Scandium trichloride complexes with tridentate N3- and S2N-donor ligands (L3) have been synthesised and characterised by IR, 1H, 13C{1H} and 45Sc NMR spectroscopy, microanalysis, and solid state and solution XAFS spectroscopy. Catalytic testing of a subset of these complexes with ethene has been undertaken in chlorobenzene with MMAO-3A and PMAO-IP at 60 °C and 40 bar ethene, giving low activity ethene polymerisation. The reactions of these complexes with MeLi and AlMe3 were studied by 1H, 13C{1H}, 27Al and 45Sc NMR spectroscopy and in situ via Sc K-edge XAFS spectroscopy. Three or four mol. equivalents of MeLi react with [ScCl3(Me3-tacn)] in THF solution to form [ScMe3(Me3-tacn)] cleanly, while complexes of type [ScCl3(R-SNS)] {R-SNS = HN(CH2CH2SC10H21)2} form two different species proposed to be [ScMe3(R-SN(Li)S)] and [ScMe2(R-SN−S)]. In contrast, in situ45Sc NMR and Sc K-edge XAFS spectroscopic studies of the reaction of [ScCl3(Me3-tacn)] with 10 mol. equivalents of AlMe3 strongly suggest that alkylation at the Sc(III) centre does not occur, instead retaining the Cl3N3 coordination environment and most likely forming Sc−Cl−AlMe3 bridging interactions. Similar studies on [ScCl3(decyl-SNS)] with 10 mol. equivalents of AlMe3 are also consistent with this, indicating that alkylation at the Sc centre does not occur except in the presence of co-catalyst [Ph3C][Al{OC(CF3)3}4] and the α-alkene, hex-1-ene.
«
Scandium trichloride complexes with tridentate N3- and S2N-donor ligands (L3) have been synthesised and characterised by IR, 1H, 13C{1H} and 45Sc NMR spectroscopy, microanalysis, and solid state and solution XAFS spectroscopy. Catalytic testing of a subset of these complexes with ethene has been undertaken in chlorobenzene with MMAO-3A and PMAO-IP at 60 °C and 40 bar ethene, giving low activity ethene polymerisation. The reactions of these complexes with MeLi and AlMe3 were studied by 1H, 13C{1H...
»