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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical chemistry accounts 54 (1979), S. 251-258 
    ISSN: 1432-2234
    Keywords: Biopolymer constituents, protonation of ∼ ; Purine bases
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Proton affinities of a large number of tautomeric adenine and guanine structures have been calculated using theab initio Hartree-Fock-Roothaan SCF method. For guanine, and to a lesser extent for adenine, it is likely that several protonated forms may co-exist in acidic solutions. Protonation at the “free” adenine and guanine positions in DNA may introduce effective acceptor levels between the energy bands of the polymer that may cause fundamental changes in the conduction properties of DNA.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The results of theoretical investigations are reported concerning the possibility of impurity-type charge carrier production in proteins. The energy band structures of the periodic protein model polyglycine calculated with the aid of the ab initio Hartree-Fock crystal orbital method and corrected afterwards for long-range correlation effects are compared with the empty levels of glyoxal, methyl-glyoxal, acrolein, and croton-aldehyde, suggested recently by Albert Szent-Györgyi as possible acceptors against proteins. The comparison with previous supermolecule calculations shows that appreciable charge transfer can be expected to glyoxal, methyl-glyoxal, and acrolein from the polypeptides, while croton-aldehyde is probably less efficient in this relation.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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