Lithium Formate for EPR Dosimetry: Radiation-Induced Radical Trapping at Low Temperatures

被引:2
|
作者
Krivokapic, Andre [1 ]
Aalbergsjo, Siv G. [1 ]
De Cooman, Hendrik [2 ]
Hole, Eli Olaug [1 ]
Nelson, William H. [3 ]
Sagstuen, Einar [1 ]
机构
[1] Univ Oslo, Dept Phys, N-0316 Oslo, Norway
[2] Univ Ghent, Dept Solid State Sci, B-9000 Ghent, Belgium
[3] Georgia State Univ, Dept Phys & Astron, Atlanta, GA 30303 USA
关键词
ELECTRON-SPIN-RESONANCE; INITIO MOLECULAR-DYNAMICS; NUCLEAR DOUBLE-RESONANCE; HYPERFINE INTERACTIONS; SINGLE-CRYSTALS; DENSITY; ENDOR; ESR; MONOHYDRATE; GEOMETRY;
D O I
10.1667/RR13582.1
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Radiation-induced primary radicals in lithium formate. A material used in EPR dosimetry have been studied using electron paramagnetic resonance (EPR), electron nuclear double resonance (ENDOR) and ENDOR-Induced EPR (EIE) techniques. In this study, single crystals were X irradiated at 6-8 K and radical formation at these and higher temperatures were investigated. Periodic density functional theory calculations were used to assist in assigning the radical structures. Mainly two radicals are present at 6 K, the well-known CO2 center dot- radical and a protonated electron-gain product. Hyperfine coupling tensors for proton and lithium interactions were obtained for these two radicals and show that the latter radical exists in four conformations with various degrees of bending at the radical center. Pairs of CO2 center dot- radicals were also observed and the tensor for the electron-electron dipolar coupling was determined for the strongest coupled pair, which exhibited the largest spectral intensity. Upon warming, both the radical pairs and the reduction product decay, the latter apparently by a transient species. Above 200 K the EPR spectrum was mainly due to the CO2 center dot- (mono) radicals, which were previously characterized as the dominant species present at room temperature and which account for the dosimetric EPR signal. (C) 2014 by Radiation Research Society
引用
收藏
页码:503 / 511
页数:9
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