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- W2069141985 abstract "A convenient method is given for the semiquantitative determination of those changes ΔSi in internal coordinates, which describe the structure of the radical cation M+(Ψ) relative to the neutral molecule M in its electronic ground state. The changes ΔSi correspond to those associated with the relaxation process which follows the ionisation M + hv → M+(Ψ) + e, M+ being in the electronic state Ψ. The method, based on the procedure originally developped by Smith & Warsop [3], uses the spacing and relative intensity of the vibrational fine-structure components of the bands in the photoelectron spectrum of M. From these data are calculated the changes ΔQk in normal coordinates, which are then transformed into the ΔSi by applying the L-matrix. The changes ΔRCX, ΔRCC and ΔRCH which describe the structure of the radical cations of the four monohaloacetylenes I(X) (X = F, Cl, Br, I) in their 2IIΩ(1) and 2IIΩ(2) states have been determined. It is shown that the results are in agreement with theoretical expectation and that they confirm the band assignement proposed in a previous communication [2]." @default.
- W2069141985 created "2016-06-24" @default.
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- W2069141985 date "1971-01-01" @default.
- W2069141985 modified "2023-09-26" @default.
- W2069141985 title "An Estimate of the Interatomic Distances in Monohaloacetylene Radical Cations from Photoelectron-spectroscopic Data" @default.
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- W2069141985 doi "https://doi.org/10.1002/hlca.19710540107" @default.
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