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Unusual neutral ligand coordination to arsenic and antimony trifluoride

Unusual neutral ligand coordination to arsenic and antimony trifluoride
Unusual neutral ligand coordination to arsenic and antimony trifluoride
The preparations and spectroscopic characterisation of the hydrolytically unstable As(III) complexes, [AsF3(OPR3)2] (R = Me or Ph) and [AsF3{Me2P(O)CH2P(O)Me2}] are described and represent the first examples of complexes of AsF3 with neutral ligands. The crystal structure of [AsF3{Me2P(O)CH2P(O)Me2}] 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 AsF3 with OAsPh3 affords Ph3AsF2, and no arsine oxide complex was formed. Reaction of SbF3 with OER3 (R = Me or Ph, E = P or As), Me2P(O)CH2P(O)Me2 and Ph2P(O)(CH2)nP(O)Ph2 (n = 1 or 2) in MeOH produces [SbF3(OER3)2], [SbF3{Me2P(O)CH2P(O)Me2}] and [SbF3{Ph2P(O)(CH2)nP(O)Ph2}] respectively. The X-ray structures reveal that the complexes contain square pyramidal SbF3O2 cores with apical F and cis disposed pnictogen oxides. However, whilst [SbF3(OER3)2] (R = Ph: E = P or As; R = Me: E = As) and [SbF3{Ph2P(O)CH2P(O)Ph2}] are monomeric, [SbF3{Me2P(O)CH2P(O)Me2}] is a dimer with bridging diphosphine dioxides producing a twelve-membered ring, and [SbF3{Ph2P(O)(CH2)2P(O)Ph2}] is a chain polymer with diphosphine dioxide bridges. In the OAsR3 reactions with SbF3, R3AsF2 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 AsF3. IR and multinuclear (1H, 19F and 31P) NMR data are reported and discussed. BiF3 does not react with pnictogen oxide ligands under similar conditions and halide exchange of bismuth chloro complexes with Me3SnF gave BiF3.

0300-9246
5291-5297
Levason, William
e7f6d7c7-643c-49f5-8b57-0ebbe1bb52cd
Light, Mark E.
cf57314e-6856-491b-a8d2-2dffc452e161
Maheshwari, Seema
276fab22-7ef8-421c-9501-ca095456ea7a
Reid, Gillian
37d35b11-40ce-48c5-a68e-f6ce04cd4037
Zhang, Wenjian
1f80ac5e-d4c2-4720-b19e-be700cd411e7
Levason, William
e7f6d7c7-643c-49f5-8b57-0ebbe1bb52cd
Light, Mark E.
cf57314e-6856-491b-a8d2-2dffc452e161
Maheshwari, Seema
276fab22-7ef8-421c-9501-ca095456ea7a
Reid, Gillian
37d35b11-40ce-48c5-a68e-f6ce04cd4037
Zhang, Wenjian
1f80ac5e-d4c2-4720-b19e-be700cd411e7

Levason, William, Light, Mark E., Maheshwari, Seema, Reid, Gillian and Zhang, Wenjian (2011) Unusual neutral ligand coordination to arsenic and antimony trifluoride. Dalton Transactions, 40 (19), 5291-5297. (doi:10.1039/C1DT10113G).

Record type: Article

Abstract

The preparations and spectroscopic characterisation of the hydrolytically unstable As(III) complexes, [AsF3(OPR3)2] (R = Me or Ph) and [AsF3{Me2P(O)CH2P(O)Me2}] are described and represent the first examples of complexes of AsF3 with neutral ligands. The crystal structure of [AsF3{Me2P(O)CH2P(O)Me2}] 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 AsF3 with OAsPh3 affords Ph3AsF2, and no arsine oxide complex was formed. Reaction of SbF3 with OER3 (R = Me or Ph, E = P or As), Me2P(O)CH2P(O)Me2 and Ph2P(O)(CH2)nP(O)Ph2 (n = 1 or 2) in MeOH produces [SbF3(OER3)2], [SbF3{Me2P(O)CH2P(O)Me2}] and [SbF3{Ph2P(O)(CH2)nP(O)Ph2}] respectively. The X-ray structures reveal that the complexes contain square pyramidal SbF3O2 cores with apical F and cis disposed pnictogen oxides. However, whilst [SbF3(OER3)2] (R = Ph: E = P or As; R = Me: E = As) and [SbF3{Ph2P(O)CH2P(O)Ph2}] are monomeric, [SbF3{Me2P(O)CH2P(O)Me2}] is a dimer with bridging diphosphine dioxides producing a twelve-membered ring, and [SbF3{Ph2P(O)(CH2)2P(O)Ph2}] is a chain polymer with diphosphine dioxide bridges. In the OAsR3 reactions with SbF3, R3AsF2 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 AsF3. IR and multinuclear (1H, 19F and 31P) NMR data are reported and discussed. BiF3 does not react with pnictogen oxide ligands under similar conditions and halide exchange of bismuth chloro complexes with Me3SnF gave BiF3.

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Published date: 2011
Organisations: Chemistry

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Local EPrints ID: 183657
URI: http://eprints.soton.ac.uk/id/eprint/183657
ISSN: 0300-9246
PURE UUID: fd67cc2a-7458-4a58-9c9c-9dd45bf1520c
ORCID for William Levason: ORCID iD orcid.org/0000-0003-3540-0971
ORCID for Mark E. Light: ORCID iD orcid.org/0000-0002-0585-0843
ORCID for Gillian Reid: ORCID iD orcid.org/0000-0001-5349-3468

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Date deposited: 03 May 2011 14:15
Last modified: 15 Mar 2024 03:01

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Contributors

Author: William Levason ORCID iD
Author: Mark E. Light ORCID iD
Author: Seema Maheshwari
Author: Gillian Reid ORCID iD
Author: Wenjian Zhang

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