Molecular term symbol

In molecular physics, the molecular term symbol is a shorthand expression of the group representation and angular momenta that characterize the state of a molecule, i.e. its electronic quantum state which is an eigenstate of the electronic molecular Hamiltonian. It is the equivalent of the term symbol for the atomic case. However, the following presentation is restricted to the case of homonuclear diatomic molecules, or other symmetric molecules with an inversion centre. For heteronuclear diatomic molecules, the u/g symbol does not correspond to any exact symmetry of the electronic molecular Hamiltonian. In the case of less symmetric molecules the molecular term symbol contains the symbol of the group representation to which the molecular electronic state belongs.

It has the general form:

${\displaystyle {}^{2S+1}\!\Lambda _{\Omega ,(g/u)}^{(+/-)}}$

where

• ${\displaystyle S}$ is the total spin quantum number
• ${\displaystyle \Lambda }$ is the projection of the orbital angular momentum along the internuclear axis
• ${\displaystyle \Omega }$ is the projection of the total angular momentum along the internuclear axis
• ${\displaystyle g/u}$ is the effect of the point group operation ${\displaystyle {\hat {i}}}$
• ${\displaystyle +/-}$ is the reflection symmetry along an arbitrary plane containing the internuclear axis

Λ quantum number

For atoms, we use S, L, J and M_J to characterize a given state. In linear molecules, however, the lack of spherical symmetry destroys the relationship ${\displaystyle [{\hat {\mathbf {L} }}^{2},{\hat {H}}]=0}$, so L ceases to be a good quantum number. A new set of operators have to be used instead: ${\displaystyle \{{\hat {\mathbf {S} }}^{2},{\hat {\mathbf {S} }}_{z},{\hat {\mathbf {L} }}_{z},{\hat {\mathbf {J} }}_{z}={\hat {\mathbf {S} }}_{z}+{\hat {\mathbf {L} }}_{z}\}}$, where the z-axis is defined along the internuclear axis of the molecule. Since these operators commute with each other and with the Hamiltonian on the limit of negligible spin-orbit coupling, their eigenvalues may be used to describe a molecule state through the quantum numbers S, M_S, M_L and M_J.

The cylindrical symmetry of a linear molecule ensures that positive and negative values of a given ${\displaystyle m_{\ell }}$ for an electron in a molecular orbital will be degenerate in the absence of spin-orbit coupling. Different molecular orbitals are classified with a new quantum number, λ, defined as

${\displaystyle \lambda =|m_{\ell }|}$

Following the spectroscopic notation pattern, molecular orbitals are designated by a lower case Greek letter: for λ = 0, 1, 2, 3,... orbitals are called σ, π, δ, φ... respectively, analogous to the Latin letters s, p, d, f used for atomic orbitals.

Now, the total z-projection of L can be defined as

${\displaystyle M_{L}=\sum _{i}{m_{\ell }}_{i}.}$

As states with positive and negative values of M_L are degenerate, we define

Λ = |M_L|,

and a capital Greek letter is used to refer to each value: Λ = 0, 1, 2, 3... are coded as Σ, Π, Δ, Φ... respectively (analogous to S, P, D, F for atomic states). The molecular term symbol is then defined as

^2S+1Λ

and the number of electron degenerate states (under the absence of spin-orbit coupling) corresponding to this term symbol is given by:

• (2S+1)×2 if Λ is not 0
• (2S+1) if Λ is 0.

Ω and spin–orbit coupling

Spin–orbit coupling lifts the degeneracy of the electronic states. This is because the z-component of spin interacts with the z-component of the orbital angular momentum, generating a total electronic angular momentum along the molecule axis J_z. This is characterized by the M_J quantum number, where

M_J = M_S + M_L.

Again, positive and negative values of M_J are degenerate, so the pairs (M_L, M_S) and (−M_L, −M_S) are degenerate: {(1, 1/2), (−1, −1/2)}, and {(1, −1/2), (−1, 1/2)} represent two different degenerate states. These pairs are grouped together with the quantum number Ω, which is defined as the sum of the pair of values (M_L, M_S) for which M_L is positive. Sometimes the equation

Ω = Λ + M_S

is used (often Σ is used instead of M_S). Note that although this gives correct values for Ω it could be misleading, as obtained values do not correspond to states indicated by a given pair of values (M_L,M_S). For example, a state with (−1, −1/2) would give an Ω value of Ω = |−1| + (−1/2) = 1/2, which is wrong. Choosing the pair of values with M_L positive will give a Ω = 3/2 for that state.

With this, a level is given by

${\displaystyle {}^{2S+1}\Lambda _{\Omega }}$

Note that Ω can have negative values and subscripts r and i represent regular (normal) and inverted multiplets, respectively.[1] For a ⁴Π term there are four degenerate (M_L, M_S) pairs: {(1, 3/2), (−1, −3/2)}, {(1, 1/2), (−1, −1/2)}, {(1, −1/2), (−1, 1/2)}, {(1, −3/2), (−1, 3/2)}. These correspond to Ω values of 5/2, 3/2, 1/2 and −1/2, respectively. Approximating the spin–orbit Hamiltonian to first order perturbation theory, the energy level is given by

E = A M_L M_S

where A is the spin–orbit constant. For ⁴Π the Ω values 5/2, 3/2, 1/2 and −1/2 correspond to energies of 3A/2, A/2, −A/2 and −3A/2. Despite of having the same magnitude, levels of Ω = ±1/2 have different energies associated, so they are not degenerate. With that convention, states with different energies are given different Ω values. For states with positive values of A (which are said to be regular), increasing values of Ω correspond to increasing values of energies; on the other hand, with A negative (said to be inverted) the energy order is reversed. Including higher-order effects can lead to a spin-orbital levels or energy that do not even follow the increasing value of Ω.

