Radical cation reactions absorption

Kawai K, Majima T (2004) Hole Transfer in DNA by Monitoring the Transient Absorption of Radical Cations of Organic Molecules Conjugated to DNA. 236 117-137 Kee TP, Nixon TD (2003) The Asymmetric Phospho-Aldol Reaction. Past, Present, and Future. 223 45-65... 

The formation of the radical-cation, PQ+ was monitored using laser photolysis techniques at its absorption maxima at 603nm. A study of the rates of PQ+" formation at different PQ++ concentrations led to kg=l.Tx109 M-1s-1. Despite the fact that this reaction is extremely fast, the rate of electron transfer for the macrobiradical is significantly slower than those for the same group in small molecules (8,11). 

The differential absorption spectra obtained in the presence of these two nucleotides are indeed similar to those obtained after reduction electrolysis of the complex in the first reduction wave, and obtained by pulse radiolysis. The prerence of the deprotonated radical cation GMI —H) can also be detected by recording the transient absorption after reaction of the reduced complex with O2. 

The oxidative degradations of binuclear azaarenes (quinoline, isoquinoline, and benzodrazines) by hydroxyl and sulfate radicals and halogen radicals have been studied under both photochemical and dark-reaction conditions. A shift from oxidation of the benzene moiety to the pyridine moiety was observed in the quinoline and isoquinoline systems upon changing the reaction from the dark to photochemical conditions. The results were interpreted using frontier-orbital calculations. The reaction of OH with the dye 3,3,6,6-tetramethyl-3,4,6,7,9,10-hexahydro-(l,8)(2//,5//)-acridinedione has been studied, and the transient absorption bands assigned in neutral solution.The redox potential (and also the pA a of the transient species) was determined. Hydroxyl radicals have been found to react with thioanisole via both electron transfer to give radical cations (73%) and OH-adduct formation (23%). The bimolec-ular rate constant was determined (3.5 x lO lmoU s ). " ... 

The solute benzene radical cation was formed on pulse radiolysis of an acidic aqueous solution of benzene. The transient optical absorption bands (A-max = 310, 350-500 nm) were assigned to the solute benzene radical cation which is formed on acid-catalysed dehydration of the OH adduct. The radical cation is able to undergo an electron-transfer reaction with Br and was found to be a strong electron oxidant. Pulse radiolysis has been used to study the complex reaction that follows electron addition to hydroxybenzophenones (HOBPs). The various radical species involved have been characterized spectrally and their p/fa values evaluated. The differences... 

In 1993, Blatter and Frei [34] extended the Aronovitch and Mazur [28] photo-oxidation into zeolitic media, which resulted in several distinctive advantages as described below. Irradiation in the visible region (633 nm) of zeolite NaY loaded with 2,3-dimethyl-2-butene, 16, and oxygen resulted in formation of allylic hydroperoxide, 17, and a small amount of acetone. The reaction was followed by in situ Fourier-transform infrared (FTlR) spectroscopy and the products were identified by comparison to authentic samples. The allylic hydroperoxide was stable at - 50°C but decomposed when the zeolite sample was warmed to 20°C [35]. In order to rationalize these observations, it was suggested that absorption of light by an alkene/Oi charge-transfer complex resulted in electron transfer to give an alkene radical cation-superoxide ion pair which collapses... 

The UV absorption spectra of radical cations such as 87 have received attention, and the ESR spectra have been studied and in some cases interpreted. Rate constants for the one-electron reduction of diquat and the salts 82 (n = 3) and 82 (n = 4) have been determined by pulse radiolysis, and kinetic studies involving reactions of the diquat radical cation at hydrogen-evolving metal electrodes have been... 

Chemical oxidation of the TTF groups in compounds 34 and 35 has been achieved by reaction with an excess of iodine in dichloromethane solution, leading to new low-energy absorptions in the UV/visible spectra which are diagnostic of TTF cation radicals the broad absorption at = 830 nm for the iodide salt of 35 suggests the formation of aggregated TTF species. A charge transfer complex formed by 35 and tetracyano-p-quinodimethane (TCNQ) has been isolated as an insoluble black powder. The stoichiometry is (35), (TCNQ)3 (i.e. 8 TTF units 3... 

The purine radical cations are strong Bronsted acids, and thus rapidly de-protonate in neutral aqueous solutions [47, 48]. For instance, the adenosine radicals generated by reaction with S04 radicals were identified as neutral radicals, A(-H) . A change in pH from 1 to 13 does not affect the transient absorption spectra of these species based on this result, it was inferred that the pKa of A is <1 [49]. The solution pH exerts pronounced effects on the transient absorption spectra of the 2AP radicals assigned to the following equilibrium ... 

However, the cell in Fig. 9.2(b) has a disadvantage in that the concentration of the electrogenerated substance decreases with increasing distance from the OTE surface. Because of this, simulation of the reaction is very difficult, except for the first order (or pseudo-first-order) reactions. For more complicated reactions, it is desirable that the concentration of the electrogenerated species is kept uniform in the solution. With a thin-layer cell, a solution of uniform concentration can be obtained by complete electrolysis, but it takes 30 s. Thus, the thin-layer cell is applicable only for slow reactions. For faster reactions, a column-type cell for rapid electrolysis is convenient. Okazaki et al. [7] constructed a stopped-flow optical absorption cell using one or two column-type cells (Fig. 9.4) and used it to study the dimerization of the radical cations (TPA +) of triphenylamine and the reactions of the radical cation (DPA +) of 9,10-diphenylanthracene with water and alcohols. Using the stopped-flow cell, reactions of substances with a half-life of 1 s can be studied in solutions of uniform concentrations. 

Pulse radiolysis has been used to afford the radical cations of thioanisole, p-methylthioanisole, and benzyl phenyl sulfides. The absorption spectra of these radicals and their reaction with a number of nucleophiles and electron donor s are reported.302 Exposure of trimethylphosphine sulfide to 60Co 7-radiation at 77 K gave the radical anion Me3PS , identified by its ESR spectrum, from which other radicals, including Me2PS, were formed at higher temperatures.303... 

Mesitylfhjorenyl anion (9MsF ) is unreactive towards Mel at temperatures below —78 °C.100 Above —60 °C the absorption spectrum of 9MsF in the presence of Mel is replaced by that of the corresponding 9-mesitylfluorenyl radical (9MsF), and 9-methyl-9-mesitylfluorene is formed in low yield, hi a study of the electron-transfer photochemistry of chrysanthemol, an intramolecular S 2 reaction of a vinylcycloprop-ane radical cation has been observed.101 hi a long series of studies of the reactivity of the acids of trivalent phosphorus and their derivatives, the behaviour of P—O nucleophiles towards arylmethyl bromide systems has been examined.102 Further evidence for an X-philic substitution/SET tandem mechanism has been obtained. 

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