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141.
Antonia Kagkoura Javier Hernandez‐Ferrer Ana M. Benito Wolfgang K. Maser Nikos Tagmatarchis 《化学:亚洲杂志》2020,15(15):2350-2356
A facile strategy for the controllable growth of CdS nanoparticles at the periphery of MoS2 en route the preparation of electron donor‐acceptor nanoensembles is developed. Precisely, the carboxylic group of α‐lipoic acid, as addend of the modified MoS2 obtained upon 1,2‐dithiolane functionalization, was employed as anchor site for the in situ preparation and immobilization of the CdS nanoparticles in an one‐pot two‐step process. The newly prepared MoS2/CdS hybrid material was characterized by complementary spectroscopic, thermal and microscopy imaging means. Absorption spectroscopy was employed to register the formation of MoS2/CdS, by observing a broad shoulder centered at 420 nm due to CdS nanoparticles, while the excitonic bands of MoS2 were also evident. Moreover, based on the efficient quenching of the characteristic fluorescence emission of CdS at 725 nm by the presence of MoS2, strong electronic interactions at the excited state between the two species within the ensemble were identified. Photoelectrochemical assays of MoS2/CdS thin‐film electrodes revealed a prompt, steady and reproducible anodic photoresponse during repeated on‐off cycles of illumination. A significant zero‐current photopotential of ?540 mV and an anodic photocurrent of 1 μA were observed, underlining improved charge‐separation and electron transport from CdS to MoS2. The superior performance of the charge‐transfer processes in MoS2/CdS is of direct interest for the fabrication of photoelectrochemical and optoelectronic devices. 相似文献
142.
Alba Covelo Sandra Rodil Edgar Oliver López-Villegas Carlos Andrés Álvarez Miguel Hernandez 《Surface and interface analysis : SIA》2020,52(12):1128-1133
The present study evaluates and correlates the morphology of poly (vinyl alcohol) (PVA) and sodium alginate (SA) nanofibres with their internal structure to determine dielectric and tensile properties for future applications as long-lasting and resistant cell scaffolds. This work generates electrospun nanofibres mixing SA concentration in a PVA solution cross-linked in calcium chloride media. The dielectric properties of the nanofibres that were obtained using electrochemical impedance spectroscopy (EIS) show that at higher amount of SA in the PVA/SA fibres, the cross-linking process occurs at shorter times, indicating the modification of the internal structure of the PVA/SA. The X-ray photoelectron spectra (XPS) demonstrate that the chemical composition of the nanofibres varies depending on the depth profile. The transmission electron microscopy (TEM) proves that the PVA/SA is formed as a core-shell coaxial nanofibre. The tensile testing demonstrates that with a higher SA concentration, the mechanical properties show brittleness. 相似文献
143.
Arpita Dey Ran Chen Feng Li Subhamita Maitra Jean-Francois Hernandez Guo-Chun Zhou Bruno Vincent 《Molecules (Basel, Switzerland)》2021,26(24)
Alzheimer’s disease (AD) is a devastating neurodegenerative disorder, one of the main characteristics of which is the abnormal accumulation of amyloid peptide (Aβ) in the brain. Whereas β-secretase supports Aβ formation along the amyloidogenic processing of the β-amyloid precursor protein (βAPP), α-secretase counterbalances this pathway by both preventing Aβ production and triggering the release of the neuroprotective sAPPα metabolite. Therefore, stimulating α-secretase and/or inhibiting β-secretase can be considered a promising anti-AD therapeutic track. In this context, we tested andrographolide, a labdane diterpene derived from the plant Andrographis paniculata, as well as 24 synthesized derivatives, for their ability to induce sAPPα production in cultured SH-SY5Y human neuroblastoma cells. Following several rounds of screening, we identified three hits that were subjected to full characterization. Interestingly, andrographolide (8,17-olefinic) and its close derivative 14α-(5′,7′-dichloro-8′-quinolyloxy)-3,19-acetonylidene (compound 9) behave as moderate α-secretase activators, while 14α-(2′-methyl-5′,7′-dichloro-8′-quinolyloxy)-8,9-olefinic compounds 31 (3,19-acetonylidene) and 37 (3,19-diol), whose two structures are quite similar although distant from that of andrographolide and 9, stand as β-secretase inhibitors. Importantly, these results were confirmed in human HEK293 cells and these compounds do not trigger toxicity in either cell line. Altogether, these findings may represent an encouraging starting point for the future development of andrographolide-based compounds aimed at both activating α-secretase and inhibiting β-secretase that could prove useful in our quest for the therapeutic treatment of AD. 相似文献
144.
