Organoscandium chemistry is the chemistry of organometallic compounds containing a carbon to scandium chemical bond. The interest in organoscandium compounds is mostly academic but several compound classes find practical application in catalysis, especially in polymerization. A common precursor is scandium chloride.
As with the other elements in group 3 – e.g. yttrium, forming organoyttrium compounds – and the lanthanides, the dominant oxidation state for scandium in organometallic compounds is +3 (electron configuration [Ar] 3d14s2). The members of this group also have large ionic radii with vacant s,p and d orbitals (88 pm for Sc3+ compared to 67 pm for Al3+ ) and as a result they behave as hard Lewis acids and tend to have high coordination numbers of 9 to 12. The metal to ligand chemical bond is largely ionic.
The majority of organoscandium compounds have at least one cyclopentadienyl (Cp) ligand. The dominant species are CpScX2, Cp2ScX and Cp3Sc. The mononuclear compounds are of limited utility because of poor steric shielding which makes them prone to nucleophilic addition and solvent attack.