Low-nuclearity magnesium hydride complexes stabilized by N-heterocyclic carbenes
Lucas A Freeman1, Jacob E Walley, Diane A Dickie
1Department of Chemistry, University of Virginia, 409 McCormick Rd./PO Box 400319, Charlottesville, VA 22904. rjg8s@virginia.edu.
Abstract:
Herein we report the synthesis and characterization of dinuclear magnesium-hydride complexes, [(IiPrMe2)Mg(μ-H)(HMDS)]2 [4, IiPrMe2 = N,N'-diisopropyl-2,3-dimethylimidazol-2-ylidine, HMDS = bis(trimethylsilyl)amide] and [(IiPrMe2)Mg(μ-H)(ASCP)]2 (5, ASCP = 2,2,5,5-tetramethyl-2,5-disila-1-azacyclopent-1-yl). Compounds 4 and 5 exhibit the lowest nuclearity of any carbene-magnesium hydride complex to date.
Related Concept Videos
Complexation Equilibria: Factors Influencing Stability of Complexes
Colors and Magnetism
When atoms or molecules absorb light at the proper frequency, their electrons are excited to higher-energy orbitals. For many main group atoms and molecules, the absorbed photons are in the ultraviolet range of the electromagnetic spectrum, which cannot be detected by the human eye. For coordination compounds, the energy difference between the d orbitals often allows photons in the visible range to be absorbed and emitted, which is seen as colors by the human...
Valence Bond Theory
Properties of Organometallic Compounds
Carbocations
Metal-Ligand Bonds
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...


