Synthesis and characterization of polyimides containing a chiral dimine link that mimics the salen ligand


SECKIN T., Koytepe S., YIGIT M., CETINKAYA E.

DESIGNED MONOMERS AND POLYMERS, vol.7, no.4, pp.377-390, 2004 (SCI-Expanded) identifier identifier

  • Publication Type: Article / Article
  • Volume: 7 Issue: 4
  • Publication Date: 2004
  • Doi Number: 10.1163/1568555041475248
  • Journal Name: DESIGNED MONOMERS AND POLYMERS
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.377-390
  • Inonu University Affiliated: Yes

Abstract

We report the synthesis of a covalently linked complex that mimics the salen ligand within the main chain of the polyimide network. The thermally-stable solid polyimides offer suitable sites for metal coordination, which is a crucially important step in establishing steroselectivity. The ligand synthesized by the sequential treatment of a chiral trans-1,2-diaminocyclohexane and p-dimethylaminobenzaldehyde was used to prepare polyimides by a one-step polymerization in the dipolar media. A series of stable polyimides was synthesized from (IS,2S)- and (1R,2R)-bis(p-dimethylaminobenzylideneamino)-1,2-cyclohexyl and various aromatic dianhydrides had inherent viscosities ranging from 1.45 to 2.21 dl/g and were soluble in polar solvents. The glass transition temperatures were 264-319degreesC, and the 10% weight loss temperatures were above 406-487degreesC.