HIGH RESOLUTION MOLECULAR BEAM SPECTROSCOPY OF THE HCNS DIMER IN THE 1.5 $\mu m$ REGION. REINVESTIGATION OF THE $\nu_{1}+\nu_{2}$ BAND AND COMPARISON WITH THEORY.
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Date
1997
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Ohio State University
Abstract
The 1.5 $\mu$ mspectrum of the $\nu_{1}+\nu_{2}$ combination band of the HCN dimmer has been reinvestigated with improved sensitivity in a molecular beam spectrometer. The $\nu_{1}$ and $\nu_{2}$ modes are nominally the free CH stretch and the hydrogen bound CH stretch respectively. The improved signal to noise has allowed us to increase the number of observed rotational states to J=24. The observed linewidths range from 12 to 60 MHz, the largest values corresponding to mixing with a perturbing state that becomes resonant around $J = 10$. Contrary to expectations, the lifetime of the upper state far from the perturbation is at least two times longer than the one observed by Jucks and Miller [JCP 88, 6059,(1988)] for the $\nu_{2}$ fundamental. This shows that changing the vibrational state of the outer CH stretch, whose lifetime is two orders of magnitude longer than that of the $\nu_{2}$ fundamental, makes it possible to control the lifetime of the hydrogen bond braking. The transition strength is measured to be about 14 times smaller than that of the $2\nu_{1}$ overtone, about, about six times larger than expected based on a simple dipole-induced dipole model for the coupling between $\nu_{1}$ and $\nu_{2}$. Five-dimensional potential energy and electric dipole moment functions have been constructed for the stretching vibrations on the basis of large-scale CEPA-1 and CCSD(T) calculations. The absolute IR intensity of the $\nu_{1}+\nu_{2}$ band is predicted to be 0.06 km $mol^{-1}$, a factor of 24 smaller than that of the $2\nu_{1}$ band ( i.e. within a factor two of the experimental value). The origin of the $2\nu_{2}$ band is predicted at $6370 cm^{-1}$ and its intensity is calculated to be 0.12 km $mol^{-1}$. This band has not been experimentally observed so far.
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$^{h}$Visiting from the University of Bonn, Institut f\""ur Angewandte Physik., Wegelerstr. 8, 53115 Bonn, Germany
Author Institution: Department of Chemistry, Princeton University; Institut f\""{u}r Physikalische Chemie der, University Gottingen
Author Institution: Department of Chemistry, Princeton University; Institut f\""{u}r Physikalische Chemie der, University Gottingen