Taichi Koike, Atsuhiro Sato, Naoki Sakurata and Takeaki Iwamoto*,
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引用次数: 0
Abstract
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 (AlI3) complex 1 and investigate its reactivity differences depending on the nucleophile of choice. While the reaction of complex 1 with the anionic nucleophile, Ph2NLi, selectively results in substitution on Al(III) to afford the CAASi-AlI2NPh2 complex (2), treatment of the neutral nucleophiles, N-heterocyclic carbenes (NHCs), results in irreversible ligand exchanges to give the corresponding NHC-AlI3 complexes. Compound 1, in the presence of 1.0 equiv of CAASi, forms an unusual AlISi2-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.
期刊介绍:
Organometallics is the flagship journal of organometallic chemistry and records progress in one of the most active fields of science, bridging organic and inorganic chemistry. The journal publishes Articles, Communications, Reviews, and Tutorials (instructional overviews) that depict research on the synthesis, structure, bonding, chemical reactivity, and reaction mechanisms for a variety of applications, including catalyst design and catalytic processes; main-group, transition-metal, and lanthanide and actinide metal chemistry; synthetic aspects of polymer science and materials science; and bioorganometallic chemistry.