化学
亲核细胞
硅烯
烷基
碘化物
铝
药物化学
立体化学
有机化学
硅
催化作用
作者
Taichi Koike,Atsuhiro Sato,Naoki Sakurata,Takeaki Iwamoto
出处
期刊:Organometallics
[American Chemical Society]
日期:2025-05-05
卷期号:44 (10): 1013-1017
标识
DOI:10.1021/acs.organomet.5c00058
摘要
Exploration of bonding motifs and reactivity modes of molecules that contain an Al–Si core is of particular interest in terms of broadening the application of two of the most abundant elements in the Earth’s crust. Here we report on the synthesis of cyclic (alkyl)(amino)silylene CAASi -ligated aluminum(III) triiodide (AlI 3 ) complex 1 and investigate its reactivity differences depending on the nucleophile of choice. While the reaction of complex 1 with the anionic nucleophile, Ph 2 NLi, selectively results in substitution on Al(III) to afford the CAASi -AlI 2 NPh 2 complex ( 2 ), treatment of the neutral nucleophiles, N-heterocyclic carbenes (NHCs), results in irreversible ligand exchanges to give the corresponding NHC-AlI 3 complexes. Compound 1, in the presence of 1.0 equiv of CAASi, forms an unusual AlISi 2 -heterocyclic compound 6 in the solid state, which was characterized by single crystal XRD analysis. DFT calculations and trapping experiments in solution revealed that 6 exists as a 1:1 equilibrium mixture of 1 and CAASi in solution.
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