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1979 (1)
1978 (2)
1Author    Walter FabianRequires cookie*
 Title    Semiempirische SCF-Rechnungen an den angeregten Zuständen von Hydroxy Cumarinen Semiempirical SCF-Calculations of the Excited States of Hydroxycoumarines  
 Abstract    Semiempirical SCF-calculations show that the fluorescence bands of 7-hydroxycoumarin at 1.87 • 10 4 -1,92 • 10 4 cm -1 are most probably due to a phototautomeric form. A topo-logical rule is evaluated to explain the dependence of the fluorescence intensity upon the position of the hydroxyl group in the various isomeric hydroxycoumarines. 
  Reference    Z. Naturforsch. 33b, 628—631 (1978); eingegangen am 16. März 1978 
  Published    1978 
  Keywords    Hydroxycoumarines, Fluorescence, Phototautomerism, PPP-Calculations 
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 TEI-XML for    default:Reihe_B/33/ZNB-1978-33b-0628.pdf 
 Identifier    ZNB-1978-33b-0628 
 Volume    33 
2Author    Walter FabianRequires cookie*
 Title    W. Fabian * Eigenschaften von Molekülen in angeregten Zuständen 348 Properties of Molecules in Excited States  
 Abstract    Using bisisochinolin derivatives and related compounds it is shown that information about the fluorescent state can be obtained by comparison of experimental fluorescence data and calculated energies of the Si-state assuming various geometries. 
  Reference    Z. Naturforsch. 33b, 332—335 (1978); eingegangen am 7. September 1977 
  Published    1978 
  Keywords    Excited States, Fluorescence, PPP-Calculations, Phototautomerism, Bisisochinolin Deri-vatives 
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 TEI-XML for    default:Reihe_B/33/ZNB-1978-33b-0332.pdf 
 Identifier    ZNB-1978-33b-0332 
 Volume    33 
3Author    Heinz Falk, Klaus ThirringRequires cookie*
 Title    On the Chemistry of Pyrrole Pigments, XXXIV [1] On the Configurations and Conformations of Diastereomeric N-Methyl-O-methyl-bilatrienes-abc  
 Abstract    of the aetiobiliverdin-IV-y-lactimether yields a lactam-N-methylated derivative the structure of which was proven by an ether cleavage and iH NMR spectro-scopy. The configuration (Z,Z,Z) was deduced from iHNMR experiments. Photo-isomerization exclusively forms the (E,Z,Z) diastereomer. By conformational analysis using the LIS technique and correlations of UV-VIS spectra and PPP-type calculations a more or less helical arrangement for the two diastereomers was confirmed. The twisting is maximal at the methine single bond adjacent to the site of N-methylation, the overall geometry seems to be much more distorted than the non methylated derivatives. 
  Reference    Z. Naturforsch. 34b, 1600—1605 (1979); eingegangen am 13. Juli 1979 
  Published    1979 
  Keywords    X H NMR, UV-VIS, Lanthanide Ion Induced Shifts, PPP-Calculations, Conformational Analysis Methylation 
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 TEI-XML for    default:Reihe_B/34/ZNB-1979-34b-1600.pdf 
 Identifier    ZNB-1979-34b-1600 
 Volume    34