Photophysical processes in aromatic polyimides. Studies with model compounds

• Published in: Journal of polymer science. Part B, Polymer physics Polymer physics, 1993-10, Vol.31 (11), p.1617-1625
• Main Authors: Hasegawa, Masatoshi, Shindo, Yoichi, Sugimura, Tokuko, Ohshima, Shigeru, Horie, Kazuyuki, Kochi, Masakatsu, Yokota, Rikio, Mita, Itaru
• Format: Article
• Language: English
• Subjects: Applied sciences; charge transfer fluorescence; Electrical, magnetic and optical properties; Exact sciences and technology; model compounds; Organic polymers; photophysical process; Physicochemistry of polymers; polyimides; Properties and characterization
• ISSN: 0887-6266; 1099-0488
• DOI: 10.1002/polb.1993.090311118

Emission mechanism in an aromatic polyimide, PI(BPDA/PDA), derived from biphenyltetracarboxylic dianhydride and p‐phenylene diamine were studied with ultraviolet visible absorption and fluorescence spectra of a series of the model compounds. The excitation spectrum of the intermolecular charge‐transfer (CT) fluorescence peaking around 550 nm of PI(BPDA/PDA) thin film was completely consistent with the absorption spectrum, indicating that the intermolecular CT fluorescence emission of PI(BPDA/PDA) film is not caused by direct excitation of the CT absorption band, but by light absorption due to structural units in the polymer backbone. The UV‐vis. absorption spectra of the model compounds corresponding to the structural units in PI(BPDA/PDA) showed that the longest wavelength absorption band is due to the biphenylbisimide moiety. The band was assigned as π, π* transition with the polarization spectrum of the model compound. The fluorescence spectra of the model compounds changed sensitively depending on the conformation around N‐phenyl bond. The lifetime measurement for the model compounds suggested that intramolecular CT process occurs very rapidly. © 1993 John Wiley & Sons, Inc.