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Optica Publishing Group
  • Applied Spectroscopy
  • Vol. 51,
  • Issue 6,
  • pp. 874-879
  • (1997)

Electron Paramagnetic Resonance and Mass Spectroscopy Study of Spin-Trapped Radicals: Styrene-Amine Photoreactions

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Abstract

The free radical intermediates from the photolysis of eleven substituted styrenes (1-11) with both tertiary and secondary amines were studied by spin trapping and the high-pressure liquid chromatography electron paramagnetic resonance (HPLC-EPR) technique. Eleven alpha -methylbenzyl radicals were trapped by 2-methyl-2-nitrosopropane (MNP) and separated by HPLC. Resolution enhancement was applied to obtain long-range hyperfine splitting constants (hfsc). The nitrogen hfsc are linearly correlated with the Hammett substituent constants. The major mass spectral fragments for the trapped aminoxyl radicals (12-22) include [M + 1]+, [M - 1]+, [MtBu]+ , [M-tBuOH]+, [M-tBuNO]+, and [(CH3) C3]+. The structures of 12-22 were also confirmed by chemical synthesis by adding Grignard reagent to alpha -phenyl- N - tert -butylnitrone (PBN) and its derivatives.

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