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Generally, the rates of ligand dissociation from low spin complexes are lower than dissociation rates from high spin complexes. In the case of octahedral complexes, electrons in the e g levels are anti-bonding with respect to the metal-ligand bonds. Famous "exchange inert" complexes are octahedral complexes of d 3 and low-spin d 6 metal ions ...
Spin crossover is sometimes referred to as spin transition or spin equilibrium behavior. The change in spin state usually involves interchange of low spin (LS) and high spin (HS) configuration. [2] Spin crossover is commonly observed with first row transition metal complexes with a d 4 through d 7 electron configuration in an octahedral ligand ...
In an octahedral complex, the molecular orbitals created by coordination can be seen as resulting from the donation of two electrons by each of six σ-donor ligands to the d-orbitals on the metal. In octahedral complexes, ligands approach along the x -, y - and z -axes, so their σ-symmetry orbitals form bonding and anti-bonding combinations ...
In octahedral complexes, the Jahn–Teller effect is most pronounced when an odd number of electrons occupy the e g orbitals. This situation arises in complexes with the configurations d 9, low-spin d 7 or high-spin d 4 complexes, all of which have doubly degenerate ground states.
Fe(acac) 3 is an octahedral complex with six equivalent Fe-O bonds with bond distances of about 2.00 Å. The regular geometry is consistent with a high-spin Fe 3+ core with sp3d2 hybridization. As the metal orbitals are all evenly occupied the complex is not subject to Jahn-Teller distortions and thus adopts a D 3 molecular symmetry.
Due to a smaller crystal field splitting energy, the homoleptic halide complexes of the first transition series are all high spin. Only [CrCl 6] 3− is exchange inert. Homoleptic metal halide complexes are known with several stoichiometries, but the main ones are the hexahalometallates and the tetrahalometallates.
Iron(III) acetylacetonate, Fe(acac) 3, is a red high-spin complex that is highly soluble in organic solvents. It is a high-spin complex with five unpaired electrons. It has occasionally been investigated as a catalyst precursor. [18] Fe(acac) 3 has been partially resolved into its Δ and Λ isomers. [19] The ferrous complex Fe(acac) 2 is ...
In this case, Orgel diagrams are restricted to only high spin complexes. [8] Tanabe–Sugano diagrams do not have this restriction, and can be applied to situations when 10Dq is significantly greater than electron repulsion. Thus, Tanabe–Sugano diagrams are utilized in determining electron placements for high spin and low spin metal complexes.