The reactivity of diatomic palladium-titanium toward carbon monoxide has been studied in solid argon by infrared spectroscopy (Fourier transform infrared) in the carbonyl stretching frequency region. Our technique of sublimation of Ti and Pd atoms from two filaments heated separately allowed the identification of five new molecules. Small polynuclear carbonyl clusters, PdTi(CO)(n) (n = 1-3), have been characterized on the basis of isotopic substitutions, metal atom and CO concentration variations, and irradiation effects. Selective irradiation in the visible region leads to conversion between two isomers distinguished by the stretching frequency of the diatomic CO: PdTiCO Ti-eo (nu(CO) = 1908.4 cm(-1)) and PdTiCO Pd-eo (nu(CO) = 2009.3 cm(-1)). The density functional theory calculations have been carried out to elucidate the geometrical and electronic structures and support the spectral assignments. The nature of the metal-carbon bonding has been discussed using the topology of the Laplacian of the electron density.