Journal
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 58, Issue 28, Pages 9425-9428Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201905198
Keywords
carbonyl compounds; ketones; Si=O bonds; silanones; silicon
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Funding
- JSPS KAKENHI [JP17H03015]
- Division for Interdisciplinary Advanced Research and Education (DIARE) Tohoku University
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Despite tremendous efforts to synthesize isolable compounds with an Si=O bond, silicon analogues of ketones that contain an unperturbed Si=O bond have remained elusive for more than 100 years. Herein, we report the synthesis of an isolable silicon analogue of a ketone that exhibits a three-coordinate silicon center and an unperturbed Si=O bond, thus representing the first example of a genuine silanone. Most importantly, this silanone does not require coordination by Lewis bases and acids and/or the introduction of electron-donating groups to stabilize the Si=O bond. The structure and properties of this unperturbed Si=O bond were examined by a single-crystal X-ray diffraction analysis, NMR spectroscopy, and theoretical calculations. Bimolecular reactions revealed high electrophilicity on the Si atom and high nucleophilicity on the O atom of this genuine Si=O bond.
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