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Purely rotational coherence effect and time-resolved sub-Doppler spectroscopy of large molecules. II. Experimental

Baskin, J. Spencer and Felker, Peter M. and Zewail, Ahmed H. (1987) Purely rotational coherence effect and time-resolved sub-Doppler spectroscopy of large molecules. II. Experimental. Journal of Chemical Physics, 86 (5). pp. 2483-2499. ISSN 0021-9606. doi:10.1063/1.452100.

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In this paper we describe the results of picosecond fluorescence polarization (sub-Doppler) experiments designed to determine the role of purely rotational coherence in two jet-cooled molecules: trans-stilbene and anthracene. Observations of the manifestations of purely rotational coherence in t-stilbene are reported. The relationship of purely rotational coherence to molecular parameters (excited state rotational constants and transition dipole directions) is confirmed by comparison of our measurements with the results of the theory described in paper I [P. M. Felker and A. H. Zewail, J. Chem. Phys. 86, 2460 (1987)]. The sum of rotational constants B[script '] and C[script '] of the t-stilbene S1 electronic state is determined with a precision of better than 1 part in 700 (B[script ']+C[script ']=0.5132±0.0007 GHz). The influence of molecular beam expansion conditions and fluorescence detection conditions on our measurements is also investigated and compared with the theroretical findings of paper I. Also measurements of time-resolved and polarization-analyzed fluorescence as a function of excess vibrational energy in the S1 electronic states of both t-stilbene and anthracene are reported. We are able to distinguish the contribution of purely rotational coherence from the contributions of purely vibrational (or rovibrational) coherence to the evolution of fluorescence from the vibrationally excited molecule. The results are first analyzed on the basis of a model in which strict separability of vibrational and rotational motion is assumed. This provides a test of the extent of coupling of these motions and its influence on intramolecular vibrational energy redistribution (IVR).

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Additional Information:Copyright © 1987 American Institute of Physics. Received 3 November 1986; accepted 24 November 1986. We thank David Semmes for helpful discussions and contributions to the experiments reported herein. Arthur Amos Noyes Laboratory of Chemical Physics, Contribution No. 7500. This work was supported by a grant from the National Science Foundation (DMR 85-21191).
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NSFDMR 85-21191
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Arthur Amos Noyes Laboratory of Chemical Physics7500
Issue or Number:5
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ID Code:11743
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Deposited On:22 Sep 2008 20:53
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