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- W4313439478 abstract "Abstract Co‐complexation of equimolar amounts of 1‐alkali‐metal‐2‐ tert butyldihydropyridines with AlMe 3 in the presence of a polydentate N ‐donor ligand has delivered four crystallographically verified alkali‐metal aluminates [donor⋅AM(μ‐ t BuDHP)AlMe 3 ] n ( 1 , AM=Li, donor=TMEDA, n=1; 2 , AM=Na, donor=PMDETA, n=1; 3 , AM=K, donor=PMDETA, n=2; 4 , AM=Cs, donor=PMDETA, n=∞; TMEDA= N , N , N′ , N′ ‐tetramethylethylenediamine; PMDETA= N , N , N′ , N′′ , N′′ ‐pentamethyldiethylenetriamine). While the monomeric complexes ( 1 , 2 ) and the polymeric complex ( 4 ) are thermally stable, the dimeric complex ( 3 ) undergoes a disproportionation process yielding the known ion‐separated homoanionic complex [K ⋅ (PMDETA) 2 ] + [AlMe 4 ] − ( 3 a ). Utilizing TMEDA as the N ‐donor resulted in the same disproportionation, but gave rise to two distinct solid‐state aggregated forms of aluminate [K ⋅ (TMEDA) 2 ] + [AlMe 4 ] − , namely monomeric ( 3 b ) and polymeric ( 3 b′ ) polymorphs, in which the anionic moiety acts as a bidentate chelator or monodentate bridge respectively to the potassium cationic moieties." @default.
- W4313439478 created "2023-01-06" @default.
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- W4313439478 date "2022-12-27" @default.
- W4313439478 modified "2023-09-27" @default.
- W4313439478 title "Incorporating Trimethylaluminium into the Structures of Alkali Metal (Li, Na, K, Cs) dihydropyridines" @default.
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- W4313439478 doi "https://doi.org/10.1002/zaac.202200356" @default.
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