Macrocyclic Binucleating β-Diketiminate Ligands and Their Lithium, Aluminum, and Zinc Complexes

The incorporation of rigid aromatic linkers into β-diketiminate ligands creates a binucleating scaffold that holds two metals near each other. This paper discloses the synthesis, characterization, and reactivity of mBin2-, which has a meta-substituted xylylene spacer, and pBin2-, which has a para-su...

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Veröffentlicht in:Organometallics 2007-07, Vol.26 (14), p.3416-3423
Hauptverfasser: Vela, Javier, Zhu, Liwei, Flaschenriem, Christine J, Brennessel, William W, Lachicotte, Rene J, Holland, Patrick L
Format: Artikel
Sprache:eng
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Zusammenfassung:The incorporation of rigid aromatic linkers into β-diketiminate ligands creates a binucleating scaffold that holds two metals near each other. This paper discloses the synthesis, characterization, and reactivity of mBin2-, which has a meta-substituted xylylene spacer, and pBin2-, which has a para-substituted xylylene spacer. Lithium, aluminum, and zinc complexes of each ligand have been isolated, and in some cases characterized by X-ray crystallography. The lithium complexes are coordinated to solvent-derived THF ligands, while the zinc and aluminum complexes have alkyl ligands. Complexes of the mBin2- ligand have an anti conformation in which the metals are on opposite sides of the macrocycle, while pBin2- complexes prefer a syn conformation. The 1H NMR spectra of the complexes demonstrate that the conformations interconvert rapidly in the lithium complexes and less rapidly in the zinc and aluminum complexes.
ISSN:0276-7333
1520-6041
DOI:10.1021/om0700258