Abstract
AbstractToluene, anisol, thioanisol, 4‐phenoxyacetophenone and N,N‐diacetyl‐4‐phenoxyaniline were subjected to a Friedel‐Crafts acylation with 2,6‐difluorobenzoyl chloride. The resulting 4′‐substituted 2,6‐difluorobenzophenones 1a–e were condensed with trimethyl silylated Bis‐phenol‐A (2) to yield homopolyethers with pendant functional groups. A series of copolyethers was analogously prepared by concondensation of 4′‐substituted 2,6‐difluorobenzophenones with a diphenol and 4,4′‐difluorobenzophenone (4a) or bis(4‐fluorophenyl) sulfone (4b), and another series by cocondensation of 2 with mixtures of 4′‐substituted 2,6‐difluorobenzophenones and 2,6‐difluorobenzonitrile (8) or 2,6‐difluoropyridine (9). All polyethers were characterized by inherent viscosities, elemental analyses and DSC‐measurements. In individual cases GPC‐measurements, thermomechanical and thermogravimetric analyses were conducted. The quantitative polymer‐analogous oxidation of methylthio groups into methylsulfinyl and finally into methylsulfonyl groups is demonstrated.
References
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Dates
Type | When |
---|---|
Created | 22 years, 4 months ago (April 16, 2003, 6:34 a.m.) |
Deposited | 1 year, 10 months ago (Oct. 22, 2023, 9:39 a.m.) |
Indexed | 11 months, 1 week ago (Sept. 19, 2024, 10:55 a.m.) |
Issued | 36 years, 3 months ago (June 1, 1989) |
Published | 36 years, 3 months ago (June 1, 1989) |
Published Online | 22 years, 5 months ago (March 12, 2003) |
Published Print | 36 years, 3 months ago (June 1, 1989) |
@article{Kricheldorf_1989, title={New polymer syntheses, 36. Functionalized aromatic polyethers derived from 4′‐substituted 2,6‐difluorobenzophenones}, volume={190}, ISSN={0025-116X}, url={http://dx.doi.org/10.1002/macp.1989.021900608}, DOI={10.1002/macp.1989.021900608}, number={6}, journal={Die Makromolekulare Chemie}, publisher={Wiley}, author={Kricheldorf, Hans R. and Delius, Ulrich}, year={1989}, month=jun, pages={1277–1288} }