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  • American Institute of Physics (AIP)  (5)
  • Blackwell Publishing Ltd  (1)
  • American Geophysical Union (AGU)
  • 1995-1999  (6)
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  • 1
    Digitale Medien
    Digitale Medien
    Woodbury, NY : American Institute of Physics (AIP)
    Chaos 5 (1995), S. 330-345 
    ISSN: 1089-7682
    Quelle: AIP Digital Archive
    Thema: Physik
    Notizen: Dissipative partial differential equations have applications throughout the sciences: models of turbulence in fluids, chemical reactions, and morphogenesis in biology can all be written in a general form which allows them to be subjected to a unified analysis. Recent results on these equations show that in many cases they are not as complex as they initially appear, and can be converted into a set of ordinary differential equations. However, most of the relevant references present a bewildering array of terms which can obscure the simple underlying ideas. The main purpose of this paper is to introduce this terminology, motivated by several major results, slowly and by example. Detailed proofs are omitted, but it is hoped that this approach will give a good understanding of and intuitive feel for the subject without recourse to technicalities. Nevertheless, sufficient mathematical detail is included to allow application of these results to many examples. © 1995 American Institute of Physics.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 81 (1997), S. 2051-2054 
    ISSN: 1089-7550
    Quelle: AIP Digital Archive
    Thema: Physik
    Notizen: We have used the inherent surface sensitivity of second-harmonic generation to develop an instrument for nonlinear optical microscopy of surfaces and interfaces. This optical technique is ideal for imaging nanometer-thick, chromophoric self-assembled monolayers (SAMs), which have been patterned using photolithographic techniques. In this paper, we demonstrate the application of second-harmonic generation microscopy to patterned SAMs of the noncentrosymmetric molecule calixarene and discuss the resolution and sensitivity limits of the technique. © 1997 American Institute of Physics.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Oxford, UK : Blackwell Publishing Ltd
    Plant breeding 116 (1997), S. 0 
    ISSN: 1439-0523
    Quelle: Blackwell Publishing Journal Backfiles 1879-2005
    Thema: Land- und Forstwirtschaft, Gartenbau, Fischereiwirtschaft, Hauswirtschaft
    Notizen: Six six-row Nordic spring barley genotypes (Hordeum vulgare L.) were assessed in the field in Finland (1994 and 1995) for resistance to Rhynchosporium secalis (Oud.) J.J. Davis, the causal pathogen of scald, in artificially inoculated plots. The barleys were known not to contain major genes for resistance to scald and the purpose of these experiments was to identify quantitative differences in resistance to scald which might be exploitable in a breeding programme. Disease development was monitored, grain yield and yield components were recorded, and these data were compared with measurements taken from plants in plots kept free of disease. Data, averaged over both years, for disease development on the uppermost three leaves — areas under disease progress curves, terminal severity and apparent infection rates — indicated that ‘Verner’, ‘Pohto’ and ‘Pokko’ were symptomatically significantly more resistant to scald than ‘Arve’, ‘Loviisa’ and Jo 1599. Grain yields, thousand-grain weights, test weights and proportions of plump grains were all significantly reduced in plots inoculated with scald compared with those kept free of disease; ‘Verner’ appeared to be the most useful genotype for use in crossing programmes to improve scald resistance in Finnish barleys.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 109 (1998), S. 5283-5289 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: The Stark effect on the qR22(0,0.5) (ν=17 682.9251 cm−1) and qP11(0,1.5) (ν=17 682.1966 cm−1) branch features of the (0,0) B 2A1–X 2A1 band system of calcium methoxide, CaOCH3, was measured and analyzed to give the magnitude of the permanent electronic dipole moments, |μ|, of 1.58(8) D and 1.21(5) D for the X 2A1 and B 2A1 states, respectively. The dipole moments are compared with other monovalent calcium compounds and those predicted from a simple electrostatic model. Pure rotational transitions in the X 2A1 state were recorded using the pump/probe microwave-optical double resonance technique. The proton magnetic hyperfine splitting pattern confirms a C3v symmetry of the ground electronic state. The determined Fermi contact and dipolar parameters are: aF=−0.421(27) MHz; Taa=1.070(45) MHz, and |Tbb−Tcc|=0.292(47) MHz. The latter parameter is associated with the lifting of the K-degeneracy of this symmetric top molecule and mixing the I0=1/2 and I0=3/2 levels. © 1998 American Institute of Physics.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 110 (1999), S. 881-889 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: The Pe(1), F″=2.5 branch feature of the (0,0) D 3Π0e–X 3Δ1 band system of 51VN was recorded as a function of an applied static electric field. The resultant Stark splitting and shifts were analyzed giving values of 3.07(7) D and 6.1(4) D for the X 3Δ1 and D 3Π0e states, respectively, for the magnitude of the permanent electric dipole moment, |μ|. Similarly, the Ree(0.5) branch feature of the (0,0) A 4Π3/2–X 4Σ− band system of 52CrN was recorded as a function of an applied static electric field and analyzed to produce |μ| values of 2.31(4) D and 5.42(2) D for the X 4Σ− and A 4Π3/2 states, respectively. In order to facilitate the dipole moment determinations for 52CrN it was necessary to record and analyze the field free spectrum of the (0,0) A 4Π3/2–X 4Σ− subband system. A comparison of the dipole moments for the first row monoxides and mononitrides is made and trends are discussed with reference to a molecular orbital correlation scheme. © 1999 American Institute of Physics.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 108 (1998), S. 2703-2711 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: The pure rotational spectrum of BaCH3(X˜ 2A1) in its ground vibrational state has been recorded using millimeter/submillimeter direct absorption techniques, the first spectroscopic information obtained for this molecule. The radical was created using Broida-type oven/d.c. discharge methods by the reaction of barium vapor and Sn(CH3)4. Twenty-eight rotational transitions of the main isotopomer 138BaCH3 were recorded, as well as five for 136BaCH3 and three for the 137BaCH3 species. Being a prolate symmetric top, K ladder structure was observed in all transitions for BaCH3, as well as fine structure splittings which arise from the unpaired electron in the molecule. For the 137Ba isotopomer, hyperfine interactions were also resolved, arising from the spin of the barium nucleus. The complete data set has been analyzed with a 2A Hamiltonian, and rotational, spin-rotational, and magnetic hyperfine/nuclear quadrupole parameters accurately determined. The fine and hyperfine structure constants established from this study suggest a predominantly ionic bond for BaCH3, but with a considerable covalent component. Structural parameters for BaCH3 derived in this work are consistent with those of other alkaline earth monomethyl species. © 1998 American Institute of Physics.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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