Cluster compounds mixed

Many novel cluster compounds have now been prepared in this way, including mixed metal clusters. Further routes involve the oxidative fusion of dicarbon metallacarborane anions to give dimetal tetracarbon clusters such as (103) and (104) O (jjg insertion of isonitriles into inetallaborane clusters to give monocarbon meiallacarboranes such as (105) and the reaction of small ii/t/o-carboranes with alane adducts such as Et3NAlH3 to give the commo species (106) ... 

The Au(I)-Au(I) distance of 330.1 pm is longer than in metallic Au (288 pm), and in view of the d configuration in Au(I) compounds, such structures as V arise by packing factors in the solid rather than by metal-metal bonding (see 8.2.2.3). Similarly long Au—Au bonds are found in other Au(I) compounds and in mixed Au(I)-Au(III) compounds. Many other cluster compounds are known . 

Magnetic field effects on the reaction kinetics or yields of photochemical reactions in the condensed phase have been studied [20-23]. They have proved powerful for verifying the mechanism of photochemical reactions including triplet states. Previously, we obtained photogenerated triplet biradicals of donor-acceptor linked compounds, and found that the lifetimes of the biradicals were remarkably extended in the presence of magnetic fields up to 1T [24]. It has been reported that Cgo and its derivatives form optically transparent microscopic clusters in mixed solvents [25,26]. The clustering behavior of fullerene (C o) is mainly associated with the strong three-dimensional hydrophobic interactions between the C o units. Photoinduced... 

The interactions of NO with the iron-sulfur cluster moieties of several enzymes generate iron-sulfur-nitrosyl cluster compounds [156]. However, synthetic nitrosyl clusters such as Roussins black salt (RBS), Roussins red salt (RRS), Roussins red ester (RRE) and [FeNOS]4 (Fig. 5.3) are well known [129, 157] and can be synthesized easily [158-164]. For example, the RBS can be prepared by mixing FeS04 with NaN03 and (NH4)2S in aqueous solution [158]. RRE salts are generally insoluble in water, but recently the water soluble sulfonated derivative, Na2[Fe2(SCH2CH2S03)2(N0)4], has been prepared [165]. 

We have restricted the discussion in the section primarily to mixed carbonyl, carbonyl-hydride, or phosphine-substituted cluster compounds. On the basis of electronegativity, there should be an enhance-... 

Unusual mixed cluster compounds of the type [RuPt2(CO)5L3] and [Ru2Pt(CO),U] (L = PPh3, PMePh2, PMejPh, or AsPh3 = PMejPh) have been prepared via the addition of Ru3(CO)j2 to PtC. The structures (2) and (3) were proposed from i.r. studies. These clusters join a growing number... 

Electric fleld gradient, 22 214-218 Electroabsorption spectroscopy, 41 279 class II mixed-valence complexes, 41 289, 291, 294-297 [j(jl-pyz)]=+, 41 294, 296 Electrocatalytic reduction, nickel(n) macro-cyclic complexes, 44 119-121 Electrochemical interconversions, heteronuclear gold cluster compounds, 39 338-339 Electrochemical oxidation, of iron triazenide complexes, 30 21 Electrochemical properties fullerene adducts, 44 19-21, 33-34 nickeljll) macrocyclic complexes, 44 112-113... 

There are several interesting families of inorganic mixed-valence compounds that we have not discussed here (see Yvon, 1979 McCarley, 1982). For example, there are metal-cluster compounds such as the Chevrel phases, M,jMo6X8(X = S or Se) and condensed metal-cluster chain compounds such as TlMojScj, TijTe, NaMo O and M PtjO. TTF halides and TTF-TCNQ complexes (Section 1.9) constitute molecular mixed-valent systems in which the mixed valency is associated with an entire molecule the charge on TTF in such compounds is nonintegral. The structure of TTF-Br(, 79 and... 

Dialkylzinc derivatives are inert towards conjugated enones (e.g. 181) in hydrocarbon or ethereal solvents. The discovery that a conjugate addition can be promoted by Cu(I) salts in the presence of suitable ligands L (e.g. sulphonamide 182) opened a new route to zinc enolates (e.g. 183), and hence to the development of three-component protocols, such as the tandem 1,4-addition/aldol addition process outlined in equation 92186. If the addition of the aldehyde is carried out at —78 °C, the single adduct 184 is formed, among four possible diastereomeric products. The presence of sulphonamide is fundamental in terms of reaction kinetics its role is supposed to be in binding both Cu(I) and Zn(II) and forming a mixed metal cluster compound which acts as the true 1,4-addition catalyst. 

Ketenyl complexes, in Ru-Os mixed-metal clusters, 6, 1080 Ketenylidenes, in iron cluster compounds, 6, 301 Ketenylidenetriphenylphosphoranes, with platinum, 8, 632 Ketimines... 

A few illustrative examples dealing with bimetallic cluster compounds will now be presented. For example, mixed cluster compounds [MjRu -CO CO qCPPI J where M = Cu, Ag, and Au have been prepared and structurally characterized. ) Metal core structures consist of a Ru4 tetrahedron with M-PPh3 groups capping two... 

The possibility of coordination of a two-electron ligand, in addition to arene, to the ruthenium or osmium atom provides a route to mixed metal or cluster compounds. Cocondensation of arene with ruthenium or osmium vapors has recently allowed access to new types of arene metal complexes and clusters. In addition, arene ruthenium and osmium appear to be useful and specific catalyst precursors, apart from classic hydrogenation, for carbon-hydrogen bond activation and activation of alkynes such compounds may become valuable reagents for organic syntheses. 

---