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  • 1
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 181 (1958), S. 1052-1053 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] THE two ideas of aromatic character and the aromatic sextet are closely bound up together in aromatic hydrocarbon theory, but their association is not invariable, either in theory or, we believe, in practice. We present an outline of the theory of a second type of aromaticity and illustrate its ...
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 171 (1953), S. 566-566 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Finding the polarization of observed band systems to check the calculations is more difficult than finding the wave-length and intensity, and has not often been attempted in aromatic hydrocarbons except in the weakest band systems, for which quite thick crystals give measurable optical ...
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 169 (1952), S. 1102-1102 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] In the upward sequence of excited states, corresponding to band systems at higher energies and shorter wave-lengths, it is to be expected that new types of atomic orbitals will be needed in the approximate molecular wave functions. Thus atomic ns and np orbitals are required in the upper states of ...
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 109 (1998), S. 1259-1263 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A new aspect of chiral discrimination is described. The rate of resonance transfer between chiral molecules at all separation distances is calculated using molecular quantum electrodynamics. The leading correction to the familiar electric dipole transfer rate is shown to be discriminatory, and is proportional to the optical rotatory strengths. In the near zone the rate and the discrimination in the rates for transfer to the two chiral enantiomers are proportional to the inverse sixth power of the separation; in the far zone to the inverse square. Results are discussed for transfer between identical and nonidentical molecules. In the latter the discrimination between the two enantiomers of the molecule excited by transfer depends on the handedness of the initially excited molecule, a property that might be exploited in practical applications. © 1998 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 158 (1946), S. 235-235 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] CALCULATIONS of the long wave-length absorption bands of aromatic molecules, such as those carried out by Sklar1 and Förster2, give good agreement with the experimental values of absorption maxima even when only nearest-neighbour exchange effects are taken into ...
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 161 (1948), S. 481-481 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] IT is an interesting fact that neitherjpentalene (1), nor heptalene (2), nor any derivatives of them have been definitely reported as being synthesized1 or found to occur naturally. Azulene (3) is, on the other hand, a substance which can be made by the established procedures of ...
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical chemistry accounts 102 (1999), S. 112-120 
    ISSN: 1432-2234
    Keywords: Key words: Chiral discrimination ; Excitation exchange ; Dispersive coupling
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract. Results in the coupling of chiral molecules are reviewed from elementary points of view and some new results are given. We show that interactions between chiral molecules can be treated by using molecular quantum electrodynamics in electric and magnetic dipole approximation in ways different from standard diagrammatic perturbation theory. The interactions are the dispersive coupling of ground-state chiral molecules and excitation transfer, with emphasis on chiral discrimination. For ground-state molecules the coupling is dealt with first by calculating the coupling, at all separation distances, of electric and magnetic dipoles induced in the two molecules by fluctuations in the vacuum radiation field. The second method is the response by one chiral molecule to the field generated by the other. Excitation transfer is treated as the response by the accepting ground-state molecule to the dipole field of the donor. A novel variant in finding the rate of excitation transfer is by using Poynting's theorem.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical chemistry accounts 89 (1994), S. 123-136 
    ISSN: 1432-2234
    Keywords: Born-Oppenheimer approximation ; Non-adiabatic corrections
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Tests of the accuracy of the Born-Oppenheimer approximation, with and without non-adiabatic corrections are made on a model system of two coupled harmonic oscillators representing electronic and nuclear motion. Two couplings are considered: bilinear and biquadratic in the displacements. For the energies of sublevels of the ground state, the transition dipole moments of the lowest vibrational transition, and the transition moment in a vibrationally perturbed forbidden electronic transition, the Born-Oppenheimer result including non-adiabatic corrections agrees with the exact result up to terms quadratic in the coupling constant. In a model of near-resonance of the coupled systems, “level crossing”, the adiabatic approximation fails, as is well-known. Even with inclusion of the non-adiabatic corrections the result does not agree to quadratic terms. However near resonance, with physically reasonable values, the methods give results that are very close. In all cases inclusion of the non-adiabatic terms is essential.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 31 (1987), S. 417-424 
    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: Pair coupling between a chiral molecule and an achiral molecule can induce weak circular dichroism in the achiral partner, as is well known in induced circular dichroism. Here the effect of the same coupling on the chiral partner is analyzed. The effect is an increase or decrease in the rotatory strength that may be detectable under conditions where the effect is enhanced by a near-resonance.
    Additional Material: 2 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 3 (1969), S. 903-911 
    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: It is shown how the leading term for very large R of the Casimir-Polder potential, that is the term varying as R-7, arises in second-order perturbation theory applied to the interaction Hamiltonian - \documentclass{article}\pagestyle{empty}\begin{document}$ - \sum\limits_\sigma {\frac{1}{2}\alpha (\sigma){\rm E}^{ \bot ^2 } (\sigma)} $\end{document}. The generalization to anisotropic molecules is calculated and the angular dependence of the long range intermolecular potential in this case is given explicitly in terms of the principal polarizabilities and their corresponding directions of the two molecules.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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