Coordination spheres optical

Although they are built from the same numbers and kinds of atoms, structural isomers have different chemical formulas, because the formulas show how the atoms are grouped in or outside the coordination sphere. Stereoisomers, on the other hand, have the same formulas, because their atoms have the same partners in the coordination spheres only the spatial arrangement of the ligands differs. There are two types of stereoisomerism, geometrical and optical. 

In the skeleton of many chelating diphosphines, the phosphorus atoms bear two aryl substituents, not least because the traditional route to this class of compounds involves the nucleophilic substitution with alkali metal diarylphosphides of enantiopure ditosylates derived from optically active natural precursors, approach which is inapplicable to the preparation of P-alkylated analogs. The correct orientation of these aryl substituents in the coordination sphere has been identified as a stereo chemically important feature contributing to the recognition ability of the metal complex [11,18-20]. 

Oligomerization and polymerization of terminal alkynes may provide materials with interesting conductivity and (nonlinear) optical properties. Phenylacetylene and 4-ethynyltoluene were polymerized in water/methanol homogeneous solutions and in water/chloroform biphasic systems using [RhCl(CO)(TPPTS)2] and [IrCl(CO)(TPPTS)2] as catalysts [37], The complexes themselves were rather inefficient, however, the catalytic activity could be substantially increased by addition of MesNO in order to remove the carbonyl ligand from the coordination sphere of the metals. The polymers obtained had an average molecular mass of = 3150-16300. The rhodium catalyst worked at room temperature providing polymers with cis-transoid structure, while [IrCl(CO)(TPPTS)2] required 80 °C and led to the formation of frani -polymers. 

Molecules in the second coordination sphere, that is, solvent or partners of an ion pair, can transfer charge to the metal ion of a coordination complex in an optically induced electronic transition. The excited states are, respectively, known as solvent to metal charge transfer (SMCT) and ion pair charge transfer (IPCT) excited states. A typical example are the ion pairs, [Cora(NH3)6]3 +, X-, formed between [Coln(NH3)6]3 + and halide and pseudohalide ions X. The UV-Vis spectrum of ion... 

In such an approach, kinetic and thermodynamic aspects and the position of the asymmetric element in the complex are of minor importance. So far the number of examples which show the properties mentioned above is very small. The optical yield in most examples of asymmetric synthesis in the coordination sphere of a metal is more or less an empirical result. 

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