Vibrational structure in magnetic circular dichroism spectra of polycyclic aromatic hydrocarbons
|Author:||Kaminský, Jakub1; Chalupský, Jakub1; Štěpánek, Petr2;|
1Institute of Organic Chemistry and Biochemistry, Academy of Sciences, Flemingovo náměstí 2, 16610 Prague, Czech Republic
2NMR Research Unit, Faculty of Science, University of Oulu, PO Box 3000, 90014 Oulu, Finland
|Online Access:||PDF Full Text (PDF, 2.4 MB)|
|Persistent link:|| http://urn.fi/urn:nbn:fi-fe2017122156013
American Chemical Society,
|Publish Date:|| 2018-11-07
Absorption and magnetic circular dichroism (MCD) spectroscopies are powerful and simple methods to discriminate among various compounds. Polycyclic aromatic hydrocarbons provide particularly strong signal, which, for example, facilitates their detection in the environment. However, interpretation of the spectra is often based on quantum-chemical simulations, providing a limited precision only. In the present work, we use time-dependent density functional theory and complete active space second-order perturbation theories to understand spectral features observed in a series of naphthalene, anthracene, phenanthrene, and three larger compounds. The electronic computations provided reasonable agreement with the experiment for the smaller molecules, while a large error persisted for the bigger ones. However, many discrepancies could be explained by vibrational splitting of the electronic transitions across the entire spectral range. Compared to plain absorption, MCD spectral bands and their vibrational splitting were more specific for each aromatic molecule. The computational tools allowing simulations of detailed vibrational features in the electronic spectra thus promise to open a qualitatively new chapter in the spectroscopy of aromatic compounds.
The journal of physical chemistry. A
|Pages:||9064 - 9073|
|Type of Publication:||
A1 Journal article – refereed
|Field of Science:||
114 Physical sciences
The work was supported by the Grant Agency of the Czech Republic (Grant No. 15-19143S, 16-05935S to P.B. and 16-00270S to J.K.).
This document is the unedited Author’s version of a Submitted Work that was subsequently accepted for publication in Journal of Physical Chemistry A, copyright © American Chemical Society after peer review. To access the final edited and published work see https://doi.org/10.1021/acs.jpca.7b10120.