Dialkyl Rare Earth Complexes Supported by Potentially Tridentate Amidinate Ligands: Synthesis, Structures, and Catalytic Activity in Isoprene Polymerization

Vassily Yu. Rad'kov, G.G. Skvortsov, Dmitry M. Lyubov, Anton V. Cherkasov, Georgy K. Fukin, Andrey S. Shavyrin, Dongmei Cui, Alexander A. Trifonov

European Journal of Inorganic Chemistry · 2012 · 35 citations · 52 references

Concepts

Abstract

Abstract Two new amidines that contain a pendant Lewis base in the side arm, 2‐MeOC 6 H 4 NC( t Bu)NH(2,6‐R 2 C 6 H 3 ) (R = Me, i Pr), were synthesized and successfully employed as tridentate ligands for the preparation of the dialkyl rare earth complexes [2‐MeOC 6 H 4 NC( t Bu)N(2,6‐R 2 C 6 H 3 )]Ln(CH 2 SiMe 3 ) 2 (L) n {Ln = Y, Lu; R = Me, i Pr; L = thf ( n = 2), dme ( n = 1)}. These ligands provided enhanced stability for the complexes. The X‐ray structure determinations revealed that intramolecular coordination of the 2‐MeOC 6 H 4 group is realized if a thf molecule is coordinated to the metal center (Ln = Y, Lu), which results in the coordination number of six. The treatment of complex [2‐MeOC 6 H 4 NC( t Bu)N(2,6‐Me 2 C 6 H 3 )]Lu(CH 2 SiMe 3 ) 2 (thf) with dme afforded a six‐coordinate dme adduct in which the methoxy group of the amidinate ligand has drifted out from the metal coordination sphere. The reaction of [2‐MeOC 6 H 4 NC( t Bu)N(2,6‐ i Pr 2 C 6 H 3 )]Y(CH 2 SiMe 3 ) 2 (thf) with 2,6‐diisopropylaniline in hexane at –70 °C, regardless of the ratio of the reagent, afforded the six‐coordinate diamido compound [2‐MeOC 6 H 4 NC( t Bu)N(2,6‐ i Pr 2 C 6 H 3 )]Y(NHC 6 H 3 ‐2,6‐ i Pr 2 ) 2 (thf), for which intramolecular coordination of the oxygen atom of the side chain was detected by an X‐ray study. Complex [2‐MeOC 6 H 4 NC( t Bu)N(2,6‐ i Pr 2 C 6 H 3 )]Y(CH 2 SiMe 3 ) 2 (thf) was evaluated as a precatalyst for isoprene polymerization. The ternary system [2‐MeOC 6 H 4 NC( t Bu)N(2,6‐ i Pr 2 C 6 H 3 )]Y(CH 2 SiMe 3 ) 2 (thf)/[Ph 3 C][B(C 6 F 5 ) 4 ]/Al i Bu 3 provided isoprene polymerization with moderate activity but without control of the regioselectivity (3,4‐regularity was slightly predominant at 52 %). Nevertheless, high 1,4‐ trans ‐selectivity was found (96 %) for the 1,4‐polyisoprenes. The obtained polyisoprene has a M n of 13.0 × 10 4 and moderate polydispersity (2.12).

References

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