Search

Hydrogenolysis of the half-sandwich penta-arylcycopentadienyl-supported rare-earth metal dibenzyl complexes [(CpAr5)Ln(p-CH2-C6H4-Me)2(THF)] (CpAr5 = C5Ar5, Ar = 3,5-iPr2-C6H3; Ln = Sc, La) afforded a bimetallic scandium complex [(CpAr5)Sc(H)(μ-OC4H9)]2 (2) with two terminal hydrido ligands, and a double-sandwich bimetallic lanthanum hydride complex [(CpAr5)La(μ-H)]2 (4) bearing the reduced CpAr5 ligand. DFT calculations were conducted to elucidate the reaction profiles. [ABSTRACT FROM AUTHOR]

The monomeric actinide dihydrido complex [(CpAr*)(Cp*)ThH2(THF)] (2) bearing the super-bulky penta-arylcyclopentadienyl (CpAr* = C5Ar*5, Ar* = 3,5-tBu2-C6H3) and pentamethylcyclopentadienyl (Cp* = C5Me5) ligands was obtained for the first time. Complex 2 underwent unique Th–H addition reactions with various unsaturated compounds to afford the corresponding five-membered metallacycles, including the first example of actinide metallacyclopentyne [(CpAr*)(Cp*)Th(PhCH–C≡C–CHPh)] (4). [ABSTRACT FROM AUTHOR]