ABSTRACT
Heterometallic hydride complexes are of growing interest due to their potential to contribute to highly active insertion-based catalysis; however, methods to modulate electron density within this class of molecules are underexplored. Addition of ancillary ligands to heterotrimetallic NiAl2H2 species (1) results in the formation of heterobimetallic NiAl-hydride complexes with varying phosphine donors (2-(L)2). Incorporation of sigma donating ancillary ligands of increasing strength led to contractions of the Ni-Al distances correlated to a strengthening of a back donation interaction to the Al-H sigma antibonding orbital, most prominently present in 2-(PMe3)2. Demethylation of the aryl ether from 2-(PMe3)2 provides access to a novel anionic nickel-aluminum complex (3) with a maintained bridged hydride moiety between Ni and Al. Increased negative charge in complex 3 results in an elongation of the Ni-Al interaction. Combined crystallographic, spectroscopic, and computational studies support a 3-center interaction within the Al-H-Ni subunits and were used to map the degree of Ni-H character of the series within the Al-H-Ni bonding continuum.