Synthesis of a new sulfonated monomer for poly(aryl ether)s
β Scribed by Scott E. McKay; Robert W. Lashlee III; Tadd P. Marshall; Robert W. Kopitzke
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 78 KB
- Volume
- 16
- Category
- Article
- ISSN
- 1042-7163
- DOI
- 10.1002/hc.20137
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β¦ Synopsis
Abstract
A new sulfonated monomer suitable for polyarylether synthesis was made. 1,1'β(pβPhenylenedioxy)bis[4β(4βfluorobenzoyl)]benzene was prepared from phosphorus pentoxide/methanesulfonic acid (PPMA), 1,4βdiphenoxybenzene, and pβfluorobenzoic acid in good yield. This compound was selectively monosulfonated on the most activated ring with fuming sulfuric acid and isolated as the sodium salt. Poly(aryl ethers) made from this monomer may find use as proton exchange membranes. Β© 2005 Wiley Periodicals, Inc. Heteroatom Chem 16:553β556, 2005; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20137
π SIMILAR VOLUMES
## Abstract A series of controlled molecular weight poly(aryl ether sulfone) oligomers with benzophenone moieties at the chain termini were prepared. The two carbonyl groups at the chain ends were converted to ethynyl groups by using trimethylsilyldiazomethane/BuLi in tetrahydrofuran. Reactions of
Three series of poly(aryl ether sulfone)s (PAESs) containing the phthalazinone moiety in the polymer backbone were synthesized by solution polycondensation of bis(4-chlorophenyl) sulfone with three commercial bisphenols and 4-(4-hydroxyphenyl)-2,3-phthalazin-1-one. Bisphenol-A, hydroquinone, and bis