No abstract

The base-free metallocenes [1,2,4-(Me 3 C) 3 C 5 H 2 ] 2 Ca, [1,2,4-(Me 3 C) 3 C 5 H 2 ] 2 Sr, and [1,2,4-(Me 3 C) 3 C 5 H 2 ] 2 Ba have been prepared by reaction of MI 2 and the sodium or potassium salt of the substituted cyclopentadiene anion in THF, while [1,2,4-(Me 3 C) 3 C 5 H 2 ] 2 Mg was prepared from the cyclopentadiene, 1,2,4-(Me 3 C) 3 C 5 H 3 , and dibutylmagnesium. The structures of the magnesocene and calcocene as well as those of the previously prepared ytterbium and samarium analgoues have been determined by X-ray crystallography. The metallocenes are slightly bent in the solid state with centroid-metal-centroid angles ranging from 163°to 173°. Adducts of the strontocene and samarocene with THF and of the barocene, samarocene, and ytterbocene with 2,6-Me 2 C 6 H 3 NC have also been prepared and characterized. The massive bulk of the [1,2,4-(Me 3 C) 3 C 5 H 2 ]ligand leads to behavior quite different from that previously observed for base-free metallocenes of the alkaline earths and divalent lanthanides.

The protonolysis reaction of [Ln(AlMe(4))(3)] with various substituted cyclopentadienyl derivatives HCp(R) gives access to a series of half-sandwich complexes [Ln(AlMe(4))(2)(Cp(R))]. Whereas bis(tetramethylaluminate) complexes with [1,3-(Me(3)Si)(2)C(5)H(3)] and [C(5)Me(4)SiMe(3)] ancillary ligands form easily at ambient temperature for the entire Ln(III) cation size range (Ln=Lu, Y, Sm, Nd, La), exchange with the less reactive [1,2,4-(Me(3)C)(3)C(5)H(3)] was only obtained at elevated temperatures and for the larger metal centers Sm, Nd, and La. X-ray structure analyses of seven representative complexes of the type [Ln(AlMe(4))(2)(Cp(R))] reveal a similar distinct [AlMe(4)] coordination (one eta(2), one bent eta(2)). Treatment with Me(2)AlCl leads to [AlMe(4)] --> [Cl] exchange and, depending on the Al/Ln ratio and the Cp(R) ligand, varying amounts of partially and fully exchanged products [{Ln(AlMe(4))(mu-Cl)(Cp(R))}(2)] and [{Ln(mu-Cl)(2)(Cp(R))}(n)], respectively, have been identified. Complexes [{Y(AlMe(4))(mu-Cl)(C(5)Me(4)SiMe(3))}(2)] and [{Nd(AlMe(4))(mu-Cl){1,2,4-(Me(3)C)(3)C(5)H(2)}}(2)] have been characterized by X-ray structure analysis. All of the chlorinated half-sandwich complexes are inactive in isoprene polymerization. However, activation of the complexes [Ln(AlMe(4))(2)(Cp(R))] with boron-containing cocatalysts, such as [Ph(3)C][B(C(6)F(5))(4)], [PhNMe(2)H][B(C(6)F(5))(4)], or B(C(6)F(5))(3), produces initiators for the fabrication of trans-1,4-polyisoprene. The choice of rare-earth metal cation size, Cp(R) ancillary ligand, and type of boron cocatalyst crucially affects the polymerization performance, including activity, catalyst efficiency, living character, and polymer stereoregularity. The highest stereoselectivities were observed for the precatalyst/cocatalyst systems [La(AlMe(4))(2)(C(5)Me(4)SiMe(3))]/B(C(6)F(5))(3) (trans-1,4 content: 95.6 %, M(w)/M(n)=1.26) and [La(AlMe(4))(2)(C(5)Me(5))]/B(C(6)F(5))(3) (trans-1,4 content: 99.5 %, M(w)/M(n)=1.18).