Different coordination modes of a tripod phosphine in gold(i) and silver(i) complexes

The following gold(I) and silver(I) complexes of the tritertiary phosphine 1,1,1- tris(diphenylphosphinomethyl)ethane, tripod , have been synthesised: Au(3)(tripod)X(3) [X = Cl(1), Br(2), I(3)]; [Au(3)(tripod)(2)Cl(2)]Cl (4); Au(tripod)X [X = Br(5), I(6)]; Ag(3)(tripod) (NO(3))(4) (7), Ag(tripod)NO(3) (8). They were characterized by X-ray diffraction (complexes 2, 3 and 4), (31)P NMR spectroscopy, electrospray and FAB mass spectrometry and infrared spectroscopy. Complexes 2 and 3 show a linear coordination geometry for Au(I), with relatively short Au-P bond distances. Complex 3 has a Au***Au intramolecular distance of 3.326 A degrees , while complex 2 had a short Au***Au intermolecular interaction of 3.048 A degrees . Complexes 4-6 were found by (31)P NMR spectroscopy studies to contain a mixture of species in solution, one of which crystallised as [Au(3)(tripod|)(2)Cl(2)]Cl which was shown by X-ray diffraction to contain both tetrahedral and linear Au(I), the first example of a Au(I) complex containing such a mixture of geometries. The reaction of [Au(3) (tripod)Cl(3)] (1) with tripod led successfully to the formation of [Au(3)(tripod|)(2)Cl(2)](+) and [Au(3)(tripod)(2)Cl(3)](+) and [Au(3)(tripod|)(3)Cl](2+). The silver(I) complexes, 7 and 8 appear to contain linear and tetrahedral Ag(I), respectively.     

Electronic and steric effects in gold(i) phosphine thiolate complexes

The unusual yellow color of Au(2)(dppm)(SR)(2) (R = 4-tolyl; dppm = diphenylphosphinomethane) is attributed to a red-shift in the S-->Au charge transfer caused by destabilization of the sulfur highest occupied molecular orbital (HOMO). Variable temperature experiments show two broad bands at -80 degrees C in the (31)P{(1)H} NMR spectrum of Au(2)(dppm)(SR)(2) and the activation energy for interconversion is 10 kcal/mol. Only one sharp band is observed down to -80 degrees C in the spectrum of the white complex, Au(2)(dppe)(SR)(2) (dppe = diphenylphosphinoethane). Molecular mechanics calculations on Au(2)(dppm)(SR)(2) and Au(2)(dppe)(SR)(2) reveal that, for Au(2)(dppe)(SR)(2), a series of maxima and minima, separated by 2.5 kcal/mol, occur every 120 degrees which is consistent with rotation around an unhindered carbon-phosphorus single bond. The Au atoms are not within bonding distance in any conformation. Computational results for Au(2)(dppm)(SR)(2) indicate one minimum energy structure in which the Au-P bonds are anti. There is a high energy conformation (9 kcal/mol above the global minimum) where overlap between golds is maximized. The implications of gold-gold bonding in this complex are discussed. The steric influence of the thiolate ligand has been examined by synthesizing a series of dinuclear gold(I) complexes in which the steric properties of the thiolate are varied: Au(2)(dppm)(SR)(2) (R = 2,6-dichlorophenyl; 2,6-dimethylphenyl; 3,5-dimethylphenyl). The 2,6-disubstituted complexes are white, while the 3,5-dimethyl complex is yellow. These results, along with VT-NMR experiments, are consistent with the conclusion that the more sterically-bulky thiolates hinder the close approach of the golds in the dinuclear complexes.     

Anti-arthritic activity in rats of some phosphinegold(i) thionucleobases and related thiolates

A number of phosphinegold(I) thiolates where, generally, the thiolate is derived from a thionucleobase, have been screened for anti-arthritic activity in Dark Agouti rats, a gold sensitive model for arthritis. Potency and toxicity data showed that, generally, the Ph(3)P derivatives and species based on thiopurines were the most effective and that with other complexes enhanced activity was accompanied by greater toxicity.     

