15min:

M. A. FLORY AND L. M. ZIURYS, Department of Chemistry, Department of Astronomy, Steward Observatory, University of Arizona, Tucson, AZ 85721.

The pure rotational spectrum of CrCN has been recorded in the frequency range 450-530 GHz. This work is the first spectroscopic study of this molecule. Ten transitions of this radical, which was created by reacting chromium vapor with cyanogen gas, were recorded. The two isotopomers ⁵²CrCN and ⁵³CrCN have been observed in their natural abundance 9:1, and substitution of ¹³C is currently underway. The spectrum clearly indicates that the electronic ground state is X ^{6 +}. Transitions arising from the excited v ₂ bending mode were measured up to (05⁵0). The bending modes show l -type doubling in v ₂ = 1 and v ₂ = 2. The vibrational progression is extremely regular, indicating a rigid structure. While many sextets are present in the spectra, they are all accounted for by isotopomers and vibrational states. Therefore, we conclude that only one structure is present in our cell, that of the linear CrCN species. The data were analyzed using a Hund case (b) Hamiltonian and rotational, spin-spin, and spin-rotation constants were determined. Trends in 3d transition metal cyanide bonding will be discussed.