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 |
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Hauptverfasser: | , , , , , |
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. |
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ISSN: | 0276-7333 1520-6041 |
DOI: | 10.1021/om0700258 |