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Efficient intermolecular energy transfer between the C–Br stretching modes ν2 and ν5 of bromoform molecules in the liquid phase has been observed directly in time-resolved experiments applying vibrational pump–probe spectroscopy with picosecond laser pulses. An analysis of results on CHBr3, CDBr3, and an isotopic mixture of both yields a typical time constant of 25±15 ps for this rather efficient, near-resonant intermolecular relaxation channel. Additional new details about the intramolecular pathways of vibrational energy relaxation have been determined for the pure substances.
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Seifert et al. (2000) studied this question.
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