Perfluorophenyl-containing verdazyl radicals

New formazans, tetrazines, and verdazyl radicals containing perfluorophenyl substituents were obtained on the basis of perfluorophenylhydrazides. The stabilities of mono-, bis-, and tris(perfluorophenyl)verdazyl radicals and their leuco compounds are compared qualitatively. The stabilities of the free radicals obtained considerably exceed the stability of the diphenylpicrylhydrazyl (DPPH) radical.Chlorohydrazone IIa was previously obtained [3] by chlorination of hydrazide Ia with phosphorus pentachloride.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1130–1133, August, 1980.     

Electrochemical studies of verdazyl radicals

The redox properties of verdazyl radicals are presented using cyclic voltammetry techniques. These radicals can be reversibly reduced as well as oxidized. Electron-donating and -withdrawing substituents have significant effects on the oxidation and reduction potentials as well as the cell potential (E(cell) = | E(ox) degrees - E(red) degrees |) for these radicals; a correlation between the electron spin distribution and redox properties is developed.     

Complex formation of verdazyl radicals with verdazilium salts

Russian Journal of General Chemistry -     

Autocatalysis in oxidation reactions of verdazyl radicals with hydroperoxides

The reaction of 2,4,6-triphenyl- and 2,3,4,6-tetraphenylverdazyl with tert-butyl hydroperoxide in acetonitrile solution and acetonitrile-water mixture was studied. This reaction was shown to be autocatalytic owing to verdazylium hydroxide formation in the course of the reaction. The main kinetic parameters were determined for the catalytic and non-catalytic reactions.     

Electronic structure and absorption spectra of verdazyl radicals,the corresponding cations,and leuco compounds

The wavelengths of transitions in electronic absorption spectra of verdazyl radicals, the corresponding cations, and leuco compounds were calculated in valence and -electron approximations with allowance for configuration interaction. It was shown that the longest-wave bands in the investigated compounds are due to ^* electron transitions. The effect of the nature of the substituents on the position of the bands in the spectrum is discussed.Translated from Teoreticheskaya i Éksperimental'naya Khimiya, Vol. 22, No. 4, pp. 473–477, July–August, 1986.     

Organic radicals based on phenalenyl and verdazyl units

Stable phenalenyl (PLY) radicals without sterically bulky substituents need to be synthesized for application as neutral organic molecular conductors. Verdazyl radicals, which have high stability even without sterically bulky substituents, were combined with PLY radicals to produce two novel radicals. The stability of the dimethylthiourea substituted PLY radical is supported by the experimental results and quantum chemical calculations.     

Reaction of superoxo Co(III) complex with stable phenoxy radicals

A typical superoxo complex [Co(CN)₅O₂][Ph₃PN

PPh₃]₃ combines with stable phenoxy radicals in CH₂Cl₂ leading to selective formation of peroxy-$\text{p}$-quinols except for 2,4,6-tri-$\text{t}$-butylphenoxy radical, representing radical reactivity of the complex.     

Probing electronic communication in stable benzene-bridged verdazyl diradicals

Two benzene-bridged N,N'-bis(isopropyl)6-oxoverdazyl diradicals 7a (1,4-benzene-bridged) and 7b (1,3-benzene-bridged) were prepared and studied by an array of physicochemical techniques aimed at elucidating the intramolecular electronic and magnetic coupling between verdazyl chromophores. The very high stability of these diradicals permits comprehensive investigations of their properties for the first time. The UV-vis spectra suggest negligible direct conjugative overlap involving the radical SOMOs, although significant differences in higher energy absorptions suggest that radical orbitals other than the SOMO are likely communicating via the central p-phenylene bridge in 7a. The electrochemical features of the two diradicals are nearly identical; in each derivative, both radicals are oxidized essentially independently while the reductions occur in a stepwise manner with differences of approximately 100 mV between the two reductions. EPR and magnetic susceptibility collectively indicate that the para-bridged diradical is weakly antiferromagnetically coupled while the meta analogue is weakly ferromagnetically coupled, in accord with the topology of the substitution pattern on the central benzene ring.     

Reaction of nitroxyl radicals with dichlorocarbene

Conclusions The reaction of aromatic nitroxyl radicals with dichlorocarbene, generated under phase transfer catalysis conditions, leads to the corresponding hydrazine derivatives through the abstraction of the oxygen atom from the nitroxyl radicals and formation of aminyl radicals.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 2, pp. 470–472, February, 1989.     

Reaction of t-butoxy radicals with norbornadiene

95 percent of the reaction of t-butoxy radical with norbornadiene occurs by radical addition followed by rearrangement to nortricyclyl and 7-t-butoxynorbornenyl products; the remainder includes a novel radical rearrangement involving a 1,3-H shift and some radical abstraction observed for the first time.     

Reaction of methyl radicals with haloalkanes

The kinetics of reactions involving halogen atom abstraction from haloalkanes by methyl radicals have been studied in the gas phase. Arrhenius parameters for halogen atom transfer were determined relative to those for methyl radical combination:

Reaction of phenyl radicals with propyne

The potential energy surface (PES) for the phenyl + propyne reaction, which might contribute to the growth of polycyclic aromatic hydrocarbons (PAHs) under a wide variety of reaction conditions, is described. The PES was characterized at the B3LYP-DFT/6-31G(d) and B3LYP-DFT/6-311+G(d,p) levels of theory. The energies of the entrance transition states, a direct hydrogen-transfer channel and two addition reactions leading to chemically activated C(9)H(9) intermediates, were also evaluated at the QCISD(T)/ 6-311G(d,p) and CCSD(T)/6-311G(d,p) levels of theory. An extensive set of unimolecular reactions was examined for these activated C(9)H(9)(dagger) intermediates, comprising 70 equilibrium structures and over 150 transition states, and product formation channels leading to substituted acetylenes and allenes such as PhCCH, PhCCCH(3), and PhCHCCH(2) were identified. The lowest energy pathway leads to indene, a prototype PAH molecule containing a five-membered ring. The title reaction thus is an example of possible direct formation of a PAH containing a five-membered ring, necessary to explain formation of nonplanar PAH structures, from an aromatic radical unit and an unsaturated hydrocarbon bearing an odd number of carbons. Extensive Supporting Information is available.