Abstract
Synthesis of the sterically crowded Tris(pentamethylcyclopentadienyl) lanthanide complexes, (C5Me5)3Ln, has demonstrated that organometallic complexes with unconventionally long metal ligand bond lengths can be isolated that provide options to develop new types of ligand reactivity based on steric crowding. Previously, the (C5Me5)3M complexes were known only with the larger lanthanides, La-Sm. The synthesis of even more crowded complexes of the smaller metals Gd and Y is reported here. These complexes allow an evaluation of the size/reactivity correlations previously limited to the larger metals and demonstrate a previously undescribed type of C5Me5-based reaction, namely C-H bond activation. (C5Me5)3Gd, was prepared from GdCl3 through (C5Me5)2GdCl2K(THF)2, (C5Me5)2Gd(C3H5), and [(C5Me5)2Gd][BPh4] and structurally characterized by x-ray crystallography. Although Gd3+ is redox-inactive, (C5Me5)3Gd functions as a reducing agent in reactions with 1,3,5,7-cyclooctatetraene (COT) and triphenylphosphine selenide to make (C5Me5)Gd(C8H8), [(C5Me5)2Gd]2Se2, and [(C5Me5)2Gd]2Se depending on the stoichiometry used. When the analogous synthetic method was attempted with yttrium in arene solvents, the previously characterized (C5Me5)2YR complexes (R=C6H5, CH2C6H5) were isolated instead, i.e., C-H bond activation of solvent occurred. To avoid this problem, (C5Me5)3Y was synthesized in high yield from [(C5Me5)2YH]2 and tetramethylfulvene in aliphatic solvents. Isolated (C5Me5)3Y was found to metalate benzene and toluene with concomitant formation of C5Me5H, a reaction contrary to the normal pKa values of these hydrocarbons. In this case, the normally inert (C5Me5)1- ligand engages in C-H bond activation due to the extreme steric crowding.