Radical cation states

Microwave or radio frequencies above 1 MHz that are appHed to a gas under low pressure produce high energy electrons, which can interact with organic substrates in the vapor and soHd state to produce a wide variety of reactive intermediate species cations, anions, excited states, radicals, and ion radicals. These intermediates can combine or react with other substrates to form cross-linked polymer surfaces and cross-linked coatings or films (22,23,29). 

Both CSs and CSs were also successfully generated by the fragmentation of ionized 4,5-dioxo-2-thioxo-l,3-dithione (65) and 2-thioxo-l,3-dithiole (66) (90JA3750). Tire three sulfur atoms in the anion and cation radicals were chemically equivalent, suggesting that they take the D h (or C2u) form (67 or 68). On the other hand, under similar conditions, 3-thioxo-1,2-dithiole (69) yielded two isomeric cation radicals the (or 2 ) form and the carbon disulfide 5-sulfide form (70). Ab initio calculations on three electronic states of CS3 at the 6-31G -l-ZPVE level indicated that the C21, form (68) was more stable than the carbon disulfide 5-sulfide form (70) in the neutral (both singlet and triplet states) and the anion radical states, but 68 was less stable than 70 in the radical cation state. 

The three highest occupied orbitals of sulfoxides are the lone pairs ns and n0, as well as the 7iso bond210. The 1,3-dithietane 1-oxide adds a lone-pair ionization and destabilizes the n0 and nso radical-cation states compared with thietane oxide. According to a hyperconjugative MO model, the ns+ combination in 1,3-dithietane is destabilized by about leV relative to the basis orbital energy a(ns) due to the combination with the... 

As already mentioned above, the oxidation of halogenated TTFs to the radical cation state is found to activate the halogen atom for entering into a halo-... 

Peroxyl radicals with a strong oxidative effect along with ROOH are continuously generated in oxidized organic compounds. They rapidly react with ion-reducing agents such as transition metal cations. Hydroxyl radicals react with transition metal ions in an aqueous solution extremely rapidly. Alkyl radicals are oxidized by transition metal ions in the higher valence state. The rate constants of these reactions are collected in Table 10.5. 

In principle, refined and relatively reliable quantum-theoretical methods are available for the calculation of the energy change associated with the process of equation 2. They take into account the changes in geometry, in electron distribution and in electron correlation which accompany the transition M(1 fio) — M+ (2 P/-), and also vibronic interactions between the radical cation states. Such sophisticated treatments yield not only reliable predictions for the different ionization energies 7 , 77 or 7 , but also rather precise Franck-Condon envelopes for the individual bands in the PE spectrum. However, the computational expenditure of these methods still limits their application to smaller molecules. We shall mention them later in connection with examples where such treatments are required. 

FIGURE 19. Correlation diagram of the jr-ionization energies /( and of cyclohexa-1,4-diene, bridged in positions 3,6 by a polymethylene chain — CCfE ), —, as a function of the dihedral angle electron ejection from the -orbitals i and 1)2 > respectively... 

Di(l-azulenyl)(6-azulenyl)methyl cation (24+) represented in Figure 17 exemplifies the cyanine-cyanine hybrid (20). Di(l-azulenyl)methylium unit in 24+ acts as a cyanine terminal group. The tropylium substructure stabilizes the cationic state (24+). Reduction of 24+ should afford the neutral radical 24, which is stabilized by capto-dative substitution effect, because 24 is substituted with azulenes in the donor and acceptor positions. The anionic state (24") is also stabilized by contribution of the cyclopentadienide substructure, which should exhibit the third color change in this system. 

Since amines generally have low oxidation potentials, they are good electron donors in their ground state, and the donor ability is further enhanced by photoexcitation. The chemical consequence of this single electron transfer (SET) is the generation of the amine radical cations (aminium radicals) and an earlier review on the aminium radicals is available1. 

The photochemical reduction of 1-methylquinolinium ions by (TMS)3SiH proceeds regioselectively to afford the corresponding 1,4-dihydroquinones in a water-acetonitrile solvent system (Reaction 4.47) [83]. Mechanistic studies demonstrated that the reactions are initiated by photoinduced electron transfer from the silane to the singlet excited states of 1-methylquinolinium ions to give the silane radical cation-quinolinyl radical pairs, followed by hydrogen transfer in the cage to yield 1,4-dihydroquinones and silicenium ion. Silyl cations are quenched by water. 

These structures may be viewed as distorted from the Bj-type geometries via a second-order JT-type mechanism or, alternatively, as Aj-type with the substituents at the wrong carbon atom. The calculations suggest that the radical cation state preference can be fine-tuned by appropriate substituents and predict substantial differences in spin-density distributions. These predictions should be verifiable by an appropriate spectroscopic technique (ESR or CIDNP) and might be probed via the chemical reactivity of the radical cations (vide infra). 

Figure 5. Minima and transition states on the potential energy surface of the radical cationic states of 1-methylcyclopropane (PMP4/6-3nCV/UMP2/6-31G + A ZPE reiative energies in kcai/moi). " ...

Figure 7. Calculated bond lengths (pm) and hyperfine couplings (G) for the syn- and ant/-conformers of vinylcyclopropane radical cationic states (MP4SDQ/6-31G )." ...

NEUTRAL MOLECULE CATION GROUND STATE RADICAL... 

Feldberg68,69 has made a valuable analysis of the relationship of the light produced in a double potential step electrochemiluminescence experiment to the current, time, and kinetic parameters involved. The analysis presumes that the reaction which produces excited states is cation-anion radical annihilation which occurs when the radical ions, separately produced, diffuse together in the solution near the electrode. The processes that Feldberg initially considered were eqs. (7)—(13). The assumptions involved are that decay of the excited state... 

These assignments are consistent with PES data ° and supported by theoretical calculations " in C2v symmetry, IS " " has two low-lying radical cationic states, and Ai. " The state is the ground state of IS " " the calculated hyperfine coupling constants (B3LYP/6-31G //MP2/6-31G ) are compatible with chemically induced dynamic nuclear polarization (CIDNP) and ESR/ENDOR results. No spin... 

Because of this difference in electron-donorand electron-acceptor properties, excited states have very different redox properties from those of related ground states. The effect is so marked that many photochemical processes begin with a complete transfer of an electron from (or to) an excited state (1.2), and the subsequent chemistry is that of radical cations and radical anions, species that are regarded as unusual in ground-state organic reactions. The importance of photochemical electron transfer is underlined by its extensive involvement in photobiological processes such as photosynthesis. 

---