Synthesis and Reactions of Silanes Containing Two Triflate Groups.

Abstract

1, 2-Bis (trifluoromethanesulfonyloxy) tetramethyldisilane (1) and dimethylsilyl-bis (trifluoromethanesulfonate) (2) were prepared viaz displacement of pheny, chloro, and methyl groups in the corresponding mono, and disilanes. Phenyl groups were displaced more rapidly than chloro and methyl groups. The unreacted groups were strongly deactivated by the presence of triflate group at the same silicon atom. The deactivation was much weaker when triflate group was present at the adjacent silicon atom. Alcohols and amines reacted more rapidly with di triflates than with monotriflates.

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Document Details

Document Type
Technical Report
Publication Date
Jul 25, 1987
Accession Number
ADA183509

Entities

People

  • Krzysztof Matyjaszewski
  • Y. L. Chen

Organizations

  • Carnegie Mellon University

Tags

Communities of Interest

  • Advanced Electronics
  • C4I
  • Materials and Manufacturing Processes

DTIC Thesaurus Topics

  • Alcohols
  • Alkenes
  • Availability
  • Chemical Reactions
  • Chemical Synthesis
  • Chemistry
  • Chlorides
  • Chlorination
  • Chlorine Compounds
  • Classification
  • Displacement
  • Materials Science
  • Military Research
  • Organic Chemistry
  • Reactivities
  • Security
  • Universities

Fields of Study

  • Chemistry

Readers

  • Organic Chemistry