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Träfflista för sökning "WFRF:(Durrant J. R.) srt2:(2010-2014)"

Sökning: WFRF:(Durrant J. R.) > (2010-2014)

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  • Eng, Mattias P, 1977, et al. (författare)
  • Concentration-Dependent Hole Mobility and Recombination Coefficient in Bulk Heterojunctions Determined from Transient Absorption Spectroscopy
  • 2010
  • Ingår i: Journal of Physical Chemistry Letters. - : American Chemical Society (ACS). - 1948-7185. ; 1:20, s. 3096-3100
  • Tidskriftsartikel (refereegranskat)abstract
    • A simple analytical function based on the multiple trapping model, is used to describe the biomolecular recombination of charge carriers in a bulk heterojunction (BHJ) film in the presence of an exponential energetic tail of localized hole "trap" states. The function is used to fit charge carrier decay data from an unannealed P3HT/PCBM film measured by transient absorption. The analysis assumes that only free holes participate in recombination and transport. This implies an effective recombination rate coefficient which varies with the ratio of free to trapped holes. The fit parameters yield a bimolecular recombination constant for free holes with free electrons (k(o) = 3.4 x 10(-12) cm(3) s(-1)) and information about the distribution of trap states (trap distribution parameter beta = 0.29) Assuming the Langevin recombination limit, the analysis yields a concentration dependent effective hole mobility saturating at mu(o) approximate to 7 x 10(-2) cm(2) V-1 s(-1). This approach should be useful to compare BHJs in a consistent and meaningful manner.
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  • Dawson, Deborah A., et al. (författare)
  • New methods to identify conserved microsatellite loci and develop primer sets of high cross-species utility - as demonstrated for birds
  • 2010
  • Ingår i: Molecular Ecology Resources. - : Wiley. - 1755-098X .- 1755-0998. ; 10:3, s. 475-494
  • Tidskriftsartikel (refereegranskat)abstract
    • We have developed a new approach to create microsatellite primer sets that have high utility across a wide range of species. The success of this method was demonstrated using birds. We selected 35 avian EST microsatellite loci that had a high degree of sequence homology between the zebra finch Taeniopygia guttata and the chicken Gallus gallus and designed primer sets in which the primer bind sites were identical in both species. For 33 conserved primer sets, on average, 100% of loci amplified in each of 17 passerine species and 99% of loci in five non-passerine species. The genotyping of four individuals per species revealed that 24-76% (mean 48%) of loci were polymorphic in the passerines and 18-26% (mean 21%) in the non-passerines. When at least 17 individuals were genotyped per species for four Fringillidae finch species, 71-85% of loci were polymorphic, observed heterozygosity was above 0.50 for most loci and no locus deviated significantly from Hardy-Weinberg proportions. This new set of microsatellite markers is of higher cross-species utility than any set previously designed. The loci described are suitable for a range of applications that require polymorphic avian markers, including paternity and population studies. They will facilitate comparisons of bird genome organization, including genome mapping and studies of recombination, and allow comparisons of genetic variability between species whilst avoiding ascertainment bias. The costs and time to develop new loci can now be avoided for many applications in numerous species. Furthermore, our method can be readily used to develop microsatellite markers of high utility across other taxa.
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  • Eng, Mattias P, 1977, et al. (författare)
  • Impact of concentration self-quenching on the charge generation yield of fullerene based donor-bridge-acceptor compounds in the solid state
  • 2011
  • Ingår i: Physical Chemistry Chemical Physics. - : Royal Society of Chemistry (RSC). - 1463-9084 .- 1463-9076. ; 13:9, s. 3721-3729
  • Tidskriftsartikel (refereegranskat)abstract
    • A fullerene based Donor-Bridge-Acceptor (DBA) compound, incorporating a pi-extended tetrathiafulvalene electron donor, is investigated with respect to its photophysics in solution versus solid state. Solid films of neat DBA are compared with blend films where the DBA compound is diluted in the inert, low dielectric, polymer poly(styrene). It is found that the moderate intermolecular electronic coupling and donor-acceptor separation (22 angstrom) in this case leads to the generation of more dissociated, intermolecular charges than a mixture of the donor and acceptor reference compounds. However, the increased intermolecular interactions in the solid state lead to the excited state of the fullerene suffering from concentration self-quenching. This is found to severely affect the charge generation yield in solid films. The impact of competing intra and intermolecular interactions in the solid state upon the film photophysics is analysed in terms of a kinetic model which includes both the effects of concentration self-quenching and the impact of film composition upon the dielectric stabilisation of charge separated states. We conclude that both concentration self-quenching and dielectric stabilisation are critical in determining the photophysics of the blend films, and discuss strategies based upon our observations to enhance the charge photogeneration properties of organic films and photovoltaic devices based upon DBA compounds.
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  • Rogers, Kathleen E., et al. (författare)
  • Novel Cruzain Inhibitors for the Treatment of Chagas' Disease
  • 2012
  • Ingår i: Chemical Biology and Drug Design. - : Wiley. - 1747-0277 .- 1747-0285. ; 80:3, s. 398-405
  • Tidskriftsartikel (refereegranskat)abstract
    • The protozoan parasite Trypanosoma cruzi, the etiological agent of Chagas disease, affects millions of individuals and continues to be an important global health concern. The poor efficacy and unfavorable side effects of current treatments necessitate novel therapeutics. Cruzain, the major cysteine protease of T.similar to cruzi, is one potential novel target. Recent advances in a class of vinyl sulfone inhibitors are encouraging; however, as most potential therapeutics fail in clinical trials and both disease progression and resistance call for combination therapy with several drugs, the identification of additional classes of inhibitory molecules is essential. Using an exhaustive virtual-screening and experimental validation approach, we identify several additional small-molecule cruzain inhibitors. Further optimization of these chemical scaffolds could lead to the development of novel drugs useful in the treatment of Chagas disease.
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