Solvent dependence of the solid-state structures of salicylaldiminate magnesium amide complexes

• Published in: Acta crystallographica. Section C, Crystal structure communications Vol. 72; no. Pt 12; p. 990
• Main Authors: Rood, Jeffrey A, Landis, Ashley M, Forster, Daniel R, Goldkamp, Timothy, Oliver, Allen G
• Format: Journal Article
• Language: English
• Published: England Wiley Subscription Services, Inc 01.12.2016
• Subjects: Chemical compounds; Crystal structure; Crystallography; Magnesium; crystal structure; magnesium; solvent effects; NMR spectroscopy; ligand redistribution; salicylaldiminate
• ISSN: 0108-2701; 2053-2296; 1600-5759
• DOI: 10.1107/S2053229616018593

There are challenges in using magnesium coordination complexes as reagents owing to their tendency to adopt varying aggregation states in solution and thus impacting the reactivity of the complexes. Many magnesium complexes are prone to ligand redistribution via Schlenk equilibrium due to the ionic character within the metal-ligand interactions. The role of the supporting ligand is often crucial for providing stability to the heteroleptic complex. Strategies to minimize ligand redistribution in alkaline earth metal complexes could include using a supporting ligand with tunable sterics and electronics to influence the degree of association to the metal atom. Magnesium bis(hexamethyldisilazide) was reacted with salicylaldimines [ L = N-(2,6-diisopropylphenyl)salicylaldimine and L = 3,5-di-tert-butyl-N-(2,6-diisopropylphenyl)salicylaldimine] in either nondonor (toluene) or donor solvents [tetrahydrofuran (THF) or pyridine]. The structures of the magnesium complexes were studied in the solid state via X-ray diffraction. In the nondonor solvent, i.e. toluene, the heteroleptic complex bis{μ-2-[(2,6-diisopropylphenyl)iminomethyl]phenolato}-κ N,O:O;κ O:N,O-bis[(hexamethyldisilazido-κN)magnesium(II)], [Mg (C H NO) (C H NSi ) ] or [ LMgN(SiMe ) ] , (1), was favored, while in the donor solvent, i.e. pyridine (pyr), the formation of the homoleptic complex {2,4-di-tert-butyl-6-[(2,6-diisopropylphenyl)iminomethyl]phenolato-κ N,O}bis(pyridine-κN)magnesium(II) toluene monosolvate, [Mg(C H NO) (C H N) ]·C H N or [{ L Mg (pyr) }·pyr], (2), predominated. Heteroleptic complex (1) was crystallized from toluene, while homoleptic complexes (2) and the previously reported [ L Mg·THF] [Quinque et al. (2011). Eur. J. Inorg. Chem. pp. 3321-3326] were crystallized from pyridine and THF, respectively. These studies support solvent-dependent ligand redistribution in solution. In-situ H NMR experiments were carried out to further probe the solution behavior of these systems.