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A Monoanionic Arsenide Source: Decarbonylation of the 2-Arsaethynolate Anion upon Reaction with Bulky Stannylenes.

ABSTRACT: We report fundamental studies on the reactivity of the 2-arsaethynolate anion (AsCO^- ), a species that has only recently become synthetically accessible. The reaction of AsCO^- with the bulky stannylene Ter₂ Sn (Ter=2,6-bis[2,4,6-trimethylphenyl]phenyl) is described, which leads to the unexpected formation of a [Ter₃ Sn₂ As₂ ]^- cluster compound. On the reaction pathway to this cluster, several intermediates were identified and characterized. After the initial association of AsCO^- to Ter₂ Sn, decarbonylation occurs to give an anion featuring monocoordinate arsenic, [Ter₂ SnAs]^- . Both species are not stable under ambient conditions, and [Ter₂ SnAs]^- rearranges to form [TerSnAsTer]^- , an unprecedented anionic mixed Group?14/15 alkene analogue.

SUBMITTER: Hinz A

PROVIDER: S-EPMC5299489 | biostudies-literature | 2016 Dec

REPOSITORIES: biostudies-literature

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A Monoanionic Arsenide Source: Decarbonylation of the 2-Arsaethynolate Anion upon Reaction with Bulky Stannylenes.

Hinz Alexander A Goicoechea Jose M JM

Angewandte Chemie (International ed. in English) 20161115 50

We report fundamental studies on the reactivity of the 2-arsaethynolate anion (AsCO- ), a species that has only recently become synthetically accessible. The reaction of AsCO- with the bulky stannylene Ter2 Sn (Ter=2,6-bis[2,4,6-trimethylphenyl]phenyl) is described, which leads to the unexpected formation of a [Ter3 Sn2 As2 ]- cluster compound. On the reaction pathway to this cluster, several intermediates were identifi ...[more]

PMID: 27862768

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