Unknown

Dataset Information

0

Photocatalytic aerobic oxidation of C(sp3)-H bonds.


ABSTRACT: In modern industries, the aerobic oxidation of C(sp3)-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 O2 and oxidation of C(sp3)-H bonds can be effectively accomplished, thus realizing efficient aerobic oxidation of C(sp3)-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(sp3)-H bonds, CeBTTD-A can also be applied to other types of aerobic oxidation reactions highlighting their potential for industrial applications.

SUBMITTER: Zhang L 

PROVIDER: S-EPMC10789790 | biostudies-literature | 2024 Jan

REPOSITORIES: biostudies-literature

altmetric image

Publications

Photocatalytic aerobic oxidation of C(sp<sup>3</sup>)-H bonds.

Zhang Lei L   Li Run-Han RH   Li Xiao-Xin XX   Wang Shengyao S   Liu Jiang J   Hong Xiao-Xuan XX   Dong Long-Zhang LZ   Li Shun-Li SL   Lan Ya-Qian YQ  

Nature communications 20240115 1


In modern industries, the aerobic oxidation of C(sp<sup>3</sup>)-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,  ...[more]

Similar Datasets

| S-EPMC10108173 | biostudies-literature
| S-EPMC9400635 | biostudies-literature
| S-EPMC10946557 | biostudies-literature
| S-EPMC5900731 | biostudies-literature
| S-EPMC10753956 | biostudies-literature
| S-EPMC3462469 | biostudies-literature
| S-EPMC8689654 | biostudies-literature
| S-EPMC5798593 | biostudies-literature
| S-EPMC6771714 | biostudies-literature
| S-EPMC5552783 | biostudies-literature