Flexible interactions of the rare-earth elements Y, La, and Lu with phosphorus in metallacyclohexane rings.

A geometrically flexible bifunctional (bis)aminophosphine ligand was synthesized in a three-component, one-pot Kabachnik-Fields reaction using tert butylphosphine, paraformaldehyde, and 3,5-dimethyl aniline. The product, bis((3,5-dimethylphenyl)aminomethyl) tert butylphosphine ( Ar BiAMP t Bu ), containing two secondary amines and a tertiary phosphine, was isolated in good yields. Deprotonation of both N-H groups with (trimethylsilyl)methylpotassium (K-CH 2 SiMe 3 ), followed by salt metathesis with LaI 3 , YI 3 , and LuI 3 generated the corresponding MI( Ar BiAMP t Bu )(thf) 3 complexes (M = Y (1), La (2), and Lu (3)) in good yields. A sterically encumbered indene, 1,3-diisopropyl-4,7-dimethyl-1 H -indene, iPrMe Ind, was deprotonated in situ and installed via salt-metathesis to generate the organometallic series of η 5 -indenide complexes, M( Ar BiAMP t Bu )(η 5-iPrMe Ind)(thf) (M = Y (4), La (5), and Lu (6)). 1 H, 31 P, 13 C, and 89 Y NMR experiments, IR spectroscopy, and single crystal X-ray diffraction (SC-XRD), were used to characterize these complexes. The Y-P coupling constant was found to be variable depending on the modifiable coordination environment of the metal center, indicating potential as both a spectroscopic handle as well as providing insight into the influence of additional ligands on the metal center.