Substituent effects on the rearrangements of cyclohexyl to cyclopentyl radicals involving avermectin-related radicals

The rearrangement of a substituted cyclohexyl radical to a cyclopentylmethyl radical on the skeleton of avermectin B1 has been investigated using density functional (UB3LYP/6-31G(d)) and G3MP2B3 computational methods. The rearrangement is preferred when highly radical stabilizing groups are present at the 2- and 3-positions of the cyclohexyl radical. A substituent on the 3-position of the cyclohexyl radical enables ring-cleavage of the cyclohexyl radical, while a radical stabilizing substituent on the 2-position of the cyclohexyl radical stabilizes the final cyclopentylmethyl radical, enabling the overall rearrangement and reversing the normal thermodynamic preference for the hexenyl radical ring closure.     

Time-resolved FT-EPR study of photoreduction of duroquinone by triethylamine in methanol

Using time resolved Fourier transform EPR spectroscopy the photoreduction of duroquinone by triethylamine in methanol solution was investigated. It is found that the spin-polarized (CIDEP) duroquinone triplet deactivates by electron transfer from triethylamine generating duroquinone radical anion and amine radical cation, and by hydrogen transfer from the solvent generating durosemiquinone radical and hydroxymethyl radical, respectively. All radicals are observed at different conditions and are spin-polarized by triplet mechanism and partially by ST₀ radical pair mechanism. The time dependence of FT-EPR intensities of radical cation and radical anion on the amine concentration is investigated in the range of 1 to 100 mM triethylamine. The contribution of the triplet mechanism to the spin polarization of radicals changes with different triethylamine concentrations. The durosemiquinone radical is found to be transformed into duroquinone radical anion in the presence of triethylamine in the solution. CIDNP experiments indicate that the hydrogen back transfer between the durosemiquinone radical and hydroxymethyl radical pair has a significant influence on the time behaviour of duroquinone radical anion. The intensity of triethylamine radical cation is found to be decreased with the increase of triethylamine concentration, which is interpreted that the triethylamine radical cation is deprotonated by the amine. Based on the FT-EPR results, a new complete mechanism is proposed.     

Ionizing radiation induced reactions of 2,6-dichloroaniline in dilute aqueous solution

In pulse radiolysis investigations the hydroxyl radical formed in water radiolysis reacts with 2,6-dichloroaniline in radical addition to the ring forming hydroxy-cyclohexadienyl radical and also in hydrogen atom abstraction from the amino group resulting in anilino radical. The hydroxy-cyclohexadienyl radical in the absence of dissolved O₂ partly transforms to anilino radical, when dissolved oxygen is present the radical transforms to peroxy radical. According to chemical oxygen demand measurements the reaction of one OH radical induces the incorporation of 0.6 O₂ into the products. It is a typical value for chlorine atom substituted aromatic molecules, and smaller than found for molecules without chlorine atom (1.0–2.0).     

Radical cyclization in heterocycle synthesis 15. Relationship between a Radical species and radical acceptors of three different types of double bond in radical addition-cyclization

Relationship between a radical species and radical acceptors of three different types of double bond in radical addition-cyclization was systematically investigated. Substrates carrying alpha,beta-unsaturated amide, isolated olefin, and oxime ether moieties underwent radical addition-cyclization to give differently substituted lactams depending upon the radicals used. The sulfanyl radical addition-cyclization of the substrate proceeded smoothly to give the 5-membered lactam having an alkoxyamino group as a result of preferable addition of an intermediary alpha-carbonyl radical to the oxime ether. On the other hand, the triethylborane-mediated radical addition-cyclization gave the lactam bearing an iodomethyl group as a result of addition to an intermediary alpha-carbonyl radical to isolated olefin. The different regioselectivity was explained by the stability of the intermediary radical and the interaction between SOMO and HOMO.     

分子间自由基正离子反应研究进展

自由基正离子含有一个正电荷和一对未成对电子,是很多有机化学反应的重要的活性中间体。文章综述了近几年自由基正离子反应研究进展,主要包括化学氧化剂诱导的自由基正离子反应、可见光诱导的自由基正离子反应、电诱导的自由基正离子反应等方面的研究。     

Laser flash photolysis kinetic studies of enol ether radical cations. Rate constants for heterolysis of alpha-methoxy-beta-phosphatoxyalkyl radicals and for cyclizations of enol ether radical cations

