In: Journal of Physics B: Atomic, Molecular and Optical Physics, 2010, vol. 43, no. 8, p. 085206
In a joint experimental and theoretical effort, we carried out a detailed study of electron scattering from Kr atoms in the energy range of the low-lying Kr⁻($4p^5 5s^2$) Feshbach resonances. Absolute angle-differential cross sections for elastic electron scattering were measured over the energy range 9.3–10.3 eV with an energy width of about 13 meV at scattering angles between 10° and...
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In: Advances in atomic, molecular, and optical physics, 2003, vol. 49, p. 85-216
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In: Physical Chemistry Chemical Physics, 2007, vol. 9, p. 3163-3173
We studied dissociative electron attachment to a series of compounds with one or two hydroxyl groups. For the monoalcohols we found, apart from the known fragmentations in the 6–12 eV range proceeding via Feshbach resonances, also new weaker processes at lower energies, around 3 eV. They have a steep onset at the dissociation threshold and show a dramatic D/H isotope effect. We assigned...
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In: Physical Chemistry Chemical Physics, 2008, vol. 10, p. 1507-1511
Dissociative electron attachment (DEA) to diethyl ether yielded primarily the C₂H₅O⁻ ion, with a strong Feshbach resonance band at 9.1 eV and a weaker shape resonance band at 3.89 eV. Very similar spectra were obtained for dibutyl ether, with C₄H₉O⁻ bands at 8.0 and 3.6 eV. Some of these primary ions subsequently lost H₂ and yielded weaker signals of the C₂H₃O⁻ and...
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In: Physical Chemistry Chemical Physics, 2008, vol. 10, p. 5232 - 5237
A difference was observed in the reactivity of alcohols and ethers toward free electrons. Whereas the lowest core-excited state of the negative ion—a ²(n,3s²) Feshbach resonance—of the alcohols readily dissociates by losing a hydrogen atom, ethers show no observable signal from this resonance. This difference in reactivity has a parallel in the anomalous shapes and energies of the...
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In: Physical Chemistry Chemical Physics, 2009, vol. 11, p. 7640-7648
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In: Physical Review Letters, 2013, vol. 111, no. 21, p. 213201
Two mechanisms for dissociative electron attachment in HCOOH, the formation of HCOO−+H, were proposed in the literature: (i) via a direct electron attachment into a σ∗ resonance, augmented by dipole binding of the incident electron [G. A. Gallup et al., Phys. Rev. A 79, 042701 (2009)], and (ii) with the 1.8 eV π∗ resonance as a doorway state, linked to the products by...
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In: Journal of the American Chemical Society, 2015, vol. 137, no. 45, p. 14329–14340
Anion photoelectron spectroscopy (PES) and electron energy-loss spectroscopy (EELS) probe different regions of the anionic potential energy surface. These complementary techniques provided information about anionic states of acetoacetic acid (AA). Electronic structure calculations facilitated the identification of the most stable tautomers and conformers for both neutral and anionic AA and...
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In: Molecular Physics, 2013, p. -
The electronic structure of TEMPO (2,2,6,6-Tetramethylpiperidine-N-oxyl) and its cation and anion were studied experimentally using the electron spectroscopy techniques, dissociative electron attachment (DEA) spectroscopy, electron energy-loss spectroscopy, measurement of elastic and vibrational excitation (VE) cross sections and HeI photoelectron spectroscopy. The experiments were supplemented...
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In: The Journal of Physical Chemistry A, 2018, vol. 122, no. 4, p. 1146–1155
We present a comprehensive study of resonance formation in electron collisions with thiophene. Detailed calculations have been performed using the ab initio R-matrix method. Absolute differential cross sections for electron impact excitation up to 18 eV and for two scattering angles, 90 and 135°, have been measured. Agreement between the calculated and measured experimental cross sections is...
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