Thermally induced homolytic scissions of interunitary bonds in a softwood lignin solution: A spin‐trapping study

Unstable chemical species, that is, radicals generated by the thermal treatment of a dimethyl sulfoxide (DMSO) solution of the lignin of a softwood, Yezo spruce (Picea jezoensis Carr.), were studied in detail with an electron spin resonance (ESR) method combined with a spin‐trapping technique. An unstable secondary carbon radical (～CH ·) in the solution was trapped as a stable nitroxide spin adduct [R? (N? O ·)? CH～ (R = tert‐butyl benzene)] when the DMSO solution was heat‐treated in the presence of a spin‐trapping reagent [2,4,6‐tri‐tert‐butylnitrosobenzene (BNB)] at about 40°C. This meant that alkyl phenyl ether bonds (～CH? O‐phenyl), known as interunitary lignin bonds, were homolytically scissioned by the thermal treatment in the lignin solution. A detailed analysis of the ESR spectrum revealed that three kinds of radicals—primary (～CH₂ ·), secondary (～CH ·), and tertiary (～C ·) carbon radicals—were trapped as stable spin adducts at about 60°C, although the phenoxy radical (Ph? O ·) was not trapped by the BNB spin trap as the counter radical of the secondary carbon radical. This suggested that a fairly large steric hindrance existed between the so‐called guaiacoxy radical with a methoxy group in the ortho position and the BNB molecule bearing two butyl groups as bulky moieties in the ortho positions. However, the phenoxy radicals in the lignin solution were stable up to about 60°C. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 93: 2136–2141, 2004     

Spin trapping of propagating radicals with 2,4,6-tri-tert-butyl-1-nitrosobenzene in radical polymerization initiated with di-tert-butyl hyponitrite

To examine the polar effect on spin trapping with 2,4,6-tri-tert-butyl-1-nitrosobenzene (BNB), propagating radicals from monomers were allowed to react with BNB to provide anilino radicals and nitroxides of which the amounts were determined by ESR spectroscopy. The proportion of the anilino radical increased with an increase in the steric congestion and electron donating character of the radical. Poly(vinyl ether) radicals exclusively gave the respective anilino radicals. Poly(vinyl ester) radicals yielded large amounts (>50%) of the anilino radicals, although the nitroxides were the main products (>85%) from the poly(alkyl acrylate) radicals. The polymer radicals of methyl methacrylate and ethyl itaconate only yielded the anilino radicals. The polymer radicals from ethyl -chloroacrylate and acrylonitrile reacted preferentially with the respective monomers leading to polymer formation, and the ESR spectra of the adducts were not observed.     

Evaluation of Reaction Efficiency of Thioacidolysis for Cleavage of β-O-4 Interunitary Linkages by Using β-O-4 Type Artificial Lignin Polymer

Abstract

Dimeric lignin model compounds with non-phenolic and phenolic moieties and a β -O-4 type artificial lignin polymer were subjected to thioacidolysis to evaluate the reaction efficiency of thioacidolysis for cleavage of β -O-4 interunitary linkage. The obtained yields of thioethylated monomeric products from the dimeric lignin model compounds reached nearly 100% under the conventional condition, whereas that from the artificial lignin polymer was as low as 74%. Neither prolonged reaction time nor increased concentration of ethanethiol (the thioacidolysis reagent) enhanced the resulting monomer yields from the polymer (69–79%). Thioacidolysis of the lignin model compounds followed by HPSEC analysis also showed the dimeric model compounds were degraded almost quantitatively, but that the artificial lignin polymer was not. Thioacidolysis followed by desulfurization gave at least one dimeric product resulting from incomplete β -O-4 cleavage at significant yield. These results suggested the conventional thioacidolysis could not achieve quantitative cleavage of β -O-4 linkages in lignin macromolecules.     

A new polymer-incorporated spin-trapping reagent aimed at environmental use. Reactions with organic free radicals

Primary and secondary alkyl free radicals in the gas phase were shown to be trapped more efficiently by poly[N-(p-vinylbenzylidene)-tert-butylamine N-oxide] and its copolymers in comparison with “monomeric” PBN. Polymer-incorporated nitrone was shown to be useful in trapping free radicals in the gas phase.     

