User:InterstellarGamer12321/Scandium compounds

Scandium chemistry is almost completely dominated by the trivalent ion, Sc3+. The radii of M3+ ions in the table below indicate that the chemical properties of scandium ions have more in common with yttrium ions than with aluminium ions. In part because of this similarity, scandium is often classified as a lanthanide-like element.
 * {|class="wikitable"


 * + Ionic radii (pm)
 * Al||Sc||Y||La||Lu
 * 53.5||74.5||90.0||103.2||86.1
 * }
 * 53.5||74.5||90.0||103.2||86.1
 * }

Oxides and hydroxides
The oxide scandium oxide and the hydroxide are amphoteric:
 * + 3 →  (scandate ion)
 * + 3 + 3  →

α- and γ-ScOOH are isostructural with their aluminium hydroxide oxide counterparts. Solutions of in water are acidic due to hydrolysis.

Halides and pseudohalides
The halides ScX3, where X= Cl, Br, or I, are very soluble in water, but ScF3 is insoluble. In all four halides, the scandium is 6-coordinated. The halides are Lewis acids; for example, ScF3 dissolves in a solution containing excess fluoride ion to form [ScF6](3−). The coordination number 6 is typical for Sc(III). In the larger Y3+ and La3+ ions, coordination numbers of 8 and 9 are common. Scandium triflate is sometimes used as a Lewis acid catalyst in organic chemistry.

Organic derivatives
Scandium forms a series of organometallic compounds with cyclopentadienyl ligands (Cp), similar to the behavior of the lanthanides. One example is the chlorine-bridged dimer, [ScCp2Cl]2 and related derivatives of pentamethylcyclopentadienyl ligands.

Uncommon oxidation states
Compounds that feature scandium in oxidation states other than +3 are rare but well characterized. The blue-black compound CsScCl3 is one of the simplest. This material adopts a sheet-like structure that exhibits extensive bonding between the scandium(II) centers. Scandium hydride is not well understood, although it appears not to be a saline hydride of Sc(II). As is observed for most elements, a diatomic scandium hydride has been observed spectroscopically at high temperatures in the gas phase. Scandium borides and carbides are non-stoichiometric, as is typical for neighboring elements.

Lower oxidation states (+2, +1, 0) have also been observed in organoscandium compounds.