Two series of enol ether radical cations were studied by laser flash photolysis methods. The radical cations were produced by heterolyses of the phosphate groups from the corresponding alpha-methoxy-beta-diethylphosphatoxy or beta-diphenylphosphatoxy radicals that were produced by 355 nm photolysis of N-hydroxypryidine-2-thione (PTOC) ester radical precursors. Syntheses of the radical precursors are described. Cyclizations of enol ether radical cations 1 gave distonic radical cations containing the diphenylalkyl radical, whereas cyclizations of enol ether radical cations 2 gave distonic radical cation products containing a diphenylcyclopropylcarbinyl radical moiety that rapidly ring-opened to a diphenylalkyl radical product. For 5-exo cyclizations, the heterolysis reactions were rate limiting, whereas for 6-exo and 7-exo cyclizations, the heterolyses were fast and the cyclizations were rate limiting. Rate constants were measured in acetonitrile and in acetonitrile solutions containing 2,2,2-trifluoroethanol, and several Arrhenius functions were determined. The heterolysis reactions showed a strong solvent polarity effect, whereas the cyclization reactions that gave distonic radical cation products did not. Recombination reactions or deprotonations of the radical cation within the first-formed ion pair compete with diffusive escape of the ions, and the yields of distonic radical cation products were a function of solvent polarity and increased in more polar solvent mixtures. The 5-exo cyclizations were fast enough to compete efficiently with other reactions within the ion pair (k approximately 2 x 10(9) s(-1) at 20 degrees C). The 6-exo cyclization reactions of the enol ether radical cations are 100 times faster (radical cations 1) and 10 000 times faster (radical cations 2) than cyclizations of the corresponding radicals (k approximately 4 x 10(7) s(-1) at 20 degrees C). Second-order rate constants were determined for reactions of one enol ether radical cation with water and with methanol; the rate constants at ambient temperature are 1.1 x 10(6) and 1.4 x 10(6) M(-1) s(-1), respectively.     

SPIN TRAPPING OF FREE RADICALS PRODUCED FROM NITROSOAMINE CARCINOGENS

Abstract— Using the spin trap 5,5-dimethylpyrroline-1-oxide we have demonstrated that the nitrosoamine carcinogen, 1-nitrosopiperidine, upon incubation with rat liver microsomes and nuclei produces two trapped free radical species. One trapped species is the hydroxyl free radical whereas the other is a free radical of unknown structure of the carcinogen itself. Three other nitrosoamine carcinogens tested, including diethylnitrosoamine, dimethylnitrosoamine and 1-nitrosopyrroline yielded similar results with the exception that the trapped carcinogen radical differs dependent upon the compound used. Oxygen was required to produce the hydroxyl free radical but its presence decreased the yield of the carcinogen radical. Both cyanide and α-tocopherol acetate caused a decrease in the yield of the carcinogen free radical. Some heat-labile inhibitor(s) of radical production was/were present in the cytosol. The amount of radical produced was not proportional to the P₄₅₀ content.     

Generation and absolute reactivity of an aryl enol radical cation in solution

Laser flash photolysis of 1-bromo-1-(4-methoxyphenyl)acetone in acetonitrile leads to the formation of the alpha-acyl 4-methoxybenzyl radical that under acidic conditions rapidly protonates to give detectable amounts of the radical cation of the enol of 4-methoxyphenylacetone. This enol radical cation is relatively long-lived in acidic acetonitrile (tau approximately equal to 200 micros), which is on the same order of magnitude as the radical cations of other 4-methoxystyrene derivatives. Rate constants for deprotonation of the radical cation and the acid dissociation constant for the enol radical cation were also determined using time-resolved absorption spectroscopy. Deprotonation is rapid, taking place with a rate constant of 3.9 x 10(6) s(-1), but the enol radical cation is found to be only moderately acidic in acetonitrile having a pK(a) = 3.2. The lifetime of the enol radical cation was also found to be sensitive to the presence of oxygen and chloride. The sensitivity toward oxygen is explained by oxygen trapping the vinyloxy radical component of the enol radical cation/vinyloxy equilibrium, while chloride acts as a nucleophile to trap the enol radical cation.     

Recent advances and perspectives on supramolecular radical cages

Supramolecular radical chemistry has been emerging as a cutting-edge interdisciplinary field of traditional supramolecular chemistry and radical chemistry in recent years. The purpose of such a fundamental research field is to combine traditional supramolecular chemistry and radical chemistry together, and take the benefit of both to eventually create new molecules and materials. Recently, supramolecular radical cages have been becoming one of the most frontier and challenging research focuses in the field of supramolecular chemistry. In this Perspective, we give a brief introduction to organic radical chemistry, supramolecular chemistry, and the emerging supramolecular radical chemistry along with their history and application. Subsequently, we turn to the main part of this topic: supramolecular radical cages. The design and synthesis of supramolecular cages consisting of redox-active building blocks and radical centres are summarized. The host–guest interactions between supramolecular (radical) cages and organic radicals are also surveyed. Some interesting properties and applications of supramolecular radical cages such as their unique spin–spin interactions and intriguing confinement effects in radical-mediated/catalyzed reactions are comprehensively discussed and highlighted in the main text. The purpose of this Perspective is to help students and researchers understand the development of supramolecular radical cages, and potentially to stimulate innovation and creativity and infuse new energy into the fields of traditional supramolecular chemistry and radical chemistry as well as supramolecular radical chemistry.

