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3106084 
Journal Article 
Fluorescence from Samarium(II) Iodide and Its Electron Transfer Quenching: Dynamics of the Reaction of Benzyl Radicals with Sm(II) 
Skene, WG; Scaiano, JC; Cozens, FL 
1996 
Yes 
Journal of Organic Chemistry
ISSN: 0022-3263
EISSN: 1520-6904 
61 
22 
7918-7921 
English 
The luminescence from SmI(2) in THF can be readily quenched by a variety of electron acceptors. In the case of organohalides, the reaction is quite fast; for example, for dichloromethane the rate constant is 2.7 x 10(8) M(-)(1) s(-)(1). Electron transfer leads to halide loss and formation of the carbon-centered radical. In the case of benzyl chloride, the benzyl radicals produced can be readily detected using laser flash photolysis techniques. This electron-transfer reaction has been used as a source of benzyl radicals in order to determine the rate constant for their reaction with SmI(2); the value obtained is (5.3 +/- 1.4) x 10(7) M(-)(1) s(-)(1) in THF at room temperature. The effect of HMPA on the spectroscopic properties of SmI(2) has also been examined.