Boosting Low‐Valent Aluminum(I) Reactivity with a Potassium Reagent

The reagent RK R=CH(SiMe3 )2 or N(SiMe3 )2 was expected to react with the low-valent (DIPP BDI)Al (DIPP BDI=HCC(Me)N(DIPP)2 , DIPP=2,6-iPr-phenyl) to give (DIPP BDI)AlR- K+ . However, deprotonation of the Me group in the ligand backbone was observed and H2 C=C(N-DIPP)-C(H)=C(Me)-N-DIPPAl- K+ (1) crystallized as a bright-yellow product (73 %). Like most anionic AlI complexes, 1 forms a dimer in which formally negatively charged Al centers are bridged by K+ ions, showing strong K+ ⋅⋅⋅DIPP interactions. The rather short Al-K bonds 3.499(1)-3.588(1) Å indicate tight bonding of the dimer. According to DOSY NMR analysis, 1 is dimeric in C6 H6 and monomeric in THF, but slowly reacts with both solvents. In reaction with C6 H6 , two C-H bond activations are observed and a product with a para-phenylene moiety was exclusively isolated. DFT calculations confirm that the Al center in 1 is more reactive than that in (DIPP BDI)Al. Calculations show that both AlI and K+ work in concert and determines the reactivity of 1.