INFRARED SPECTRA OP SELENIUM OXIDES IN SOLID ARGON.

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1994

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Ohio State University

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Codeposition of O2 with the superheated vapors of selenium from a Knudsen cell yields Se2O2, with bonds at 1404, 391 and 361cm−1. The presence of the O2 fragment is confirmed by scrambled 0-16/0-18 experiments; a triplet with very narrow lines, is obtained, suggesting that the two oxygens are equivalent and/or poorly vibrationally coupled to the Se2 moiety. The presence of the Se2 fragment is suggested by the locations of the observed bands, the subsequent chemistry in the matrix, and the correspondence with the sulfur-oxygen system, in which S2O2 is found. Subsequent photolysis at λ>490 nm yields SeO (883cm−1) (SeO)2 (the vander Waals dimer, 875cm−1), SeO2Se (perturbed SeO2, 960, 921, 365cm−1), and SeOSeO (966, 636, and 294cm−1). In each of these product molecules, the individual lines due to the selenium isotopes, occurring in natural abundance, were resolved. Codeposition of O3 with the superheated selenium vapors yields, in addition to SeO, a broad band which is assigned to Se2O(903cm−1); this feature is also obtained when one traps the products of a microwave discharge in argon seeded with oxygen and selenium vapor.

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Author Institution: Department of Chemistry, University of Virginia

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