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- W2126738364 abstract "Singlet oxygen fuels anthracenes and forces an axial rotation of aryl substituents during the oxidation. The molecular switch can be synthesized in only one step from commercially available starting materials. Thermal cleavage of the resulting endoperoxides proceeds quantitatively and affords a simple 180° switch with oxygen as the only waste product. The initial trans state is attained by heating, and repetitive cycles are possible. Supporting information for this article is available on the WWW under http://www.wiley-vch.de/contents/jc_2002/2007/z700443_s.pdf or from the author. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article." @default.
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- W2126738364 date "2007-10-08" @default.
- W2126738364 modified "2023-10-02" @default.
- W2126738364 title "Molecular Switches Flipped by Oxygen" @default.
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- W2126738364 doi "https://doi.org/10.1002/anie.200700443" @default.
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