124 research outputs found
Shape Control of Highly Crystallized Titania Nanorods for Dye-Sensitized Solar Cells Based on Formation Mechanism
<Abstract of published report>Heparin-induced release of extracellular-superoxide dismutase form(V) to plasma.
Evidence and mechanism of efficient thermally activated delayed fluorescence promoted by delocalized excited states
The design of organic compounds with nearly no gap between the first excited singlet (S1) and triplet (T1) states has been demonstrated to result in an efficient spin-flip transition from the T1 to S1 state, that is, reverse intersystem crossing (RISC), and facilitate light emission as thermally activated delayed fluorescence (TADF). However, many TADF molecules have shown that a relatively appreciable energy difference between the S1 and T1 states (~0.2 eV) could also result in a high RISC rate. We revealed from a comprehensive study of optical properties of TADF molecules that the formation of delocalized states is the key to efficient RISC and identified a chemical template for these materials. In addition, simple structural confinement further enhances RISC by suppressing structural relaxation in the triplet states. Our findings aid in designing advanced organic molecules with a high rate of RISC and, thus, achieving the maximum theoretical electroluminescence efficiency in organic light-emitting diodes
<Abstract of published report>Quantitative Analysis of Extracellular-Superoxide Dismutase in Serum and Urine by ELISA with Monoclonal Antibody.
<Abstract of published report>Quantitative and qualitative changes of extracellular-superoxide dismutase in patients with various diseases.
<Abstract of published report>An arginine-213 to glycine mutation in human extracellularsuperoxide dismutase reduces susceptibility to trypsin-like proteinases.
<Abstract of published report>Molecular analysis of extracellular-superoxide dismutase gene associated with high level in serum.
<Abstract of published report>Substitution of glycine for arginine-213 in extracellular-superoxide dismutase impairs affinity for heparin and endothelial cell surface.
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