Electron paramagnetic resonance and electron nuclear double resonance studies of X-irradiated crystals of cytosine hydrochloride. Part I: Free radical formation at 10 K after high radiation doses
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Hole, EO
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机构:Univ Oslo, Dept Phys, N-0316 Oslo, Norway
Hole, EO
Nelson, WH
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机构:Univ Oslo, Dept Phys, N-0316 Oslo, Norway
Nelson, WH
Sagstuen, E
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机构:Univ Oslo, Dept Phys, N-0316 Oslo, Norway
Sagstuen, E
Close, DM
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机构:Univ Oslo, Dept Phys, N-0316 Oslo, Norway
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[1] Univ Oslo, Dept Phys, N-0316 Oslo, Norway
[2] Georgia State Univ, Dept Phys & Astron, Atlanta, GA 30303 USA
[3] E Tennessee State Univ, Dept Phys, Johnson City, TN 37614 USA
Anhydrous single crystals of cytosine hydrochloride (protonated at N3) have been X-irradiated at 10 K and studied using K-band EPR, ENDOR and FSE spectroscopy, At least seven radicals were present at 10 K after X irradiation with a dose of about 150 kGy. Two different protonation states of the one-electron reduced cytosine cation were observed: an amino-protonated species (R1) and the pristine one-electron reduced species (R2) with zero net charge. Apparently three deprotonated versions of the one-electron oxidized cytosine cation were formed: the amino-deprotonated cation (R3), an N3-deprotonated cation (R4) and an N1-deprotonated cation (R5). Finally, two products formed by net hydrogen addition to the cytosine base were observed: a C5 hydrogen-addition radical (R6) and a C6 hydrogen-addition radical (R7). The crystalline lattice of cytosine hydrochloride is characterized in part by a cytosine base initially protonated at the N3-position, thus forming a cytosine base cation, and in part by an extended network of hydrogen bonding involving the chlorine anions. Proton transfer properties of pristine one-electron oxidation and reduction base products in this lattice are discussed and are suggested as explanations of the unusual multitude of positions for deprotonation of the one-electron oxidized species as well as for the two protonation states of the reduction product observed. The magnetic parameters for the amino-protonated species R1 agree well with those extracted from previous studies of cytosine derivatives in frozen solutions and in various glasses. (C) 1998 by Radiation Research Society.