Progress in Polyarsolyl Chemistry.

ABSTRACT: The synthesis of heteroatom analogues of the cyclopentadienyl anion Cp^- is a fascinating and challenging field of research. The replacement of methine moieties by phosphorus is well investigated for the synthesis of mono-, tri- and pentaphospholyl ligands. On the other hand, arsenic derivatives are rare and 1,2,4-triarsolyl and tetraarsolyl salts are unknown. Herein, we report on the synthesis of Cs[E₃ C₂ (trip)₂ ] (1 a: E=P; 1 b: E=As; trip=2,4,6-triisopropylphenyl) and Cs[E₄ C(trip)] (2 a: E=P; 2 b: E=As). Compound 1 b represents the first 1,2,4-triarsolyl and 2 b the first tetraarsolyl anion. All salts are obtained in one-pot syntheses using E(SiMe₃ )₃ , 2,4,6-triisopropylbenzoyl chloride and CsF. The products 1 a⋅2 C₄ H₈ O₂ , 2 a⋅Et₂ O and 2 b⋅3 C₄ H₈ O₂ were characterized by X-ray structural analysis, which revealed planar heterocycles. Nucleus-independent chemical shifts (NICS) confirmed the aromaticity of these anions. Notably, compound 2 a⋅Et₂ O is only the second tetraphospholyl ligand which is structurally characterized.

SUBMITTER: Heindl C 

PROVIDER: S-EPMC5053250 | biostudies-literature | 2016 Feb

REPOSITORIES: biostudies-literature