| タイトル | Infrared Spectroscopy of Matrix-Isolated Polycyclic Aromatic Compounds and their Ions |
| 本文（外部サイト） | http://hdl.handle.net/2060/20020079825 |
| 著者（英） | Allamandola, L. J.; Rosi, M.; Bauschlicher, C. W., Jr.; Mattioda, A. L.; Hudgins, Douglas M.; DeVincenzi, D. |
| 著者所属（英） | NASA Ames Research Center |
| 発行日 | 2002-08-01 |
| 言語 | eng |
| 内容記述 | The matrix-isolation technique has been employed to measure the mid-infrared spectra of several polycyclic aromatic nitrogen heterocycles in both neutral and cationic forms. The species studied include: 7,8 benzoquinoline (C13H9N); 2-azapyrene (C15H9N); 1- and 2-azabenz(a)anthracene (C17H11N); and 1-, 2-, and 4-azachrysene (also C17H11N). The experimentally measured band frequencies and intensities for each molecule are tabulated and compared with their theoretically calculated values computed using density functional theory at the B3LYP/4-31G level. The overall agreement between experiment and theory is quite good, in keeping with previous investigations involving the parent aromatic hydrocarbons. Several interesting spectroscopic trends are found to accompany nitrogen substitution into the aromatic framework of these compounds. First, for the neutral species, the nitrogen atom produces a significant increase in the total integrated infrared intensity across the 1600 - 1100/cm region and plays an essential role in the molecular vibration that underlies an uncharacteristically intense, discrete feature that is observed near 1400/cm in the spectra of 7,8 benzoquinoline, 1-azabenz(a)anthracene, and 4-azachrysene. The origin of this enhanced infrared activity and the nature of the new 1400/cm vibrational mode are explored. Finally, in contrast to the parent hydrocarbon species, these aromatic nitrogen heterocycles possess a significant permanent dipole moment. Consequently, these dipole moments and the rotational constants are reported for these species in their neutral and ionized forms. |
| NASA分類 | Chemistry and Materials (General) |
| レポートNO | SSA-113 |
| 権利 | No Copyright |
| URI | https://repository.exst.jaxa.jp/dspace/handle/a-is/224205 |
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