Antitumor activity of gold(i), silver(i) and copper(i) complexes containing chiral tertiary phosphines

The in vitro cytotoxicities of a number of gold(I), silver(I) and copper(I) complexes containing chiral tertiary phosphine ligands have been examined against the mouse tumour cell lines P815 mastocytoma, B16 melanoma [gold(I) and silver(I) compounds] and P388 leukaemia [gold(I) complexes only] with many of the complexes having IC(50) values comparable to that of the reference compounds cis-diamminedichloroplatinum(ll), cisplatin, and bis[1,2-bis(diphenylphosphino) ethane]gold(I) iodide. The chiral tertiary phosphine ligands used in this study include (R)-(2-aminophenyl)methylphenylphosphine; (R,R)-, (S,S)- and (R(*),R(*))-1,2-phenylenebis(methylphenylphosphine); and (R,R)-, (S,S)- and (R(*),R(*))-bis{(2-diphenylphosphinoethyl)phenylphosphino}ethane. The in vitro cytotoxicities of gold(I) and silver(I) complexes containing the optically active forms of the tetra(tertiary phosphine) have also been examined against the human ovarian carcinoma cell lines 41M and CH1, and the cisplatin resistant 41McisR, CH1cisR and SKOV-3 tumour models. IC(50) values in the range 0.01 - 0.04 muM were determined for the most active compounds, silver(I) complexes of the tetra(tertiary phosphine). Furthermore, the chirality of the ligand appeared to have little effect on the overall activity of the complexes: similar IC(50) data were obtained for complexes of a particular metal ion with each of the stereoisomeric forms of a specific ligand.     

Electronic structure of dinuclear gold(i) complexes

Cyclic voltammetry (CV) experiments on LL(AuSR *)(2) complexes [LL = diphenylphosphinomethane (dppm), diphenylphosphinopentane (dpppn); R(*) = p-SC(6)H(4)CH(3)] show anodic sweeps that broaden by about 25 mV on going from the longer (dpppn) to the shorter (dppm) bidentate phosphine ligand. Changing concentrations had no effect on the shape of the waveform. The result suggests a weak intramolecular metal-metal interaction in dppm(AuSR *)(2) that correlates well with rate acceleration occurring in the reaction of dppm(AuSR *)(2) with organic disulfides. Quantum yields for cis-dppee(AuX)(2) [dppee = 1,2-bis(diphenylphosphino)ethylene; X = Cl, Br, I] complexes, (disappearance) Phi , are significantly higher in complexes with a softer X ligand, a trend that correlates well with aurophilicity. This result also suggests that electronic perturbation caused by Au(I)-Au(I) interactions is important in explaining the reactivity of some dinuclear gold(I) complexes. The crystal structure for cis-dppee(Aul)(2) shows short intramolecular Au(I)-Au(I) interactions of 2.9526 (6) A degrees , while the structure of trans-dppee(AuI)(2) , shows intermolecular Au(I)-Au(I) interactions of 3.2292 (9) A degrees . The substitution of .As for P results in a ligand, cis-diphenylarsinoethylene (cis-dpaee), that is photochemically active, in contrast to the cis-dppee ligand. The complexes, cis-dpaee(AuX)(2), are also photochemically active but with lower quantum yields than the cis-dppee(AuX)(2) complexes.     

Reactions of organic disulfides and gold(i) complexes

Gold-thiolate/disulfide exchange reactions of (p-SC(6)H(4)Cl)(2) with Ph(3)PAu(SC(6)H(4)CH(3)), dppm(AuSC(6)H(4)CH(3))(2), and dppe(AuSC(6)H(4)CH(3)) (2) were investigated. The rate of reactivity of the gold-thiolate complexes with (p-SC(6)H(4)Cl)(2) is: dppm(AuSC(6)H(4)CH(3))(2)> dppe(AuSC(6)H(4)CH(3))(2)>Ph(2)PAu (SC(6)H(4)CH(3)). This order correlates with conductivity measurements and two ionic mechanisms have been evaluated. (1)H NMR experiments demonstrate that in the reaction of dppm(AuSC(6)H(4)CH(3))(2) with (p-SC(6)H(4)Cl)(2), the mixed disulfide, ClC(6)H(4)SSC(6)H(4)CH(3), forms first, followed by the formation of (p-SC(6)H(4)CH(3))(2). The rate law is first order in (pp-SC(6)H (4)Cl)(2) and partial order in dppm(AuSC(6)H(4)CH(3))(2). Results from electrochemical and chemical reactivity studies suggest that free thiolate is not involved in the gold-thiolate/disulfide exchange reaction. A more likely source of ions is the dissociation of a proton from the methylene backbone of the dppm ligand which has been shown to exchange with D(2)O. The implications of this are discussed in terms of a possible mechanism for the gold-thiolate/disulfide exchange reaction.     

Structures of gold(i) and silver(i) thiolate complexes of medicinal interest: a review and recent results

We review the crystal structures, electrospray ionization mass spectra (ESI-MS) data and chiral HPLC data for the racemic and optically pure mononuclear AuL2 complexes, and for racemic [AuLI]n and optically pure [AgLII]n polymers (LI = thiomalate, LII = D-penicillamine). We postulate an equilibrium between polymeric, mononuclear and free ligand species for [AuLII]n (gold sodium thiomalate or GST). The ESI-MS results clearly show a tetrameric principal species in the 1:1 gold polymers, [AuLI]n. For the 1:1 silver: D-penicillamine complex, [AgLII]n, a non-molecular crystal of double helical structure, the ESI-MS results show multi-ligand-silver species, including tetramers, pentamers and hexamers. Other, relevant gold, silver and copper complexes are compared.     

