Organolanthanide chemistry

Organolanthanide chemistry is the field of chemistry that studies organolanthanides, compounds with a lanthanide-to-carbon bond. Organolanthanide compounds are different from their organotransition metal analogues in the following ways: They are far more air- and water-sensitive and are often pyrophoric. Chemistry in the 0 oxidation state is far more limited. In fact, their electropositive nature makes their organometallic compounds more likely to be ionic. They form no stable carbonyls at room temperature; organolanthanide carbonyl compounds have been observed only in argon matrices, and decompose when heated to 40 K. Metal-carbon σ bonds are found in alkyls of the lanthanide elements such as [LnMe6]3− and Ln[CH(SiMe3)2]3. Methyllithium dissolved in THF reacts in stoichiometric ratio with LnCl3 (Ln = Y, La) to yield Ln(CH3)3 probably contaminated with LiCl. If a chelating agent (L-L), such as tetramethylethylenediamine (tmed or tmeda) or 1,2-dimethoxyethane (dme) is mixed with MCl3 and CH3Li in THF, this forms [Li(tmed)]3[M(CH3)6] and [Li(dme)]3[M(CH3)6]. Certain powdered lanthanides react with diphenylmercury in THF to yield octahedral complexes: 2 Ln + 3 Ph2Hg + 6 THF → 2 LnPh3(THF)3 + Hg (Ln = Ho, Er, Tm, Lu). Cyclopentadienyl complexes, including several lanthanocenes, are known for all lanthanides. All, barring tris(cyclopentadienyl)promethium(III) (Pm(Cp)3), can be produced by the following reaction scheme: 3 Na[Cp] + MCl3 → M[Cp]3 + 3 NaCl Pm(Cp)3 can be produced by the following reaction: 2 PmCl3 + 3 Be[Cp]2 → 3 BeCl2 + 2 Pm[Cp]3 These compounds are of limited use and academic interest.