The dinuclear cyclometallated gold(I) complex [Au2(μ-2-C6F4PPh2)2] was prepared in high yield from the reaction of 2-LiC6F4PPh2 with either [AuBr(AsPh3)] or [AuCl(tht)], and from the reaction of 2-Me3SnC6F4PPh2 with [AuCl(tht)]. The digold(I) complex undergoes oxidative addition reactions with halogens to give the metal-metal bonded dihalodigold(II) complexes [Au2IIX2(μ-2-C6F4PPh2)2] (X = Cl, Br, I), which on warming or exposure to light, isomerise to give the heterovalent gold(I)-gold(III) species [XAu(µ-2-C6F4PPh2)(κ2-2-C6F4PPh2)AuX] containing a four-membered cyclometallated ring on a gold(III) centre. Unlike its protio analogue, [Au2(μ-2-C6F4PPh2)2] did not undergo oxidative addition of methyl iodide or dibenzoyl peroxide. The dihalodigold(II) [Au2IIX2(μ-2-C6F4PPh2)2] and gold(I)-gold(III) compounds [XAu(µ-2-C6F4PPh2)(κ2-2-C6F4PPh2)AuX] (X = Cl, Br) are further oxidised by halogens to give the digold(III) species [Au2X4(μ-2-C6F4PPh2)2] and [X3Au(μ-2-C6F4PPh2)(κ2-2-C6F4PPh2)AuX], respectively. The complexes [Au2X4(μ-2-C6F4PPh2)2] are reduced to the dihalodigold(II) complexes in the presence of one equivalent of zinc powder; further addition of zinc gave the parent digold(I) dimer. Treatment of [Au2IICl2(μ-2-C6F4PPh2)2] and [ClAu(µ-2-C6F4PPh2)(κ2-2-C6F4PPh2)AuCl] with an excess of silver nitrate, benzoate, acetate, trifluoroacetate or triflate gave the corresponding oxyanion complexes. Slow crystallisation of the di(benzoato)digold(II) complex from dichloromethane and methanol gave the parent digold(I) complex derived by reductive elimination. The di(triflato)digold(II) complex behaved similarly, although in this case the novel gold(I) tetramer [Au4(μ-2-C6F4PPh2)4] was formed together with the dimer. Two closely related gold complexes containing the chelating κ2(C,O) phosphine oxide ligand, 2-C6F4P(O)PPh2, were isolated from the reaction of [ClAu(µ-2-C6F4PPh2)(κ2-2-C6F4PPh2)AuCl] with an excess of silver nitrate. The reaction of [Au2IICl2(μ-2-C6F4PPh2)2] with two equivalents of potassium trifluoroethoxide failed to give the corresponding digold(II) bis(alkoxo) complex; instead, reduction took place to form the digold(I) dimer [Au2(μ-2-C6F4PPh2)2]. Treatment of a solution of the di(benzoato)digold(II) complex with C6F5Li gave the pentafluorophenyl complex [Au2(C6F5)2(μ-2-C6F4PPh2)2] which, when heated in toluene, rearranged to the gold(I)-gold(III) complex [(C6F5)Au(µ-2-C6F4PPh2)(κ2-2-C6F4PPh2)Au(C6F5)], analogous to the behaviour of the dihalodigold(II) complexes. The heterovalent, gold(I)-gold(III) dimethyl compound [Au2I,III(CH3)2(μ-2-C6F4PPh2)2] was obtained from the reaction of the di(benzoato)digold(II) complex with dimethylzinc. This compound is structurally similar to its tetraprotio analogue. The cycloaurated dinuclear gold complexes [Au2(μ-C6H3-n-F-2-PPh2)2] (n = 5, 6) were made similarly to the 2-C6F4PPh2 analogue from the appropriate lithium or tin reagents, though in some cases the dimers were formed in admixture with the corresponding gold(I) tetramers. Like their tetrafluoro analogues, the 6-fluoro complexes [Au2X2(μ-C6H3-6-F-2-PPh2)2] (X = Cl, Br, I) rearrange on heating to give the heterovalent gold(I)-gold(III) species [XAu(µ-C6H3-6-F-2-PPh2)(κ2-C6H3-6-F-2-PPh2)AuX]. Thus, the presence of a fluorine atom in place of hydrogen in the 6-position of the bridging aryl group is sufficient to stop the isomerisation of the digold(II) complexes [Au2X2(μ-2-C6H4PPh2)2] at the gold(I)-gold(III) stage and to prevent subsequent C-C coupling of the aryl groups at the gold(III) centre. In contrast, the dihalodigold(II) complexes containing the 5-fluoro substituted ligand undergo reductive elimination and coupling of the metallated aryl groups to give the digold(I) biphenyldiyl complexes [Au2X2(2,2'-Ph2P-5-FC6H3C6H3-5-F-PPh2)] (X = Cl, Br, I). The described complexes were characterised using 1H NMR, 31P NMR, 19F NMR spectroscopy, elemental analysis, mass spectroscopy, IR spectroscopy, X-ray diffraction and 197Au Mössbauer spectroscopy.
Identifer | oai:union.ndltd.org:ADTP/210486 |
Date | January 2008 |
Creators | Mirzadeh, Nedaossadat, s3114476@student.rmit.edu.au |
Publisher | RMIT University. Applied Sciences |
Source Sets | Australiasian Digital Theses Program |
Language | English |
Detected Language | English |
Rights | http://www.rmit.edu.au/help/disclaimer, Copyright Nedaossadat Mirzadeh |
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