Abstract
Three of a kind: The directional O-O/S-S heteroclonor ligand H 4-1 reacts with TiIV to give the triple-stranded dinuclear tetra-anion [Ti2(1)3]4- (see picture, acac = 2,4-pentanedione). The reaction yields exclusively the regioisomer with a parallel orientation of the ligands and only one pair of enantiomers is obtained.
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Hahn, F. E., Isfort, C. S., & Pape, T. (2004). A dinuclear, triple-stranded helicate with a diamide-bridged catechol/benzenedithiol ligand. Angewandte Chemie - International Edition, 43(36), 4807–4810. https://doi.org/10.1002/anie.200460188
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