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Synthesis and characterisation of WVI complexes of phosphane oxide ligands, [WO2X2(OPR3)2] (X = F, Cl or Br; R = Me or Ph), and of the [MoO2F2(OPR3)2]

Synthesis and characterisation of WVI complexes of phosphane oxide ligands, [WO2X2(OPR3)2] (X = F, Cl or Br; R = Me or Ph), and of the [MoO2F2(OPR3)2]
Synthesis and characterisation of WVI complexes of phosphane oxide ligands, [WO2X2(OPR3)2] (X = F, Cl or Br; R = Me or Ph), and of the [MoO2F2(OPR3)2]
Phosphane oxide complexes of dioxidotungstenVI, [WO2X2(OPR3)2] (X = Cl or Br, M = Ph or Me) have been prepared under anhydrous conditions from the reaction of WX6 with (Me3Si)2O in CH2Cl2, followed by addition of OPR3. Some diphosphane dioxide analogues have been made similarly, viz, [WO2X2(L-L)] {L-L = Ph2P(O)(CH2)nP(O)Ph2 (n = 1 or 2), o-C6H4[P(O)Ph2]2}. The complexes have been characterised by elemental analysis, IR and NMR (1H and 31P{1H}) spectroscopy, and the structures of [WO2Br2(OPPh3)2] and [WO2Cl2(OPMe3)2] determined, revealing distorted six-coordinate tungsten centres with cis-WO2 and trans-WX2 units. The difluorido-dioxido complexes [MO2F2(OPR3)2] (M = Mo or W) and [WO2F2(L-L)] (L-L = 2,2-bipyridyl, 1,10-phenanthroline) have been prepared by fluorination of the corresponding chlorido complexes with Me3SnF in CH2Cl2. These are characterised similarly and by 19F{1H} NMR spectroscopy. Attempts to make [MO2I2(OPR3)2] were unsuccessful. No adduct formation occurs between CrO2Cl2 and OPPh3 under rigorously anhydrous conditions. Crystal structures of [Me3SnCl(OPPh3)] and two forms of [WO2Cl2(1,10-phen)] are also reported and discussed.
1434-1948
306-313
Davis, Martin F.
72f26f03-4bbe-482e-b8a5-6c792b22fcc3
Levason, William
e7f6d7c7-643c-49f5-8b57-0ebbe1bb52cd
Ratnani, Raju
0a86c56f-00c6-4c9f-8aa0-52667938ba70
Reid, Gillian
37d35b11-40ce-48c5-a68e-f6ce04cd4037
Rose, Tim
082b9daf-4f68-4b7a-83d5-2bea8a15660c
Webster, Michael
f26c6e36-cb2e-486e-b2ed-b0d25a3a71f7
Davis, Martin F.
72f26f03-4bbe-482e-b8a5-6c792b22fcc3
Levason, William
e7f6d7c7-643c-49f5-8b57-0ebbe1bb52cd
Ratnani, Raju
0a86c56f-00c6-4c9f-8aa0-52667938ba70
Reid, Gillian
37d35b11-40ce-48c5-a68e-f6ce04cd4037
Rose, Tim
082b9daf-4f68-4b7a-83d5-2bea8a15660c
Webster, Michael
f26c6e36-cb2e-486e-b2ed-b0d25a3a71f7

Davis, Martin F., Levason, William, Ratnani, Raju, Reid, Gillian, Rose, Tim and Webster, Michael (2006) Synthesis and characterisation of WVI complexes of phosphane oxide ligands, [WO2X2(OPR3)2] (X = F, Cl or Br; R = Me or Ph), and of the [MoO2F2(OPR3)2]. European Journal of Inorganic Chemistry, 2007 (2), 306-313. (doi:10.1002/ejic.200600823).

Record type: Article

Abstract

Phosphane oxide complexes of dioxidotungstenVI, [WO2X2(OPR3)2] (X = Cl or Br, M = Ph or Me) have been prepared under anhydrous conditions from the reaction of WX6 with (Me3Si)2O in CH2Cl2, followed by addition of OPR3. Some diphosphane dioxide analogues have been made similarly, viz, [WO2X2(L-L)] {L-L = Ph2P(O)(CH2)nP(O)Ph2 (n = 1 or 2), o-C6H4[P(O)Ph2]2}. The complexes have been characterised by elemental analysis, IR and NMR (1H and 31P{1H}) spectroscopy, and the structures of [WO2Br2(OPPh3)2] and [WO2Cl2(OPMe3)2] determined, revealing distorted six-coordinate tungsten centres with cis-WO2 and trans-WX2 units. The difluorido-dioxido complexes [MO2F2(OPR3)2] (M = Mo or W) and [WO2F2(L-L)] (L-L = 2,2-bipyridyl, 1,10-phenanthroline) have been prepared by fluorination of the corresponding chlorido complexes with Me3SnF in CH2Cl2. These are characterised similarly and by 19F{1H} NMR spectroscopy. Attempts to make [MO2I2(OPR3)2] were unsuccessful. No adduct formation occurs between CrO2Cl2 and OPPh3 under rigorously anhydrous conditions. Crystal structures of [Me3SnCl(OPPh3)] and two forms of [WO2Cl2(1,10-phen)] are also reported and discussed.

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Published date: 14 November 2006
Organisations: Chemistry

Identifiers

Local EPrints ID: 147007
URI: http://eprints.soton.ac.uk/id/eprint/147007
ISSN: 1434-1948
PURE UUID: 6c2f4169-804f-4cca-a2d1-f73d17b7efa9
ORCID for William Levason: ORCID iD orcid.org/0000-0003-3540-0971
ORCID for Gillian Reid: ORCID iD orcid.org/0000-0001-5349-3468

Catalogue record

Date deposited: 03 Jun 2010 11:26
Last modified: 17 Sep 2019 01:11

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