NiII by pteroylglutamic acid have been studied in the 545 ∘C range, the ionic strength
(0.6 M) being regulated with KNO3, in the 5.5–7.0pH range, using the stopped-flow method. Under the experimental conditions
two processes were observed. The faster process was detected in the millisecond range and is associated with the reaction
between NiII and the ligand. The slower is observed within a few seconds. Complementary equilibrium studies were made at 25
∘C. The results are consistent with the formation of a 1:1 complex between the reactants, and a mechanism is proposed to account
for the observed behaviour. Equilibrium constants for the NiII plus pteroylglutamic acid system, as well as activation parameters,
are reported.
This revised version was published online in June 2006 with corrections to the Cover Date. 相似文献
27.
Dr. Andre Nicolai Petelski Josefina Marquez Silvana Carina Pamies Prof. Dr. Gladis Laura Sosa Prof. Dr. Nélida María Peruchena 《Chemphyschem》2021,22(7):665-674
Due to their potential binding sites, barbituric acid (BA) and its derivatives have been used in metal coordination chemistry. Yet their abilities to recognize anions remain unexplored. In this work, we were able to identify four structural features of barbiturates that are responsible for a certain anion affinity. The set of coordination interactions can be finely tuned with covalent decorations at the methylene group. DFT-D computations at the BLYP-D3(BJ)/aug-cc-pVDZ level of theory show that the C−H bond is as effective as the N−H bond to coordinate chloride. An analysis of the electron charge density at the C−H⋅⋅⋅Cl− and N−H⋅⋅⋅Cl− bond critical points elucidates their similarities in covalent character. Our results reveal that the special acidity of the C−H bond shows up when the methylene group moves out of the ring plane and it is mainly governed by the orbital interaction energy. The amide and carboxyl groups are the best choices to coordinate the ion when they act together with the C−H bond. We finally show how can we use this information to rationally improve the recognition capability of a small cage-like complex that is able to coordinate NaCl. 相似文献
28.
Lipases and esterases are important catalysts with wide varieties of industrial applications. Although many methods have been established for detecting their activities, a simple and sensitive approach for picogram detection of lipolytic enzyme quantity is still highly desirable. Here we report a lipase detection assay which is 1000-fold more sensitive than previously reported methods. Our assay enables the detection of as low as 5 pg and 180 pg of lipolytic activity by direct spotting and zymography, respectively. Furthermore, we demonstrated that the detection sensitivity was adjustable by varying the buffering capacity, which allows for screening of both high and low abundance lipolytic enzymes. Coupled with liquid chromatography-mass spectrometry, our method provides a useful tool for sensitive detection and identification of lipolytic enzymes. 相似文献
29.
Marjorie C. L. C. Freire Gabriela D. Noske Natlia V. Bitencourt Paulo R. S. Sanches Norival A. Santos-Filho Victor O. Gawriljuk Eduardo P. de Souza Victor H. R. Nogueira Mariana O. de Godoy Aline M. Nakamura Rafaela S. Fernandes Andre S. Godoy Maria A. Juliano Bianca M. Peres Cecília G. Barbosa Carolina B. Moraes Lucio H. G. Freitas-Junior Eduardo M. Cilli Rafael V. C. Guido Glaucius Oliva 《Molecules (Basel, Switzerland)》2021,26(16)
The COVID-19 outbreak has rapidly spread on a global scale, affecting the economy and public health systems throughout the world. In recent years, peptide-based therapeutics have been widely studied and developed to treat infectious diseases, including viral infections. Herein, the antiviral effects of the lysine linked dimer des-Cys11, Lys12,Lys13-(pBthTX-I)2K ((pBthTX-I)2K)) and derivatives against SARS-CoV-2 are reported. The lead peptide (pBthTX-I)2K and derivatives showed attractive inhibitory activities against SARS-CoV-2 (EC50 = 28–65 µM) and mostly low cytotoxic effect (CC50 > 100 µM). To shed light on the mechanism of action underlying the peptides’ antiviral activity, the Main Protease (Mpro) and Papain-Like protease (PLpro) inhibitory activities of the peptides were assessed. The synthetic peptides showed PLpro inhibition potencies (IC50s = 1.0–3.5 µM) and binding affinities (Kd = 0.9–7 µM) at the low micromolar range but poor inhibitory activity against Mpro (IC50 > 10 µM). The modeled binding mode of a representative peptide of the series indicated that the compound blocked the entry of the PLpro substrate toward the protease catalytic cleft. Our findings indicated that non-toxic dimeric peptides derived from the Bothropstoxin-I have attractive cellular and enzymatic inhibitory activities, thereby suggesting that they are promising prototypes for the discovery and development of new drugs against SARS-CoV-2 infection. 相似文献
30.
Tatiana Monaretto Andre Souza Tiago Bueno Moraes Victor Bertucci-Neto Corinne Rondeau-Mouro Luiz Alberto Colnago 《Magnetic resonance in chemistry : MRC》2019,57(9):616-625
The traditional way to enhance signal-to-noise ratio (SNR) of nuclear magnetic resonance (NMR) signals is to increase the number of scans. However, this procedure increases the measuring time that can be prohibitive for some applications. Therefore, we have tested the use of several post-acquisition digital filters to enhance SNR up to one order of magnitude in time domain NMR (TD-NMR) relaxation measurements. The procedures were studied using continuous wave free precession (CWFP-T1) signals, acquired with very low flip angles that contain six times more noise than the Carr–Purcell–Meiboom–Gill (CPMG) signal of the same sample and experimental time. Linear (LI) and logarithmic (LO) data compression, low-pass infinity impulse response (LP), Savitzky–Golay (SG), and wavelet transform (WA) post-acquisition filters enhanced the SNR of the CWFP-T1 signals by at least six times. The best filters were LO, SG, and WA that have high enhancement in SNR without significant distortions in the ILT relaxation distribution data. Therefore, it was demonstrated that these post-acquisition digital filters could be a useful way to denoise CWFP-T1, as well as CPMG noisy signals, and consequently reducing the experimental time. It was also demonstrated that filtered CWFP-T1 method has the potential to be a rapid and nondestructive method to measure fat content in beef and certainly in other meat samples. 相似文献