Abstract
Laser ablation of transition metal targets with concurrent 4 K codeposition of CO2/Ne mixtures produces metal independent infrared absorptions at 1658.2 and 1421.6 cm−1 due to CO2− and CO2+. Additional metal independent absorptions at 2130.8 and 1274.4 cm−1, and at 1852.4, 1189.2, and 679.2 cm−1 increase on annealing to 8 K. Isotopic substitution shows that both band sets involve two equivalent CO2 subunits. Based on density functional theory calculations of structures and vibrational frequencies, the 2130.8 and 1274.4 cm−1 bands are assigned to the C2O4+ cation with C2h symmetry, and the 1852.4, 1189.2, and 679.2 cm−1 bands are assigned to the C2O4− anion with D2d symmetry. Evidence is also obtained for (CO2−)(CO2)x(x=1,2) anion complexes.
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Dates
Type | When |
---|---|
Created | 23 years, 1 month ago (July 26, 2002, 8:17 a.m.) |
Deposited | 1 year, 6 months ago (Feb. 6, 2024, 1:24 a.m.) |
Indexed | 1 month, 3 weeks ago (July 3, 2025, 3:32 a.m.) |
Issued | 26 years, 4 months ago (April 8, 1999) |
Published | 26 years, 4 months ago (April 8, 1999) |
Published Print | 26 years, 4 months ago (April 8, 1999) |
@article{Zhou_1999, title={Infrared spectra of the C2O4+ cation and C2O4− anion isolated in solid neon}, volume={110}, ISSN={1089-7690}, url={http://dx.doi.org/10.1063/1.478586}, DOI={10.1063/1.478586}, number={14}, journal={The Journal of Chemical Physics}, publisher={AIP Publishing}, author={Zhou, Mingfei and Andrews, Lester}, year={1999}, month=apr, pages={6820–6826} }