This Perspective summarizes the recent developments of supramolecular radical cages including the design and synthesis of radical cages, their interesting host–guest spin–spin interactions and applications in radical-mediated/catalyzed reactions.     

Reactions of hydrated electron with various radicals: spin factor in diffusion-controlled reactions

The reactions of hydrated electron (eaq-) with various radicals have been studied in pulse radiolysis experiments. These radicals are hydroxyl radical (*OH), sulfite radical anion (*SO3-), carbonate radical anion (CO3*-), carbon dioxide radical anion (*CO2-), azidyl radical (*N3), dibromine radical anion (Br2*-), diiodine radical anion (I2*-), 2-hydroxy-2-propyl radical (*C(CH3)2OH), 2-hydroxy-2-methyl-1-propyl radical ((*CH2)(CH3)2COH), hydroxycyclohexadienyl radical (*C6H6OH), phenoxyl radical (C6H5O*), p-methylphenoxyl radical (p-(H3C)C6H4O*), p-benzosemiquinone radical anion (p-OC6H4O*-), and phenylthiyl radical (C6H5S*). The kinetics of eaq- was followed in the presence of the counter radicals in transient optical absorption measurements. The rate constants of the eaq- reactions with radicals have been determined over a temperature range of 5-75 degrees C from the kinetic analysis of systems of multiple second-order reactions. The observed high rate constants for all the eaq- + radical reactions have been analyzed with the Smoluchowski equation. This analysis suggests that many of the eaq- + radical reactions are diffusion-controlled with a spin factor of 1/4, while other reactions with *OH, *N3, Br2*-, I2*-, and C6H5S* have spin factors significantly larger than 1/4. Spin dynamics for the eaq-/radical pairs is discussed to explain the different spin factors. The reactions with *OH, *N3, Br2*-, and I2*- have also been found to have apparent activation energies less than that for diffusion control, and it is suggested that the spin factors for these reactions decrease with increasing temperature. Such a decrease in spin factor may reflect a changing competition between spin relaxation/conversion and diffusive escape from the radical pairs.     

Polymerization of coordinated monomers. XXII. Ab initio molecular orbital study on the binary radical complexes of 2-methoxycarbonyl propyl radical with boron trichloride and with boron trifluoride as a model of growing radical end

The geometrical and electronic structures of the binary radical complexes of 2-methoxycarbonyl propyl radical with boron trichloride and with boron trifluoride were determined by using an ab initio molecular orbital method. The 2-methoxycarbonyl propyl radical complex was a model of the growing radical end in the copolymerization of methyl methacrylate in the presence of boron halides. The most stable structure of the binary radical complex composed of 2-methoxycarbonyl propyl radical with boron trichloride was a twisted form in which the dihedral angle between the vinyl group and the ester group was 32°, while that of the binary radical complex composed of methyl methacrylate radical with boron trifluoride was a planar form as the free radical. The frontier orbital energy of 2-methoxycarbonyl propyl radical was lowered by 0.06 au by the coordination of boron trichloride, while that was lowered only by 0.02 au by the coordination of boron trifluoride. The polymerization mechanism was elucidated on the basis of these predictions. © 1993 John Wiley & Sons, Inc.     

Hypocrellin A与二苄胺和N-甲基苄胺的光化学反应

In order to discuss the free radicals formation mechanism of Hypocrellin A（HA）with amino derivatives,the electron-spin resonance（ ESR） spectroscopy was adopted to study the photochemistry on HA with dibenzyl amine（DBA）and N-methyl benzyl amine（NMBA）,respectively. When HA with DBA or NMBA in chloroform solution was illuminated with visible light,singlet oxygen,semiquinone radical and oxynitride radical were formed depending on the condition of the solvent system containing the amino-substituted and solved oxygen. The signal intensity of oxynitride radical decreased with increasing the illumination time,and the signal intensity of semiquinone radical increased with increasing the illumination time. The oxynitride radical content was in inverse ratio with the semiquinone radical generated by being irradiated. In the aerobic system of chloroform solution containing DBA/HA,smiquinone radical was the main radical irradiated. The results indicated that HA induced amino derivatives into HA semiquinone radical.     

