Infrared spectroscopy, infrared photoconversion, and ultraviolet photodissociation of NO dimers in neon and nitrogen matrices

Abstract

The nitric oxide dimers isolated in neon or nitrogen matrices have been irradiated in the infrared by selected lines of a cw CO laser and in the UV at 193 nm by an ArF excimer laser. IR excitation of the antisymmetric mode of the cis dimer in neon induces a conversion to a special van der Waals dimer. At T<6 K UV irradiation dissociates the dimers mainly to NO monomers and, in smaller proportion, to NO2 in the neon matrix or to N2O in the nitrogen matrix. NO2 is formed exclusively from the cis dimer and N2O from the trans dimer. At higher temperature in nitrogen, the oxygen atoms produced in the N2O formation migrate and react with NO to form NO2. The vibrational spectroscopy in nitrogen reveals several new features. The symmetrical vibrational mode of planar trans-(NO)2, normally IR inactive, becomes observable at 5.8 K owing to the matrix strain. cis-(NO)2 is trapped in two sites and the energy difference between them changes abruptly around 14 K, suggesting a structural transformation in the neighborhood of the sites. Cooling at 5.8 K induces a reversible decrease of the cis dimer bands, correlated with the appearance of vdW dimer bands. In both matrices, the antisymmetric band of the cis dimer is broadened by a predissociation effect as in the gas phase.