J. Phys. Chem. A, 110 (38), 10925 -10928, 2006. 10.1021/jp0645061 S1089-5639(06)04506-3
Web Release Date: August 31, 2006

Copyright © 2006 American Chemical Society

Field-Resolved Coherent Raman Spectroscopy of High Frequency Vibrational Resonances

Andrew M. Moran, Rene A. Nome, and Norbert F. Scherer*

Department of Chemistry and the James Franck Institute, The University of Chicago, 5735 South Ellis Avenue, Chicago, Illinois 60637

Received: July 16, 2006

In Final Form: August 15, 2006

Abstract:

Electric fields of coherent Raman signals are resolved with sensitivity for high-frequency vibrational resonances utilizing a four-pulse, trapezoidal beam geometry in a diffractive optic-based interferometer. Our experiments show that the heterodyne detected signal phase is stabilized for particular terms in the third-order response function by the cancellation of inter-pulse phases. The C-H stretching modes of cyclohexane and benzene are studied under two polarization conditions. The temporal profiles of signal fields for cyclohexane exhibit a low-frequency recurrence due to the interference between the signals associated with the symmetric and asymmetric C-H stretching modes. In contrast, the electronically nonresonant polarizability response of benzene gives rise to a significant broadband signal component in addition to that associated with its C-H vibrational resonance. Time-frequency shapes of the Raman signal fields are strongly dependent on the properties of the liquid and the polarizations of the laser pulses.


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