4.8 Article

An isolable silanoic ester by oxygenation of a stable silylene

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 129, Issue 23, Pages 7268-+

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja072425s

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The first silicon analogue of a carbonic ester, compound 2, and the novel cyclodisiloxane 4 have been synthesized by remarkably clean mono- and dioxygenation reactions of the stable siloxysilylene 1 with N2O (CO2) and O-2, respectively. Ester 2 represents a unique donor-supported SiO complex with an intriguing thermal stability up to 200 degrees C. The addition of MeOH at the SiO bond in 2 furnishes the corresponding adduct 3.

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