New Ferrocene Schiff base compounds based on the strong ferrocene moity and hydroxy benzaldehyde derivatives exhibited increased electron donor ability were synthesized via described methods. The acceptors used in this investigation are 2,3-dichloro-5,6-dicyano-1,4- benzoquinone (DDQ), p-chloranil (CHL) and chloranilic acid (CHLC). The reactions of donor and acceptor indicate the formation of 1:1 charge-transfer complexes based on the electronic absorption and the spectroscopic studies reveal that charge-transfer unstable in solution and required some time for stabilization. Electrochemical properties of these new compounds were studied using conductometric technique and ultra violet- visible spectra. The absorption spectra showed a red-shift with a slight increase in the absorption intensities. Kinetic studies of the reaction in ethanol at different temperatures reveal that the rate of reaction is k dependence. The energy of activation Ea was determined further more the thermodynamic parameters, enthalpy of reactions H and entropy DS were calculated.