The 130-500 GHz rotational spectroscopy of cyanopyrazine (C4H3N2-CN)

The rotational spectrum of cyanopyrazine (2-pyrazinecarbonitrile, p-C4H3N2-CN) has been obtained from 130 to 500 GHz. Rotational transitions of cyanopyrazine have been measured, assigned, and least-squares fit for the first time. Over 7000 transitions of the ground vibrational state have been least-squares fit to partial octic, A-and S -reduced Hamiltonians with low statistical uncertainty (sigma fit = 34 kHz). Similar to other cyanoarenes, the first two fundamental modes are the out-of-plane (nu 27, A '') and in-plane (nu 19, A ') nitrile bending modes, which form an a -and b-axis Coriolis-coupled dyad. Greater than 5800 transitions from each of these vibrational modes were fit to a partial octic, A-reduced Hamiltonian (sigma fit = 38 kHz), and the analysis reveals the precise energy separation, Delta E27,19, between the coupled vibrational states, as well as values for eight a- and b-type Coriolis-coupling co-efficients, Ga, GJa, GKa, GJaJ, FKbc, Gb, GJb, and Fac. Cyanopyrazine is a strongly polar derivative of pyrazine, thus cyanopyrazine can serve as a potential tracer molecule for its nonpolar parent compound in extraterrestrial environments. The transition frequencies and spectroscopic constants provided in this work, combined with theoretical or experimental nuclear quadrupole coupling constants, provide the foundation for future radio -astronomical searches for cyanopyrazine.

Automated summary

The rotational spectrum of cyanopyrazine has been investigated, providing insights into its vibrational states and coupling coefficients. Cyanopyrazine, a polar derivative of pyrazine, can potentially serve as a tracer molecule for its nonpolar parent compound in extraterrestrial environments.