SOME ONE ELECTRON REDUCTION PRODUCTS OF FLAVIN ANALOGS: CYANOISOALLOXAZINES AND DEAZAISOALLOXAZINES

Abstract— 8-Cyanoisoalloxazines have been previously shown to form highly stable radical species at basic pH. We have measured the electron spin resonance (EPR) spectra of the radical forms of 8-cyano-10-methyl-3-sulfopropylisoalloxazine (I) at both acidic and basic pH. In both cases. the EPR spectra are similar to those obtained from unsubstituted isoalloxazines. with no indication of hyperfine splitting due to the cyano nitrogen. Laser photolysis of I in the presence of EDTA at basic pH generates two radical species. One of these decays rapidly by a first-order process to produce thc stable radical. The rate of this decay depends upon the initial flavin concentration, thus suggesting a reaction of the radical with oxidized isoalloxazine. The rates of reaction of the radical species with added oxidants (O₂, ferricyanide), and the pH-dependence of stable radical formation, indicate that the rapidly-decaying species is the anion radical of I, and that the stable radical is formed by its reaction with oxidized flavin. Laser photolysis of I at acidic pH, as well as of 8-cyano-5-deaza-isoalloxazine at acidic or basic pH, does not generate stable radical species. I-Deazaisoalloxazines do not give radical transients at all upon laser photolysis.     

Wellenmechanische Absolutrechnung an einer intramolekularen Radikalreaktion an einem methyl– und hydroxylsubstituierten ungesättigten Kohlenwasserstoff

An energy surface for the intramolecular radical reaction oxygen radical ? methylene radical has been estimated on an important part of the α-Tocopherol molecule (Vitamin E), using the SCF –MO –LC (LCGO ) method. The total energy of the oxygen radical is greater than that of the methylene radical by about 49.6 kcal/Mol. The height of the potential barrier between the two tautomeric radicals was calculated to be 54.6 kcal/Mol. The calculated life time of the oxygen radical was 5.3 sec.     

Radical heterolysis reactions. Dynamics of formation, collapse, and solvation of ion pairs determined by a competition kinetic method

The kinetics of radical heterolysis reactions, including rate constants for radical cation-anion contact ion pair formation, collapse of the contact pair back to the parent radical, and separation of the contact pair to a solvent-separated ion pair or free ions were obtained in several solvents for a beta-mesyloxy radical. Rate constants were determined from indirect kinetic studies using thiophenol as both a radical trapping agent via H-atom transfer and an alkene radical cation trapping agent via electron transfer. [reaction: see text].     

The first ESR observation of radical species in subcritical water

Triphenylmethanol was treated in subcritical and supercritical water. A radical species, triphenylmethyl radical, was directly generated from triphenylmethanol in subcritical and supercritical water without using any radical initiator. The radical formation was confirmed by direct electron spin resonance (ESR) measurement in high-temperature and high-pressure subcritical water and by capturing the radical intermediate using hydrogen donors in supercritical water.     

Reactivity of 4-vinylphenol radical cations in solution: implications for the biosynthesis of lignans

Nanosecond laser flash photolysis studies of the radical cation of 4-hydroxy-3-methoxystyrene show that the radical cation reacts with neutral 4-hydroxy-3-methoxystyrene and non-phenolic styrenes with rate constants that range from 1 x 10(8) to 5 x 10(8) M(-1) s(-1). Similar 4-vinylphenol radical cations such as the radical cations of isoeugenol and coniferyl alcohol display reduced reactivity, presumably due to the presence of beta-alkyl substituents. Overall, the results show that the reactivity of 4-vinylphenol radical cations with neutral styrenes parallels the reactivity of non-phenolic styrene radical cations, which are known to undergo efficient radical cation mediated dimerization reactions to give lignan-like compounds. The possibility that the biosynthesis of some lignans may follow a radical cation mediated mechanism is discussed.     

丙烯与HBr/Br·发生自由基加成和取代反应的机理和竞争

含有α-H的烯烃可以与溴自由基发生自由基加成和自由基取代反应。本文以丙烯为例,论述了自由基加成和取代反应的机理和竞争关系,从而帮助读者更好地理解反应条件对优势反应及产物的影响。     

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.     

Spectroscopic detection, reactivity, and acid-base behavior of ring-dimethoxylated phenylethanoic acid radical cations and radical zwitterions in aqueous solution

A product and time-resolved kinetic study of the one-electron oxidation of ring-dimethoxylated phenylethanoic acids has been carried out at different pH values. Oxidation leads to the formation of aromatic radical cations or radical zwitterions depending on pH, and pK(a) values for the corresponding acid-base equilibria have been measured. The radical cations undergo decarboxylation with first-order rate constants (k(dec)) ranging from <10(2) to 5.6 x 10(4) s(-1) depending on radical cation stability. A significant increase in k(dec) (between 10 and 40 times) is observed on going from the radical cations to the corresponding radical zwitterions. The results are discussed in terms of the ease of intramolecular side chain to ring electron transfer required for decarboxylation, in both the radical cations and radical zwitterions.