The porphyrin derivatives, 5,10,15,20-tetra(4-(N-pentane-carboxamide) phenyl) porphyrin(4 NC5-TPP), 5,10,15,20-tetra(4-(N-dodecane-carboxamide) phenyl) porphyrin(4 NC12-TPP) and their zinc-complexes(4 NC5-TPPZn and 4 NC12-TPPZn), have been synthesized. Their thermal properties and morphologies were investigated via thermal gravity analysis(TGA), differential scanning calorimetry(DSC) and polarized optical microscopy(POM). It was found that the 4 NC5-TPP was amorphous and the 4 NC5-TPPZn was crystalline at room temperature, while the 4 NC12-TPP formed the columnar liquid crystal and the 4 NC12-TPPZn showed the spherulite texture. The electron state density distributions and the optimum configuration of the porphyrin derivatives were calculated by chemical simulation. The electrochemical oxidation and reduction abilities of the porphyrin derivatives were studied by cyclic voltammetry(CV). It was indicated that the porphyrin derivatives had the potential to develop organic photovoltaic(OPV) devices. Using the porphyrin derivatives as donor materials and the 3,4,9,10-perylenetetracarboxylic dianhydride(PTCDA) as the acceptor material, the OPV devices were fabricated. The device structure is ITO/porphyrin derivatives:PTCDA/Al. The relationship between the morphology and performance of OPV was studied. It was found that the crystalline morphology of the film was beneficial to improve the efficiency of the devices.
The water-soluble conjugated polyelectrolyte, poly[3-(1′-ethyloxy-2′-N- methylimidazole)thiophene](PEOIMT), was prepared. Its photophysical and electrochemical properties, and response characteristics to the external condition(e g, temperature response, solvent response and pH response), were investigated. The results show the PEOIMT belongs to the organic semiconductor. The interaction between the PEOIMT and the bovine serum albumin(BSA) was investigated using UV-vis spectroscopy. It was found that the PEOIMT could interact with the BSA. The PEOIMT can be used as a biosensor to detect the BSA.