2017
DOI: 10.1016/j.synthmet.2017.06.011
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Polythianthrene ladder oligomers function as an organic battery electrode with a high oxidation potential

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Cited by 10 publications
(8 citation statements)
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“…The heteroatom (S) containing polymer, polythianthrene, also acts as a p-type organic cathode to lose four outer-shell electrons at high reaction potentials and provide a high theoretical capacity of 388 mAh g −1 . 36 To enable this anion insertion reaction, two or more thioether groups should be connected with a conjugated structure, such as a benzene ring. During the anion insertion process, intramolecular electron transfer is triggered in the conjugated structure, and each sulfur atom loses an electron and possesses a positive charge.…”
Section: Reaction Mechanisms In Organic Batteriesmentioning
confidence: 99%
See 1 more Smart Citation
“…The heteroatom (S) containing polymer, polythianthrene, also acts as a p-type organic cathode to lose four outer-shell electrons at high reaction potentials and provide a high theoretical capacity of 388 mAh g −1 . 36 To enable this anion insertion reaction, two or more thioether groups should be connected with a conjugated structure, such as a benzene ring. During the anion insertion process, intramolecular electron transfer is triggered in the conjugated structure, and each sulfur atom loses an electron and possesses a positive charge.…”
Section: Reaction Mechanisms In Organic Batteriesmentioning
confidence: 99%
“…The heteroatom (S) containing polymer, polythianthrene, also acts as a p-type organic cathode to lose four outer-shell electrons at high reaction potentials and provide a high theoretical capacity of 388 mAh g –1 . To enable this anion insertion reaction, two or more thioether groups should be connected with a conjugated structure, such as a benzene ring.…”
Section: Reaction Mechanisms In Organic Batteriesmentioning
confidence: 99%
“…Intramolecular Friedel-Crafts electrophilic substitution represents perhaps one of the most common ladderization strategies, broadly used in the construction of ladder-type p-phenylenes and subsequently expanded to other frameworks. [24][25][26][27] A pendant group is usually required to serve as the electrophile and is typically activated in acidic conditions. Electron-rich aromatic units which can function as nucleophiles are required to facilitate the reaction.…”
Section: Kinetic Annulationsmentioning
confidence: 99%
“…This performance outperformed almost all of the reported thianthrene-based molecules (Table S2, ESI†). 38,39…”
mentioning
confidence: 99%
“…32 Theoretically, thianthrene can be electrochemically oxidized to a double cation in two steps, with an onset potential of 0.74 V vs. Fc/Fc + , corresponding to 3.9 V vs. Li/Li + for the first oxidation. [33][34][35] Although the chemical and electrochemical properties of thianthrene-based materials have been investigated as cathodes, [36][37][38][39][40][41] they mainly include soluble small molecules or polymers which are insoluble but require complex synthesis (limiting the potentially large-scale applications with low cost).…”
mentioning
confidence: 99%