Spin Chemistry is a sub-field of chemistry and physics, positioned at the intersection of chemical kinetics, photochemistry, magnetic resonance and free radical chemistry, and dealing with magnetic and spin effects in chemical reactions. The examples of phenomena that Spin Chemistry deals with are Chemically Induced Dynamic Nuclear and Electron Polarization (CIDNP and CIDEP), magnetic isotope effects in chemical reactions, as well as the environmental, health effects of static and oscillating electromagnetic fields, and avian magnetoreception, particularly as radical-pair reaction kinetics are dependent on the direction of magnetic fields.
Some of the prominent scientists in the field (in alphabetical order) are:
- E. G. Bagryanskaya (Novosibirsk, Russia),
- K.-P. Dinse (Darmstadt, Germany),
- S. A. Dzuba (Novosibirsk, Russia),
- M. D. E. Forbes (Chapel Hill, USA),
- P. Gast (Leiden, Netherlands),
- P. J. Hore (Oxford, UK),
- G. Jeschke (Zurich, Switzerland),
- R. Kaptein (Utrecht, Netherlands),
- C. W. M. Kay (London, UK),
- K. Möbius (Berlin, Germany),
- Yu. N. Molin (Novosibirsk, Russia),
- J. R. Norris (Chicago, USA),
- R. Z. Sagdeev (Novosibirsk, Russia),
- K. M. Salikhov (Kazan, Russia),
- U. Steiner (Konstanz, Germany),
- S. Tero-Kubota (Sendai, Japan),
- C. R. Timmel (Oxford, UK),
- A. J. van der Est (St. Catharines, Canada)
- H.-M. Vieth (Berlin, Germany),
- S. Weber (Freiburg, Germany).
- 1 The Radical-Pair Mechanism
- 2 References
The Radical-Pair Mechanism
The radical-pair mechanism explains how a magnetic field can affect reaction kinetics by affecting electron spin dynamics. Most commonly demonstrated in reactions of organic compounds involving radical intermediates, a magnetic field can speed up a reaction by decreasing the frequency of reverse reactions.
History of the Theory and Circumstances of Proposal
Radicals and Radical-Pairs
A radical, of course, is a molecule with an odd number of electrons, and is induced in a variety of ways, including ultra-violet radiation. A sun burn is largely due to radical formation from this radiation. The radical-pair, however, is not simply two radicals. This is because radical-pairs (specifically singlets) are quantum entangled, even as separate molecules. More fundamental to the radical-pair mechanism, however, is the fact that radical-pair electrons both have spin, short for spin angular momentum, which gives each separate radical a magnetic moment. Therefore, spin states can be altered by magnetic fields.
Singlet versus Triplet Spin States
The radical-pair is characterized as triplet or singlet by the coupled spin state of the two lone electrons. The spin relationship is such that the two unpaired electrons, one in each radical molecule, may have opposite spin (singlet; anticorrelated), or the same spin (triplet; correlated). The singlet state is called such because there is only one way for the electrons’ spins to anticorrelate (S), whereas the triplet state is called such because the electron’s spin may be correlated in three different fashions (T+1, T0,T−1).
Relevance to Reaction Kinetics and the Zeeman Interaction
Spin states relate to chemical and biochemical reaction mechanisms because bonds can only be formed between two electrons of opposite spin (Hund’s Rule). Sometimes when a bond is broken in a particular manner, for example, when struck by photons, each electron in the bond relocates to each respective molecule, and a radical-pair is formed. Furthermore, the spin of each electron previously involved in the bond is conserved, which means that the radical-pair now formed is a singlet (each electron has opposite spin, as in the origin bond). As such, the reverse reaction, i.e. the reforming of a bond, called recombination, readily occurs. The radical-pair mechanism explains how external magnetic fields can prevent radical-pair recombination with Zeeman interactions, the interaction between spin and an external magnetic field, and shows how a higher occurrence of the triplet state accelerates radical reactions because triplets can only proceed to products, and singlets are in equilibrium with the reactants as well as with the products.
The Zeeman interaction is an interaction between spin and external magnetic field,
and is given by the equation,
where ∆E is the energy of the Zeeman interaction, in Joules, vL is the Larmor frequency, in hertz, B is the external magnetic field, in teslas, µB is the Bohr magneton constant, h is Planck’s constant, and g is the g-value of a free electron, 2.002319, which is slightly different in different radicals.
It is common to see the Zeeman Interaction formulated in other ways.
Zeeman Interactions and Magnetoreception
Because the Zeeman Interaction is a function of magnetic field and Larmor frequency, it can be obstructed or amplified by altering the external magnetic or the Larmor frequency with experimental instruments that generate oscillating fields. This is interesting because migratory birds lose their navigational abilities in similar conditions where the Zeeman interaction is obstructed in radical-pairs, and researchers can control these conditions to probe the importance of Zeeman Interactions in Magnetoreception, implicating the presence of a radical-pair mechanism.
- Hore, P. J.; Mouritsen, Henrik (2016-01-01). "The Radical-Pair Mechanism of Magnetoreception". Annual Review of Biophysics. 45 (1): 299–344. PMID 27216936. doi:10.1146/annurev-biophys-032116-094545.
- Vyushkova, Maria (April, 2011). "Basic Principles and Applications of Spin Chemistry" (PDF). www.nd.edu. Notre Dame University. Retrieved November, 2016. Check date values in:
- "ＨＰ of Hisaharu Hayashi：Introduction to Dynamic Spin Chemistry". www015.upp.so-net.ne.jp. Retrieved 2016-12-05.