2014
DOI: 10.1016/j.cplett.2014.08.053
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Photoinduced rotamerization and dissociation of o -fluorobenzoyl chloride in solid Ar

Abstract: UV light-induced reactions of o-fluorobenzoyl chloride (FBC) were investigated using infrared spectroscopy in a cryogenic Ar matrix. Photoinduced rotational isomerization from anti-to gauche-FBC was confirmed by comparison with calculated spectra. In addition, photolysis products were found to be ketene specieso-chlorofluorobenzene, m-chlorofluorobenzene and CO.

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“…Unlike the photoinduced reactions of chloroacetyl chloride [24] and o-fluorobenzoyl chloride [30] in solid Ar, where the rotational isomerisation reached an equilibrium and the less stable conformer was decomposed upon further irradiation, in our case the concentration of syn-chloroacetone continued to grow during the entire irradiation period, as shown in Figure 2. This might indicate that in the photolysis of Fig.…”
Section: Identification Of Additional Productsmentioning
confidence: 79%
“…Unlike the photoinduced reactions of chloroacetyl chloride [24] and o-fluorobenzoyl chloride [30] in solid Ar, where the rotational isomerisation reached an equilibrium and the less stable conformer was decomposed upon further irradiation, in our case the concentration of syn-chloroacetone continued to grow during the entire irradiation period, as shown in Figure 2. This might indicate that in the photolysis of Fig.…”
Section: Identification Of Additional Productsmentioning
confidence: 79%