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Sökning: L773:1359 7345

  • Resultat 61-70 av 514
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61.
  • Castelletto, Valeria, et al. (författare)
  • Structure of single-wall peptide nanotubes: in situ flow aligning X-ray diffraction
  • 2010
  • Ingår i: Chemical Communications. - : Royal Society of Chemistry (RSC). - 1364-548X .- 1359-7345. ; 46:34, s. 6270-6272
  • Tidskriftsartikel (refereegranskat)abstract
    • The structure of single wall peptide nanotubes is presented for the model surfactant-like peptide A(6)K. Capillary flow alignment of a sample in the nematic phase at high concentration in water leads to oriented X-ray diffraction patterns. Analysis of these, accompanied by molecular dynamics simulations, suggests the favourable self-assembly of antiparallel peptide dimers into beta-sheet ribbons that wrap helically to form the nanotube wall.
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62.
  • Castoldi, Laura, et al. (författare)
  • Transition metal-free and regioselective vinylation of phosphine oxides and H-phosphinates with VBX reagents
  • 2020
  • Ingår i: Chemical Communications. - : Royal Society of Chemistry (RSC). - 1359-7345 .- 1364-548X. ; 56:92, s. 14389-14392
  • Tidskriftsartikel (refereegranskat)abstract
    • A series of phosphine oxides and H-phosphinates were vinylated in the presence of the iodine(iii) reagents vinylbenziodoxolones (VBX), providing the corresponding alk-1-enyl phosphine oxides and alk-1-enyl phosphinates in good yields with complete chemo- and regioselectivity. The vinylation proceeds in open flask under mild and transition metal-free conditions.
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63.
  • Cellini, Andrea, 1991, et al. (författare)
  • Structural basis of the radical pair state in photolyases and cryptochromes
  • 2022
  • Ingår i: Chemical Communications. - : Royal Society of Chemistry (RSC). - 1359-7345 .- 1364-548X. ; , s. 4889-4892
  • Tidskriftsartikel (refereegranskat)abstract
    • We present the structure of a photoactivated animal (6-4) photolyase in its radical pair state, captured by serial crystallography. We observe how a conserved asparigine moves towards the semiquinone FAD chromophore and stabilizes it by hydrogen bonding. Several amino acids around the final tryptophan radical rearrange, opening it up to the solvent. The structure explains how the protein environment stabilizes the radical pair state, which is crucial for function of (6-4) photolyases and cryptochromes.
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64.
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65.
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66.
  • Chen, Chih-Yao, et al. (författare)
  • High-voltage honeycomb layered oxide positive electrodes for rechargeable sodium batteries
  • 2020
  • Ingår i: Chemical Communications. - : Royal Society of Chemistry (RSC). - 1364-548X .- 1359-7345. ; 56:65, s. 9272-9275
  • Tidskriftsartikel (refereegranskat)abstract
    • Honeycomb layered oxides from Na2Ni2-xCoxTeO6 family were assessed for use as positive electrodes in rechargeable sodium batteries at ambient and elevated temperatures using ionic liquids. Substitution of nickel with cobalt increases the discharge voltage to nearly 4 V (versus Na+/Na), surpassing the average voltages of most Na based layered oxide positive electrodes.
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67.
  • Chen, Fei-Jian, et al. (författare)
  • Structure-direction towards the new large pore zeolite NUD-3
  • 2021
  • Ingår i: Chemical Communications. - : Royal Society of Chemistry (RSC). - 1359-7345 .- 1364-548X. ; 57:2, s. 191-194
  • Tidskriftsartikel (refereegranskat)abstract
    • The new zeolite NUD-3 possesses a three-dimensional system of large pore channels that is topologically identical to those of ITQ-21 and PKU-14. However, the three zeolites have distinctly different frameworks: a particular single 4-membered ring inside the denser portion of the zeolite is missing in PKU-14, disordered in ITQ-21 and fully ordered in NUD-3. We document these differences and use molecular simulations to unravel the mechanism by which a particular structure directing agent dication, 1,1′-(1,2-phenylenebis(methylene))bis(3-methylimidazolium), is able to orient this inner ring.
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68.
  • Chen, H., et al. (författare)
  • A Cu2Se-Cu2O film electrodeposited on titanium foil as a highly active and stable electrocatalyst for the oxygen evolution reaction
  • 2018
  • Ingår i: Chemical Communications. - : Royal Society of Chemistry. - 1359-7345 .- 1364-548X. ; 54:39, s. 4979-4982
  • Tidskriftsartikel (refereegranskat)abstract
    • Many nonprecious metal-selenide-based materials have been reported as electrocatalysts with high activity for the oxygen evolution reaction (OER). Herein, a hybrid catalyst film composed of Cu2Se and Cu2O nanoparticles directly grown on Ti foil (Cu2Se-Cu2O/TF) was prepared through a simple and fast cathodic electrodeposition method. Surprisingly, this electrode required a relatively low overpotential of 465 mV to achieve a catalytic current density of 10 mA cm-2 for the OER in 0.2 M carbonate buffer (pH = 11.0). Furthermore, a long-term constant current electrolysis test confirmed the high durability of the Cu2Se-Cu2O/TF anode at a current density of 10 mA cm-2 over 20 h. The XRD, TEM and XPS analysis of the sample after the OER indicated that a CuO protective layer formed on the surface of the Cu2Se-Cu2O catalyst, which effectively suppressed further oxidation of the Cu2Se-Cu2O catalyst during the OER and resulted in sustained catalytic oxidation of water.
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69.
  • Chen, Yun, et al. (författare)
  • Immobilization of a cobalt catalyst on fullerene in molecular devices for water reduction
  • 2015
  • Ingår i: Chemical Communications. - : Royal Society of Chemistry (RSC). - 1359-7345 .- 1364-548X. ; 51:57, s. 11508-11511
  • Tidskriftsartikel (refereegranskat)abstract
    • A cobalt-based molecular catalyst was successfully grafted to a fullerene derivative via 'click' chemistry on an electrode for both electro-catalytic and light driven water reduction. Using an organic photovoltaic electrode immobilized with a cobalt catalyst as the photocathode, the photoelectrochemical cell displayed a stable photocurrent.
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70.
  • Chien, Yu-Chuan, 1990-, et al. (författare)
  • Towards reliable three-electrode cells for lithium–sulfur batteries
  • 2022
  • Ingår i: Chemical Communications. - : Royal Society of Chemistry (RSC). - 1359-7345 .- 1364-548X. ; 58:5, s. 705-708
  • Tidskriftsartikel (refereegranskat)abstract
    • Three-electrode measurements are valuable to the understanding of the electrochemical processes in a battery system. However, their application in lithium–sulfur chemistry is difficult due to the complexity of the system and thus rarely reported. Here, we present a simple three-electrode cell format with relatively good life time and minimum interference with the cell operation.
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