Jm. Stegge et al., THE SOLVENT-INITIATED PHOTOCHEMISTRY OF TRIS(N,N-DIETHYLDITHIOCARBAMATO)IRON(III), Inorganica Chimica Acta, 250(1-2), 1996, pp. 385-388
The photolysis of [Fe(Et(2)dtc)(3)],Et(2)dtc = diethyldithiocarbamate,
in chloroform to yield [Fe(Et(2)dtc)(2)Cl] proceeds under 313 nm irra
diation through a metal complex excited state, as expected. Under 254
nm irradiation, however, the dominant pathway is through a solvent-ini
tiated reaction in which radicals formed after absorption of light by
CHCl3 react thermally with [Fe(Et(2)dtc)(3)]. The initial rate varies
linearly with the light intensity at 313 nm, but at 254 nm varies with
the square root of the intensity.