Synthesis of Perfluoroaliphatic Ether Monomers
Abstract
Perfluoroalkyl ether alpha, omega-diiodides were hydrolyzed in fuming sulfuric acid to the corresponding symmetrical diacyl fluorides. Under certain conditions the intermediate hydrolysis product omega-iodoacyl fluoride was obtained as the major product. Addition of tetrafluoroethylene oxide to the diacyl fluorides gave a series of oligomer diacyl fluorides.
Document Details
- Document Type
- Technical Report
- Publication Date
- Jul 01, 1977
- Accession Number
- ADB026706
Entities
People
- Theodore Psarras