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Bioelectromagnetism

2012; Lau et al., 2012; Wiltschko and Wiltschko, 2014, Bolte et al., 2016; Kerpal et al., 2019; Wiltschko

et al., 2021). In this CRY, a favoprotein, “favin adenine dinucleotide (FAD)” is a photofunctional mol­

ecule, and it is bound to the site buried in the helix domain by intermolecular interaction. When FAD

is excited by blue light, electron transfer occurs from nearby tryptophan (Trp) that is charge-separated,

and the consequent radical pair induces the efciency of reaction to be detected, albeit with a weak

magnetic feld. Using such highly sensitive magnetic receptors (magnetoreceptors), migratory birds are

assumed to be able to migrate in their intended proper direction.

Here, the historical background study of the “radical pair (recombination) mechanism (RPM)” mod­

els for quantum-assisted magnetic sensing and recent studies on both natural and artifcial in vitro

systems related to favoproteins such as FAD are introduced. Te forming processes of radical pairs dif­

fered between natural favoproteins and artifcial systems, which were focused in this review. Te latter

system was expected to provide advantages for precisely controlling the experimental condition. Te

avian magnetic compass is currently being actively investigated in the feld of “Quantum Biology” (Ball,

2011; Al-Khalili and McFadden, 2014; Solov’yov et al., 2014).

4.2 Historical Background Study of the Radical

Pair Mechanism Models

As historical background studies of spin chemistry, it has been generally considered difcult to con­

trol chemical and biological reactions using magnetic felds. Te reason is that the electronic energy

involved in the magnetic felds is extremely smaller than that in the chemical reactions. For example,

the Zeeman splitting of electron spins by 1 T magnetic feld is 0.935 cm−1, while the thermal energy is

about 200 cm−1, and the activation energy of chemical reactions is usually 3.000 cm−1 or more (Hayashi,

1982). In spite of this historical background, however, it has been mainly published by Japanese research­

ers that when radical pairs are included in the reaction process, even relatively weak magnetic felds in

the feld range below 1 T could afect the chemical reaction rate and yield (Hata, 1976, 1978, 1985, 1986;

Tanimoto et al., 1976; Hayashi and Nagakura, 1978; Hata et al., 1979; Sakaguchi et al., 1980a, b, 1981;

Sakaguchi and Hayashi, 1982; Hata and Yagi, 1983; Hata and Nishida, 1985).

4.2.1 Magnetic Field Effects on Chemical Reactions

via Radical Pair Recombination

Even in the 1 T magnetic feld, it is difcult to thermodynamically change the chemical reaction at

room temperature for the above-mentioned reasons, i.e., the Zeeman splitting energy in the magnetic

feld. Regarding the chemical magnetic feld efects, from the 1970s to the 1980s, chemical reactions

through unstable radical pairs or biradicals have been proved to be infuenced by an external magnetic

feld (Kaptein, 1972; Sagdeev et al., 1973; Hata, 1976, 1978, 1985, 1986; Tanimoto et al., 1976; Hayashi and

Nagakura, 1978; Hata et al., 1979; Turro and Chow, 1979; Sakaguchi et al., 1980a, b, 1981; Hayashi, 1982;

Sakaguchi and Hayashi, 1982; Hata and Yagi, 1983; Hata and Nishida, 1985). Te magnetic feld efect

on chemical reactions was interpreted in terms of the fact that a magnetic feld enhances or reduces

the singlet-triplet (S-T) conversion of intermediate radical pairs or biradicals (Kaptein, 1972; Hayashi

and Nagakura, 1978) through the electronic Zeeman and electron-nuclear hyperfne coupling (HFC)

interactions (Hayashi et al., 1966; Itoh et al., 1969). In particular, as one of the pioneer studies, Japanese

researchers observed and found the magnetic feld efects on the reaction yield and rate of the chemical

reaction proceeding via a radical-pair intermediate in the solution from both experimental and theo­

retical perspectives (Hata, 1976, 1978, 1985, 1986; Tanimoto et al., 1976; Hayashi and Nagakura, 1978;

Hata et al., 1979; Sakaguchi et al., 1980a, b, 1981; Hayashi, 1982; Sakaguchi and Hayashi, 1982; Hata and

Yagi, 1983; Hata and Nishida, 1985).

Photochemical reaction proceeding via a radical-pair intermediate in the solution can generally be

expected to show an external magnetic feld efect which arises from an electric Zeeman interaction