Unusual neutral ligand coordination to arsenic and antimony trifluoride.

The preparations and spectroscopic characterisation of the hydrolytically unstable As(III) complexes, [AsF(3)(OPR(3))(2)] (R = Me or Ph) and [AsF(3){Me(2)P(O)CH(2)P(O)Me(2)}] are described and represent the first examples of complexes of AsF(3) with neutral ligands. The crystal structure of [AsF(3){Me(2)P(O)CH(2)P(O)Me(2)}] contains dimers with bridging diphosphine dioxide, but there are also long contacts between the dimers to neighbouring phosphine oxide groups, completing a very distorted six-coordination at arsenic and producing a weakly associated polymer structure. The reaction of AsF(3) with OAsPh(3) affords Ph(3)AsF(2), and no arsine oxide complex was formed. Reaction of SbF(3) with OER(3) (R = Me or Ph, E = P or As), Me(2)P(O)CH(2)P(O)Me(2) and Ph(2)P(O)(CH(2))(n)P(O)Ph(2) (n = 1 or 2) in MeOH produces [SbF(3)(OER(3))(2)], [SbF(3){Me(2)P(O)CH(2)P(O)Me(2)}] and [SbF(3){Ph(2)P(O)(CH(2))(n)P(O)Ph(2)}] respectively. The X-ray structures reveal that the complexes contain square pyramidal SbF(3)O(2) cores with apical F and cis disposed pnictogen oxides. However, whilst [SbF(3)(OER(3))(2)] (R = Ph: E = P or As; R = Me: E = As) and [SbF(3){Ph(2)P(O)CH(2)P(O)Ph(2)}] are monomeric, [SbF(3){Me(2)P(O)CH(2)P(O)Me(2)}] is a dimer with bridging diphosphine dioxides producing a twelve-membered ring, and [SbF(3){Ph(2)P(O)(CH(2))(2)P(O)Ph(2)}] is a chain polymer with diphosphine dioxide bridges. In the OAsR(3) reactions with SbF(3), R(3)AsF(2) are also formed. Notably the Sb-O(P) bonds are shorter than As-O(P), despite the covalent radii (As < Sb), consistent with very weak coordination of the AsF(3). IR and multinuclear ((1)H, (19)F and (31)P) NMR data are reported and discussed. BiF(3) does not react with pnictogen oxide ligands under similar conditions and halide exchange of bismuth chloro complexes with Me(3)SnF gave BiF(3).