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Reactive vibrational excitation spectroscopy of formic acid in solid argon: Quantum yield for infrared induced trans→cis isomerization and solid state effects on the vibrational spectrum
Author(s) -
Ermelinda Maçôas,
Leonid Khriachtchev,
Mika Pettersson,
Jonas Jusélius,
Rui Fausto,
Markku Räsänen
Publication year - 2003
Publication title -
the journal of chemical physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.071
H-Index - 357
eISSN - 1089-7690
pISSN - 0021-9606
DOI - 10.1063/1.1624598
Subject(s) - excited state , isomerization , chemistry , conformational isomerism , molecular vibration , excitation , infrared spectroscopy , molecular physics , atomic physics , materials science , molecule , physics , biochemistry , organic chemistry , quantum mechanics , catalysis
Formic acid molecules are trapped in two predominant local environments (sites) when isolated in an argon matrix at 8 K. Using narrowband tunable infrared (IR) radiation, we performed site-selective excitation of various vibrational modes of the lower-energy trans conformer. For all excited modes, ranging from 7000 to 2950 cm−1, we detected site-selective isomerization to the higher-energy cis form. By measuring the IR absorption of a selected band of the cis conformer as a function of the excitation frequency, the reactive vibrational excitation (RVE) spectra were obtained. The trans→cis isomerization quantum yields for the excited modes were determined. Remarkably, very high absolute values were obtained for the quantum yield (up to 40%) at excitation energies above the reaction barrier. The efficiency of the photoinduced isomerization is essentially independent of the excited vibrational mode in a broad energy interval. Even when the excitation energy was below the reaction barrier, IR-induced rotation...

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