Log in

Relevant bibliographies by topics / Phenoxyl-radicals / Journal articles

To see the other types of publications on this topic, follow the link: Phenoxyl-radicals.

Journal articles on the topic 'Phenoxyl-radicals'

Author: Grafiati

Published: 4 June 2021

Last updated: 22 June 2024

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the top 50 journal articles for your research on the topic 'Phenoxyl-radicals.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Browse journal articles on a wide variety of disciplines and organise your bibliography correctly.

1

Manderville, Richard A. "Ambident reactivity of phenoxyl radicals in DNA adduction." Canadian Journal of Chemistry 83, no. 9 (2005): 1261–67. http://dx.doi.org/10.1139/v05-121.

Full text

Abstract:

Phenols are a class of compounds that can create beneficial effects in vivo owing to their antioxidant properties (through radical scavenging), or they can display hazardous effects owing to their pro-oxidant properties. The mechanism by which phenols act as pro-oxidants stems from their one-electron oxidation into reactive phenoxyl radicals by peroxidase enzymes or redox-active transition metals. In the presence of thiols and molecular oxygen, these reactive phenoxyl radicals stimulate an oxidative stress and cause oxidative damage to biomolecules, which is proposed to contribute to the occur

APA, Harvard, Vancouver, ISO, and other styles

2

Shukla, D., N. P. Schepp, N. Mathivanan, and L. J. Johnston. "Generation and spectroscopic and kinetic characterization of methoxy-substituted phenoxyl radicals in solution and on paper." Canadian Journal of Chemistry 75, no. 12 (1997): 1820–29. http://dx.doi.org/10.1139/v97-615.

Full text

Abstract:

A number of methoxy-substituted phenoxyl radicals have been generated and characterized by laser flash photolysis techniques in solution and on paper. The radicals have been produced by three routes in solution: hydrogen abstraction from phenols by tert-butoxyl radical, photolysis of α-aryloxyacetophenones, and direct excitation of phenols. Most of the phenoxyl radicals studied have a characteristic absorption near 400 nm; the ortho-substituted radicals have an additional broad absorption in the visible in non-hydroxylic solvents (e.g., 650 nm for 2-methoxyphenoxyl radical). The relative inten

APA, Harvard, Vancouver, ISO, and other styles

3

Aotake, Tatsuya, Mitsuharu Suzuki, Naoki Aratani, et al. "Correction: 9,9′-Anthryl-anthroxyl radicals: strategic stabilization of highly reactive phenoxyl radicals." Chemical Communications 51, no. 24 (2015): 5124. http://dx.doi.org/10.1039/c5cc90112j.

Full text

APA, Harvard, Vancouver, ISO, and other styles

4

de Jonge, Cornelis R. H. I. "Reactions with Stable Phenoxyl Radicals." Liebigs Annalen der Chemie 1986, no. 2 (1986): 299–304. http://dx.doi.org/10.1002/jlac.198619860210.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

Teng, Zhuochao, Xianwei Zhao, Hetong Wang, et al. "Mechanism and kinetic properties for the complete series reactions of chloro(thio)phenols with O(3P) under high temperature conditions." RSC Advances 11, no. 29 (2021): 17683–93. http://dx.doi.org/10.1039/d1ra02407h.

Full text

Abstract:

Under pyrolysis or combustion conditions, chlorophenols (CPs) and chlorothiophenols (CTPs) can readily form chlorophenoxy radicals (CPRs) and chlorotriophenoxy radicals (CTPRs) by abandoning the phenoxyl-H and sulfydryl-H, respectively.