Chemical intermediates and derivatives from oleyl alcohol

Several series of compounds were prepared from oleyl alcohol which may prove useful as lubricants and plasticizers. The reactions involved addition to the double bond and replacement of the hydroxyl moiety. One series of compounds is characterized l-R′, 9(10)R octadecane where l-R′ signifies the replacement of hydroxyl by ethoxy,tert-butylphenyl,tert-butoxy and phenyl. Examples of additions across the double bond 9(10)R, include hydrogen, methoxy,tert-butoxy,tert-butylphenyl, and phenyl. Other test series were 9(10)-R, 27(28)-R-hexatriacontane andbis [9(10)-R-octadecyl] ether where R signifies additions across a pair of double bonds. Additions in these series include methoxy, ethoxy,tert-butoxy,tert-butylphenyl, 2-ethylhexoxy, and phenyl. Derivatives of octadecane were fluid and several had fairly low pour points. The derivatives of hexatriacontane and dioctadecyl ether were either low-melting solids or liquids. Details concerning the synthesis and several physical properties are presented.     

利用ESR技术研究α—蒎烯β—蒎烯光敏氧化反应机理

本文主要利用电子顺磁共振自旋捕获技术研究９,１０－二氰基蒽敏化α－蒎烯,β－蒎烯光氧化反应,提供了在乙腈中α－蒎烯和β－蒎烯的光氧化反应过程中存在超氧负离子基和单重 氧的直接证据;在四氯化碳溶剂中只捕获到＾１Ｏ２;在正己烷中没有捕获到Ｏ＾－２或＾１Ｏ２．ＥＳＲ实验结果进一步证明在乙腈中光敏氧化反应的＾１Ｏ２可能来自Ｏ＾－２和反应底物α－β,蒎烯正离子自由基之间的电荷复合。     

Stabilization of photo-induced radicals in hematoporphyrin-IX-doped chitosan film

Induction and stabilization of free radicals were investigated in hematoporphyrin-IX (Hp)-doped chitosan (Hp-Ch) film by electron spin resonance (ESR) following photo-irradiation. Induced radicals were more stable in chitosan and 6-O-carboxymethyl chitin films than in carboxymethyl cellulose and sodium alginate films. Hydroxyl groups on D-glucosamine residues in chitosan are suggested as participating in accepting radicals, since spin trapping was absorbed in ESR spectra of Hp-Ch film by the use of oxygen sensitive spin trapping reagent. An induced circular dichroism spectrum was observed only for Hp-doped chitosan film over a range 360–450 nm among seven pairs of polymers and dyes; it is suggested that Hp molecules are arranged parallel along the carbohydrate backbone of chitosan, resulting in the highest acceptance of photo-induced radicals in the polymer film.     

ESR study of the effect of ferric chloride on the photodegradation of model compound for polypropylene

In our previous article on the photodegradation of polypropyle (PP), the effect of ferric chloride (FeCl₃) accelerating the formation of peroxy radical and depressing the formation of alkyl radical were reported. In the present article, the influence of FeCl₃ on model compounds of PP was examined using electron spin resonance (ESR) spectrometry. The following compounds were employed as models of PP, including its irregular structures: 2-methylpentane (2-MP), 2,4-dimethylpentane (2,4-DMP), 2-methyl-4-pentanone (2-M4P), 2,6-dimethyl-4-heptanone (2,6-DM4H), 2-methyl-1-pentene (2-M1P), and tert-butylhydroperoxide (t-BuO₂H). FeCl₃ accelerated the formation of alkyl radicals for 2-MP and 2,4-DMP, alkyl and acyl radicals for 2-M4P and 2,6-DM4H, and alkyl radicals for 2-M1P. As no definite effect of FeCl₃ was observed for n-pentane and 2-octanone, FeCl₃ was assumed to attack saturated hydrocarbons, ketones at a tertiary carbon-hydrogen bond, and hydrocabons at an allylic hydroge, leading to easier photodegradations. FeCl₃ was also effective for the photodegradation of t-BuO₂H using λ >300 nm, so that FeCl₃ is believed to contribute also to the photodegradation of PP under the same irradation conditions. The catalytic effect of FeCl₃ in photodegradation seems to origirate in a redox reaction.     

