Synthesis and characterization of thermally stable polyimides with a pendent phenothiazine unit based on new diamine 10-(3,5-diaminobenzoyl)phenothiazine

• Published in: High performance polymers 2016-02, Vol.28 (1), p.26-33
• Main Authors: Ghorpade, Ravindra V., Thorave, Asmita K., Rajan, C. R., Chavan, Nayaku N., Ponrathnam, S.
• Format: Article
• Language: English
• Subjects: Chains (polymeric); Diamines; Dianhydrides; Molecular orbitals; Phenothiazines; Polyimide resins; Polymers; Thermal stability
• ISSN: 0954-0083; 1361-6412
• DOI: 10.1177/0954008314568877

A novel diamine 10-(3,5-diaminobenzoyl)phenothiazine (DBPT) with a side chain containing phenothiazine unit was synthesized. A new family of polyimides (PIs) containing phenothiazine unit in the side chains has been successfully synthesized by direct polycondensation of DBPT with pyromellitic dianhydride, 3,3′,4,4′-benzophenone tertacarboxylic dianhydride, and 4,4′-oxydiphthalic anhydride (ODA) via a conventional two-step chemical imidization process. The yield of polymers was good enough, which were soluble in most organic solvents. The molecular orbital energy gaps, thermal stability, and crystallinity of PIs were investigated by molecular modeling, thermogravimetric analysis, and wide-angle X-ray scattering, respectively. Thermal properties of polymers were good enough to permit the use of these PIs in various applications; only 49% weight loss is detected at 900°C in nitrogen atmosphere. X-Ray diffraction clearly reveals the amorphous nature of PIs. A quantum modeling study (density functional theory) has shown the influence of dianhydride structure on the energy difference of highest occupied molecular orbital and lowest unoccupied molecular orbital energy levels.