Photocatalytic aerobic oxidation of C(sp3)-H bonds
In modern industries, the aerobic oxidation of C(sp 3 )-H bonds to achieve the value-added conversion of hydrocarbons requires high temperatures and pressures, which significantly increases energy consumption and capital investment. The development of a light-driven strategy, even under natural sunl...
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Veröffentlicht in: | Nature communications 2024-01, Vol.15 (1), p.537-537, Article 537 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | In modern industries, the aerobic oxidation of C(sp
3
)-H bonds to achieve the value-added conversion of hydrocarbons requires high temperatures and pressures, which significantly increases energy consumption and capital investment. The development of a light-driven strategy, even under natural sunlight and ambient air, is therefore of great significance. Here we develop a series of hetero-motif molecular junction photocatalysts containing two bifunctional motifs. With these materials, the reduction of O
2
and oxidation of C(sp
3
)-H bonds can be effectively accomplished, thus realizing efficient aerobic oxidation of C(sp
3
)-H bonds in e.g., toluene and ethylbenzene. Especially for ethylbenzene oxidation reactions, excellent catalytic capacity (861 mmol g cat
−1
) is observed. In addition to the direct oxidation of C(sp
3
)-H bonds, CeBTTD-A can also be applied to other types of aerobic oxidation reactions highlighting their potential for industrial applications.
The authors report a family of photocatalysts containing Ce active sites and perylene diimide ligands for the aerobic oxidation of substituted toluene, ethylbenzene, benzyl alcohol, thioanisole, and benzylamine in acetonitrile. |
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ISSN: | 2041-1723 2041-1723 |
DOI: | 10.1038/s41467-024-44833-y |