Redox properties of titanocene-pyrrole derivative and its electropolymerization

A new titanocene dichloride derivative in which one cyclopentadienyl ligand (Cp) is functionalized with a pyrrolyl ring, Tc3Py (Cl2TiCpC5H4(CH2)3NC4H4), has been synthesized and characterized with NMR. Its redox properties have been studied by CV in acetonitrile (AN), tetrahydrofurane (THF) and dichloromethane (DCM), in comparison with unsubstituted titanocene dichloride (Tc) and pyrrole. Ti(IV/III) transition observed within the negative potential range is a quasi-reversible reaction in THF and DCM (but without a complete recuperation of the initial reagent in the back scan) while the reoxidation peak in AN is strongly shifted in the positive direction. These results are interpreted within…