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 |
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Format: | Artikel |
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;
−
. |
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ISSN: | 1359-7345 1364-548X 1364-548X |
DOI: | 10.1039/d4cc02374a |