Abstract
New diphenylmethane [4‐tBu‐2‐(C3H2N2Me‐1)C6H3]2CH2 (1) bearing pendant imidazolyl groups in ortho‐positions of aromatic rings of diphenylmethane skeleton was synthesized using Stille cross‐coupling reaction between bis(4‐(tert‐butyl)‐2‐iodophenyl)methane and Bu3Sn(C3H2N2Me) in the presence of Pd(PPh3)4. Potassium diphenylmethanide [{[4‐tBu‐2‐(C3H2N2Me‐1)C6H3]2CH}K(OEt2)]2 (2K) was prepared by treatment of 1 with an equimolar amount of Lochmann‐Schlosser super base. Rare‐earth metal heteroalkyl complexes {[4‐tBu‐2‐(C3H2N2Me‐1)C6H3]2CH}Ln(CH2SiMe3)2(THF)n (Ln = Sc, n = 0 (2Sc); Y, n = 1 (2Y)) with NCsp3N pincer type diphenylmethanido ligand were synthesized by the selective sp3 CH‐bond activation of the central CH2 group in 1 by Ln(CH2SiMe3)3(THF)2. According to the X‐ray data the diphenylmethanido ligands in 2K and 2Sc perform a tridentate pincer‐type κ3‐N,C,N coordination. Complexes 2Ln were evaluated as catalysts for isoprene polymerization and hydrosilylation of alkenes and alkynes.
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