| Autor: |
Barclay, A. J., Lauzin, C., Sheybani-Deloui, S., Michaelian, K. H., Moazzen-Ahmadi, N. |
| Zdroj: |
Physical Chemistry Chemical Physics (PCCP); 1/14/2017, Vol. 19 Issue 2, p1610-1613, 4p |
| Abstrakt: |
Infrared spectra in the carbon monoxide CO stretch region (∼2150 cm−1) and in the ν3 asymmetric stretch region of N2O (∼2223 cm−1) are assigned to the previously unobserved O-bonded form of the CO–N2O dimer (“isomer 2”). This van der Waals complex has a planar skewed T-shaped structure like that of the previously observed C-bonded form (“isomer 1”), but with the CO rotated by 180°. The effective intermolecular distance between the centers of mass is 3.51 Å for isomer 2 as compared to 3.88 Å for isomer 1. In addition to the fundamental band, two combination bands are observed for isomer 2, yielding values for two intermolecular vibrational modes: 14.502(5) cm−1 for the coupled disrotatory motion or the uncoupled CO rock and 21.219(5) cm−1 for the out-of-plane rock. We show that the published ab initio study on this system is inadequate in predicting the intermolecular frequencies for isomer 2 of CO–N2O. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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