Pulse Radiolysis and Computational Studies on a Pyrrolidinium Dicyanamide Ionic Liquid: Detection of the Dimer Radical Anion.

A pulse radiolysis study on pyrrolidinium cation based ionic liquids is presented herein. Time-resolved absorption spectra for 1-methyl-1-propylpyrrolidinium dicyanamide (DCA) at 500 ns after the electron pulse show broad absorption bands at wavelengths below 440 nm and at 640 nm. In pyrrolidinium bis(trifluoromethylsulfonyl)imide (NTf) and tris(perfluoroethyl)trifluorophosphate (FAP) ILs, the transient absorption below 440 nm is much weaker.

Hydrogen production in aromatic and aliphatic ionic liquids.

The radiolytic production of molecular hydrogen in the ionic liquids N-trimethyl-N-butylammonium bis(trifluoromethanesulfonyl)imide ([N1114][Tf2N]) and 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([emim][Tf2N]) has been examined with γ-rays, 2-10 MeV protons, and 5-20 MeV helium ions to determine the functional dependence of the yield on particle track structure. Molecular hydrogen is the dominant gaseous radiolysis product from these ionic liquids, and the yields with γ-rays are 0.73 and 0.

Antioxidant activity and free radical scavenging reactions of hydroxybenzyl alcohols. Biochemical and pulse radiolysis studies.

Comparative studies on free radical scavenging by isomers of hydroxybenzyl alcohols (HBAs) were carried out to understand the molecular mechanisms involved in the antioxidant action. Using rat liver mitochondria as model systems, we have examined the radioprotective and antioxidant effects of hydroxybenzyl alcohols. Apart from their ability to scavenge free radicals and ferric reducing power, HBAs have shown good protection against radiation and oxidative stress.

Addition-elimination in the reaction of alpha-hydroxyalkyl radicals with 3,5-pyridinedicarboxylic acid and nicotinic acid: example of inner sphere organic electron transfer.

Reactions of alpha-hydroxyalkyl radicals with 3,5-pyridinedicarboxylic acid (3,5-PDCA) and nicotinic acid (NA) were studied at appropriate pHs in aqueous solutions by pulse radiolysis technique. At pH 1, CH(3)C*HOH and *CH(2)OH radicals were found to react with 3,5-PDCA by rate constants of 2.2 x 10(9) and 5.