APA, Harvard, Vancouver, ISO, and other styles

6

Wojnárovits, L., A. Kovács, and G. Földiák. "Spectral characteristics of monosubstituted phenoxyl radicals." Radiation Physics and Chemistry 50, no. 4 (1997): 377–79. http://dx.doi.org/10.1016/s0969-806x(97)00053-4.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

Thomas, Fabrice. "ChemInform Abstract: Metal-Coordinated Phenoxyl Radicals." ChemInform 42, no. 41 (2011): no. http://dx.doi.org/10.1002/chin.201141217.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

Dol, Cyrielle, Guillaume Gerbaud, Bruno Guigliarelli, Emily Bloch, Stéphane Gastaldi, and Eric Besson. "Modulating lifetimes and relaxation times of phenoxyl radicals through their incorporation into different hybrid nanostructures." Physical Chemistry Chemical Physics 21, no. 29 (2019): 16337–44. http://dx.doi.org/10.1039/c9cp03052b.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

Kasumov, Veli T., Bünyamin Karabulut, Ibrahim Kartal, and Fevzi Köksal. "Synthesis And Spectroscopic Studies Of New Bis(N-1-hydroxy-2,6-Di-Fe/Tf-Butylphenyl- Salicylideneaminato)Cobalt(Ii) Complexes And Their Oxidation With PbO2." Zeitschrift für Naturforschung B 56, no. 8 (2001): 778–86. http://dx.doi.org/10.1515/znb-2001-0811.

Full text

Abstract:

A series of new bis[N-(1-OH-2,6-di-tert-butylphenyl)salicylaldiminato]cobalt(II) complexes possessing one or two HO- and CH3O - substituents on the salicylaldehyde moiety were prepared, and their spectroscopic properties as well as their oxidation with PbO2 were examined. ESR data indicate that oxidation of the complexes produces stable phenoxyl radicals. All phenoxyl radicals have similar g-values and hyperfine coupling constants, which are influenced very little by the substituents and by coordination. The experimental observations indicate that the Co(L·x)2 radicals are ligand-localized and

APA, Harvard, Vancouver, ISO, and other styles

10

Molloy, J. K., O. Jarjayes, C. Philouze, L. Fedele, D. Imbert, and F. Thomas. "A redox active switch for lanthanide luminescence in phenolate complexes." Chemical Communications 53, no. 3 (2017): 605–8. http://dx.doi.org/10.1039/c6cc07942c.

Full text

APA, Harvard, Vancouver, ISO, and other styles

11

d’Alessandro, Nicola, Giorgio Bianchi, Xingwang Fang, Famin Jin, Heinz-Peter Schuchmann, and Clemens von Sonntag. "Reaction of superoxide with phenoxyl-type radicals." Journal of the Chemical Society, Perkin Transactions 2, no. 9 (2000): 1862–67. http://dx.doi.org/10.1039/b003346o.

Full text

APA, Harvard, Vancouver, ISO, and other styles

12

Foti, M., K. U. Ingold, and J. Lusztyk. "The Surprisingly High Reactivity of Phenoxyl Radicals." Journal of the American Chemical Society 116, no. 21 (1994): 9440–47. http://dx.doi.org/10.1021/ja00100a005.

Full text

APA, Harvard, Vancouver, ISO, and other styles

13

Ye, Mingyu, and Robert H. Schuler. "Second-order combination reactions of phenoxyl radicals." Journal of Physical Chemistry 93, no. 5 (1989): 1898–902. http://dx.doi.org/10.1021/j100342a040.

Full text

APA, Harvard, Vancouver, ISO, and other styles

14

Jonsson, M., J. Lind, T. Reitberger, T. E. Eriksen, and G. Merenyi. "Free radical combination reactions involving phenoxyl radicals." Journal of Physical Chemistry 97, no. 31 (1993): 8229–33. http://dx.doi.org/10.1021/j100133a018.

Full text

APA, Harvard, Vancouver, ISO, and other styles

15

Bolton, J. "Quinoids, quinoid radicals, and phenoxyl radicals formed from estrogens and antiestrogens." Toxicology 177, no. 1 (2002): 55–65. http://dx.doi.org/10.1016/s0300-483x(02)00195-6.

