## Abstract The ability to use calculated OH frequencies to assign experimentally observed peaks in hydrogen bonded systems hinges on the accuracy of the calculation. Here we test the ability of several commonly employed model chemistries—HF, MP2, and several density functionals paired with the 6‐3
Vibrational predissociation in hydrogen-bonded OH…O complexes via OH stretch-OO stretch energy transfer
✍ Scribed by Arnulf Staib; James T. Hynes
- Publisher
- Elsevier Science
- Year
- 1993
- Tongue
- English
- Weight
- 817 KB
- Volume
- 204
- Category
- Article
- ISSN
- 0009-2614
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✦ Synopsis
A theory for vibrational predissociation of hydrogen-bonded OH...0 complexes via OH stretch-00 stretch energy transfer is constructed, motivated by a recent experiment on vibrational predissociation of hydrogen-bonded ethanol dimer in solution. The theory employs a vibrationally adiabatic perspective, exploiting the frequency separation between the OH and 00 stretches. The nonadiabatic coupling responsible for the hydrogen bond rupture subsequent to OH stretch excitation is found analytically. A lifetime for ethanol dimer of % 10 ps is estimated, which is within a factor of two of the experimental result. General trends are predicted and discussed for other OH...0 complexes.
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