Preparation and mass spectral characterization of pentafluorobenzyl derivatives of alkyl and hydroxyalkyl-nucleobase DNA adducts

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Abstract
Pentafluorobenzyl (PFBz) derivatives of the following nucleobases were prepared: cytosine, 5‐methylcytosine, O2‐methylcytosine, O2‐ethylthymine, O4‐ethylthymine, 5‐hydroxymethyluracil, N6‐methyladenine, O6‐methylguanine, O6‐hydroxyethylguanine and O6‐hydroxyethylpurine. 13C nuclear magnetic resonance was diagnostic for O‐ versus N‐attachment of the PFBz moiety: the resonance of the methylene carbon appeared in the range 29.15–42.13 ppm for NCH2C6F5, and 58.45–69.01 for OCH2C6F5. Considerable structural information was provided by mass spectrometry with ionization by electron impact. All of the derivatives were detected with high sensitivity and specificity by gas chromatography with detection by electron capture negative ion mass spectrometry, reflecting not only their chemical and physical stability, but also their strong tendency to form a structurally diagnostic anion, [M – PFBz]−, in high yield under these ionization conditions. PFBz derivatives are therefore attractive forms of alkyl‐substituted nucleobases for analysis by mass spectrometry.