Redox chemistry of H2S oxidation by the British gas Stretford process part V: Aspects of the process chemistry

Stretford processes use air to oxidize H₂S in process and natural gases to elemental sulphur, by absorption in aqueous solution at about pH 9 and reaction of the resulting HS^– ions with dissolved oxygen, in the presence of anthraquinone disulphonates (AQDS) and vanadium (v) species, which act as catalysts. Kinetic measurements of the reactions (AQ27DS + HS^– ions), (V(v) + HS^– ions) and (AQ27DSH^– + O₂), primarily used stopped flow spectrophotometry, as reported here, following papers on the electrochemical behaviour of the individual redox couples in Stretford Processes. The course of reaction (AQ27DS + HS^– ions) was also followed with a gold bead indicator electrode, the potential of which was determined essentially by the AQ27DS/AQ27DSH^– couple as the former species were reduced to the latter. Attempts to use⁵¹V NMR to characterize aqueous vanadium-sulphur complexes were inconclusive. A possible mechanism for Stretford Processes is postulated, involving polysulphide (S _n ^2–) ions as intermediates, which are oxidized to elemental sulphur by another intermediate, H₂O₂, formed by reaction of AQ27DSH^– ions and dissolved oxygen.     

相转移催化氧化合成双(对羧苯基)苯基氧化膦

以双(对甲苯基)苯基硫化膦为原料,高锰酸钾为氧化剂,通过相转移催化氧化反应合成了标题化合物,并采用DSC、红外光谱、核磁共振等对结构进行了表征.     

Redox chemistry of H2S oxidation by the British Gas Stretford process part IV: V-S-H2O thermodynamics and aqueous vanadium (v) reduction in alkaline solutions

The thermodynamics of V-H₂O and V-S-H₂O systems at 298 K are summarized in the form of potential-pH and activity-pH diagrams calculated from recently published critically assessed standard Gibbs energies of formation. At pH 9, as used in Stretford Processes, V-H₂O potential-pH diagrams predicted that the V(v)/V(iv) couple involves HV₂O₇ ^3–/V₄O₉ ^2– ions. However, in neutral and alkaline solutions there is difficulty in discriminating between kinetic intermediates and thermodynamically stable solution species, some with V(v)/V(iv) mixed oxidation states. Hence, V₁₈O₄₂ ^12– ions may be the stable V(iv) species, depending on the concentration, though no thermodynamic data are available to enable them to be included in potential-pH calculations. Potential-pH diagrams for V-S-H₂O systems predicted an area of stability for VS₄ in the pH range 2–8 and over a restricted potential range; neither VS nor VS₂ were predicted to be stable under any conditions considered. In cyclic voltammetric experiments at Hg, Au and vitreous carbon electrodes, reduction of vanadium (v) species (probably HV₂O₇ ^3– ions) was found to be irreversible on a variety of electrode surfaces and, at lower potentials, led predominantly to the formation of solid oxide films (V₃O₅, V₂O₃ and VO) rather than to V(iv) solution species, of which V₁₈O₄₂ ^12– ions probably predominate at equilibrium. In the presence of the large excess of HS^– ions required to form VS₄ ^3– ions, the electrochemical behaviour of a gold electrode was dominated by the former species.     

Redox chemistry of H2S oxidation by the British Gas Stretford Process Part. II: Electrochemical behaviour of aqueous hydrosulphide (HS−) solutions

Electrochemical techniques were used to study the oxidation of HS^– ions at pH 9.3. Voltammetry of gold electrodes in HS^– -containing solutions showed that multilayers of sulphur and soluble oxidation products were formed. As a known HS^– oxidation product, thiosulphate solutions were also studied voltammetrically, but found to be electro-inactive at mildly oxidising potentials. The voltammetric behaviour of polysulphide ions, S _n ^2– (n = 2 to 5), was similar to that of HS^– solutions on oxidation, though they could be reduced to HS^– ions at low potentials. Ring-disc electrode experiments, extending the HS^– concentration range that had been studied previously, confirmed that polysulphide ions were produced on reduction of anodically deposited elemental sulphur. This was demonstrated in both cyclic Volammetry and potential step experiments. By comparison of the charges passed producing polysulphides from sulphur and reducing them to HS^– ions, an average polysulphide chain length of 1.8 was calculated, indicating a mixture of species was produced. Ion chromatography confirmed that polysulphide solutions do contain a number of species, consistent with thermodynamic predictions.     

