Aminodimethylalanes (R1R2NAlMe2) as Useful Synthetic Precursors of Aminoalane Difluorides Using Trimethyltin Fluoride: Crystal Structures of (2,6-i-Pr2
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AminodimethylalanesR1R2NAlMe2 (R1 =2,6-i-Pr2C6H3,2,6-Me2C6H3; R2 =SiMe3, Si(i-Pr)Me2, Si(t-Bu)Me2,Si(2,4,6-Me3C6H2)Me2)are prepared in high yield via reaction of therespective amine R1R2NH withtrimethylaluminum in n-hexane. Further reaction of(2,6-i-Pr2C6H3)N(SiMe3)AlMe2with 2 equiv of trimethyltin fluoride in toluene affordstheaminoalane difluoride(2,6-i-Pr2C6H3)N(SiMe3)AlF2.An X-ray structural determination of(2,6-i-Pr2C6H3)N(SiMe3)AlMe2shows it to be dimeric with bridging methyl and terminalamino groups. The aminoalane difluoride(2,6-i-Pr2C6H3)N(SiMe3)AlF2is trimeric with asix-membered alternating aluminum-fluorine ring. Terminalfluorine atoms are locatedabove and below the ring. Reactions of aminoalanesR1R2NAlMe2 with 2 equiv oftrimethyltinfluoride in THF yield the monomeric THF adductsR1R2NAlF2·THF.

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