TMP (2,2,6,6-tetramethylpiperidide)-aluminate bases: lithium-mediated alumination or lithiation-alkylaluminium-trapping reagents?

The lithium TMP-aluminate bases "LiTMP center dot Al(Bu-i)(3)" 1 and "LiTMP center dot Al(TMP)(Bu-i)(2)" 2, where TMP is 2,2,6,6-tetramethylpiperidide, have recently come under the spotlight as "aluminating" reagents in that they can perform aluminium-hydrogen exchange on a wide variety of aromatic substrates. Previous studies have intimated that 1 existed as a single species in THF solution formulated as [(THF)center dot Li(mu-TMP)(mu-Bu-i)Al(Bu-i)(2)]1 center dot THF, having a contacted ion pair structure as evidenced by an X-ray crystallographic study of isolated crystals. But here using anisole as a case substrate it is revealed that pre-crystallised 1 center dot THF cannot deprotonate anisole at all whether in hexane or THF solution contradicting earlier in situ applications of 1 which revealed near quantitative metallation of anisole. NMR spectroscopic studies of 1 made in situ in THF solution ascribe this reactivity distinction from 1 center dot THF to complex equilibria involving five major species in LiTMP center dot THF, Al(Bu-i)(3)center dot THF, [{Li(THF)(4)}(+){Al(TMP)(Bu-i)(3)}(-)] 1 center dot(THF)(4), [(THF)center dot Li(mu-TMP)(mu-OC4H7)-Al(Bu-i)(2)], 4, and (TMP)Al(Bu-i)(2)center dot THF. Reagent 2 in contrast is found to exist as only two separated homometallic species in LiTMP center dot THF and (TMP)Al(Bu-i)(2)center dot THF in THF solution. The constitutions of 1 and 2 in non-polar hexane solution are also revealed. With the aid of DFT calculations, discussion focuses on the fact that none of the aluminate species present in THF solutions of 1 or 2 can deprotonate/metallate anisole, instead the metallation processes appear to be LiTMP lithiations followed immediately by trapping by an alkylaluminium complex, in a metal exchange which drives the reaction to the product (arylaluminated) side.