有机锡化合物光解活泼自由基的ESR研究

本文用自旋捕捉技术与ESR相结合的方法,研究了六种有机锡化合物的光解反应历程。结果表明:有机锡化合物紫外光照时,碳—锡键发生均裂,产生碳中心和锡中心自由基。其中碳中心自由基易被捕捉剂α-苯基-N-特丁基氮氧化物(PBN)或2,3,5,6-四甲基亚硝基苯(ND)所捕获;而锡中心自由基可与菲醌形成稳定的环状加合物。由于环状加合物中配体的不同,产生的空间效应也不同,从而导致加合物中的未偶电子云密度发生变化,给出相异的ESR信号。     

Radicals generated in autoxidized methyl linoleate by light irradiation

The structure of free radicals generated in the autoxidation of methyl linoleate (ML) was studied by the spin trapping technique using deuterated nitrosodurene, (CD₃)₄C₆HNO, as the spin trap. The secondary alkyl radicals were trapped after irradiation of ML with UV light. The formation rate of secondary alkyl radicals increased upon shortening the wavelength of irradiation light and was closely correlated with the peroxide value of autoxidized ML when a UV light longer than 250 nm was employed. When hydroperoxides separated from autoxidized ML were added to ML, the relationship between the formation rate of secondary alkyl radicals and the amounts of added hydroperoxides was nearly linear. These results suggest that secondary alkyl radicals are generated by proton abstraction of the active radicals, such as RO and HO, which are produced by the photolysis of hydroperoxides with UV light. The spin trapping technique can be applied to the study of lipid oxidation and/or photolysis of autoxidized lipid.     

Investigation of oxygen diffusion into contact lenses using electron spin resonance spectroscopy

Oxygen permeability is the most important parameter of contact lenses, as lack of oxygen causes corneal edema and threatens the vision of the patient. This study was unique in that it used an electron spin resonance (ESR) technique to determine the oxygen diffusion coefficient (D) of contact lenses. Although there are many methods and techniques for investigating oxygen diffusion into contact lenses, ESR was used for the first time in this study. The ESR technique is based on the scavenging of radicals produced in lenses by oxygen. As a contact lens is not a paramagnetic substance, it cannot give an ESR spectrum. But it does produce an ESR spectrum after γ irradiation. When a vacuum‐irradiated contact lens is exposed to air, the radicals trapped in the lens are transformed into peroxide radicals by the addition of molecular oxygen to the free radicals, and the ESR spectrum begins to change with time. This effect can be used as a tool to measure oxygen uptake in irradiated contact lenses. The oxygen diffusion coefficient of a contact lens was determined from changes in ESR signal intensity varying with time. The diffusion coefficients of oxygen for a contact lens were determined for rapid decay [(1.5 + 0.4) × 10^?8 cm²/s] and slow decay [(1.3 + 0.3) × 10^?9 cm²/s] in this study. These values are in agreement with the D values given in the literature for polymeric materials used for contact lenses. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 2937–2941, 2006     

Up to 96% Enantioselectivities in the Hydrogenation of Fluorine Substituted (E)‐2,3‐Diphenylpropenoic Acids over Cinchonidine‐Modified Palladium Catalyst

