Abstract
The preparation and reaction chemistry of β-diketiminato aluminum complexes are described. (TTP)AlCl2 (1) (TTPH = 2-(p-tolylamino)-4-(p-tolylimino)-2-pentene) is formed by the treatment of AlCl3 with LiTTP. Sequential alkylation of 1 with CH3Li results in the formation of the mono- and dimethyl aluminum complexes (TTP)AlMeCl (2) and (TTP)AlMe2 (3), respectively. Only monoalkyl complexes are produced when more hindered alkyllithium reagents are used. Compounds 2 and 3 are more conveniently prepared by treating Al(CH3)3 with TTPH·HCl and TTPH, respectively. The more sterically hindered β-diketimine ligand 2-((2,6-diisopropylphenyl)amino)-4-((2,6-diisopropylphenyl)imino)-2-pentene (DDPH) also reacts smoothly with Al(CH3)3 to yield (DDP)Al(CH3)2 (4). Compound 3 undergoes methyl abstraction reactions upon addition of B(C6F5)3 or AgOTf. Cationic species formed from 3 and B(C6F5)3 are unstable and decompose to (TTP)Al(CH3)(C6F5) and MeB(C6F5)2. In contrast, (TTP)Al(CH3)(OTf) (6) is thermally stable, but the trif...
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