EPR, ENDOR and DFT study of L-lysine • HCl • 2H2O single crystals X-irradiated at 66 K

被引:8
作者
Zhou, Yiying [1 ]
Nelson, William H. [1 ]
机构
[1] Georgia State Univ, Dept Phys & Astron, Atlanta, GA 30302 USA
关键词
EPR; ENDOR; DFT; L-lysine monohydrochloride dehydrate; Irradiation; Single crystal; ELECTRON-SPIN-RESONANCE; HYDROGEN-BONDED PROTONS; DENSITY-FUNCTIONAL THEORY; CARBOXYL RADICAL-ANIONS; SUPERHYPERFINE COUPLINGS; NEUTRON-DIFFRACTION; MAGNETIC-RESONANCE; RADIATION PRODUCTS; DNA; PROTEIN;
D O I
10.1016/j.radphyschem.2009.09.006
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Electron Paramagnetic Resonance (EPR), Electron-Nuclear DOuble Resonance (ENDOR) and ENDOR-Induced EPR (EIE) results indicated at least three radicals produced in L-lysine center dot HCl center dot 2H(2)O crystals irradiated at 66 K. EPR from radical R1 dominated the spectra and it was identified as the carboxyl anion, (H2OO(C) over dot) CH (NH3)(+) (CH2)(4) (NH3)(+). Density-Functional Theory (DFT) calculations supported the assignment and indicated that the carboxyl group transformed from planar to a pyramidal configuration following electron trapping. Two small couplings detected from R1 were ascribed to protons transferred to the carboxyl group from neighboring molecules through intermolecular hydrogen bonds. Radical R2 was identified as the product of decarboxylation, (C) over dotH (NH3)(+)(CH2)(4) (NH3)(+). Although it was not possible to obtain R2 s alpha-coupling tensor from the experiment, EPR simulations and DFT calculations provided strong support for the identification. Radical R3 exhibited several P-couplings but could be detected only in one plane and could not be identified. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:479 / 489
页数:11
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