Femtosecond degenerate four-wave mixing of carbon disulfide: High-accuracy rotational constants

Abstract

Femtosecond degenerate four-wave mixing (fs-DFWM) rotational coherence spectroscopy (RCS) has been used to determine the rotational and centrifugal distortion constants of the 00 (0)0 ground and 01 (1)0 vibrationally excited states of gas-phase CS(2). RCS transients were recorded over the 0-3300 ps optical delay range, allowing the observation of 87 recurrences. The fits yield rotational constants B(00 (0)0)=3.271 549 2(18) GHz for (12)C(32)S(2) and B(00 (0)0)=3.175 06(21) GHz for the (12)C(32)S(34)S isotopomer. The rotational constants of the degenerate 01 (1)0 bending level of (12)C(32)S(2) are B(01 (1)0)=3.276 72(40) and 3.279 03(40) GHz for the e and f substrates, respectively. These fs-DFWM rotational constants are ten times more accurate than those obtained by CO(2) laser/microwave heterodyne measurements and are comparable to those obtained by high-resolution Fourier transform infrared spectroscopy. Ab initio calculations were performed at two levels, second-order Moller-Plesset theory and coupled-cluster singles, doubles, and iterative triples [CCSD(T)]. The equilibrium and vibrationally averaged C=S distances were calculated using large Dunning basis sets. An extrapolation procedure combining the ab initio rotational constants with the experiment yields an equilibrium C=S bond length of 155.448 pm to an accuracy of +/-20 fm. The theoretical C=S bond length obtained by a complete basis set extrapolation at the CCSD(T) level is r(e)(C=S)=155.579 pm, or 0.13 pm longer than that in the experiment.