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An unpaired electron has a magnetic dipole moment, while an electron pair has no dipole moment because the two electrons have opposite spins so their magnetic dipole fields are in opposite directions and cancel. Thus an atom with unpaired electrons acts as a magnetic dipole and interacts with a magnetic field. Only elements with unpaired ...
The manganese (Mn) atom has a 3d 5 electron configuration with five unpaired electrons all of parallel spin, corresponding to a 6 S ground state. [4] The superscript 6 is the value of the multiplicity, corresponding to five unpaired electrons with parallel spin in accordance with Hund's rule.
Octahedral low-spin: 2 unpaired electrons, paramagnetic, substitutionally inert. d 5 High-spin [Fe(NO 2) 6] 3− crystal field diagram Low-spin [Fe(NO 2) 6] 3− crystal field diagram Octahedral high-spin: 5 unpaired electrons, paramagnetic, substitutionally labile. Octahedral low-spin: 1 unpaired electron, paramagnetic, substitutionally inert.
Each has two electrons of opposite spin in the π* level so that S = 0 and the multiplicity is 2S + 1 = 1 in consequence. In the first excited state, the two π* electrons are paired in the same orbital, so that there are no unpaired electrons. In the second excited state, however, the two π* electrons occupy different orbitals with opposite spin.
The multiplicity is equal to + , where is the total spin angular momentum for all electrons. The multiplicity is also equal to the number of unpaired electrons plus one. [ 4 ] Therefore, the term with lowest energy is also the term with maximum S {\displaystyle S\,} and maximum number of unpaired electrons with equal spin angular momentum ...
With one unpaired electron μ eff values range from 1.8 to 2.5 μ B and with two unpaired electrons the range is 3.18 to 3.3 μ B. Note that low-spin complexes of Fe 2+ and Co 3+ are diamagnetic. Another group of complexes that are diamagnetic are square-planar complexes of d 8 ions such as Ni 2+ and Rh + and Au 3+.
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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.