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Oriented molecule beams: Focusing and orientation of t-butyl iodide with analysis by polarized laser photofragmentation

Journal Article · · J. Chem. Phys.; (United States)
DOI:https://doi.org/10.1063/1.455106· OSTI ID:6934561
The tert-butyl iodide molecule is readily focused with the electrostatic hexapole, via its first-order Stark effect as a pseudo-symmetric top. The pulsed, seeded supersonic focused beam, characterized by = V/sub th// V/sub 0/ (where theta is the angle between the molecular dipole axis ..mu.. and the electric field E; +- V/sub 0/ the hexapole ''rod voltage,'' and V/sub th/ the so-called threshold voltage), passes into a small homogeneous electric field in which it is oriented. The degree of laboratory orientation achieved is measured using the method of linearly polarized laser-induced photofragmentation (S. R. Gandhi, T. J. Curtiss, and R. B. Bernstein, Phys. Rev. Lett. 59, 2951 (1987)), operating (at three laser wavelengths) on the I(/sup 2/P/sub 3//sub ///sub 2/) and I(/sup 2/P/sub 1//sub ///sub 2/) as well as the t-C/sub 4/H/sub 9/ radical photofragments. The results show that the oriented beam molecules of t-butyl iodide (at a rotational temperature near 15 K) have a higher degree of orientation than the prototype CH/sub 3/I molecules (JKM state-selected and focused similarly), explainable by the greater importance of the so-called hyperfine disorientation effect for the prolate symmetric top (CH/sub 3/I) than for the t-C/sub 4/H/sub 9/I. For the latter, orientations with photofragment up--down asymmetry ratios as large as a factor of 10 can be achieved, suggesting that t-C/sub 4/H/sub 9/I is an excellent candidate reagent for reactive asymmetry studies.
Research Organization:
Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90024-1569
OSTI ID:
6934561
Journal Information:
J. Chem. Phys.; (United States), Journal Name: J. Chem. Phys.; (United States) Vol. 89:4; ISSN JCPSA
Country of Publication:
United States
Language:
English