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Journal ArticleDOI

Resonances in Electron Impact on Diatomic Molecules

George J. Schulz
- 01 Jul 1973 - 
- Vol. 45, Iss: 3, pp 423-486
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TLDR
In this article, the energies, configuration, and other properties of resonances (also called "compound states" and "temporary negative ions") in diatomic molecules are presented in the form of tables and energy level diagrams.
Abstract
In this review we present the energies, configuration, and other properties of resonances (also called "compound states" and "temporary negative ions") in diatomic molecules. Much of the information is presented in the form of tables and energy level diagrams. Vibrational, rotational, and electronic excitation are discussed whenever these processes have given information on resonances; often these excitation processes proceed via resonances. The paper is divided according to molecular species (${\mathrm{H}}_{2}$, ${\mathrm{N}}_{2}$, CO, NO, ${\mathrm{O}}_{2}$), but the main conclusions are discussed by the nature of the processes involved.

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Citations
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Surface-enhanced spectroscopy

TL;DR: The surface-enhanced Raman scattering (SERS) effect was first discovered by Fleischmann, Van Duyne, Creighton, and Creighton as discussed by the authors, who showed that molecules adsorbed on specially prepared silver surfaces produce a Raman spectrum that is at times a millionfold more intense than expected.
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Atomic and molecular electron affinities: photoelectron experiments and theoretical computations.

TL;DR: Theoretical D determination of Electron Affinities and Statistical Analysis of DFT Results ThroughComparisons to Experiment and Other theoretical Methods and Specific Theoretical Successes 251E.
Journal ArticleDOI

Anisotropic scattering of electrons by N2 and its effect on electron transport.

TL;DR: The changes in the commonly measured transport and reaction coefficients resulting from the introduction of anisotropic elastic and inelastic scattering, while keeping the elastic momentum-transfer cross section constant, are less than 1%.
Journal ArticleDOI

The theory of electron-molecule collisions

TL;DR: The current state of the theory and its application to low-energy electron-molecule collisions is reviewed in this paper, where the emphasis is on elastic scattering and vibrational and rotational excitation of small diatomic and polyatomic molecules.
Journal ArticleDOI

Adsorption of oxygen on Ag(110) studied by high resolution ELS and TPD

TL;DR: In this paper, a tentative model is presented, according to which the molecule is adsorbed in the grooves of the (110) surface with its axis parallel to the surface.
References
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Journal ArticleDOI

Unified theory of nuclear reactions

TL;DR: In this article, a new formulation of the theory of nuclear reactions based on the properties of a generalized "optical" potential is presented, where the real and imaginary part of this potential satisfy a dispersion type relation while its poles give rise to resonances in nuclear reactions.
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A Unified Theory of Nuclear Reactions, II

TL;DR: In this paper, the effective Hamiltonian method for nuclear reactions described in an earlier paper with the same title, part I, is generalized so as to include all possible reaction types, as well as the effects arising from the identity of particles.
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Potential‐Energy Curves for the X 1Σg+, b3Σu+, and C 1Πu States of the Hydrogen Molecule

TL;DR: In this article, the ground-state energy of H2 has been extended to include large internuclear distances and accurate potential energy curve for 0.4≤R≤4.0 a.u.
Journal ArticleDOI

The Relation Between the Internuclear Distances and Force Constants of Molecules and Its Application to Polyatomic Molecules

TL;DR: In this article, the relation between the internuclear distances and force constants found for diatomic molecules is discussed, and it is shown that the relation can carry over to polyatomic molecules, with considerable accuracy.
Journal ArticleDOI

Potential energy curves for N2, NO, O2 and corresponding ions

TL;DR: In this paper, potential energy curves for the observed electronic states of N2, N2+), NO, NO(+), O2 and O2+ were calculated from published spectroscopic data by a numerical modification of the Rydberg-Klein method.