In chemistry, the selection rule (also known as the transition rule) formally restricts certain reactions, known as spin-forbidden reactions, from occurring due to a required change between two differing quantum states. When a reactant exists in one spin state and the product exists in a different spin state, the corresponding reaction will have an increased activation energy when compared to a similar reaction in which the spin states of the reactant and product are isomorphic. As a result of this increased activation energy, a decreased rate of reaction is observed.
Case of some cobalt carbonyls
Singlet and triplet states can occur within organometallic complexes as well, such as Tpi-Pr,MeCo(CO)2 and Tpi-Pr,MeCo(CO), respectively.
Changing spin states
When a reaction converts a metal from a singlet to triplet state (or vice versa): The energy of the two spin states must be nearly equal, as dictated by temperature, A mechanism is required to change spin states. Strong spin-orbital coupling can satisfy the 2nd condition. Parameter 1, however, can lead to very slow reactions due to large disparities between the metal complex's potential energy surfaces, which only cross at high energy leading to a substantial activation barrier.
Spin-forbidden reactions formally fall into the category of electronically non-adiabatic reactions. In general, potential energy surfaces fall into either the adiabatic and diabatic classification. Potential Energy Surfaces that are adiabatic rely on the use of the full electronic Hamiltonian, which includes the spin-orbit term. Those that are diabatic are likewise derived by solving the eigenvalues of the Schrödinger equation, but in this case one or more terms are omitted.
Non-adiabatic transition
Once a minimum energy crossing point is reached and parameter 1 above is satisfied, the system needs to hop from one diabatic surface to the other, as stated above by parameter 2. At a given energy (E), the rate coefficient [k(E)] of a spin-forbidden reaction can be calculated using the density of rovibrational states of the reactant [ρ(E)] and the effective integrated density of states in the crossing seam between the two surfaces [Ner(E)].
where
The probability of hopping (psh) is calculated from Landau-Zener theory giving
where
in which the spin-orbit coupling derived off the diagonal Hamiltonian matrix element between two electronic states (H12), the relative slope of the two surfaces at the crossing seam [F(Δ)], the reduced mass of the system through its movement along the hopping coordinate (μ), and the kinetic energy of the system passing through the crossing point (E) are used.
It is useful to note that when Eh < Ec (when below the minimum energy crossing point) the probability of hopping between spin states is null.
An example of a spin-forbidden reaction
One example showing the slowing effect of spin-forbidden reaction takes place when Fe(CO)x is placed under CO pressure. Transitions from x = 2,3,4 to x = 3,4,5 demonstrate a slowing rate when the reactant is in a triplet ground state but the product is in a singlet ground state. In the case of Fe(CO)x, when x = 2, 3, 4 the iron exists as a triplet in ground state; when x = 5, the iron exists as a singlet in ground state. The kinetics of said system can be represented by: Fe(CO)2->[{ k_{ 23}}][CO]Fe(CO)3->[{ k_{ 34}}][CO]Fe(CO)4->[{ k_{ 45}}][CO]Fe(CO)5
where: , , and .
The rate constants above are notably temperature independent, tested at 55 °C, 21 °C, and 10 °C, indicating, according to the authors, that the observed 500 fold reduction in rate occurs due to the spin-forbidden nature of the latter equation and not due to the kinetics of adding an additional ligand.
Application to catalysis
Ligand association and dissociation from metal centers involve a fundamental change in the coordination sphere of that metal. This change in certain reactions also requires a change in spin state to occur, which can retard the rate of ligand association. Oxidative addition and reductive elimination can be thought of in a similar manner to ligand association and dissociation, respectively. Mathematically, the rate ligand dissociation can increase when the reaction proceeds from one spin state to another, although it must be noted that this effect is often small in comparison with other factors such as sterics around the metal center.