15min:
COMBINATION BANDS OF THE NONPOLAR N2O DIMER AND INFRARED SPECTRA OF (C2D4)2 AND (C2D4)3 USING A QUANTUM CASCADE LASER.

M. REZAEI, N. MOAZZEN-AHMADI, Department of Physics and Astronomy, University of Calgary, Calgary, AB T2N 1N4, Canada; A. R. W. MCKELLAR, Steacie Institute for Molecular Sciences, National Research Council of Canada, Ottawa, ON K1A 0R6, Canada; K. H. MICHAELIAN, Natural Resources Canada, CANMET Western Research Center, 1 Oil Patch Drive, Suite A202 Devon Alberta T9G 1A8, Canada..

Our pulsed-jet supersonic apparatus has been retrofitted by an infrared cw external-cavity quantum cascade laser (QCL) manufactured by Dayligh Slutions to study infrared spectra of weakly-bound complexes. The QCL is used in the rapid-scan signal-averaging mode. Although the repetition rate of the QCL is limited by its PZT scan rate, which is 100 Hz, we describe a simple technique to increase the effective repetition rate to 625 Hz. In addition, we have significantly reduced the long term frequency drift of the QCL by locking the laser frequency to the sides of a reference line. Performance of the apparatus is illustrated by recording spectra of the combination bands of the nonpolar (14N2O)2 and (15N2O)2 and infrared spectra of ethylene dimer and trimer.

Spectra of ethylene dimer and trimer were studied in the nu11 fundamental band region of C2D4 ( sim 2200 cm-1). The dimer spectrum is that of a prolate symmetric top perpendicular band, with a distinctive appearance because the A rotational constant is almost exactly equal to six times the B constant. The analysis supports the previously determined cross-shaped dimer structure with D2h symmetry. Ethylene trimer has not previously been observed with rotational resolution. The spectrum is that of an oblate symmetric top parallel band. It leads to a proposed trimer structure which is barrel shaped and has C3h or C3 symmetry, with the ethylene monomer C—C axes approximately aligned along the trimer symmetry axis.