The photoelectron energy spectrum of benzene has been measured with monochromatic rarliation of wavelengths between 1253 and 584A. The first two ionization potentials are shown to be 9.25 and 12.5 eV. Explanations are given which account for previously observed structure lying between the first two
Electronic Ground and Excited State Spectroscopy of C6H and C6D
β Scribed by H. Linnartz; T. Motylewski; O. Vaizert; J.P. Maier; A.J. Apponi; M.C. McCarthy; C.A. Gottlieb; P. Thaddeus
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- English
- Weight
- 226 KB
- Volume
- 197
- Category
- Article
- ISSN
- 0022-2852
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β¦ Synopsis
Rotational transitions in the X 2 βΈ ground state of C 6 H and C 6 D have been measured by Fourier transform microwave and millimeter-wave absorption spectroscopy. More than 150 rotational lines in the ground 2 βΈ 3/2 and 2 βΈ 1/2 ladders have been observed, allowing an accurate determination of the rotational, fine structure, lambda-doubling, and hyperfine coupling constants using a standard effective Hamiltonian for a molecule in an isolated 2 βΈ electronic state. The molecular ground state constants are used to characterize the rotationally resolved origin band of the 2 βΈ 4 X 2 βΈ electronic transition observed by cavity ring-down laser absorption spectroscopy in a pulsed supersonic slit-jet discharge source. From these data, spectroscopic constants for the excited electronic state are determined.
π SIMILAR VOLUMES
Large-scale open-shell coupled cluster calculations have been carried out for the four lowest doublet states of C~ and the ground state of linear C 6. They strongly support the assignment of the peaks at 607.7 and 586.5 nm observed in neon matrix isolation experiments to the 0 Β° and 31 transitions w
The structure and energetics of the C H ΠΈ I complex have been studied 6 6 2 1 1.55 eV difference between the vertical and adiabatic excitation energies of 4 AΠ and the dramatic geometry change in the CT state.