Abstract
Electron Paramagnetic Resonance (EPR), Electron-Nuclear DOuble Resonance (ENDOR) and ENDOR-Induced EPR (EIE) results indicated at least three radicals produced in l-lysine·HCl·2H 2O crystals irradiated at 66 K. EPR from radical R1 dominated the spectra and it was identified as the carboxyl anion, (H 2OOĊ) CH (NH 3) + (CH 2) 4 (NH 3) +. 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, ĊH (NH 3) +(CH 2) 4 (NH 3) +. Although it was not possible to obtain R2's α-coupling tensor from the experiment, EPR simulations and DFT calculations provided strong support for the identification. Radical R3 exhibited several β-couplings but could be detected only in one plane and could not be identified.
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