When Λ = 0 there is no spin–orbit splitting to first order in perturbation theory, as the associated energy is zero. So for a given S, all of its M_S values are degenerate. This degeneracy is lifted when spin–orbit interaction is treated to higher order in perturbation theory, but still states with same |M_S| are degenerate in a non-rotating molecule. We can speak of a ⁵Σ₂ substate, a ⁵Σ₁ substate or a ⁵Σ₀ substate. Except for the case Ω = 0, these substates have a degeneracy of 2.

Reflection through a plane containing the internuclear axis

There are an infinite number of planes containing the internuclear axis and hence there are an infinite number of possible reflections. For any of these planes, molecular terms with Λ > 0 always have a state which is symmetric with respect to this reflection and one state that is antisymmetric. Rather than labelling those situations as, e.g., ²Π^±, the ± is omitted.

For the Σ states, however, this two-fold degeneracy disappears, and all Σ states are either symmetric under any plane containing the internuclear axis, or antisymmetric. These two situations are labeled as Σ⁺ or Σ⁻.

Reflection through an inversion center: u and g symmetry

Taking the molecular center of mass as origin of coordinates, consider the change of all electrons' position from (x_i, y_i, z_i) to (−x_i, −y_i, −z_i). If the resulting wave function is unchanged, it is said to be gerade (German for even); if the wave function changes sign then it is said to be ungerade (odd). For a molecule with a center of inversion, all orbitals will be symmetric or antisymmetric. The resulting wavefunction for the whole multielectron system will be gerade if an even number of electrons are in ungerade orbitals, and ungerade if there are an odd number of electrons in ungerade orbitals, regardless of the number of electrons in gerade orbitals.

An alternative method for determining the symmetry of the MO is to rotate the orbital about the line joining the two nuclei and then rotate the orbital about the line perpendicular to this. If the sign of the lobes remains the same, the orbital is gerade, and if the sign changes, the orbital is ungerade.[2]

Wigner-Witmer correlation rules

In 1928 Eugene Wigner and E.E. Witmer proposed rules to determine the possible term symbols for diatomic molecular states formed by the combination of a pair of atomic states with given atomic term symbols.[3][4][5] For example, two like atoms in identical ³S states can form a diatomic molecule in ¹Σ_g⁺, ³Σ_u⁺, or ⁵Σ_g⁺ states. For one like atom in a ¹S_g state and one in a ¹P_u state, the possible diatomic states are ¹Σ_g⁺, ¹Σ_u⁺, ¹Π_g and ¹Π_u.[4]

Simplified correlation rules for diatomic molecules

Atomic Term Symbols	Molecular Term Symbols
Sg + Sg or Su + Su	Σ^+
Sg + Su	Σ^−
Sg + Pg or Su + Pu	Σ^−, Π
Sg + Pu or Su + Pg	Σ^+, Π
Pg + Pg or Pu + Pu	Σ^+(2), Σ^−, Π(2), Δ
Pg + Pu	Σ^+, Σ^−(2), Π(2), Δ

Alternative empirical notation

Electronic states are also often identified by an empirical single-letter label. The ground state is labelled X, excited states of the same multiplicity (i.e., having the same spin quantum number) are labelled in ascending order of energy with capital letters A, B, C...; excited states having different multiplicity than the ground state are labelled with lower-case letters a, b, c... In polyatomic molecules (but not in diatomic) it is customary to add a tilde (e.g. ${\displaystyle {\tilde {X}}}$, ${\displaystyle {\tilde {a}}}$) to these empirical labels to prevent possible confusion with symmetry labels based on group representations.

See also

• Molecular orbital theory

References

1. p. 337, Molecular Spectra and Molecular Structure, Vol I - Spectra of Diatomic Molecules, G. Herzberg, Reprint of Second Edition w/corrections, Malabar, Florida: Krieger Publishing Company, 1989. ISBN 0-89464-268-5
2. Lee, John David (2008). Concise Inorganic Chemistry (5th ed.). Wiley and Sons. ISBN 978-0-632-05293-6.
3. "Wigner-Witmer rules". Oxford Reference. Retrieved 26 August 2019.
4. Herzberg, Gerhard (1950). Molecular Spectra and Molecular Structure, Volume I.Spectra of Diatomic Molecules (2nd ed.). van Nostrand Reinhold. pp. 315–322. Reprint 2nd ed. with corrections (1989): Krieger Publishing Company. ISBN 0-89464-268-5
5. Wigner, Eugene (1928). "Über die Struktur der zweiatomigen Molekelspektren nach der Quantenmechanik". Zeitschrift für Physik (in German). 51 (11–12): 859–886. Bibcode:1928ZPhy...51..859W. doi:10.1007/BF01400247. S2CID 122110014.