Cationic Tropidinyl Scandium Catalyst: A Perfectly Acceptable Substitute for Cationic Half-Sandwich Scandium Catalysts in cis-1,4-Polymerization of Isoprene and Copolymerization with Norbornene

Different nonmetallocene rare earth metal alkyl complexes such as monotropidinyl (Trop) scandium diallcyl complex (Trop)Sc(CH2SiMe3)(2)(THF) (1), ditropidinyl yttrium alkyl complex (Trop)(2)Y(CH2SiMe3)(THF) (3) as well as binuclear lutetium alkyl complex bearing one tetradentate dianionic 6-N-methyl-1,4-cycloheptadienyl (NMCH) ligand [(NMCH)Lu(CH2SiMe3)(THF)](2) (2) have been synthesized in high yields via one-pot acid-base reaction by using of the tris(trimethylsilylmethyl) rare earth metal complexes with the readily available natural product tropidine. The polymerization experiments indicate that the monotropidinyl scandium diallcyl complex 1 displays reactivity akin to that of the analogous monocyclopentadienyl scandium diallcyl complexes. In the presence of activator and a small amount of AlMe3, complex 1 exhibits similar activities (up to 1.6 x 10(6) g mol(Sc)(-1) h(-1)) but higher cis-1,4-selectivities (up to 100%) than (C5H5)Sc(CH2SiMe3)(2)(THF) (cis-1,4-selectivity as 95%) in the isoprene polymerization, yielding the pure cis-1,4-PIPs with moderate molecular weights (M-n = 0.5-11.2 x 10(4) g/mol) and bimodal molecular weight distributions (M-w/M-n = 1.48-6.07). Moreover, the complex 1/[Ph3C][B(C6F5)(4)/(AlBu3)-Bu-i ternary system also shows good comonomer incorporation ability in the copolymerization of isoprene and norbomene similar to the [C5Me4(SiMe3)]Sc(eta(3)-CH2CHCH2)(2)/activator binary system, affording the random isoprene/norbornene copolymers with a wide range of isoprene contents around 57-91 mol % containing cis-1,4 configuration up to 88%.