Syntheses and optoelectronic properties of amino/carboxyphenylporphyrins for potential use in dye-sensitizedTiO2solar cells

New mixed-substituent amino/carboxyphenylporphyrins for a dye-sensitized TiO 2 solar cell were prepared using several synthetic routes. The reaction of 4-carbomethoxy- and 4-acetamidobenzaldehydes with pyrrole in propionic acid under aerobic conditions afforded mixtures of mixed amide/ester substituted tetraphenylporphyrins which were separated using centrifugal chromatography then deprotected to give the target compounds. Condensation of p-nitrophenyldipyrromethane with 4-carbomethoxybenzaldehyde in CH 2 Cl 2 catalyzed by trifluoroacetic acid, followed by oxidation with dichlorodicyanoquinone gives trans-dicarbomethoxy/dinitrophenylporphyrin, which when treated with SnCl 2 and HCl affords the trans-diamino/dicarboxy derivative, trans- TA 2 C 2 PP . Commercially available tetrakis-5,10,15,20-(4-carboxyphenyl)porphyrin (TCPP) was converted to mixtures of mixed amino/carbomethoxyphenylporphyrins using hydroxylamine hydrochloride in polyphosphoric acid with methanol workup. Relative yields and product distributions from each route are discussed and the optoelectronic characteristics of the synthesized porphyrins were studied using UV-visible spectroscopy and cyclic voltammetry.