Distinguishing from radicals

The term primary radical used in this context should be distinguished from that used when describing the substitution pattern of alkyl radicals, t For example, in PS the initiator-derived end groups will account for ca 0.2% of units in a sample of molecular weight 100,000 (termination is mainly by combination). 

While nitroxides give overwhelmingly combination in their reaction with carbon-centered radicals, the amount of disproportionation is finite (Scheme 9.24). Disproportionation cannot always be rigorously distinguished from elimination and it is possible that both reactions occur. The combinatiomdisproportionation ratio (or extent of elimination) depends on the nitroxide and radical structure and within a scries of structurally related systems appears to increase as... 

The inner-sphere nature of the ion-radical pair may render the biradical (or zwitterionic) intermediate difficult to assess and distinguish from a concerted... 

Single Electron Transfer A single electron transfer (SET) mechanism is often difficult to distinguish from an SN2 reaction because the principal product of these two pathways is the same, apart from the stereochemistry at carbon (race-mization instead of inversion). The radicals formed can recombine rapidly in a solvent cage (inner-sphere ET) [2, 193, 194]. The [HFe(CO)5] -catalyzed deiodina-tion of iodobenzene may serve as an example [179] (Eq. (13)). 

A special property of captodative radicals can neither be recognized in Leroy s nor in Pasto s work. The substituents may show additivity, less than additivity or, even, more than additivity in the calculated stabilization. If we combine the results in both schemes it has to be concluded that captodative radicals are not a distinguishable class of radicals. They should not obey different rules from radicals stabilized by non-captodative substituents. Radicals can be stabilized by all kinds of substituents, although to a different... 

Formaldonitrone, CH2=N(H)—O (3), the elusive simplest organic nitrone, has been prepared transiently in the gas phase by femtosecond collisional neutralization of its cation radical, CH2—N(H)—0+". The latter was generated by dissociative ionization of 1,2-oxazolidine. Nitrone 3 showed negligible dissociation upon collisional neutralization and was distinguished from its tautomers formaldoxime 2 and nitrosomethane 1 that gave different NR mass spectra. The enthalpy of formation was calculated from enthalpies of atomization and two isodesmic reactions as Af//29s(3) = 58 1 kJmol . The calculated, large activation barriers for isomerization of 3 (179 and 212 kJmoH for 3 anti-2 and 3 1, respectivelyindicate that once 3 is formed and diluted in the gas phase it should not isomerize unimolecularly to either 1 or (syn/anti) 2. 

DNA, laced with an intercalator characterized by a high electron affinity, is y-ir-radiated and observed by EPR. The one-electron reduced intercalator presents an EPR spectrum that is readily distinguishable from that of the DNA-trapped radicals. A key example is mitoxantrone (MX), with an electron affinity of 6.25 eV and a radical anion spectrum that is a sharp singlet. Charges are injected into the DNA by y-irradiation at a preselected temperature (4 130 K). Holding the temperature constant, the EPR spectrum changes as a function of time (0.5-30 h). Thereby, a direct measure of the rate of electron transfer from one-electron reduced pyrimidines (Pryre) to the intercalator, e.g., MX, is measured. The turmeling rate is observed to depend on the electron affinity (EA) of the... 

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