• Media type: E-Article
  • Title: Cyclodextrins in polymer synthesis: Dimethyl-β-cyclodextrin as thermosensitive retardant for the radical polymerization of N-methacryloyl-L-tyrosine derivatives in water
  • Contributor: Tabatabai, Monir; Ritter, Helmut; Schmelzer, Monika
  • Published: Walter de Gruyter GmbH, 2002
  • Published in: e-Polymers, 2 (2002) 1
  • Language: Without Specification
  • DOI: 10.1515/epoly.2002.2.1.551
  • ISSN: 1618-7229; 2197-4586
  • Keywords: Polymers and Plastics ; Physical and Theoretical Chemistry ; General Chemical Engineering
  • Origination:
  • Footnote:
  • Description: AbstractThe synthesis and characterization of N-methacryloyl-L-tyrosine methyl ester (3a) and ethyl ester (3b), and their acetyl derivatives O-acetyl-N-methacryloyl- L-tyrosine methyl ester (4a) and ethyl ester (4b) are described. Monomers 3 and 4 were complexed with RAMEB (randomly methylated ß-cyclodextrin) yielding water soluble host-guest complexes 5a-d. The radical polymerization of monomers 3 and 4 was investigated in the presence as well as in the absence of RAMEB in aqueous medium at room temperature and also at 60°C. It is shown that the polymerization tendency of complexes 5a-d at room temperature is lower, leading to polymers of higher molecular weight, compared to the free monomers 3 and 4. Furthermore, the polymerization of monomers 3 and 4 was carried out in homogenous organic solution using 2,2’-azoisobutyronitrile as initiator, and the results are discussed.
  • Access State: Open Access