Raman and ROA spectra of (-)- and (+)-2-Br-hexahelicene: experimental and DFT studies of a π-conjugated chiral system.

Christian Johannessen, Ewan W Blanch, Claudio Villani, Sergio Abbate, Giovanna Longhi, Nisha R Agarwal, Matteo Tommasini, David A Lightner

Faculty of Life Sciences and Manchester Institute of Biotechnology, John Garside Building, University of Manchester, 131 Princess Street, Manchester M1 7DN, UK.

The journal of physical chemistry. B 2013 Feb 21

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The Raman optical activity (ROA) spectra of both enantiomers of 2-Br-hexahelicene in chloroform solution have been measured in the range 1700-300 cm(-1). Density functional theory (DFT) calculations accurately reproduce the observed features. The most intense ROA features are also the most intense Raman features, in the region 1350-1400 cm(-1), and correspond to the so-called D-modes, which play a major role in coronene and other PAHs (polycyclic aromatic hydrocarbons). Together with a detailed analysis of the normal mode structure, the polarizability tensors for the intense Raman features are investigated and related to the principal characteristics of helicene systems, namely, chirality and π-conjugation. Through electron-phonon coupling analysis, we propose a mechanism that justifies the intense ROA signals.

Citation

Christian Johannessen, Ewan W Blanch, Claudio Villani, Sergio Abbate, Giovanna Longhi, Nisha R Agarwal, Matteo Tommasini, David A Lightner. Raman and ROA spectra of (-)- and (+)-2-Br-hexahelicene: experimental and DFT studies of a π-conjugated chiral system. The journal of physical chemistry. B. 2013 Feb 21;117(7):2221-30