Full text

APA, Harvard, Vancouver, ISO, and other styles

16

Aotake, Tatsuya, Mitsuharu Suzuki, Naoki Aratani, et al. "9,9′-Anthryl-anthroxyl radicals: strategic stabilization of highly reactive phenoxyl radicals." Chemical Communications 51, no. 31 (2015): 6734–37. http://dx.doi.org/10.1039/c4cc10104a.

Full text

APA, Harvard, Vancouver, ISO, and other styles

17

Tomilin, O. B., O. V. Boyarkina, and B. S. Tanaseichuk. "One-Electron Transfer during Dimerization of Phenoxyl Radicals." Russian Journal of Organic Chemistry 58, no. 5 (2022): 637–47. http://dx.doi.org/10.1134/s1070428022050013.

Full text

APA, Harvard, Vancouver, ISO, and other styles

18

Nishide, Hiroyuki, Makoto Miyasaka, Ryuji Doi, and Takashi Araki. "Poly(1,2-phenylenevinylene) Ferromagnetically 3,5-Bearing Phenoxyl Radicals." Macromolecules 35, no. 3 (2002): 690–98. http://dx.doi.org/10.1021/ma011209f.

Full text

APA, Harvard, Vancouver, ISO, and other styles

19

Xie, Chunping, and Paul M. Lahti. "Highly stabilized phenoxyl radicals with hydrogen-bonding capability." Tetrahedron Letters 40, no. 23 (1999): 4305–8. http://dx.doi.org/10.1016/s0040-4039(99)00784-4.

Full text

APA, Harvard, Vancouver, ISO, and other styles

20

Sakihama, Yasuko, Jun'ichi Mano, Satoshi Sano, Kozi Asada, and Hideo Yamasaki. "Reduction of Phenoxyl Radicals Mediated by Monodehydroascorbate Reductase." Biochemical and Biophysical Research Communications 279, no. 3 (2000): 949–54. http://dx.doi.org/10.1006/bbrc.2000.4053.

Full text

APA, Harvard, Vancouver, ISO, and other styles

21

Forni, L. G., and R. L. Willson. "Thiyl and phenoxyl free radicals and NADH Direct observation of one-electron oxidation." Biochemical Journal 240, no. 3 (1986): 897–903. http://dx.doi.org/10.1042/bj2400897.

Full text

Abstract:

Absolute rate constants for the reaction of NADH with thiyl free radicals derived from various sulphur-containing compounds of biological significance were measured by using the technique of pulse radiolysis. These and related reactions with phenoxyl free radicals are believed to occur through one-electron-transfer processes. Further evidence comes from studies with deuterated NADH. The results support the possibility that, in biochemical systems, thiols may act as catalysts linking hydrogen-atom and electron-transfer reactions.

APA, Harvard, Vancouver, ISO, and other styles

22

Adounkpe, Julien, Martin Aina, Daouda Mama, and Brice Sinsin. "Gas Chromatography Mass Spectrometry Identification of Labile Radicals Formed during Pyrolysis of Catechool, Hydroquinone, and Phenol through Neutral Pyrolysis Product Mass Analysis." ISRN Environmental Chemistry 2013 (December 29, 2013): 1–8. http://dx.doi.org/10.1155/2013/930573.

Full text

Abstract:

Catechol, hydroquinone, and phenol are known to be environmental pollutants due to their ability to generate environmentally free radicals, which cause millions of deaths worldwide. Recently, efforts have been done to precisely identify the origin and the nature of those free radicals employing EPR-LTMI technique. All the three precursors generate cyclopentadienyl radical as major pyrolysis products and phenoxyl radical as both pyrolysis and photolysis products which were obtained from phenol; ortho-semiquinone and para-semiquinone were seen, respectively, from the pyrolysis of catechol and hy

APA, Harvard, Vancouver, ISO, and other styles

23

Bordwell, Frederick G., and Jinpei Cheng. "Substituent effects on the stabilities of phenoxyl radicals and the acidities of phenoxyl radical cations." Journal of the American Chemical Society 113, no. 5 (1991): 1736–43. http://dx.doi.org/10.1021/ja00005a042.

