Dipnictenes of the type RPn=PnR (Pn=P, As, Sb, Bi) can be viewed as dimers of the corresponding pnictinidenes R-Pn. Phosphanylidene- and arsanylidenephosphoranes (R-Pn(PMe); Pn=P, As) have been shown to be versatile synthetic surrogates for the delivery of pnictinidene fragments. We now report that thermal treatment of 1 : 1 mixtures of R-P(PMe) and R'-As(PMe) gives access to arsaphosphenes of the type RP=AsR'. Three examples are presented and the properties and reactivity of Mes*P=AsTer (1) (Mes*=2,4,6-tBu-CH; Ter=2,6-(2,6-iPrCH)-CH) were studied in detail. Solid state P NMR spectroscopy revealed a large P NMR chemical shift anisotropy with a span of ca. 920 ppm for 1 while computational methods were employed to investigate this pronounced magnetic deshielding of the P atom in 1. In the presence of the carbene IMe (IMe=:C(MeNCMe)) 1 is shown to be split into the corresponding NHC adducts Mes*P(IMe) and TerAs(IMe), which is additionally shown for diarsenes.
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http://dx.doi.org/10.1002/cplu.202400120 | DOI Listing |
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