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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 ...
The metal also has six valence orbitals that span these irreducible representations - the s orbital is labeled a 1g, a set of three p-orbitals is labeled t 1u, and the d z 2 and d x 2 −y 2 orbitals are labeled e g. The six σ-bonding molecular orbitals result from the combinations of ligand SALCs with metal orbitals of the same symmetry.
Thus aquo complex ([Fe(H 2 O) 6] 3+ has only five unpaired electrons. It is high-spin. With chloride, iron(III) forms tetrahedral complexes, e.g. ([Fe(Cl) 4] −. Tetrahedral complexes are high spin. The magnetism of ferric complexes can show when they are high or low spin.
Low-spin [Fe(NO 2) 6] 3− crystal field diagram. The Δ splitting of the d orbitals plays an important role in the electron spin state of a coordination complex. Three factors affect Δ: the period (row in periodic table) of the metal ion, the charge of the metal ion, and the field strength of the complex's ligands as described by the spectrochemical series.
A d 1 octahedral metal complex, such as [Ti(H 2 O) 6] 3+, shows a single absorption band in a UV-vis experiment. [7] The term symbol for d 1 is 2 D, which splits into the 2 T 2g and 2 E g states. The t 2g orbital set holds the single electron and has a 2 T 2g state energy of -4Dq.
Mössbauer spectrum of Fe 2 (C 2 O 4) 3 · 4 H 2 O exhibits an isomer shift of 0.38 mm/s and a quadrupole splitting of 0.40 mm/s, suggesting a high spin Fe 3+ in octahedral coordination. [ 1 ] [ 2 ] Production
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.
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.