Reversible borohydride formation from aluminium hydrides and {H(9-BBN)}2: structural, thermodynamic and reactivity studies. Issue 29 (8th March 2019)

• Record Type: Journal Article
• Authors: Caise, Alexa; Kolychev, Eugene L.; Hicks, Jamie; Fuentes, M. Ángeles; Goicoechea, Jose M.; Aldridge, Simon
• Is Part Of: Dalton transactions. Volume 48:Issue 29(2019)
• Page Start: 10845
• Page End: 10852
• Publication Date: 2019-03-08
• Subjects: Chemistry, Inorganic -- Periodicals; Chemistry, Physical and theoretical -- Periodicals; Chemistry, Inorganic -- Periodicals; 546.05
• DOI: 10.1039/c9dt00535h
• Languages: English
• ISSNs: 1477-9226

Abstract

Abstract : Aluminium borohydrides of the type (Nacnac)Al(R){H2 (9-BBN)} are characterized by borane dissociation in solution under ambient conditions. This behaviour is critical to the ability of such complexes to reduce CO2 . Abstract : A series of novel β-diketiminate stabilised aluminium borohydrides of the type (Nacnac)Al(R){H2 (9-BBN)} has been synthesised offering variation in both the auxiliary R substituent and in the Nacnac backbone itself. A number of these complexes show unusual dissociation of the borane from the aluminium hydride in solution under ambient conditions. The lability of the borane is shown (by variable temperature NMR analyses) to be influenced by the electronic character of both the aluminium-bound R substituent and the Nacnac ligand itself, such that electron-withdrawing substituents lead to greater dissociation of the borane. Comparison of these complexes with related systems featuring the tetrahydroborate [BH4 ] − ligand illustrates the impact of the boron-bound substituents on the ability of the borane fragment to dissociate from the aluminium hydride. This dissociative behaviour is shown to be highly influential on the ability of the borohydride complexes to reduce carbon dioxide in a stoichiometric manner.