15min:
ROTATIONALLY RESOLVED SPECTRA OF THE B2 Pi - X2 Pi 000 AND µ2 Sigma - µ2 Sigma 1111 TRANSITIONS OF C6H AND C6D.

D. ZHAO, M. A. HADDAD, Institute for Lasers, Life and Biophotonics Amsterdam, De Boelelaan-1081, NL 1081 HV Amsterdam, Netherlands; H. LINNARTZ, Raymond and Beverly Sackler Laboratory for Astrophysics, Leiden Observatory, Leiden University, P.O. Box 9513, NL-2300 RA Leiden, and Institute for Lasers, Life and Biophotonics Amsterdam, De Boelelaan 1081, NL-1081 HV Amsterdam, Netherlands; W. UBACHS, Institute for Lasers, Life and Biophotonics Amsterdam, De Boelelaan-1081, NL 1081 HV Amsterdam, Netherlands.

The linear carbon chain radicals have been topic of a series of spectroscopic studies. The hexatriynyl radical C6H (and deuterated equivalent C6D), a member of the linear CnH series, has attracted renewed interest in recent years after the astronomical identification of its chemically related anion C6H- and its low-lying 111 µ2 Sigma vobronic state.

In this talk, rotationally resolved spectra of the B2 Pi - X2 Pi 000 and 1111 transitions of both C6H and C6D are presented. Cavity ringdown spectroscopy is used to record the spectra in direct absorption through a supersonically expanding planar plasma. The µ2 Sigma - µ2 Sigma 1111 vobronic hot bands are observed for the first time. Heavy rotational perturbations are found in the upper levels of C6D. Precise spectroscopic parameters for the 111 µ2 Sigma levels of both C6H and C6D are determined for the first time, and the spectroscopic parameters for the B2 Pi 00 states are also improved. The Renner-Teller interaction is also discussed to estimate the excitation energies of the low-lying 111 µ2 Sigma vibronic states.