Peer-reviewedCC BY-NCRSC advances
Mechanochemical generation of chlorine dioxide radical for solvent-free oxygenation of dibenzothiophenes
4 affiliations
- 1aGraduate School of Pharmaceutical Sciences, The University of Osaka, 1-6 Yamadaoka, Suita, Osaka 565-0871, Japan.
- 2bInstitute for Open and Transdisciplinary Research Initiatives (OTRI), The University of Osaka, 1-6 Yamadaoka, Suita, Osaka 565-0871, Japan.
- 3aGraduate School of Pharmaceutical Sciences, The University of Osaka, 1-6 Yamadaoka, Suita, Osaka 565-0871, Japan.bInstitute for Open and Transdisciplinary Research Initiatives (OTRI), The University of Osaka, 1-6 Yamadaoka, Suita, Osaka 565-0871, Japan.
- 4bInstitute for Open and Transdisciplinary Research Initiatives (OTRI), The University of Osaka, 1-6 Yamadaoka, Suita, Osaka 565-0871, Japan.cOrganization for Carbon Neutrality Collaboration (OCNC), The University of Osaka, 1-6 Yamadaoka, Suita, Osaka 565-0871, Japan.
Abstract
Herein, we present a method for generating chlorine dioxide radical Alt-text is not available for this image. under solvent-free conditions by ball milling sodium chlorite with silica gel. The mechanochemical formation of Alt-text is not available for this image. was supported by UV-vis absorption spectroscopy and ESR measurements. The in situ-generated Alt-text is not available for this image. was directly used for the selective monooxygenation of dibenzothiophenes, including a poorly soluble π-extended benzothiophene derivative. This method provides a practical solvent-free platform for Alt-text is not available for this image.-mediated oxygenation of poorly soluble organosulfur compounds.
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BibTeX
@article{sekiguchi2026mechanochemical,
title = {{Mechanochemical generation of chlorine dioxide radical for solvent-free oxygenation of dibenzothiophenes}},
author = {Kensho Sekiguchi and Yuki Itabashi and Tsuyoshi Inoue and Kei Ohkubo and Haruyasu Asahara},
journal = {RSC advances},
year = {2026},
month = oct,
doi = {10.1039/d6ra07225a},
url = {https://europepmc.org/article/PMC/PMC13656216},
note = {CC BY-NC},
}
RIS
TY - JOUR
TI - Mechanochemical generation of chlorine dioxide radical for solvent-free oxygenation of dibenzothiophenes
AU - Kensho Sekiguchi
AU - Yuki Itabashi
AU - Tsuyoshi Inoue
AU - Kei Ohkubo
AU - Haruyasu Asahara
PY - 2026
DA - 2026/10/12
JO - RSC advances
DO - 10.1039/d6ra07225a
UR - https://europepmc.org/article/PMC/PMC13656216
AB - Herein, we present a method for generating chlorine dioxide radical Alt-text is not available for this image. under solvent-free conditions by ball milling sodium chlorite with silica gel. The mechanochemical formation of Alt-text is not available for this image. was supported by UV-vis absorption spectroscopy and ESR measurements. The in situ-generated Alt-text is not available for this image. was directly used for the selective monooxygenation of dibenzothiophenes, including a poorly soluble π-extended benzothiophene derivative. This method provides a practical solvent-free platform for Alt-text is not available for this image.-mediated oxygenation of poorly soluble organosulfur compounds.
SN - 2046-2069
ER -