期刊
ORGANIC LETTERS
卷 12, 期 22, 页码 5116-5119出版社
AMER CHEMICAL SOC
DOI: 10.1021/ol102263w
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资金
- La Sapienza University of Rome
- University of Pisa
A study of the reaction of thioanisole with singlet oxygen in different ionic liquid acetonitrile binary mixtures has shown that ILs are able to accelerate the thioanisole sulfoxidation when used as additives. With imidazolium ILs, the maximum efficiency is reached at X-IL similar to 0.1-0.2, whereas for the pyrrolidinium IL a plateau is reached. These results are discussed in terms of the ILs' tendency to form ionic aggregates and of differences in sulfoxidation reaction mechanism.
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