Tribenzo-1,4,5,8,9,12-hexathiatriphenylene Dication and Dibenzo-1,4,5,8-tetrathiaphenanthrene Dication
Takeo Nakai, Masatoshi Kozaki, Kazunobu Sato, Daisuke Shiomi, Takeji Takui, Koichi Itoh, Keiji Okada
Abstract
Takeo Nakai, Masatoshi Kozaki, Kazunobu Sato, Daisuke Shiomi, Takeji Takui, Koichi Itoh, Keiji Okada
Abstract
Abstract Tribenzo-1,4,5,8,9,12-hexathiatriphenylene dication (12+) and dibenzo-1,4,5,8-tetrathiaphenanthrene dication (22+) were generated in concentrated sulfuric acid. Their zero-field splitting parameters were determined as D = 0.012 cm−1, E ≈ 0.00 cm−1 for 12+, and D = 0.012 cm−1, E ≈ 0.00 cm−1 for 22+. The dication 12+ was found to be a triplet in the ground state, whereas 22+ to be a singlet ground state with the singlet-triplet energy gap of −35 ± 2 J/mol.
OpenAlex reports 4 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Abstract Tribenzo-1,4,5,8,9,12-hexathiatriphenylene dication (12+) and dibenzo-1,4,5,8-tetrathiaphenanthrene dication (22+) were generated in concentrated sulfuric acid. Their zero-field splitting parameters were determined as D = 0.012 cm−1, E ≈ 0.00 cm−1 for 12+, and D = 0.012 cm−1, E ≈ 0.00 cm−1 for 22+. The dication 12+ was found to be a triplet in the ground state, whereas 22+ to be a singlet ground state with the singlet-triplet energy gap of −35 ± 2 J/mol.
Key concepts: Dication, Chemistry, Medicinal chemistry, Stereochemistry, Photochemistry, Organic chemistry, Ion