The enantioselective hydrogenation of methoxy‐ and fluorine‐substituted (E)‐2,3‐diphenylpropenoic acid derivatives was studied over cinchonidine‐modified, supported palladium catalysts in the absence and presence of benzylamine as additive. The fluorine substituent in the appropriate position was even more efficient than the methoxy group in increasing the optical purity of the saturated product. High enantioselectivities, up to 96%, were obtained in the hydrogenation of some disubstituted derivatives, unprecedented in the hydrogenation of prochiral unsaturated carboxylic acids over modified heterogeneous catalyst. The best optical purities were reached in the hydrogenation of derivates bearing a para‐substituent on the β phenyl and an ortho‐substituent on the α phenyl ring, respectively. The influence of the substituent on the β phenyl ring was attributed to the increase in the efficiency of the modifier‐substrate interaction by electronic effects or to a decrease in the adsorption strength of the substituted acid over modified surface sites. The beneficial effect of the ortho‐substituent on the α phenyl ring was assumed to be due to the additional interaction of this substituent with the modifier on the surface, its steric hindrance contributing only in a small part to the observed effect. These suggestions were supported by results obtained in the hydrogenations of some methyl‐substituted derivatives.     

Oxidative Stability of Lipids by Means of EPR Spectroscopy and Chemiluminescence

The aim of this study was to investigate the oxidation of selected vegetable oils (CLSO, CCSO, CBO) at accelerated oxidation rates. Several seldom used analytical methods were applied including electron paramagnetic resonance (EPR), spin trapping with α-(4-pyridyl-1-oxide)-N-tert-butylnitrone (POBN) and 5,5-dimethyl-1-pyrroline-N-oxide (DMPO), Fe²⁺-induced chemiluminescence, Rancimat tests, and the determination of conjugated diens at λ = 233 nm. The antioxidative properties of POBN and DMPO were also investigated. The time required for each method was determined. EPR spectrometry of trapped radicals generated during oxidation turned out to be the fastest method to determine oxidative stability. Chemiluminometric determination of oxidation kinetics showed that POBN has a very strong anti-oxidative potential: it significantly (by 160–277%) lengthened the time to the chemiluminescence peak, as well as the induction time in the Rancimat test (by 110–140%). Photo-oxidation studies showed that superoxide anion radicals are the main factor responsible for the oxidation of lipids in the investigated oils.     

Antioxidant activity of Magnolol, honokiol, and related phenolic compounds

The antioxidant activity of 10 Japanese and Chinese crude drugs (Kampo drugs) was determined in vitro. Extract of Magnolia cortex, which had the highest antioxidant activity, contained phenolic compounds magnolol and honokiol. However, inhibitory effects of these compounds on lipid oxidation were weaker than that of α-tocopherol as measured by thiobarbituric acid assay. The structure-activity relationship of phenolic compounds showed that antioxidant activities were in the order 4-allyl-2,6-dimethoxyphenol ≥ p,p′-biphenol > eugenol > 2-allyl-6-methylphenol > honokiol > magnolol > caffeic acid > p-ethylphenol > guaiacol. As expected, these results showed that an electron donor and/or bulky groups at the ortho- or para-position of the phenol were required for inhibition of lipid oxidation. Electron spin resonance spin trapping experiments showed that phenol compounds with an allyl substituent on their aromatic rings directly scavenged superoxide (O ₂ ⁻ ), and that only eugenol trapped hydroxyl radicals. These findings suggest that phenolic compounds that contain allyl groups may be effective antioxidants because of the scavenging ability of O ₂ ⁻ or hydroxyl radical, whereas other phenols, without an allyl moiety such as α-tocopherol, may play a role in the termination of free radical chain reactions.     

Conversion of alkyl radicals to allyl radicals in irradiated single crystal mats of polyethylene

The decay of alkyl radicals, the conversion of alkyl radicals to allyl radicals and the trapping of allyl radicals in irradiated single crystal mats of polyethylene have been studied by electron spin resonance (e.s.r.). It has been suggested that in the crystal core alkyl radicals react with trans-vinylene double bonds and are converted into trans-vinylene allyl radicals; at the crystal surface, alkyl radicals react with vinyl end groups and are converted into allyl radicals with vinyl end groups. The decay of radical pairs and the formation of trans-vinylene double bonds are discussed.     