Full text

APA, Harvard, Vancouver, ISO, and other styles

24

Lahti, Paul M., Burak Esat, Jacqueline R. Ferrer, et al. "Polymeric, H-Bonded, and Chelatable Phenoxyl and Nitroxide Radicals." Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals 334, no. 1 (1999): 285–94. http://dx.doi.org/10.1080/10587259908023326.

Full text

APA, Harvard, Vancouver, ISO, and other styles

25

Xu, Jing, Xinguo Wu, Wei Yan, Ruxiu Cai, and Zhixin Lin. "A new kinetic method for quantification phenoxyl free radicals." Talanta 70, no. 2 (2006): 323–29. http://dx.doi.org/10.1016/j.talanta.2006.02.055.

Full text

APA, Harvard, Vancouver, ISO, and other styles

26

Neta, Pedatsur, and Jan Grodkowski. "Rate Constants for Reactions of Phenoxyl Radicals in Solution." Journal of Physical and Chemical Reference Data 34, no. 1 (2005): 109–99. http://dx.doi.org/10.1063/1.1797812.

Full text

APA, Harvard, Vancouver, ISO, and other styles

27

Xie, Chunping, Paul M. Lahti, and Clifford George. "Modulating Spin Delocalization in Phenoxyl Radicals Conjugated with Heterocycles." Organic Letters 2, no. 22 (2000): 3417–20. http://dx.doi.org/10.1021/ol0063407.

Full text

APA, Harvard, Vancouver, ISO, and other styles

28

Chekalov, A. K., A. I. Prokof'ev, N. N. Bubnov, S. P. Solodovnikov, and M. I. Kabachnik. "EPR spectra of some substituted 2-(?-hydroxyethoxy)phenoxyl radicals." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 36, no. 6 (1987): 1155–59. http://dx.doi.org/10.1007/bf00956652.

Full text

APA, Harvard, Vancouver, ISO, and other styles

29

Grampp, Günter, Stephan Landgraf, and Claudia Mureşanu. "Redox properties and bond dissociations energies of phenoxyl radicals." Electrochimica Acta 49, no. 4 (2004): 537–44. http://dx.doi.org/10.1016/j.electacta.2003.09.007.

Full text

APA, Harvard, Vancouver, ISO, and other styles

30

Folkes, Lisa K., Madia Trujillo, Silvina Bartesaghi, Rafael Radi, and Peter Wardman. "Kinetics of reduction of tyrosine phenoxyl radicals by glutathione." Archives of Biochemistry and Biophysics 506, no. 2 (2011): 242–49. http://dx.doi.org/10.1016/j.abb.2010.12.006.

Full text

APA, Harvard, Vancouver, ISO, and other styles

31

JONSSON, M., J. LIND, T. REITBERGER, T. E. ERIKSEN, and G. MERENYI. "ChemInform Abstract: Free Radical Combination Reactions Involving Phenoxyl Radicals." ChemInform 24, no. 47 (2010): no. http://dx.doi.org/10.1002/chin.199347094.

Full text

APA, Harvard, Vancouver, ISO, and other styles

32

Wanke, Riccardo, Laurent Benisvy, Maxim L. Kuznetsov, M. Fátima C. Guedes da Silva, and Armando J. L. Pombeiro. "Persistent Hydrogen-Bonded and Non-Hydrogen-Bonded Phenoxyl Radicals." Chemistry - A European Journal 17, no. 42 (2011): 11882–92. http://dx.doi.org/10.1002/chem.201101509.

Full text

APA, Harvard, Vancouver, ISO, and other styles

33

Johnston, Linda J., N. Mathivanan, Fabrizia Negri, Willem Siebrand, and Francesco Zerbetto. "Assignment and vibrational analysis of the 600 nm absorption band in the phenoxyl radical and some of its derivatives." Canadian Journal of Chemistry 71, no. 10 (1993): 1655–62. http://dx.doi.org/10.1139/v93-206.

