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A hexagonal cobalt(ii) metallacycle and its "lipid packaged" derivatives, [Co6(R-bisterpy)6]X12 (R = H, OC16H33, OC27H55; X = BF4, C12-Glu), have been synthesized and characterized. The compounds incorporating BF4- anions formed sphere-like aggregates while the compounds with C12-Glu lipid anions gave double-layered honeycomb architectures composed of hexagonal stacked tubular structures, which exhibit spin crossover behaviour.Two-dimensional materials play a vital role in next-generation microelectronics, optoelectronics and flexible electronics due to their novel physical properties caused by quantum-confinement effects. In this work, we investigate the stability and the possibility of exfoliation of monolayer Bi2Se3-xTex (x = 0, 1, 2) using first-principles calculations. Our calculations show that these materials are indirect bandgap semiconductors, and the elastic modulus is smaller than other conventional materials, which indicates better flexibility. We find that the electron mobility of monolayer Bi2SeTe2 along the armchair direction is higher than that of black phosphorene, reaching 2708 cm2 V-1 s-1, and the electron mobility of monolayer Bi2Se3 along the zigzag direction is about 24 times larger than the hole mobility. The remarkable electron mobilities and highly anisotropic properties of these new monolayers pave the way for future applications in high-speed (opto)electronic devices.A variety of pulse sequences have been described for converting nuclear spin magnetisation into long-lived singlet order for nuclear spin-1/2 pairs. Existing sequences operate well in two extreme parameter regimes. The magnetisation-to-singlet (M2S) pulse sequence performs a robust conversion of nuclear spin magnetisation into singlet order in the near-equivalent limit, meaning that the difference in chemical shift frequencies of the two spins is much smaller than the spin-spin coupling. Other pulse sequences operate in the strong-inequivalence regime, where the shift difference is much larger than the spin-spin coupling. However both sets of pulse sequences fail in the intermediate regime, where the chemical shift difference and the spin-spin coupling are roughly equal in magnitude. We describe a generalised version of M2S, called gM2S, which achieves robust singlet order excitation for spin systems ranging from the near-equivalence limit well into the intermediate regime. Abraxane manufacturer This closes an important gap left by existing pulse sequences. The efficiency of the gM2S sequence is demonstrated numerically and experimentally for near-equivalent and intermediate-regime cases.Plasmas in contact with liquids represent a green chemistry method for the synthesis of metal oxides. In this work, underwater plasma was used for the synthesis of molybdenum and tungsten oxides. The obtained samples were analyzed by various techniques. Results showed that underwater plasma with Mo electrodes allows obtaining non-stoichiometric molybdenum oxide (MoOx). In the case of tungsten electrodes, monoclinic WO3 was formed. The synthesized oxides have a wide band gap (3.21 eV for MoOx and 3.27 eV for WO3). The photocatalytic and sorption activities of the synthesized oxides towards the decomposition of cationic and anionic dyes (Methylene Blue, Rhodamine B, and Reactive Red 6C) were studied. MoOx shows excellent photocatalytic performance under UV and visible light irradiation. The photocatalytic activity of WO3 under visible light is less than that under UV irradiation.Six new ruthenium(ii) complexes with lapachol (Lap) and lawsone (Law) with the general formula [Ru(L)(P-P)(bipy)]PF6, where L = Lap or Law, P-P = 1,2'-bis(diphenylphosphino)ethane (dppe), 1,4'-bis(diphenylphosphino)butane (dppb), 1,1'-bis(diphenylphosphino)ferrocene (dppf) and bipy = 2,2'-bipyridine, were synthesized, fully characterized by elemental analysis, molar conductivity, NMR, cyclic voltammetry, UV-vis, IR spectroscopies and three of them by X-ray crystallography. All six complexes were active against breast (MCF-7 and MDA-MB-231) and prostate (DU-145) cancer cell lines with lower IC50 values than cisplatin. Complex [Ru(Lap)(dppe)(bipy)]PF6 (1a) showed significant selectivity for MDA-MB-231, a model of triple-negative breast cancer (TNBC), as compared to the "normal-like" human breast epithelial cell line, MCF-10A. Complex (1a) inhibited TNBC colony formation and induced loss of cellular adhesion. Furthermore, the complex (1a) induced mitochondrial dysfunction and generation of ROS, as is involved in the apoptotic cell death pathway. Preferential cellular uptake of complex (1a) was observed in MDA-MB-231 cells compared to MCF-10A cells, consistent with the observed selectivity for tumorigenic vs. non-tumorigenic cells. Taken together, these results indicate that ruthenium complexes containing lapachol and lawsone as ligands are promising candidates as chemotherapeutic agents.Penetratin is a short Trojan peptide that attracts great interest in biomedical research for its capacity to translocate biological membranes. Herein, we study in detail both self-assembly and intracellular delivery of DNA by the heptamer KIWFQNR, a truncated peptide derived from Penetratin. This shortened sequence possesses a unique design with bolaamphiphilic characteristics that preserves the longest noncationic amino acid portion found in Penetratin. These features convey amphipathicity to assist self-assembly and make it a suitable model for exploring the role of hydrophobic residues for peptide interaction and cell uptake. We show that the fragment forms peptiplexes (i.e., peptide-DNA complexes), and aggregates into long nanofibers with clear β-sheet signature. The supramolecular structure of nanofibers is likely composed of DNA cores surrounded by a peptide shell to which the double helix behaves as a template and induces fibrillization. A nucleation and growth mechanism proceeding through liquid-liquid phase separation of coacervates is proposed for describing the self-assembly of peptiplexes. We also demonstrate that peptiplexes deliver double-stranded 200 bp DNA into HeLa cells, indicating its potential for preparing non-viral vectors for oligonucleotides through noncovalent strategies. Since the main structural features of native Penetratin are conserved in this simpler fragment, our findings also highlight the role of uncharged amino acids for structuration, and thus for the ability of Penetratin to cross cell membranes.
Here's my website: https://www.selleckchem.com/products/abraxane-nab-paclitaxel.html
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