Study of Structure of Industrial Acid Hydrolysis Lignin,Oxidized in the H2O2-H2SO4 System

Products of oxidation of industrial acid hydrolysis lignin in the H₂O₂-H₂SO₄ system were studied using ¹³C NMR (in solution and solid state), MALDI-MS, and MS(ESI) techniques. Oxidation of hydrolysis lignin leads to the opening of aromatic rings of lignin, yielding carboxylic groups. Alkyl aryl ether linkages (β-O-4-bonds) between lignin phenyl propane units are not significantly affected by the oxidation. The structure of oxidized hydrolysis lignin is proposed. The basic structural unit of oxidized hydrolysis lignin is a muconic acid derivative.     

Electron spin resonance spectroscopy for evaluation of early oxidative events in semisolid palm oil

Electron spin resonance (ESR) spectroscopy was applied to study early oxidative events in semisolid palm oil in bulk. Oil was stored at mildly accelerated conditions of 50°C for 7 days and the free radical formation was followed with the addition of spin trap N‐tert‐butyl‐α‐phenyl‐nitrone. Dissolution of the oil samples in isooctane prior to ESR measurements stabilized the ESR signal allowing the changes in relative free radical concentrations during oil storage to be monitored. Formation of lipid hydroperoxides as primary lipid oxidation products was found to correlate with the tendency for the formation of free radicals in the oil during the storage and accordingly, ESR spectroscopy may be used to detect the early events in lipid oxidation in palm oil. However, the interference of added rosemary extract (RE) in ESR analyses was seen as an increased ESR signal while the efficiency of RE as antioxidant in palm oil was confirmed by isothermal DSC. Practical applications : ESR spectroscopy may be used to evaluate early events of oxidation in semisolid oils such as palm fat, which is widely used in food industry.     

Carbon radicals generated by solid polymers: Electron spin resonance spectroscopy for detection of species in water

Radicals generated in plastic medical devices (solid phase) by γ-rays or electron-beam irradiation during sterilization are known to cause oxidation of protein drugs, resulting in a loss or reduction in drug efficacy. The generation of radical species in water by the radical species in solid polymers has not been proved. Using electron spin resonance (ESR) spectroscopy, we confirm the generation of new radicals in water by γ-ray irradiated cyclic olefin polymers (COP). ESR measurements are obtained using 4-hydroxy-2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPOL) as a spin probe and 5-(2,2-dimethyl-1,3-propoxycyclophosphoryl)-5-methyl-1-pyrroline N-oxide (CYPMPO) as a spin trap, in which the irradiated COP was immersed. The ESR signals indicate the TEMPOL radicals decline over time, suggesting the generation of new radicals. Conversely, the characteristic ESR signals of the adduct formed by the reaction between CYPMPO and the hydroxyl radical are observed. Thus, hydroxyl radicals are generated because of the migration of the radicals from COP to water. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48604.     

苯甲醛及对溴苯甲醛光解初级过程自由基的ESR研究

苯甲醛的光解与其在放置过程中的自氧化引发机理密切相关,因此确定光解过程的主要中间产物有重要意义。自氧化的全过程比较复杂,但单纯的光解本身显然相对简单一些。本文用自旋捕捉-ESR技术研究了苯甲醛及与其相类似的对溴苯甲醛在紫外和可见光作用下生成的活泼中间体,并讨论了在本文实验条件下的光解初级过程。 苯甲醛为色谱纯样品,对溴苯甲醛和二苯酮经两次重结晶提纯,溶剂苯经重蒸馏后     

Thermomechanical Pulp and Light -Photoactivity of α-Carbonyl Group in Solid Lignin

Interaction of sunlight and UV light with thermomechanical (TMP) pulps, milled wood lignin (MWL) and various lignin model compounds in solid state was studied. It was found that TMP fibers were sensitive to these lights. During exposure, TMP lost its brightness as a function of irradiation time and increased its yellowness. The α-carbonyl group functioned as a light absorption center to promote photocleavage of C_α—C_β and β–0–4 linkages. Electron spin resonance (ESR) studies demonstrated that free radicals were generated in the interim. Phenoxy radicals appeared to be important radical intermediates that ultimately transformed into o—quinonoid structures.