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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 73 (1969), S. 2964-2969 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 74 (1970), S. 1508-1511 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical chemistry accounts 61 (1982), S. 193-202 
    ISSN: 1432-2234
    Keywords: Polymer orbitals ; Periodic perturbations ; Band structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract By combining the one-dimensional “crystal orbitals” of a simple polymer under the action of a perturbation which extends the repeating segment from one site to n sites a perturbation method allows the band structure of the new chain to be calculated. As well as estimating the band gaps to a fairly good agreement with the results of the “direct” method the present technique shows how specific gaps created by the symmetry-lowering will respond to the characteristics of the perturbations imposed.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical chemistry accounts 1 (1963), S. 458-462 
    ISSN: 1432-2234
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Résumé La diffraction électronique indique qu'en vapeur les anneaux phényles du diphényle s'inclinent à 42° approximativement. Cet angle est un compromis entre le recouvrement des orbitales P zqui tend à maintenir plan la molécule entière, et l'encombrance des atomes d'hydrogène 2∶2′ et 6∶6′ qui font tordre les anneaux pour réduire la répulsion stérique. On a dérivé une fonction potentielle, d'une forme exponentielle, qui a un minimum à l'angle observé.
    Abstract: Zusammenfassung Die Elektronenbeugung zeigt, daß die beiden Ringe des Diphenyls im Gaszustand um einen Winkel von etwa 42° gegeneinander verdreht sind. Dieser Zustand stellt einen Kompromiß dar zwischen der Überlappung der p z-Orbitale einerseits, die das ganze Molekül planar zu halten sucht, und der Pressung der van der Waals-Radien der 2,2′ und 6,6′-Wasserstoffatome andererseits, die die Ringe aus der gemeinsamen Ebene herausdreht, um die sterische Hinderung abzumindern. Für die potentielle Energie wurde eine e-Funktion mit einem Minimum am beobachteten Winkel hergeleitet.
    Notes: Abstract Electron diffraction shows that in the vapour the phenyl rings of diphenyl are inclined at about 42°. This is a compromise between the P z-orbital overlap, which tends to keep the whole molecule planar, and overcrowding of the 2∶2′ and 6∶6′ hydrogen atoms which causes twisting of the rings to reduce the steric repulsion. A potential function, having an exponential form, has been derived, which gives a minimum at the observed angle.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical chemistry accounts 65 (1984), S. 13-22 
    ISSN: 1432-2234
    Keywords: Virtual charge model ; solvation effects ; protonation of amines
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Relative protonation energies in the primary, secondary and tertiary aliphatic series of amines are calculated by a semiempirical method employing the virtual charge model. The method accounts quite well for the observed differences between the gas-phase protonation affinities and the protonation enthalpies in solution, but when allowance is made for steric shielding from the bulk solvent for “non-edge” atoms, some anomalies in the uncorrected model are removed. The calculated solute-solvent interactions are related to experimental enthalpies of solution and to trends expected from the Born model.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical chemistry accounts 2 (1964), S. 75-83 
    ISSN: 1432-2234
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenfassung Eine Beobachtung von Clar hat gezeigt, daß die Spektren der Benzologen des Triphenylens, wie z. B. II, III, IV außerordentlich ähnlich sind denen der Phene, die ausgehend vom zentralen Ring und den beiden längsten Armen der obigen Systeme gebildet werden. Daher ähnelt das Spektrum von II stark dem des Tetraphens I und die von III und IV dem des Pentaphens V. Es wird gezeigt, daß dieser Beobachtung durch eine einfache Modifikation der Hückelschen MO-Theorie Rechnung getragen werden kann.
    Abstract: Résumé Clar a observé que les spectres d'absorption des dérivés annelés du triphénylène tels que, II, III et IV montrent une ressemblance extraordinaire à ceux des phènes définis par l'anneau central du triphényléne et ses deux armes les plus longues. Ainsi le spectre de II ressemble à celui du tétraphène et ceux de III et de IV à celui du pentaphène V. Nous avons démontré qu'on peut expliquer cette observation par une modification simple de la méthode des orbitales moléculaires d'Hückel.
    Notes: Abstract Clar has observed that the spectra of annellated derivatives of triphenylene such as II, III, IV below show remarkable resemblance to those of the phenes defined by the central ring of the triphenylene and its two longest acene limbs, II resembling tetraphene I, and III and IV pentaphene V. We show that this observation can be explained in terms of a simple modification of the Hückel molecular-orbital method.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical chemistry accounts 68 (1985), S. 389-405 
    ISSN: 1432-2234
    Keywords: Polynuclear aromatic hydrocarbons ; Lithium π complexes ; Graphite-lithium intercalates ; Barriers to migration ; Charge transfer
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract In a preliminary investigation of the bonding between the sub-lattices of lithium and of graphite in intercalation compounds, molecular orbital calculations are performed on systems of Li atoms π complexed to one or both sides of polynuclear aromatic hydrocarbons. Energy wells calculated reveal possible sites offered to the Li atoms above the aromatic plane to form complexes in both central and edge regions of the molecule. The influence of additional complexed Li atoms on the migratory tendency of a given Li atom is also investigated, and observations made on the effect of the complexed Li atoms on the C-C bonds of the hydrocarbon.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical chemistry accounts 65 (1984), S. 13-22 
    ISSN: 1432-2234
    Keywords: Virtual charge model ; solvation effects ; protonation of amines
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Relative protonation energies in the primary, secondary and tertiary aliphatic series of amines are calculated by a semiempirical method employing the virtual charge model. The method accounts quite well for the observed differences between the gas-phase protonation affinities and the protonation enthalpies in solution, but when allowance is made for steric shielding from the bulk solvent for “non-edge” atoms, some anomalies in the uncorrected model are removed. The calculated solute-solvent interactions are related to experimental enthalpies of solution and to trends expected from the Born model.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 18 (1980), S. 937-951 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In an attempt to apply band-structure calculations to polymers with “reduced” symmetries, and simultaneously to examine some of the causes of band gaps in semiconducting polymers, two types of symmetry reduction are applied on the all-trans polyacetylene chain. Using a neighboring-segment approximation the consequent perturbations were used to calculate changes to the band structure of the undistorted chain and the energy gaps compared with those obtained from a direct calculation on the distorted polymer.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 18 (1980), S. 1405-1413 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Semiempirical MO calculations of the self-consistent charge and configuration (SCCC) method are reported for the acetonitrile-metal solvated species (CH3CN)xMn+, where M = Be2+ and Mg2+. Comparison of the delocalization energies for various chemical structures x = 1, 2, 3, 4, 6 leads to an expectation of a tetrahedral structure for the Be2+ species and an octahedral structure for the Mg2+ species. The electronic nature of the donor-acceptor interaction is also discussed.
    Additional Material: 8 Tab.
    Type of Medium: Electronic Resource
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