Abstract

Competition between intramolecular vibrational energy redistribution (IVR) and intermolecular vibrational energy transfer (VET) of excited methylene iodide (CH2I2) in solution has been measured in real time. After excitation of the C−H− stretch overtone and C−H− stretch containing combination bands of CH2I2 between 1.7 and 2.4 μm an increase followed by a decrease in the transient electronic absorption at 400 nm has been monitored. The transient absorption has been attributed to vibrational energy flow from the initially excited degrees of freedom to vibrational states with larger Franck-Condon (FC) factors for the electronic transition (long wavelength wing) and energy loss due to energy transfer to the solvent. A model based upon the dependence of the electronic absorption on the internal energy 〈E〉 of CH2I2 has been used to determine the times for intramolecular vibrational energy redistribution and intermolecular energy transfer to the solvent. In the simplest version of our model the internal energy ...

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