نتایج جستجو برای: selenide
تعداد نتایج: 2194 فیلتر نتایج به سال:
Artificial enzymes capable of achieving tunable catalytic activity through stimuli control of enzymatic structure transition are of significance in biosensor and biomedicine research. Herein we report a novel smart glutathione peroxidise (GPx) mimic with modulatory catalytic activity based on redox-induced supramolecular self-assembly. First, an amphiphilic Fmoc-phenylalanine-based selenide was...
The intensity of a He–Ne laser ~633 nm, 5 mW! transmitted by different GaSe samples is observed to change in correlation with a Nd-yttrium–aluminum–garnet laser pulse ~532 nm, 7.8 ns, 3 mJ! which excites them. Such time response has been attributed to a nonlinear optical effect, i.e., a decrease in the refractive index due to the exciton screening by the photogenerated carriers. A calculation o...
Articles you may be interested in Aging and reduced bulk conductance in thin films of the topological insulator Bi2Se3 Comment on " The role of Bi3+ ions in magneto-optic Ce and Bi comodified epitaxial iron garnet films " [Appl. The role of Bi 3 + ions in magneto-optic Ce and Bi comodified epitaxial iron garnet films Appl.
Impurity doping in two-dimensional (2D) materials can provide a route to tuning electronic properties, so it is important to be able to determine the distribution of dopant atoms within and between layers. Here we report the tomographic mapping of dopants in layered 2D materials with atomic sensitivity and subnanometer spatial resolution using atom probe tomography (APT). APT analysis shows tha...
In situ lithiation-delithiation treatment enables high oxygen reduction activity in palladium selenide without serious structural or phase change; resulting an optimum balance of catalytic and stability.
Oxo-sulfido- and oxo-selenido-molybdenum(VI) complexes with an ene-1,2-dithiolate ligand are generated as models of the active sites of molybdenum hydroxylases. The sulfide and selenide groups are highly reactive toward triphenylphosphine in the order of Se > S.
A strategy for photochemical cleavage of peptide and protein backbones is described, which is based on a selenide-mediated cleavage of a backbone ester moiety. Studies in model systems establish the viability of the chemistry and suggest the method could be a valuable tool for chemical biology studies of proteins.
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