Redox chemistry of H2S oxidation in the British Gas Stretford Process Part I: Thermodynamics of sulphur-water systems at 298 K

The thermodynamics of aqueous sulphur-water systems are summarized in the form of potential-pH diagrams, calculated from recently reported critically assessed standard Gibbs energies of formation of the species considered. However, there is convincing evidence from the literature that a value of pK _a(HS^–) = 17–19 is appropriate, whereas a value of 13 is widely accepted; hence, the higher value of 19, corresponding to G _f ⁰ (S^2–) = 120.5 kJ mol^–1 , was used in these calculations, rather than G _f ⁰ (S2-) = 86.31 kJ mol^–1 quoted in the main data source.Under ambient conditions, only – 2 (sulphide), 0 (elemental sulphur) and + 6 (sulphate) oxidation states are thermodynamically stable in water, which is predicted to be oxidized by peroxodisulphate (H₂ S₂ O₈/SO ₈ ^2– and peroxomonosulphate (HSO ₅ ^– /SO ₅ ^2– ). However, when sulphate is excluded from the calculations to allow for the large energy of activation/slow kinetics of its formation from sulphide, then other sulphoxy species appear on the diagram for what is then a metastable system. Similarly, if all sulphoxy species (i.e. any species with oxidation states > 0) are excluded, then polysulphide ions (S _n ^2– , 2 n 5) have areas of predominance at high pH, each with a narrow potential window of predominance. Hence, this information is complemented with S _n ^2– /HS^– activity-potential diagrams at pH 9 and 14.Some species have no area of stability even on the metastable diagrams. Hence, potential-pH diagrams are also presented for the sulphite-dithionite system (excluding elemental sulphur), and that involving peroxomonosulphate (HSO ₅ ^– /SO ₅ ^2– ) in place of peroxodisulphate (H₂S₂O₈/SO ₈ ^¨– ).     

单体三(4-氟苯基)膦氧化物和三(4-羟基苯基)膦氧化物的新合成方法

以4-氟溴苯和三氯氧磷为起始原料,经格氏反应可直接合成三官能团单体三(4-氟苯基)膦氧化物(TFPPO),该单体进一步与氢氧化钾反应可得到三(4-羟基苯基)膦氧化物(TOHPPO)。该合成方法安全、简便,利于实际应用中扩大规模生产。     

The selective adsorption of gold (III) and palladium (II) on new phosphine sulphide-type chelating polymers bearing different spacer arms: Equilibrium and kinetic characterisation

New resins, with a functional group based on triisobutyl phosphine sulphide and containing different spacer arms between the polymeric matrix and the functional group, are evaluated in order to determine and characterise the mechanism of the metal adsorption process. These polymers are selective towards gold and palladium from other noble (Pt, Rh and Ir) and base (Fe, Cu, Ni and Zn) metals. Selectivity is higher in the case of gold (2.8 mmol Au/g resin for polymer 3 and 6.5 for polymer 4) than for palladium (0.5 mmol Pd/g resin for polymer 3 and 0.7 for polymer 4). The application of the Langmuir model to the data permits the determination of the adsorption mechanism, which we found to be a chelating process. The result shows that spacer heteroatoms become involved in the adsorption process. The kinetics of the adsorption is faster for palladium than for gold. The elution of these two metals is accomplished by the use of sodium nitrite and thiourea as eluting compounds.     

Redox chemistry of highly dispersed rhodium in zeolite NaY

NaY zeolite exchanged with [Rh(NH₃)₅Cl]²⁺ ions have been studied using temperature programmed oxidation (TPO), temperature programmed reduction (TPR), and Fourier transformed infrared spectroscopy. The TPO profiles show that ammine ligands in NaY encaged [Rh(NH₃)₅Cl]²⁺ are destroyed above 300 °C, whereas the Rh precursor ion remains intact after calcination at 200 °C. TPR profiles in conjunction with the CO_ads IR spectra show that the reducibility of Rh by H₂ is largely controlled by the concentration of the surface protons, i.e. Rh³⁺+H₂Rh⁺+2H⁺ Rh⁺ + 1/2H₂Rh⁰+H⁺ In the presence of ammonia, the protons are neutralized and Rh³⁺ is reduced to Rh⁰. However, reduction remains incomplete when the concentration of protons is high. The ammonia was provided either by NH₃ admission or by conservation of ammine ligands by controlled calcination. CO adsorption does not lead to reoxidation of Rh⁰ particles to Rh⁺ ions.