Full text

Abstract:

An experimental and theoretical study is reported of the 600 nm band system of phenoxyl and several methoxy substituted phenoxyls. These radicals, generated in freon, show a diffuse band in this region with a vibrational structure that is incompletely resolved but consistent with the 500 cm−1 "progression" observed earlier for phenoxyl in the vapour and in a rigid matrix. The low intensity of this band is considerably enhanced by ortho-methoxy substitution. To establish its assignment and analyze its structure, semi-empirical and ab initio quantum chemical calculations have been performed. It

APA, Harvard, Vancouver, ISO, and other styles

34

BORDWELL, F. G., and J. P. CHENG. "ChemInform Abstract: Substituent Effects on the Stabilities of Phenoxyl Radicals and the Acidities of Phenoxyl Radical Cations." ChemInform 22, no. 25 (2010): no. http://dx.doi.org/10.1002/chin.199125068.

Full text

APA, Harvard, Vancouver, ISO, and other styles

35

WINTERBOURN, Christine C., Helena N. PARSONS-MAIR, Silvia GEBICKI, Janusz M. GEBICKI, and Michael J. DAVIES. "Requirements for superoxide-dependent tyrosine hydroperoxide formation in peptides." Biochemical Journal 381, no. 1 (2004): 241–48. http://dx.doi.org/10.1042/bj20040259.

Full text

Abstract:

Superoxide reacts rapidly with other radicals, but these reactions have received little attention in the context of oxidative stress. For tyrosyl radicals, reaction with superoxide is 3-fold faster than dimerization, and forms the addition product tyrosine hydroperoxide. We have explored structural requirements for hydroperoxide formation using tyrosine analogues and di- and tri-peptides. Superoxide and phenoxyl radicals were generated using xanthine oxidase, peroxidase and the respective tyrosine derivative, or by γ-radiation. Peroxides were measured using FeSO4/Xylenol Orange. Tyrosine and t

APA, Harvard, Vancouver, ISO, and other styles

36

Porkhun, V. I., Yu V. Aristova, and E. V. Porkhun. "Quantum chemical study of the rearrangement of phenoxyl-hydroxyphenyl radicals." Russian Journal of Physical Chemistry A 91, no. 3 (2017): 472–75. http://dx.doi.org/10.1134/s0036024417030220.

Full text

APA, Harvard, Vancouver, ISO, and other styles

37

Amorati, Riccardo, and Gian Franco Pedulli. "Hydrogen bond donating ability of meta and parahydroxy phenoxyl radicals." Org. Biomol. Chem. 10, no. 4 (2012): 814–18. http://dx.doi.org/10.1039/c1ob06502e.

Full text

APA, Harvard, Vancouver, ISO, and other styles

38

Iida, Toshiyuki, Joji Ohshita, Nobuaki Ohta та ін. "Spin–spin interaction between phenoxyl radicals through σ–π system". Journal of Organometallic Chemistry 688, № 1-2 (2003): 192–99. http://dx.doi.org/10.1016/j.jorganchem.2003.09.004.

Full text

APA, Harvard, Vancouver, ISO, and other styles

39

Tripathi, G. N. R. "Proton Reactivity and Electronic Structure of Phenoxyl Radicals in Water†." Journal of Physical Chemistry A 102, no. 13 (1998): 2388–97. http://dx.doi.org/10.1021/jp9808633.

Full text

APA, Harvard, Vancouver, ISO, and other styles

40

Janzen, Edward G., Allan L. Wilcox, and Vinothane Manoharan. "Reactions of nitric oxide with phenolic antioxidants and phenoxyl radicals." Journal of Organic Chemistry 58, no. 14 (1993): 3597–99. http://dx.doi.org/10.1021/jo00066a001.

