VIBRATIONAL SPECTRA OF $NO^{+}$ AND $NO_{2}^{+}$

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1975

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Ohio State University

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Interest in the oxides of nitrogen has increased rapidly as speculation about their effects in the upper atmosphere has gained publicity. In considering the reactions which may occur, extensive data has been available on NO2=, NO2, and NO2. Very little information has been published on the chemically reactive NO2= species. The infrared spectrum of NO2+ has been studied in the solid compound NO2BF4 and in alkali halide solid solutions. The fundamental assignments in NO2BF4 are ν1 = 1043 cm−1 (Raman), ν2 = 593 cm−1 (I.R.), ν3 2382 cm−1 (I.R.). ν2 had not been observed previously, while ν3 had been misassigned. The chemical reactivity of NO2+ is so great that it is difficult to prepare, and to maintain, at high purity. The NO2BF4 was found to contain appreciable quantities of NO+, and the spectra were separated by controlled thermal decomposition of the NO2BF4. The frequencies observed for NO+ are 2337 cm−1 (I.R.) and 2343 cm−1 (Raman), both in NO2BF4. In the isolation of NO2+ and NO+ in alkali halide matrices, quantities of NOX and NO2X were produced (X = halogen), as wel as other reaction products which have not been fully identified.

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The Oak Ridge National Laboratory is operated by the Union Carbide Corporation for the USEC.


Author Institution: Oak Ridge National Laboratory; Fisk University, Nashville, Tennessee 37203.

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