Selective oxidation of thiacalix[4]arenes to the sulfinyl- and sulfonylcalix[4]arenes and their coordination ability to metal ions
β Scribed by Nobuhiko Iki; Hitoshi Kumagai; Naoya Morohashi; Kohki Ejima; Mitsuharu Hasegawa; Setsuko Miyanari; Sotaro Miyano
- Book ID
- 104259951
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 248 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Thiacalix[4]arenes, in which the four methylene bridges of calix[4]arenes are replaced by sulfide linkages, were selectively oxidized to sulfinyl-or sulfonylcalix[4]arene under mild conditions with control of the stoichiometry of the oxidant. Solvent extraction of the transition and alkaline earth metal ions with these hosts showed that the metal binding ability was governed by the oxidation state of the sulfur functionalities.
π SIMILAR VOLUMES
The complexation abilities of different thiacalix [4]arene derivatives towards some rare earth metal ions, metallic pollutants, and noble metals have been investigated in liquid-liquid experiments. Thiacalix[4]arene dissolved in chloroform effectively extracts Pd(II) (in acidic chloride media) and a
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Dye-sensitised photo-oxidation of cz-phellandrene (3) yields, besides the expected endoperoxides, the cyclohexadienyl hydroperoxides ( ) and ( ); reduction of these latter gives the unstable arene 1,4-hydrates ( ) and ( ).