A supramolecular naphthalenediimide radical anion through host-guest interactions for photooxidation of alkylarenes to carbonyls

A supramolecular naphthalenediimide radical anion was developed through host-guest interactions between NDI and cucurbit[7]uril (CB[7]), which can be greatly promoted in the presence of chloride ions to obtain Cl&z.rad; and NDI-2CB[7]&z.rad; − . Under the synergistic action of Cl&z.rad;...

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2024-08, Vol.6 (67), p.8924-8927
Hauptverfasser: Li, Xin-Long, Niu, Kai-Kai, Yu, Shengsheng, Liu, Hui, Xing, Ling-Bao
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Sprache:eng
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Zusammenfassung:A supramolecular naphthalenediimide radical anion was developed through host-guest interactions between NDI and cucurbit[7]uril (CB[7]), which can be greatly promoted in the presence of chloride ions to obtain Cl&z.rad; and NDI-2CB[7]&z.rad; − . Under the synergistic action of Cl&z.rad; as a hydrogen atom transfer (HAT) agent and NDI-2CB[7]&z.rad; − transferring electrons to O 2 to produce O 2 &z.rad; − , the photocatalytic oxidation reactions of alkylarenes to carbonyls can be realized with universal applicability. A supramolecular naphthalenediimide radical anion was developed through host-guest interactions between NDI and cucurbit[7]uril (CB[7]), which can be greatly promoted in the presence of chloride ions to obtain Cl&z.rad; and NDI-2CB[7]&z.rad; − .
ISSN:1359-7345
1364-548X
1364-548X
DOI:10.1039/d4cc02374a