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  • 1
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 86 (1982), S. 488-494 
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 86 (1982), S. 3293-3294 
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    Journal of the American Chemical Society 107 (1985), S. 253-254 
    ISSN: 1520-5126
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    Journal of the American Chemical Society 102 (1980), S. 4536-4537 
    ISSN: 1520-5126
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie
    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 88 (1988), S. 386-393 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: Results of ab initio band structure calculations of completely mislinked (α–β linked) polypyrrole, polythiophene, and polyfuran are reported. Comparison of the important electronic properties such as ionization potential, electron affinity, and band gap of these mislinked polymers with those of the normally linked (α–α' linked) polymer chains indicates that the introduction of mislinkages in the normally linked polymer chains makes them more insulating and less dopantphilic. Both the ionization potential and the electron affinity values of the mislinked polymer chains are found to be sensitive to both the nature of the heteroatom and substitution at the backbone. The effect of the distributions (both periodic and random) of the mislinkages on the conduction properties of normally linked heterocyclic polymers is also investigated using negative factor counting method in its tight binding approximation. A random distribution of mislinkages, in general, has been found to produce polymer chains which are less insulating and have better prospects for forming conductive materials on doping with both electron acceptors and electron donors than the corresponding periodic distribution of mislinkages. The possible effects of the distribution of mislinkages on the conduction properties of copolymers of the heterocyclic compounds are also discussed.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    Springer
    Theoretical chemistry accounts 22 (1971), S. 403-406 
    ISSN: 1432-2234
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract In the radical anions of styrene, 4-vinyl pyridine and p-fluoro-styrene it has been found earlier by ESR experiments that the two ortho protons, as well as the two meta protons of the six-membered ring are not equivalent. We have made a systematic theoretical study of these systems by using the unrestricted Hartree-Fock method. Satisfactory agreement with the experimental results has been obtained without invoking the so called “α effect” or “β effect”.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 7
    Digitale Medien
    Digitale Medien
    Springer
    Theoretical chemistry accounts 8 (1967), S. 306-311 
    ISSN: 1432-2234
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Zusammenfassung Bei früheren ESR-Untersuchungen an trans-Stilben, trans-Dipyridyläthylen, Terephthalaldehyd und Benzaldehyd wurde gefunden, daß sowohl die ortho- wie die meta-ständigen Ringprotonen nicht gleichwertig sind. Wir haben die Spindichten in diesen Systemen mit der UHF- und der UHFAA-Methode untersucht. Befriedigende Übereinstimmung mit experimentellen Ergebnissen wurde erzielt, ohne daß dazu der sogenante α- oder β-Effekt herangezogen werden mußte.
    Kurzfassung: Résumé Dans les anions radicalaires du trans-stilbène, du trans-l,2-bis(4-pyridyl)-éthylène, des aldéhydes térephtaliques cis et trans, et de l'aldéhyde benzo'que, des expériences de r.p.e avaient montré que les deux protons en méta n'étaient pas équivalents. Nous avons effectué une étude systématique des distributions de spin dans ces systèmes en utilisant les méthodes U.H.F. (Hartree-Fock sans restriction) et U.H.F.A.A. (U.H.F. comportant l'annihilation de la composante quartet de spin). On a obtenu un accord satisfaisant avec les résultats expérimentaux dans le cadre de ces théories sans faire appel à de soi-disants effects α ou β.
    Notizen: Abstract In the radical anions of trans-stilbene, trans-1,2-bis(4-pyridyl)-ethylene, cis and transterephthalaldehyde and benzaldehyde it has been found earlier by ESR experiments that the two ortho protons, as well as the two meta protons of the six-membered ring are not equivalent. We have made a systematic study of spin distributions in these systems by employing the UHF (Unrestricted Hartree Fock) and UHFAA (UHF incorporating the annihilation of the quartet spin component) methods. Satisfactory agreement with the experimental results has been obtained within the framework of these theories and without invoking the so called “α effect” or “β effect”.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 8
    Digitale Medien
    Digitale Medien
    Springer
    Theoretical chemistry accounts 9 (1968), S. 268-274 
    ISSN: 1432-2234
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Conclusion The quantitative agreement with experimental barrier height and the extra stabilization energy of cis-N2F2 over trans-N2F2 may not be considered to be very good, but this is only to be expected as small differences between large quantities are being calculated. It appears from our present calculations that the use of Cusachs relation for evaluating the off-diagonal matrix elements in this system is open to question since the experimentally observed planarity of N2F2 is not correctly predicted by the use of this relation. We therefore prefer the use of the Wolfsberg-Helmholz relation in this system. A value of K= 1.75 appears to be preferable. The results of all the E.H.T. calculations made here for difluorodiazine clearly show that a twisted transition state is more probable than a linear one (LT or LC) in the isomerization of trans-N2F2 to cis-N2F2. This conclusion also receives further support from a consideration of the high preexponential factor in the rate equation [1] and the multiplicity of the transition state.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 9
    ISSN: 1432-2234
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract Spin density distributions in the radial anions of some heterocycles derived from thiophene, furan and pyrrole have been obtained using the unrestricted Hartree-Fock method. Good agreement between the calculated results and experimental data has been observed.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 10
    Digitale Medien
    Digitale Medien
    Springer
    Theoretical chemistry accounts 23 (1971), S. 111-114 
    ISSN: 1432-2234
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract The floating spherical gaussian orbital method is employed for predicting the shape of C2H 7 + . The pentavalency of carbon may be explained by the presence of a two-electron three-centre bond in addition to the standard two-electron two-centre bonds in this ion.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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