Full text

APA, Harvard, Vancouver, ISO, and other styles

41

Philibert, Aurélie, Fabrice Thomas, Christian Philouze, Sylvain Hamman, Eric Saint-Aman, and Jean-Louis Pierre. "Galactose Oxidase Models: Tuning the Properties of CuII–Phenoxyl Radicals." Chemistry - A European Journal 9, no. 16 (2003): 3803–12. http://dx.doi.org/10.1002/chem.200304880.

Full text

APA, Harvard, Vancouver, ISO, and other styles

42

Kuznetsova, N. A., A. Y. Krupnova, A. O. Sergeev, and V. I. Porkhun. "KINETICS OF THE REACTION OF PHENOXYL RADICALS WITH METAL IONS." Izvestia Volgograd State Technical University, no. 12 (2022): 73–77. http://dx.doi.org/10.35211/1990-5297-2022-12-271-73-77.

Full text

APA, Harvard, Vancouver, ISO, and other styles

43

Coronel, Marta E. J., and Agustin J. Colussi. "Entropic and enthalpic effects of 4-methoxy substitution in phenoxyl radicals." Journal of the Chemical Society, Perkin Transactions 2, no. 4 (1994): 785. http://dx.doi.org/10.1039/p29940000785.

Full text

APA, Harvard, Vancouver, ISO, and other styles

44

O'Malley, Patrick J. "Hybrid Density Functional Studies of Phenoxyl Free Radicals Modeling α-Tocopheroxyl". Journal of Physical Chemistry B 106, № 47 (2002): 12331–35. http://dx.doi.org/10.1021/jp025754+.

Full text

APA, Harvard, Vancouver, ISO, and other styles

45

Denisova, T. G., and E. T. Denisov. "The reactivity of phenoxyl radicals of bioantioxidants in the abstraction reactions." Russian Chemical Bulletin 58, no. 8 (2009): 1609–15. http://dx.doi.org/10.1007/s11172-009-0221-1.

Full text

APA, Harvard, Vancouver, ISO, and other styles

46

Sadykov, R. A., G. D. Safina, I. Yu Chukicheva, R. R. Kinzyabulatov, and A. V. Kuchin. "ESR spectra of phenoxyl radicals derived from 2,6-diisobornyl-4-methylphenol." Russian Chemical Bulletin 61, no. 8 (2012): 1667–68. http://dx.doi.org/10.1007/s11172-012-0229-9.

Full text

APA, Harvard, Vancouver, ISO, and other styles

47

Stolze, Klaus, and Hans Nohl. "Formation of Methemoglobin and Phenoxyl Radicals from P-Hydroxyanisole and Oxyhemoglobin." Free Radical Research Communications 11, no. 6 (1991): 321–28. http://dx.doi.org/10.3109/10715769109088930.

Full text

APA, Harvard, Vancouver, ISO, and other styles

48

Allard, Marco M., Jason A. Sonk, Mary Jane Heeg, Bruce R. McGarvey, H. Bernhard Schlegel, and Cláudio N. Verani. "Bioinspired Five-Coordinate Iron(III) Complexes for Stabilization of Phenoxyl Radicals." Angewandte Chemie International Edition 51, no. 13 (2011): 3178–82. http://dx.doi.org/10.1002/anie.201103233.

Full text

APA, Harvard, Vancouver, ISO, and other styles

49

Lahti, Paul M., Burak Esat, Jacqueline R. Ferrer, et al. "ChemInform Abstract: Polymeric, H-Bonded, and Chelatable Phenoxyl and Nitroxide Radicals." ChemInform 31, no. 10 (2010): no. http://dx.doi.org/10.1002/chin.200010270.

Full text

APA, Harvard, Vancouver, ISO, and other styles

50

Omelka, Ladislav, and Jana Kováčová. "Spin trapping of sterically unhindered phenoxyl radicals with nitrosobenzene and nitrosodurene." Magnetic Resonance in Chemistry 32, no. 9 (1994): 525–31. http://dx.doi.org/10.1002/mrc.1260320905.

Full text

APA, Harvard, Vancouver, ISO, and other styles

We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!