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. 2021 Feb 24;11:4411. doi: 10.1038/s41598-021-83863-0

Table 3.

Oxidative cleavage of alkenes to corresponding aldehydes in the presence of A-CQDs/W catalyst.

Entry Structure Product Conversion (%)a Yield (%) b
1 graphic file with name 41598_2021_83863_Figc_HTML.gif graphic file with name 41598_2021_83863_Figd_HTML.gif 95 86
2 graphic file with name 41598_2021_83863_Fige_HTML.gif graphic file with name 41598_2021_83863_Figf_HTML.gif 78 69
3c graphic file with name 41598_2021_83863_Figg_HTML.gif graphic file with name 41598_2021_83863_Figh_HTML.gif 72 63
4 graphic file with name 41598_2021_83863_Figi_HTML.gif graphic file with name 41598_2021_83863_Figj_HTML.gif 100 94
5 graphic file with name 41598_2021_83863_Figk_HTML.gif graphic file with name 41598_2021_83863_Figl_HTML.gif 96 89
6 graphic file with name 41598_2021_83863_Figm_HTML.gif graphic file with name 41598_2021_83863_Fign_HTML.gif 91 84
7c graphic file with name 41598_2021_83863_Figo_HTML.gif graphic file with name 41598_2021_83863_Figp_HTML.gif 83

42

38

8c graphic file with name 41598_2021_83863_Figq_HTML.gif graphic file with name 41598_2021_83863_Figr_HTML.gif 76 63
9c graphic file with name 41598_2021_83863_Figs_HTML.gif graphic file with name 41598_2021_83863_Figt_HTML.gif 74 74

Reaction conditions: Substrate (1 mmol), H2O2 (3 mmol), H2O (1.5 mL), A-CQDs/W (1 mol %), 3 h, 90 °C.

bConversions were calculated based on initial mmol of substrate.

cIsolated Yields.

dIn the presence of 0.25 mmol CH3COOH.