The Raman optical activity (ROA) spectra of both enantiomers of 2-Brhexahelicene 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.
Raman and ROA Spectra of (−)- and (+)-2-Br-Hexahelicene: Experimental and DFT Studies of a π‑Conjugated Chiral System
ABBATE, Sergio;LONGHI, Giovanna;
2013-01-01
Abstract
The Raman optical activity (ROA) spectra of both enantiomers of 2-Brhexahelicene 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.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
