Synthesis and reactivity of metal complexes supported by the tetradentate monoanionic ligand bis(2-picolyl)(2-hydroxy-3,5-di-tert-butylbenzyl)amide (BPPA) |
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Authors: | Chomitz Wayne A Minasian Stefan G Sutton Andrew D Arnold John |
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Affiliation: | Department of Chemistry, University of California, Berkeley, CA 94720-1460, USA. |
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Abstract: | Metal-halide complexes of Ti, V, Y, Zr, Al, Ga, and U supported by the tetradentate monoanionic (TDMA) ligand bis(2-picolyl)(2-hydroxy-3,5-di-tert-butylbenzyl)amine, H(BPPA), were synthesized and spectroscopically characterized. In addition, the complexes (BPPA)TiCl2, (BPPA)VBr2, [(BPPA)YCl2]2, (BPPA)AlCl2, (BPPA)GaCl2, and (BPPA)UI3 were characterized by single-crystal X-ray crystallography. In all cases the ligand is bound kappa4 to the metal center. All structurally characterized compounds are monomeric in the solid-state with the exception of [(BPPA)YCl2]2, which exists as a dimer in the solid-state. The metal-alkyl complexes (BPPA)AlMe2 and (BPPA)Zr(CH2Ph)3 were also synthesized and characterized, and an X-ray structure of (BPPA)Zr(CH2Ph)3 was obtained. The transformation of BPPA from a monoanionic to a dianionic ligand via proton abstraction was observed and monitored by NMR spectroscopy. |
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