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In octahedral complex

Similarity with cobalt is also apparent in the affinity of Rh and iH for ammonia and amines. The kinetic inertness of the ammines of Rh has led to the use of several of them in studies of the trans effect (p. 1163) in octahedral complexes, while the ammines of Ir are so stable as to withstand boiling in aqueous alkali. Stable complexes such as [M(C204)3], [M(acac)3] and [M(CN)5] are formed by all three metals. Force constants obtained from the infrared spectra of the hexacyano complexes indicate that the M--C bond strength increases in the order Co < Rh < [r. Like cobalt, rhodium too forms bridged superoxides such as the blue, paramagnetic, fCl(py)4Rh-02-Rh(py)4Cll produced by aerial oxidation of aqueous ethanolic solutions of RhCL and pyridine.In fact it seems likely that many of the species produced by oxidation of aqueous solutions of Rh and presumed to contain the metal in higher oxidation states, are actually superoxides of Rh . ... [Pg.1127]

Octahedral To understand how geometric isomerism can arise in octahedral complexes, refer back to Figure 15.4. Notice that for any given position of a ligand, four other positions are at the same distance from that ligand, and a fifth is at a greater distance. [Pg.415]

Give the number of unpaired electrons in octahedral complexes with strong-field ligands for... [Pg.427]

Rate parameters for ligand replacement processes in octahedral complexes of metals in oxidation state three. J. O. Edwards, F. Monacelli and G. Ortaggi, Inorg. Chim. Acta, 1974,11,47-104 (368). [Pg.66]

In octahedral complexes, the e -orbitals (dz< and dx2 -yi) lie higher in energy than the t2 -orbitals (dxy, dyz, and dzx). The opposite is true in a tetrahedral complex, for which the ligand field splitting is smaller. [Pg.802]

We are now ready to apply the ideas in the preceding three sections to the construction of molecular orbitals in octahedral complexes. [Pg.107]

At this point, it is appropriate to mention some of the evidence that indicates a trans effect in octahedral complexes, but only a brief description will be given. In the reaction of Mo(CO)6 with pyridine, only three CO ligands undergo replacement, and the product has the structure... [Pg.724]

In addition to the indications of an octahedral trans effect presented, there exists structural information in the form of bond lengths and spectral data similar to that described earlier for square planar complexes. Although the trans effect in octahedral complexes is not the dominant influence that it is in square planar complexes, there is no doubt that there is such an effect. [Pg.725]

The molecular orbital model can also be applied to complexes of the d-block elements. In octahedral complexes the d-orbitals of the metal are not degenerate, as they are in the free metal, because of the interaction between the ligand and metal orbitals. The five d-orbitals are split into three t2g (nonbonding) and two e (antibonding) MOs that is ... [Pg.11]


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See also in sourсe #XX -- [ Pg.108 ]

See also in sourсe #XX -- [ Pg.108 ]




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Bond Lengths in Octahedral Complexes

Bonding in Octahedral Complexes

Configurational in octahedral complexes

Crystal field splitting in octahedral complexes

Crystal field theory d-orbital splitting in octahedral and tetrahedral complexes

D Orbitals in octahedral complexes

Electron configuration in octahedral complexes

Field Splitting in Octahedral Complexes

Geometric isomerism, in octahedral complexes

Group theoretical aspects of band intensities in octahedral complexes

Isomerism in octahedral complexes

Isomerization in octahedral complexes

Lability and Inertness in Octahedral Complexes

Ligand substitution in octahedral complexes

Molecular orbitals in octahedral complexes

Nucleophilic substitution in octahedral complexes

Rates of water exchange in octahedral aqua complexes

Stereoisomerism in Octahedral Complexes

Substitution and racemization in octahedral complexes

Substitution reactions in octahedral complexes

Trans effect in octahedral complexes

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