Divalent Lanthanide Tetraisobutylaluminates: Reactivity and Living Isoprene Polymerization
Eric C Moinet1, Benjamin M Wolf1, Olivier Tardif2
1Institut für Anorganische Chemie, Eberhard Karls Universität Tübingen, Auf der Morgenstelle 18, 72076, Tübingen, Germany.
Abstract:
Lanthanide (Ln) tetraisobutylaluminates constitute key components in commercial 1,3-diene polymerization catalysts, and likewise are the homogeneous rare-earth-metal catalysts of prime industrial importance. Discrete divalent rare-earth-metal complexes [Ln(AliBu4 )2 ] (Ln=Sm, Eu, Yb) reported here display the first structurally characterized homoleptic metal tetraisobutylaluminates. Treatment of [Ln(AliBu4 )2 ] with C2 Cl6 gives access to SmII /SmIII mixed-valence cluster [Sm6 Cl8 (AliBu4 )6 ] and the YbII cluster [Yb4 Cl4 (AliBu4 )4 ], respectively. Reaction with B(C6 F5 )3 leads to hydride abstraction and formation of arene-coordinated hydroborates such as [Sm{HB(C6 F5 )3 }2 (toluene)2 ]. Complexes [Ln(AliBu4 )2 ] engage in single-component isoprene polymerization, affording high cis-1,4 polyisoprenes with narrow molecular weight distributions. Binary [Yb(AliBu4 )2 ]/[HNPhMe2 ][B(C6 F5 )4 ] fabricates polyisoprene in a perfectly living manner. The catalytically active species are scrutinized by NMR spectroscopy.
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