Ungapped Local Multiple Alignment is a widely used procedure in bioinformatics. It roughly consists of locating in a given set of nucleotide (DNA) or amino acid (proteins) sequences, a number of non-overlapping fixed-size factors (also called occurrences), that are likely to have evolved from a common ancestor. In addition to the widely known statistical approaches, we define the problem from a pure combinatorial optimization point of view, by defining specific neighborhood functions and a hill-climbing strategy for each of four particular instances of this problem: (1) one occurrence per sequence, (2) at most one occurrence per sequence, (3) at least one occurrence per sequence, and (4) any number of occurrences per sequence. The method is implemented in a tool called Nomad (Neighborhood Optimization for Multiple Alignment Discovery) and a web interface is available at www.expasy.org/tools/nomad.html. 相似文献
145.
146.
Juan Sebastian Trujillo Hernandez Alberto Aragn-Muriel Willinton Corrales Quintero Juan Camilo Castro Velsquez Natalia Andrea Salazar-Camacho German Antonio Prez Alczar Jesús Anselmo Tabares 《Molecules (Basel, Switzerland)》2022,27(24)
The aim of this study is to evaluate the applicability of the catalytic activity (CA) of the Fe3O4 magnetic system in the adsorption/degradation of methylene blue and esterification. The thermal decomposition method allowed the preparation of Fe3O4 nanoparticles. The crystallites of the Fe3O4 structural phase present an acicular form confirmed by X-ray diffraction. Transmission electron microscopy results identified the acicular shape and agglomeration of the nanoparticles. Mössbauer spectroscopy showed that the spectrum is composed of five components at room temperature, a hyperfine magnetic field distribution (HMFD), two sextets, a doublet, and a singlet. The presence of the HMFD means that a particle size distribution is present. Fluorescence spectroscopy studied the CA of the nanoparticles with methylene blue and found adsorption/degradation properties of the dye. The catalytic activity of the nanoparticles was evaluated in the esterification reaction by comparing the results in the presence and absence of catalyst for the reaction with isobutanol and octanol, where it is observed that the selectivity for the products MIBP and MNOP is favored in the first three hours of reaction. 相似文献
147.
Haibin Gu Roberto Ciganda Ricardo Hernandez Patricia Castel Pengxiang Zhao Jaime Ruiz Didier Astruc 《Macromolecular rapid communications》2016,37(7):630-636
Diblock metallopolymer polyelectrolytes containing the two redox‐robust cationic sandwich units [CoCp′Cp]+ and [FeCp′(η6‐C6Me6)]+ (Cp = η5‐C5H5; Cp′ = η5‐C5H4‐) as hexafluorophosphate ([PF6]−) salts are synthesized by ring‐opening metathesis polymerization using Grubbs' third generation catalyst. Their electrochemical properties show full chemical and electrochemical reversibilities allowing fine determination of the copolymer molecular weight using Bard–Anson's electrochemical method by cyclic voltammetry.
148.
D. Fink G. Muñoz Hernandez N.L. Ruiz J. Vacik V. Hnatowicz H. García-Arellano 《辐射效应与固体损伤》2013,168(5):396-417
Etching of continuous nuclear tracks in thin polymer foils from both sides is known to lead to the formation of double-conical nanopores. In this work and related ones we try to find out how this etching kinetics is modified when materials are added which react with each other upon their contact towards some new product that influences the etching. For that purpose we have chosen here Li+ and F? ions as the additions, which react with each other to form LiF precipitations. The coupled etching and precipitation kinetics is recorded by measuring the electrical current that is transmitted through the foils upon application of a low-frequency alternating sinusoidal voltage. Depending on the etchant concentrations, the etching temperature and the time of Li+ and F? addition, different effects are found that range from (a) no alteration of the transmitted current at all, via (b) the emergence of an alternating current with a temperature-dependent amplitude, and (c) the complete vanishing of any transmitted current at all, towards (d) chaotic transmitted current histories with phases with strong current spike emission and (e) rather quiet phases, alternating with each other in a rather unsystematic way. The observed effects are ascribed to (a) the enhanced penetration efficiency of both the Li+ and F? ions through the polymeric bulk and/or latent ion tracks after the removal of the polymer's protective surface layer by the etchant, (b) the high mobility of preferentially the F? ions within the polymer, (c) the LiF precipitation within the polymer or on its surface upon encounter of Li+ and F? ions, (d) the nanofluidic properties of narrow etched tracks covered with Li+ ions on the wall surfaces and F? ions beyond, and/or (e) the formation of LiF membranes within the etched tracks. 相似文献
149.
150.
[reaction: see text] Common sugar derivatives can be transformed in a few steps into chiral-substituted furyl carbinols. The mildness of the reaction conditions and the good yields obtained make this procedure an interesting alternative to the conventional processes. 相似文献