Metal-containing ligands

By far the most important metal containing dyes are derived from OjO-dUiydroxyazo stmctures in which one of the two azo nitrogen atoms and the two hydroxyl oxygen atoms are involved in bonding with the metal ion. Thus these dyes serve as terdentate ligands. In the case of metal ions with a coordination number of four, eg, Cu(H), the fourth position is usuaUy occupied by a solvent molecule (47). 

Bis(phosphonio)isophosphindolium cations were expected to act as attractive ambidentate ligands toward the transition-metal-containing moieties. These expectations did not materialize with respect to CpM(CO)3 (M = Mo, W), since the anionic metathesis occurred to yield the ionic products 178 (96PSS125). 

In principle, any molecule or anion with an unshared pair of electrons can act as a Lewis base. In other words, it can donate a lone pair to a metal cation to form a coordinate covalent bond. In practice, a ligand usually contains an atom of one of die more electronegative elements (C, N, O, S, F, Cl, Br, I). Several hundred different ligands are known. Those most commonly encountered in general chemistry are NH3 and HzO molecules and CN , Cl-, and OH- ions. 

The nature of the donor atoms in the chelating agent. Ligands which contain donor atoms of the soft-base type form their most stable complexes with the relatively small group of Class B metal ions (i.e. soft acids) and are thus more selective reagents. This is illustrated by the reagent diphenylthiocarbazone (dithizone) used for the solvent extraction of metal ions such as Pd2+, Ag+, Hg2+, Cu2+, Bi3+, Pb2+, and Zn2 +. ... 

Ruthenium probably forms more nitrosyl complexes [115] than any other metal. Many are octahedral Ru(NO)Xs systems, where X5 can represent a combination of neutral and anionic ligands these contain a linear (or very nearly) Ru-NO grouping and are regarded as complexes of ruthenium(II). They are often referred to as (Ru(NO) 6 systems. 

Recently some information became available on a new type of highly active one-component ethylene polymerization catalyst. This catalyst is prepared by supporting organometallic compounds of transition metals containing different types of organic ligands [e.g. benzyl compounds of titanium and zirconium 9a, 132), 7r-allyl compounds of various transition metals 8, 9a, 133), 7r-arene 134, 185) and 71-cyclopentadienyl 9, 136) complexes of chromium]. 

The scope of the present paper is limited to those cyclopentadienyl ligands that contain more than two bulky substituents and transition metal complexes derived thereof in order to be able to focus on the specific effects of these ligand systems. A selection of some mono-substituted cyclopentadienyl ligands will be treated also. Among the numerous reviews highlighting special aspects of cyclopentadienyl... 

Can a chiral catalyst containing the same ligand/metal components promote the formation of both enantiomers enantioselectively The bis(oxazoline)magnesium perchlorate-catalyzed asymmetric Diels-Alder reaction [103]... 

Simple alkyl and aryl cr-bonded complexes are conveniently prepared by reaction of an alkylating reagent with a halocobalt(II) precursor. All-alkyl systems are rare, but the penta-methylcobaltate(II) anion is known.197 More typically, the coordination sphere of the metal contains additional co-ligands, particularly with P, S, or N donors. Some examples that reflect the style of reactions extant appear below. 

The hydroformylation of styrene using rhodium systems containing the four structurally related diphosphines dppe, dppp, (86), and (87) has been studied. A systematic analysis of the effect of the pressure, temperature, and the ligand metal molar ratio shows that the five- and six-membered ring chelating diphosphines behave differently from one another.347 An analysis of the effect of pressure, temperature, and ligand metal molar ratio on the selectivity of styrene hydroformylation catalyzed... 

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