Amino Acid and Dipeptide Functionalized Polyolefins

N-protected amino acid and dipeptide branched, chiral polyolefins have been prepared using acyclic diene metathesis polycondensation chemistry. The polymerizations were performed in THF using Grubbs' second-generation catalyst. The polymers bearing CBz-protected amino acids and dipeptides are s...

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Veröffentlicht in:Macromolecules 2003-04, Vol.36 (7), p.2206-2214
Hauptverfasser: Hopkins, Timothy E, Wagener, Kenneth B
Format: Artikel
Sprache:eng
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Zusammenfassung:N-protected amino acid and dipeptide branched, chiral polyolefins have been prepared using acyclic diene metathesis polycondensation chemistry. The polymerizations were performed in THF using Grubbs' second-generation catalyst. The polymers bearing CBz-protected amino acids and dipeptides are semicrystalline with melt transitions of up to 150 °C, whereas the polymers bearing BOC-protected amino acids and dipeptides are primarily amorphous with the exception of the di-BOC-protected lysine polymer, which is semicrystalline.
ISSN:0024-9297
1520-5835
DOI:10.1021/ma021668w