148

Bioelectromagnetism

External magnetic feld efects on the photosubstitution reaction (1→3) in cyclohexane are shown by

Hata and Nishida (1985). Here, 1, 4-methyl-2-quinolinecarbonitrile; 3, 2-cyclohexyl-4-methylquinoline. In

the case of the chemical yield of 2-cyclohexyl-4-methylquinoline 3, the results are plotted against the feld

strength in either the absence or presence of 1,3-pentadiene. In either case, the conversion was almost inde­

pendent of the feld strength (19%–21%). In the absence of 1,3-pentadiene, as shown by curve (a), the chemi­

cal yield of 3 was ca. 65% at the zero feld. However, it decreased steeply upon the application of a magnetic

feld of 40 mT to be ca. 54% (the magnetic feld efect due to HFI mechanism). Further increase in the feld

strength resulted in the quadratic recovery in the chemical yield to reach a constant value of ca. 63% (the

magnetic feld efect due to Δg mechanism). However, the addition of 1,3-pentadiene as shown by curve

(b) caused a complete disappearance of these magnetic feld efects. Consequently, the chemical yield of 3

became independent of the feld strength to show ca. 67%. Tis means that both HFI and Δg magnetic feld

efects observed in this reaction can be assigned to the feld dependence of the chemical yield of the T1-born

cage product. Also, the fact that product 3 was obtained in a high feld (ca. 67%), even in the of 1,3-pentadi­

ene, suggests strongly that the photosubstitution reaction proceeds from the S1 state as well as the T1 state.

Tanimoto et al. (1976) examined the photodegradation reaction at room temperature under magnetic

felds of up to 4.2 T to determine the relative magnetic feld change of the cage product. Tis study is

the frst study to confrm the magnetic feld efect on the reaction yield of the chemical reaction in the

solution. Dissipative product yields and chemical reactions from triplet precursors can be treated in the

same way (Hayashi and Nagakura, 1978; Sakaguchi et al., 1980a, b).

Furthermore, regarding the rate of the chemical reaction proceeding, it is theoretically estimated that

the singlet-triplet (S-T) conversion rate (kST) (in the coherent mixing between singlet and triplet spin

states) may be decreased by the magnetic feld (Hayashi and Nagakura, 1978; Sakaguchi et al., 1980a,

b). In order to measure kST experimentally, the research team devised a method of measuring the time

change of the absorption intensity of the electron spectrum in the radical pair (Sakaguchi et al., 1980a, b,

1981; Sakaguchi and Hayashi, 1982). Tey used a pulsed laser as the excitation light source to examine the

magnetic feld efects on kST in photochemical reactions in a micelle for the frst time (Sakaguchi et al.,

1980a, b, 1981; Hayashi, 1982; Sakaguchi and Hayashi, 1982).

When benzophenone (BP) in a sodium dodecyl sulfate (SDS) micelle is laser excited, the triplet excited

state (3BP*) abstracts hydrogen from the micelle molecule (RH) to form a triplet radical pair (Sakaguchi

et al., 1980a, b).

3

*

3

BP + RH ° (K• •R)

(4.1)

Here, BP

= (C H

)2 CO, K• = (C H )2 COH, R• = •C H SO . kST can be obtained from the time change

6

5

6

5

12

24

4

of the absorption intensity of K•. Since these kST values are similar to T1

1 of electrons in radicals, kST could

be afected by T1. Magnetic feld strength dependence of the S-T conversion constant (kST) at remote pairs

of 4,4-difuorobenzophenone ketyl radical, (C6H4F)2 COH, and alkyl radical, C H SO , in an SDS

12

24

4

micelle is shown by Hayashi (1982), modifed from Sakaguchi and Hayashi (1982). Te experimental

results suggested magnetic feld strength dependence of the S-T conversion constant. Surprisingly, the

kST value at 13.4 kg (1.34 T) is about 1/10 of the kST value at 0 kg, and such a large magnetic feld efect on

kST has not been reported so far (Hayashi, 1982). Te reason is thought to be that radical-pair interme­

diates can exist for a long time in micelles (Hayashi, 1982). Since the reaction in the micelle is similar

to the reaction in the living systems, the magnetic feld efects on the biological reaction can be greatly

expected (Hayashi, 1982).

4.2.2 Magnetic Field Effects on Biological Systems

via Radical Pair Recombination

With regard to magnetic feld efects on radical pair recombination in biological systems, the yield of

excited triplet electronic states in the photosynthetic reaction center was frst shown to be magnetic