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  • 1
    Digitale Medien
    Digitale Medien
    Springer
    The visual computer 2 (1986), S. 367-378 
    ISSN: 1432-2315
    Schlagwort(e): Molecular polymodelling ; POLYMOD ; 3D Grid stage ; COOBOX ; Geometric and Boolean operations ; Composite images
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Informatik
    Notizen: Abstract A polymodelling system (POLYMOD) is presented for varied 2D or 3D displays of chemical shapes, whether structural (molecular volumes distances, surfaces...) or electronic (molecular electrostatic potential, electron densities ...). The POLYMOD system manages reversible correspondences between calculation and representation spaces by immersing the molecules studied in a unique represetation space structured by a 3D grid box. This box, called COOBOX, defined by its point internal coordinates, is used to transform other coordinates into its own. Direct multi-slice images along thex, y, z axis provide access to a variety of derived operations around a molecular shape or set of shapes disposed in various manners. Interactive sub systems ensure Boolean operations and compare property shapes through the 3D grid. Clear separation of graphic routine and of downstream modelling programs leads to rapid and original generation of varied images (subimages, direct or composite images) which are then available for simulation strategies.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 14 (1983), S. 83-86 
    ISSN: 0377-0486
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The time-resolved resonance Raman spectrum (excitation: 532 nm, 30 ns laser pulse; optical multichannel detection) of the short-lived species generated by UV flash irradiation of a benzooxazolinic spiropyran in toluene or benzene, has been obtained. The CW resonance Raman spectrum of a related permanent benzooxazolinic merocyanine closely resembles the spectrum of the transient species. A tentative assignment of the Raman bands is proposed in order to characterize the bonds directly involved in the π-electron delocalization of the merocyanines.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 15 (1983), S. 855-866 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: A new couloamperometric apparatus has been designed to extend the range of this kinetic technique to the measurement of very high rate constants, 108M-1s-1, by using TFCR-EXSEL conditions (TFCR - very low reactant concentration; EXSEL - salt excess), which give half-lives of a few seconds for very fast second-order reactions. Very low faradaic currents, in the nanoampere range for halogens, corresponding to very low reactant concentrations of 10-8-10-9M, are measured selectively by compensating the eddy currents, principally the residual and the induced currents. When the electroactive species is bromine, the concentration is demonstrated to be linearly related to the limiting reduction current in the very low concentration range. The upper limit of this technique for bromination is at present 3 × 108M-1s-1. The method is applied to the kinetic study of highly reactive enol ethers EtO-C(R) = CH-R′, where R and R′ are H or Me. A value of 2.2 × 108M-1s-1 is obtained for kBr2, the rate constant for free bromine addition to EtO-CH = CH2, by extrapolating the kinetic bromide ion effects to [Br-] = 0. An α-methyl effect (kα-Me/kH)EtO of 15 is found; this is a small decrease in the methyl effect compared to the marked increase in the double bond reactivity. For the enol acetate MeCOO-CH = CH2, whose rate constant is 6 × 102M-1s-1, (kα-Me/kH)OCOMe is 21. The dependence of substituent effects on reactivity is discussed in terms of the Hammond effect on the transition state position and of charge delocalization by group G of olefins G-CH = CH2.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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