RESUMO
The near-infrared electronic transition of CuCl, occurring in the region of 745 nm, was recorded using intracavity laser absorption spectroscopy. The (0, 0), (1, 1), and (2, 2) vibronic bands were analyzed, and from this the molecular constants for the two electronic states were derived. Originally assigned as A' (3)Sigma(+)-X(1)Sigma(+), we have confirmed that this transition does not connect to the ground state, but occurs between two unknown excited states. The excited CuCl molecules were produced in a copper hollow cathode, operated using argon and a small amount of CCl(4). Line positions were referenced to iodine spectra observed from a heated extracavity cell using the broadband spectral output of the intracavity laser as the light source. Copyright 2000 Academic Press.
RESUMO
The intracavity laser spectroscopy (ILS) technique has been shown to be a very sensitive method for observing absorption spectra. By considering quantitative results (line-strengths and pressure broadening coefficients) obtained using the ILS method with a dye laser, the technique has been shown to provide quantitative information that is in excellent agreement with the values afforded by use of more traditional methods for acquiring absorption spectra. A similar investigation has been conducted for an ILS system based on a Ti:sapphire laser. Presented here are quantitative results for water vapor transitions occurring around 795 nm. Line intensities are determined as a function of water vapor pressure and effective path length (i.e., generation time). The line-strengths are compared with values determined by R. A. Toth [J. Mol. Spectrosc. 166, 176-183 (1994)] who used a multipass cell and the Fourier transform spectrometer at the Kitt Peak National Observatory. The good agreement between the results demonstrates that quantitatively accurate data can be obtained using the ILS technique with a Ti:sapphire laser. Copyright 1998 Academic Press.
