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Hyperbranched Poly(ether ketone) with Carboxylic Acid Terminal Groups: Synthesis, Characterization, and Derivatization
A new procedure is described for the formation of a hyperbranched poly(ether ketone) with carboxylic acid terminal groups. This preparation was based on the one-step synthesis of an AB2-type monomer 5-phenoxyisophthalic acid using phosphorus pentoxide/methanesulfonic acid as the condensing agent and...
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Published in: | Macromolecules 1999-01, Vol.32 (1), p.100-105 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | A new procedure is described for the formation of a hyperbranched poly(ether ketone) with carboxylic acid terminal groups. This preparation was based on the one-step synthesis of an AB2-type monomer 5-phenoxyisophthalic acid using phosphorus pentoxide/methanesulfonic acid as the condensing agent and solvent. The electrophilic aromatic substitution reaction led to the formation of the aryl ketone linkage. With the help of model compounds, 1H NMR studies revealed that the degree of branching of the poly(ether ketone) was about 55%. The terminated carboxylic acid groups were readily functionalized, yielding hyperbranched polymers with a variety of different functional chain ends. The nature of the chain ends was shown to dramatically affect physical properties of the hyperbranched macromolecules. The ammonium derivative was soluble in water and behaved as a unimolecular micelle. |
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ISSN: | 0024-9297 1520-5835 |
DOI: | 10.1021/ma981114m |