Abstract

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).

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.