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  • Digitale Medien  (9)
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  • Digitale Medien  (9)
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  • 1
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 95 (1991), S. 7846-7853 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: Recent analyses have led to an experimentally based potential energy curve for the ground state of HF which includes nonadiabatic corrections and which joins smoothly to the long-range potential at an accurately determined dissociation limit (De=49 362±5 cm−1). Using this potential curve and a new ab initio dipole moment function (in excellent agreement with experiment), accurate radiative transition probabilities among all vibrational levels (v=0–19 known, v=20 predicted) of the ground state of HF have been calculated for selected rotational quantum numbers. Comparisons of Einstein A spontaneous emission coefficients, dipole moment absorption matrix elements, and Herman–Wallis factors for absorption bands are presented.
    Materialart: Digitale Medien
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  • 2
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 97 (1993), S. 2053-2058 
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
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  • 3
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 100 (1994), S. 2661-2670 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: This paper critically surveys the best available data for the two lowest states (X 1Σ+g and a 3Σ+u) of Na2. Since both states are known up to near dissociation, they can be used to determine the separate Coulomb and exchange contributions to the intermediate and long range interaction potentials. The multipolar expansion representation of the Coulomb (dispersion) energy at long range (−∑nCn/Rn) and the exponential representation of the exchange energy at long range (Ae−aR) are tested.
    Materialart: Digitale Medien
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  • 4
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 101 (1994), S. 10382-10387 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: This paper critically surveys the best available spectroscopic data for the two lowest electronic states (X 1Σ+g and a 3Σ+u) of K2. Since both states are known up to dissociation, they can be used to determine Coulomb and exchange contributions to the intermediate and long range interaction potentials. The multipolar expansion representation of the Coulomb (dispersion) energy at long range (−ΣnCnR−n) and the exponential representation of the exchange energy (Ae−αR) as well as a variety of theoretical calculations are compared with these empirical results. Finally, dissociation energy values are discussed and improved dissociation energies for the X 1Σ+g (De=4449.1±1.0 cm−1) and the a 3Σ+u state (De=252.9±1.1 cm−1) proposed. © 1994 American Institute of Physics.
    Materialart: Digitale Medien
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  • 5
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: Resolved fluorescence from the K2 43 Σ+g state to the a3 Σ+u state has been measured by the perturbation-facilitated optical–optical double resonance (PFOODR) technique. Data have been fit to an improved set of molecular constants for the a3 Σ+u state. In particular, the new Te value for this state has been determined as 4197.935±0.047 cm−1, nearly 1.8 cm−1 higher than previously reported. By combining the new results for the a3 Σ+u state and the recent results for the ground X1 Σ+g state [J. Chem. Phys. 103, 3350 (1995)], we report in this paper an improved analysis of long-range dispersion and exchange interactions between two K atoms and of the X1 Σ+g and a3 Σ+u state dissociation energies De of 4450.674±0.072 cm−1 and 252.74±0.12 cm−1, respectively. © 1996 American Institute of Physics.
    Materialart: Digitale Medien
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  • 6
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 111 (1999), S. 4962-4965 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: Recently experimentally-based asymptotic exchange energies ΔVE between ground state atoms in Li2, Na2, K2, and NaK have been determined from spectroscopically-determined potential energy curves. These empirical results are shown to be well fit by the expression −CRαe−βR of Smirnov and Chibisov, where C is a positive constant and α and β can be readily calculated from the atomic ionization energies. The expression should be useful for estimating the exchange energy in other alkali dimers. © 1999 American Institute of Physics.
    Materialart: Digitale Medien
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  • 7
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 111 (1999), S. 4956-4961 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: This article critically surveys spectroscopic data for the two lowest states (X 1Σ+ and a 3Σ+) of NaK. These states both dissociate to ground state Na and K atoms. Since both states are known precisely to near dissociation, they can be used to determine experimental values of the separate Coulombic and exchange contributions to the long-range interaction potentials, which agree reasonably well with theory. We also discuss the dissociation energy of both of the states and recommend De(X 1Σ+)=5273.65±0.10 cm−1 and De(a 3Σ+)=207.79±0.10 cm−1. © 1999 American Institute of Physics.
    Materialart: Digitale Medien
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  • 8
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 114 (2001), S. 10811-10815 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: This article critically examines spectroscopic data for the two lowest states (X 1Σ+ and a 3Σ+) for NaRb, which dissociate to ground state Na and Rb atoms. A more precise triplet state RKR potential curve is reported. A complete hybrid potential for the triplet state is determined, based on the improved RKR curve plus Coulombic and exchange contributions at long range. A new, more precise dissociation energy for the a 3Σ+ state is determined: De=183.0±0.10 cm−1. Previously unpublished and improved Dunham coefficients for the singlet state are reported, which cover the bottom 57% of the well. A complete hybrid potential energy curve for the singlet state is determined, based on the RKR curve plus Coulombic and exchange contributions at long range. The X 1Σ+ state potential curve now covers 100% of the well and a new, precise dissociation energy is determined: De=5030.75±0.10 cm−1. Three additional unobserved energy levels are predicted for the a 3Σ+ state of 23Na85Rb, all within 1.1 cm−1 of the dissociation limit. © 2001 American Institute of Physics.
    Materialart: Digitale Medien
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  • 9
    Digitale Medien
    Digitale Medien
    Springer
    Theoretical chemistry accounts 22 (1971), S. 23-38 
    ISSN: 1432-2234
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Zusammenfassung Die niedrig liegenden Π-Zustände des H2 bestehen aus einem Rumpfelektron σ und einem Valenzelektron π und ermöglichen eine direkte Auswertung der σ-π-Wechselwirkung zwischen zwei Schalen. Nach der Zerlegung der elektronischen Energie in σ-,π- und σ-π-Anteile wird gezeigt, daß eine elektronische Veränderung in diesem Modellsystem nur auf eine Veränderung des π-Elektronenanteils zurückgeht. Die einfache Hückeltheorie wird untersucht. Wenn der Molekülrumpf geeignet dargestellt wird, so sind, unabhängig von der π-Wellenfunktion, die berechneten Parameter α und β in guter Übereinstimmung mit den empirischen Parametern. Diese Übereinstimmung scheint auf eine starke Auslöschung von Energieanteilen zurückzugehen.
    Kurzfassung: Résumé Les états inférieurs π de H2 consistent en un électron de coeur (σ) et un électron de valence (π) et fournissent une évaluation directe de l'interaction entre couches σ-π. Après expression de l'énergie électronique en parties σ, π et σ-π, on montre qu'une modification électronique de ce système modèle est due seulement à une modification des électrons π. La théorie de Hückel simple est examinée. Si le coeur moléculaire est convenablement représenté, quelle que soit la fonction d'onde π, les paramètres α at β calculés sont en accord raisonnable avec les paramètres empiriques. Cet accord apparaît comme le résultat d'une compensation fortuite de contributions énergétiques.
    Notizen: Abstract The low-lying Π states of H2 consist of one core (σ) and one valence (π) electron and afford a direct evaluation of intershell σ-π interaction. After resolution of the electronic energy into σ only, π only, and σ-π parts, it is shown that an electronic change in this model system is due solely to a change in the π electrons. Simple Hückel theory is examined. If the molecular core is represented properly, regardless of the π wave function the calculated α and β parameters are in reasonable agreement with the “empirical” parameters. This agreement appears to be due to a fortuitous cancellation of energy contributions.
    Materialart: Digitale Medien
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