Structurally well-defined conjugated -aminoporphyrin oligomers analogous to polyanilines.

Polyaniline, which is formed by the oxidative polymerization of aniline, is a widely explored conducting polymer with several stable oxidation states, and can be applied in advanced materials, including sensing devices and electrochemical catalysts. The marriage of polyanilines with the diverse chemistry of porphyrins is expected to confer new properties, including a combination of electrical, optical, magnetic and chemical properties. Herein, we demonstrate that -aminodiarylporphyrin, a porphyrin analogue of aniline, undergoes oxidative oligomerization in an acidic solution under an oxygen atmosphere to yield stable oligomeric products that are analogous to fully oxidized polyanilines. The so-formed oligomers are composed of the same number of electron-rich porphyrinoid and electron-deficient quinoid moieties, and they exhibit a broad electronic absorption band in the near infrared (NIR) region, which is attributable to intramolecular charge transfer (ICT) transition from electron-rich porphyrinoid moieties to electron-deficient quinoid ones. The quinoid moieties in the oligomers could be reversibly reduced using sodium ascorbate to obtain all-porphyrinoid oligomers that resemble fully reduced polyanilines. The fully reduced oligomers do not exhibit the NIR ICT band. Furthermore, three types of partially reduced tetramers consisting of a single quinoid moiety were also obtained, among which two interconverted in solution. Their interconversion was significantly accelerated in the presence of a protic solvent. This result is consistent with the high electron conductivity of partially oxidized polyanilines following their protonation.