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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<sup>-</sup> ), a species that has only recently become synthetically accessible. The reaction of AsCO<sup>-</sup> with the bulky stannylene Ter<sub>2</sub> Sn (Ter=2,6-bis[2,4,6-trimethylphenyl]phenyl) is described, which leads to the unexpected formation of a [Ter<sub>3</sub> Sn<sub>2</sub> As<sub>2</sub> ]<sup>-</sup> cluster compound. On the reaction pathway to this cluster, several intermediates were identifi  ...[more]

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