| Autor: |
Vogelhuber KM; JILA and Department of Chemistry and Biochemistry, University of Colorado, 440 UCB, Boulder, Colorado 80309, USA., Wren SW, McCoy AB, Ervin KM, Lineberger WC |
| Jazyk: |
angličtina |
| Zdroj: |
The Journal of chemical physics [J Chem Phys] 2011 May 14; Vol. 134 (18), pp. 184306. |
| DOI: |
10.1063/1.3585606 |
| Abstrakt: |
We report the 364-nm negative ion photoelectron spectra of CHX(2)(-) and CDX(2)(-), where X = Cl, Br, and I. The pyramidal dihalomethyl anions undergo a large geometry change upon electron photodetachment to become nearly planar, resulting in multiple extended vibrational progressions in the photoelectron spectra. The normal mode analysis that successfully models photoelectron spectra when geometry changes are modest is unable to reproduce qualitatively the experimental data using physically reasonable parameters. Specifically, the harmonic normal mode analysis using Cartesian displacement coordinates results in much more C-H stretch excitation than is observed, leading to a simulated photoelectron spectrum that is much broader than that which is seen experimentally. A (2 + 1)-dimensional anharmonic coupled-mode analysis much better reproduces the observed vibrational structure. We obtain an estimate of the adiabatic electron affinity of each dihalomethyl radical studied. The electron affinity of CHCl(2) and CDCl(2) is 1.3(2) eV, of CHBr(2) and CDBr(2) is 1.9(2) eV, and of CHI(2) and CDI(2) is 1.9(2) eV. Analysis of the experimental spectra illustrates the limits of the conventional normal mode approach and shows the type of analysis required for substantial geometry changes when multiple modes are active upon photodetachment. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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