4.5 Article

Acid-Catalyzed Condensation Reaction of Phenylsilanetriol: Unexpected Formation of cis,trans-1,3,5-Trihydroxy-1,3,5-triphenylcyclotrisiloxane as the Main Product and Its Isolation

Journal

ORGANOMETALLICS
Volume 33, Issue 22, Pages 6278-6281

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/om500691c

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Funding

  1. Future Pioneering Projects Development of Innovative Catalytic Processes for Organosilicon Functional Materials
  2. New Energy and Industrial Technology Development Organization (NEDO)

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cis,trans-1,3,5-Trihydroxy-1,3,5-triphenylcyclotrisiloxane was successfully isolated and fully characterized by spectroscopic methods and single-crystal X-ray diffraction. This compound was believed to be highly unstable and only exist as a transient species in low concentration during the condensation reaction of phenylsilanetriol or its precursors. The isolated pure cyclotrisiloxane is, however, surprisingly stable even in acidic solution and partially isomerizes to the cis,cis isomer.

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