Metal clusters phosphine reactions

The first mixed-metal cluster of Os-Pd, [Os6Pd(bipy)(CO)i8], was reported in 1994, and since then a variety of mixed-metal cluster that contain various Os Pd ratios have been created. Palladium-pyridine complexes appear to be useful reagents in the synthesis of mixed-metal clusters with osmium carbonyl compounds. " The reaction of the coordinately unsaturated cluster [Os3(yu-H)2(CO)io] with [Pd(NH3)2l2] afforded a number of Os-Pd clusters with a high hydride content. " Both palladium phosphine and bidentate phosphine complexes are useful in the preparation of high-nuclearity mixed-metal clusters. The reaction of [Os3(/i-H)2(CO)io] with [Pd2(/i-dppm)2Cl2] gave 258 and 259, in addition to 260, with the same metal core, " in which the molecule contains a twofold symmetry axis. " " ... 

Syntheses in which a reaction of a mononuclear metal complex precursor gives a tethered metal cluster are rare an early example is the formation of a tetrairidium carbonyl on a phosphine-fimctionaUzed polymer [17]. 

Several mixed-metal clusters containing platinum and cobalt are known and some of them have been employed as methanol homologation catalysts.1 Among them, the title compound2 was first prepared unambiguously from the reaction of dichloro[l,2-ethanediylbis(diphenylphosphine)]platinum with sodium tetracarbonylcobaltate, Na[CO(CO)4]. The compound also may be prepared by the reaction of [l,2-ethanediylbis(diphenyl-phosphine)]bis(phenylethynyl)pIatinum with Co COJg.1... 

It has been found in the meantime that reaction (1) is generalizable (752), and that oxidative additions of this type occur for such widely differing substrates H2Y as ethylene, benzene 130), cyclic olefins, alkyl and aryl phosphines, aniline 337, 406), and H2S 130), ail of which give the same product structure with a triply-bridging Y ligand. The stability of these third-row transition metal clusters has stiU prevented catalytic reactions of these species, but it is likely that similar ones are involved in olefin and acetylene reactions catalyzed by other metal complexes. 

Modified carbonylcobalt complexes can catalyze the PKR. One or more CO can be substituted by phosphines, and these can be immobilized in resins thus giving anchored cobalt complexes (27), that were able to catalyze the reaction of 28 giving 29 with good yield and minor amounts of 30 (Scheme 10) [76]. Other cobalt metal clusters like Co4(CO)i2 [77] or methyl-idynetricobalt nonacarbonyl [78] have exhibited high reactivity in the catalytic PKR. 

Complexes in the 0 oxidation state may be obtained either by reduction of halides such as RuCl2(PPh3)3 with Na or Zn in the presence of CO or other ligands such as RNC, or by reaction of metal carbonyls with phosphines. Reactions of polynuclear carbonyls such as Ru3(CO)12 (Section 18-F-13) with phosphines tend to preserve the cluster structure. 

Although the reactions between alkynes or alkenes and metal clusters are the main source of alkyne-substituted complexes, there are other reagents which can produce similar products. Two such reagents are tetraphenylcyclopentadienone, which in the reaction with Ru3(CO)i2 produces Ru3(CO)10(PhCCPh) (167), and dimethyl-vinylarsine, which has been made to react with several carbonyl clusters [Eq. (8)] (168, 169). In the reaction of M3(CO)12 (M = Ru, Os) with a number of tertiary phosphines and aromatic alcohols, an oxidative addition takes place and benzyne-triosmium compounds are obtained (170-176). The fact that Os3(CO)uPEt3 can be converted into an alkyne compound (177) suggests that the conversion goes through substituted intermediates. Carbene derivatives of clusters have also... 

Similar studies in an organic solvent yielded almost the same product [66]. Nanostructured particles of amorphous carbon-activated palladium metallic clusters have been prepared (in situ) at room temperature by ultrasound irradiation of an organometallic precursor, tris-//-[dibenzylideneacetone]dipalladium [(p-CH= CH-CO-CH=CH-5 )3Pd2] in mesitylene. Characterization studies show that the product powder consists of nanosize particles, agglomerated in clusters of approximately 800 A. Each particle is found to have a metallic core, covered by a carbonic shell that plays an important role in the stability of the nanoparticles. The catalytic activity in a Heck reaction, in the absence of phosphine ligands, has been demonstrated. 

Catalysis by Supported Metal-cluster Compounds. Further work has been reported recently on methods of chemically binding cluster compounds to supports and on the characterization of the resulting materials by various spectroscopic techniques. For example, the reaction of Rh6(CO)i6 with amine- and phosphine-modified silicas has been examined by infrared spectroscopy and has shown that cluster breakdown occurs giving L Rh(CO)2 and Lfn I (CO), where L comprizes the surface attached ligands. This behaviour is similar to that observed with Rh4(CO)i2 on unmodified silica where cluster breakdown occurs readily, particularly in the presence of traces of water and/or oxygen. ... 

The second type includes a functionalized monomer copolymerized with styrene and DVB. For example, j)-bromostyrene may be included in the reaction mixture to provide the desired concentration of functional groups in the support. These groups may eventually be converted into phosphines by reaction with lithium diphenylphosphide. Such resins with low phosphine concentrations are the supports of choice for attachment of monophosphine-substituted metal clusters because the ligands are sparsely and almost randomly distributed in the polymers (5). 

Another area of major interest in the field is that of mixed metal cluster systems. Hieber very early in the study of metal carbonyl chemistry was able to prepare mercury complexes of the type Fe(CO)4(HgCl)2. The related gold ° compounds were prepared in the 1960s by reaction of phosphine gold halides with carbonyl anions. 

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