The chemistry and spectroscopy of the iron(II) phenylterpyrazine complex, [Fe(phtpz) 2 ] 2+ , were investigated in comparison with the analogous phenylterpyridine species, Fe(phtpy) 2 ] 2+ , and the results indicated a strong electronic delocalization on the Fe(II) terimine chromophore encompassing the lateral pyrazyl groups. The delocalized nature of the molecular orbitals involved in the electronic excitation precluded a direct assignment of the pyridine and pyrazine vibrations in the complex. However, the capability of the terpyrazine complex to bind transition metal ions, such as the [Fe(CN) 5 ] 3species, allowed to generate pentanuclear complexes displaying characteristic charge-transfer and resonance Raman spectra, revealing the pyrazine vibrations in the complex. The [Fe(CN) 5 ] 3containing species also yielded polymeric compounds in presence of transition metal ions, exhibiting intervalence transfer bands and chemical similarities with the Prussian Blue complex.