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Träfflista för sökning "WFRF:(Yu DM) srt2:(2000-2004)"

Search: WFRF:(Yu DM) > (2000-2004)

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1.
  • Johansson, DM, et al. (author)
  • Influence of polymerization temperature on molecular weight, photoluminescence, and electroluminescence for a phenyl-substituted poly(p-phenylenevinylene)
  • 2001
  • In: Macromolecules. - 0024-9297 .- 1520-5835. ; 34:11, s. 3716-3719
  • Journal article (peer-reviewed)abstract
    • We present the synthesis and characterization of poly(2-(2",5'-bis(2"-ethylhexyloxy)phenyl)-1,4-phenylenevinylene) (BEHP-PPV) polymerized at different temperatures. The photoluminescence efficiencies in the solid state of BEHP-PPV obtained at 144 and 0 degreesC are 28% and 60%, respectively. H-1 NMR measurements showed a lower concentration of structural defects for BEHP-PPV obtained at lower temperatures, which can explain the increased photoluminescence efficiencies for these polymers. Polymerization temperatures below 0 degreesC decrease the molecular weight without changing the photoluminescence efficiency to any large extent. The electroluminescence efficiencies follow the trend in the photoluminescence efficiencies.
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2.
  • Johansson, DM, et al. (author)
  • Synthesis of soluble phenyl-substituted poly(p-phenylenevinylenes) with a low content of structural defects
  • 2002
  • In: Macromolecules. - : American Chemical Society (ACS). - 0024-9297 .- 1520-5835. ; 35:13, s. 4997-5003
  • Journal article (peer-reviewed)abstract
    • The synthesis and characterization of two new soluble poly(p-phenylenevinylenes) (PPVs) are reported. The polymers are poly(2-2',5'-bis(octyloxy)benzene)-1,4-phenylenevinylene) (BOP-PPV) and poly(2-(2',5'-bis(octyloxy)benzene)-5-methoxy-1,4-phenylenevinylene) (BOPM-PPV). Both polymers have been polymerized at high and low temperatures to study the formation of structural defects. It is shown that both methoxy groups as side chains and low polymerization temperatures decrease the content of defects in the final polymer. As a consequence, the polymers with lower concentration of defects exhibit higher electroluminescence yields in light-emitting diodes. In addition to this, the polymers with a low content of defects exhibited longer operational lifetimes in these devices. The highest photoluminescence quantum yield in the solid state and electroluminescence efficiency were found to be 72% and 1.74%, respectively.
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3.
  • Ryder, JW, et al. (author)
  • Isomer-specific antidiabetic properties of conjugated linoleic acid. Improved glucose tolerance, skeletal muscle insulin action, and UCP-2 gene expression
  • 2001
  • In: Diabetes. - : American Diabetes Association. - 0012-1797 .- 1939-327X. ; 50:5, s. 1149-1157
  • Journal article (peer-reviewed)abstract
    • Conjugated linoleic acid (CLA) isomers have a number of beneficial health effects, as shown in biomedical studies with animal models. Previously, we reported that a mixture of CLA isomers improved glucose tolerance in ZDF rats and activated peroxisome proliferator–activated receptor (PPAR)-γ response elements in vitro. Here, our aim was to elucidate the effect(s) of specific CLA isomers on whole-body glucose tolerance, insulin action in skeletal muscle, and expression of genes important in glucose and lipid metabolism. ZDF rats were fed either a control diet (CON), one of two CLA supplemented diets (1.5% CLA) containing differing isoforms of CLA (47% c9,t11; 47.9% c10,t12, 50:50; or 91% c9,t11, c9,t11 isomers), or were pair-fed CON diet to match the intake of 50:50. The 50:50 diet reduced adiposity and improved glucose tolerance compared with all other ZDF treatments. Insulin-stimulated glucose transport and glycogen synthase activity in skeletal muscle were improved with 50:50 compared with all other treatments. Neither phosphatidlyinositol 3-kinase activity nor Akt activity in muscle was affected by treatment. Uncoupling protein 2 in muscle and adipose tissue was upregulated by c9,t11 and 50:50 compared with ZDF controls. PPAR-γ mRNA was downregulated in liver of c9,t11 and pair-fed ZDF rats. Thus, the improved glucose tolerance in 50:50 rats is attributable to, at least in part, improved insulin action in muscle, and CLA effects cannot be explained simply by reduced food intake.
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