A metal carbonyl compound consists of carbon monoxide coordinated to a zero valent metal. For a long time, it had been unclear why such bonding was possible, let alone stable at all. The belief that normal coordination bonds were formed by the donation of electrons from highly basic ligands to a metal formed the basis of the coordination theory of A. Werner. Because the basicity of carbon monoxide is very low,and transition metal-carbon bonds are generally not very stable, a suitable explanation for the stability of metal carbonyl compounds was sought. If the shape and symmetry of them etal d orbital and of the CO π (antibonding) orbital for the carbon-oxygen bond are suitable for overlap, a bonding interaction between the metal and carbon is expected. the bonding scheme shown was proposed from this point of view. The mechanism by which electrons are donated to the vacant carbon monoxide π* orbitable from the filled metal d orbital is called back donation. Since accumulation of superfluous electrons on a low oxidation state metal atom is prevented, back donation leads to the stabilization of the M-C bond.