The kinetic stability provided by the sterically demanding {SiNDipp}2− dianion (SiNDipp = {CH2SiMe2NDipp}2; Dipp = 2,6-i-Pr2C6H3) is intrinsic to the isolation of not only the group 1 alumanyl reagents ([{SiNDipp}AlM]2; M = K, Rb, Cs) but also facilitates the completely selective oxidative addition of a C-H bond of 1,2-C2B10H12 to the aluminium centre. In each case, the resultant compounds comprise a four-coordinate o-carboranyl (hydrido)aluminate anion, [(SiNDipp)Al(H)(1,2-C2B10H11)]−, in which the carboranyl cage is bonded to aluminium by an Al-C σ bond. Although the anions further assemble as extended network structures based on Al-H∙∙∙M, B-H∙∙∙M, and C-H∙∙∙M interactions, each structure is unique due to the significant variation in M+ ionic radius as group 1 is descended. The potassium derivative crystallises as a one-dimensional polymer, its rubidium analogue is a dimer due to the polyhapto-sequestration of a molecule of benzene solvent within the alkali metal coordination sphere, and the caesium species is a two-dimensional assembly of hexameric aggregates.

Oxidative Addition to Group 1 (K, Rb, Cs) Alumanyl Anions as a Route to o-Carboranyl (hydrido)aluminates

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