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13C-selective infrared multiple-photon decomposition study of CBrClF2

Research paper by M. Hattori, Y. Ishikawa, K. Mizuta, S. Arai, S. Sugimoto, Y. Shimizu, S. Kawanishi, N. Suzuki

Indexed on: 01 Nov '92Published on: 01 Nov '92Published in: Applied Physics B



Abstract

The infrared multiple-photon single-frequency decomposition (IRMPD) of CBrClF2 was examined as functions of laser wavenumber, laser fluence, and partial pressure of CBrClF2. The initial step was the scission of a C-Br bond. In the presence of O2 the carbon-containing product was CF2O and its subsequent hydrolysis gave CO2. The initial dissociation was highly 13C selective at wavenumbers below 1014 cm−1. CBrClF2 decomposed at relatively low fluences as compared to CHClF2. However, the decomposition yield rapidly decreased with increasing pressure. In the large-scale irradiation experiment using about 8 J pulse at 1 Hz, we obtained a carbon yield of 0.41 μmol per pulse at a 13C-atom fraction of 17% for a mixture of 10 Torr CBrClF2 and 10 Torr O2, and a carbon yield of 0.17 μmol per pulse at a fraction of 29% for a mixture of 20 Torr CBrClF2 and 20 Torr O2. The IRMPD of CHClF2 gave a carbon yield of 0.18 μmol per pulse at 48% for 10 Torr neat CHClF2 and yield of 0.25 μmol at 52% for 20 Torr CHClF2. The large-scale irradiation experiment was also carried out for mixtures of CBr2F2 and O2. CHClF2 is the most productive of 13C.