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In Situ Ozone Generated on the Surface of Water Microdroplets Mediates Selective Aromatic Oxidation

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Abstract Microdroplet-mediated ozone (O 3 ) oxidation offers an alternative route for organic transformations compared to the commonly studied hydrogen peroxide (H 2 O 2 )-dominated systems. Here, we demonstrate efficient O 3 oxidation at the microdroplet interface, achieving selective conversion of naphthalene (NA) to dimethyl phthalate (DP) with 11.6% yield. When an aqueous methanol solution of NA is atomized into ~ 7.0 µm microdroplets under O 2 atmosphere, the system operates without external catalysts or oxidants while outperforming typical microdroplet oxidation methods. The generation of O 3 is unequivocally confirmed by indigo disulfonate spectrophotometry and high-resolution mass spectrometry. Combined with radical trapping experiments and DFT calculations, these results establish a surface-activated O 3 -mediated oxidation mechanism. Key intermediates were further confirmed by mass spectrometry. This work not only advances microdroplet O 3 chemistry beyond analytical detection to preparative synthesis, but also provides new insights into interfacial oxidative processes.
Title: In Situ Ozone Generated on the Surface of Water Microdroplets Mediates Selective Aromatic Oxidation
Description:
Abstract Microdroplet-mediated ozone (O 3 ) oxidation offers an alternative route for organic transformations compared to the commonly studied hydrogen peroxide (H 2 O 2 )-dominated systems.
Here, we demonstrate efficient O 3 oxidation at the microdroplet interface, achieving selective conversion of naphthalene (NA) to dimethyl phthalate (DP) with 11.
6% yield.
When an aqueous methanol solution of NA is atomized into ~ 7.
0 µm microdroplets under O 2 atmosphere, the system operates without external catalysts or oxidants while outperforming typical microdroplet oxidation methods.
The generation of O 3 is unequivocally confirmed by indigo disulfonate spectrophotometry and high-resolution mass spectrometry.
Combined with radical trapping experiments and DFT calculations, these results establish a surface-activated O 3 -mediated oxidation mechanism.
Key intermediates were further confirmed by mass spectrometry.
This work not only advances microdroplet O 3 chemistry beyond analytical detection to preparative synthesis, but also provides new insights into interfacial oxidative processes.

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