1976
DOI: 10.1086/154509
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Predissociation effects in the A, B, and C states of CH and the interstellar formation rate of CH via inverse predissociation

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Cited by 180 publications
(90 citation statements)
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“…We calculated line positions of other satellite branches after we calculated B state energy levels using the line positions of the main branch lines and X state energy levels. For an oscillator strength value, we used 3.1 ± 0.2 x 10-3, which was derived from an average of four lifetime measurements (Brooks and Smith, 1974;Anderson et al, 1975;Brzozowski et al, 1976;Ortiz and Campos, 1982). The ratio of adopted oscillator strengths for the B-X (0-0) and A-X (0-0) bands is 0.61, which is in excellent agreement with experimental values (Linevsky, 1967;Garland and Crosley, 1985) and a theoretical estimate (Hinze et al, 1975).…”
Section: Modelingsupporting
confidence: 66%
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“…We calculated line positions of other satellite branches after we calculated B state energy levels using the line positions of the main branch lines and X state energy levels. For an oscillator strength value, we used 3.1 ± 0.2 x 10-3, which was derived from an average of four lifetime measurements (Brooks and Smith, 1974;Anderson et al, 1975;Brzozowski et al, 1976;Ortiz and Campos, 1982). The ratio of adopted oscillator strengths for the B-X (0-0) and A-X (0-0) bands is 0.61, which is in excellent agreement with experimental values (Linevsky, 1967;Garland and Crosley, 1985) and a theoretical estimate (Hinze et al, 1975).…”
Section: Modelingsupporting
confidence: 66%
“…We used formulae presented in Table 1 of Schadee (1975) for the calculations of the Holn-London factors for the first rotational lines. After a thorough search through the literature, we conclude that the best oscillator strength is 5.1 ± 0.15 x 10-3, which was derived from an average of the best four lifetime measurements (Brzozowski et al, 1976;Becker et al, 1980;Ortiz and Campos, 1982;Bauer et al, 1989). This value is in excellent agreement with a refined and extensive theoretical treatment by Larsson and Siegbahn (1983).…”
Section: Modelingmentioning
confidence: 95%
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“…Therefore, we have calculated the synthetic CH spectrum utilizing the LIFBASE molecular spectra simulation program [31] with the use of vibrational and rotational constants of the A 2 Δ, B 2 Σ + and X 2 Π r electronic states of CH from [32][33][34][35][36][37]. Similar computer procedure, employed in the analysis of spectra of diatomic molecules, occurring in cation-and photoninduced fragmentation of five-and six-membered heterocycles, has been recently proven to be efficient and dependable [15,18,27,28,38].…”
Section: Hementioning
confidence: 99%
“…This region includes the band head of the (0-0), (1-1), (2-2) bands of the A 2 D-X 2 P transitions of CH. The dissociation potential used was 3.465 eV from Brzozowski et al (1976), and the log gf values of the electronic transitions were modified to reproduce the solar spectrum by using the solar abundance of carbon from Anders & Grevesse (1989) and the Kurucz solar spectrum. We found a corrective factor of À0.3 dex in log gf and a shift of À0.05 Å in wavelength.…”
Section: Abundancementioning
confidence: 99%