Experimental and theoretical studies on protonation of thioketones
Tokio Yamabe, S. Nagata, K. Akagi, Ryuichi Hashimoto, Koichi Yamashita, Kenichi Fukui, Astuyoshi Ohno, Kaoru Nakamura
Abstract
Tokio Yamabe, S. Nagata, K. Akagi, Ryuichi Hashimoto, Koichi Yamashita, Kenichi Fukui, Astuyoshi Ohno, Kaoru Nakamura
Abstract
The site of protonation in two classes of thioketones, (RC6H4)2CS (R = H or OCH3) and But2CS, was investigated by 1H and 13C n.m.r. spectroscopy. For aromatic thioketones, protonation occurs on the thiocarbonyl carbon from the side of the π-plane, whereas for the aliphatic compound, protonation of the sulphur atom occurs from the side of the σ-plane as in the case of carbonyl compounds. Electronic absorption spectra also provide information on sites of protonation in these molecules. Results are discussed in terms of total energies, charge-density distributions, and excitation energies of R2CS and its protonated derivative elucidated by semi-empirical SCF-MO calculations in the CNDO/2 approximation.
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The site of protonation in two classes of thioketones, (RC6H4)2CS (R = H or OCH3) and But2CS, was investigated by 1H and 13C n.m.r. spectroscopy. For aromatic thioketones, protonation occurs on the thiocarbonyl carbon from the side of the π-plane, whereas for the aliphatic compound, protonation of the sulphur atom occurs from the side of the σ-plane as in the case of carbonyl compounds. Electronic absorption spectra also provide information on sites of protonation in these molecules. Results are discussed in terms of total energies, charge-density distributions, and excitation energies of R2CS and its protonated derivative elucidated by semi-empirical SCF-MO calculations in the CNDO/2 approximation.
Key concepts: Protonation, CNDO/2, Chemistry, Molecule, Computational chemistry, Carbon fibers, Sulfur, Atom (system on chip)