Journal
ORGANOMETALLICS
Volume 32, Issue 24, Pages 7509-7519Publisher
AMER CHEMICAL SOC
DOI: 10.1021/om400997b
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Funding
- Australian Research Council
- Monash University
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In this systematic study six new chiral alkali-metal complexes derived from (S)-alpha-(methylbenzyl)benzylamine (alpha-mmba) have been synthesized and characterized in the solution state, with five successfully analyzed by single-crystal X-ray diffraction. The reaction products observed are highly dependent on the choice of alkali metal and Lewis donor used, affording either the amido deprotonation complex [Li{PhCH(Me)NCH2Ph}center dot HMPA](2) (3) when using nBuLi or the aza-allyl complexes [Na{PhC(Me)NCHPh}center dot TMEDA](infinity) (4), [Na{PhC(Me)NCHPh}center dot 3THF] (5), [Na{PhC(Me)NCHPh}center dot THF center dot TMEDA] (6), and [K{PhC(Me)NCHPH}center dot PMDETA](infinity) (8) via hydrogen elimination reactions. Unexpectedly a co- secondary product is also obtained when tridentate or pseudo-tridentate donor ligands are used in the reaction of a-mbba with either nBuNa or nBuK to give the unexpected 1, 3-dipheny1-2-aza-ally1 complexes[M{(PhCH)(2)N}center dot L] [M = Na, L = 3 THF (5a) or TMEDA/THF (6a); M = K, L = PMDETA (8a)] in various ratios. Reinforcing the experimental findings, formation of the methane elimination complex was confirmed via GC-headspace analysis experiments, while theoretical DTF calculations on model systems reinforce the experimental findings showing that thermodynamic gas elimination pathways trend toward the larger alkali metals with H2 elimination kinetically favored over CH4.
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