Polyimides from a novel monomer 3,6-bis(dimethylamino) acridine(p-cymene)dichlororuthenium(II) for a catalytic application


Seckin T., Koytepe S., Ozdemir I., Gurbuz N., CETINKAYA B.

JOURNAL OF INORGANIC AND ORGANOMETALLIC POLYMERS AND MATERIALS, vol.14, no.3, pp.177-190, 2004 (Peer-Reviewed Journal) identifier identifier

  • Publication Type: Article / Article
  • Volume: 14 Issue: 3
  • Publication Date: 2004
  • Doi Number: 10.1023/b:joip.0000039366.65792.68
  • Journal Name: JOURNAL OF INORGANIC AND ORGANOMETALLIC POLYMERS AND MATERIALS
  • Journal Indexes: Science Citation Index Expanded, Scopus
  • Page Numbers: pp.177-190

Abstract

Tricyclic heteroaraomatic dye-based monomer containing NMe2 units, 6-bis(dimethylamino)acridine(p-cymene)dichlororuthenium (II), was used to prepare novel polyimides via a one-stage solution polycondensation due to their stability under a variety of oxidative and reductive conditions. The Ru(II) complex monomer was synthesized starting from [RuCl2(p-cymene)](2) and 3,6-bis(dimethylamino)acridine. A series of stable polyimides was synthesized from the Ru(II) complex of 3,6-bis(dimethylamino)acridine and various aromatic dianhyrides. The polymers had inherent viscosities ranging from 1.72 to 2.11 dL/g and were soluble in polar solvents. The glass transition temperatures were 192-278degreesC, and the 10% weight loss temperatures were above 503-635degreesC. Ruthenium-substituted polyimides were tested for catalytic activity in the furan formation reaction of (Z)-3-methylpent-2-en-4-yn-1-ol. The polymeric catalyst was added to (Z)-3-methylpent-2-en-4-yn-1-ol without a solvent and the pure furan was isolated by distillation under reduced pressure. The conversion of the starting, enynol, was determined by gas chromatography (GC).