Bibliografias temáticas / Aminojíl

Literatura científica selecionada sobre o tema "Aminojíl"

Autor: Grafiati
Publicado: 4 de junho de 2021
Última modificação: 5 de fevereiro de 2022

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  1. Artigos de revistas
  2. Teses / dissertações
  3. Livros
  4. Capítulos de livros
  5. Trabalhos de conferências

Artigos de revistas sobre o assunto "Aminojíl":

1

Zhang, Yong-Kang, e De-Kang Shen. "Synthesis of a Dihydroxy-Substituted Aminoxyl Spin Label and its Crown Ether and Cyclic Diester Derivatives". Zeitschrift für Naturforschung B 48, n.º 4 (1 de abril de 1993): 505–10. http://dx.doi.org/10.1515/znb-1993-0417.

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A novel dihydroxy-substituted aminoxyl spin label, 4-hydroxy-3-(3'-hydroxypropyl)-2,2,6,6-tetramethylpiperidine-1-oxy (5), has been prepared. From this aminoxyl radical, a spin-labeled crown ether, 16,16,18,18-tetramethyl-2,5,8,11-tetraoxa-17-azabicyclo[ 13,4,0]-nonadecane-17-oxy (12), and a spin-labeled cyclic diester, 16,16,18,18-tetramethyl-3,10-dioxo-2,5,8,11-tetraoxa-17-azabicyclo[13,4,o]nonadecane-17-oxy (13), have been acquired. Other four new stable aminoxyl radicals 8,9,10, and 11 have also been obtained within the synthetic approach. It has been demonstrated that the cyclic ether compound (7) is generated by the reduction of its corresponding lactone which is sidely derived from the oxo-reduced species of 3 by intramolecular cyclization.
2

Shil, Suranjan, Debojit Bhattacharya, Anirban Misra e Douglas J. Klein. "A high-spin organic diradical as a spin filter". Physical Chemistry Chemical Physics 17, n.º 36 (2015): 23378–83. http://dx.doi.org/10.1039/c5cp03193a.

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3

Parrot, Arnaud, Yuma Morimoto, Sayantan Paria, Hideki Sugimoto, Nobutaka Fujieda e Shinobu Itoh. "Generation and characterisation of a stable nickel(ii)-aminoxyl radical complex". Dalton Transactions 46, n.º 25 (2017): 8013–16. http://dx.doi.org/10.1039/c7dt01789h.

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4

Berliner, Lawrence J., Helmut Görner e Heinz-Peter Schuchmann. "Evaluation of EPR monitoring of singlet oxygen production using the photosensitizer chloroboron subphthalocyanine". Journal of Porphyrins and Phthalocyanines 15, n.º 02 (fevereiro de 2011): 118–21. http://dx.doi.org/10.1142/s1088424611003057.

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Singlet molecular oxygen produced in the presence of 2,2,6,6-tetramethyl-4-piperidone (TMPD) in 1,4-dioxan, by boron subphthalocyanine chloride as the sensitizer, was monitored by Electron Paramagnetic Resonance (EPR) via the oxidation of TMPD to the corresponding aminoxyl radical. This radical product is formed in low yields along the singlet oxygen pathway. A kinetic analysis of the process allows one to understand the reasons behind this, while affording more accurate quantitative insights into the mechanistic details. A crucial aspect of this reaction system, which explains the low aminoxyl radical yields along the singlet oxygen pathway, is the disappearance of the sensitizer triplet state in a reaction with TMPD, which has a rate constant of 1 × 109 M-1.s-1.
5

Zhang, Yong-Kang, e De-Kang Shen. "Notizen: Synthesis of Novel Hydroxy-Substituted Aromatic Aminoxyl Esters and their Azo Derivatives". Zeitschrift für Naturforschung B 48, n.º 6 (1 de junho de 1993): 849–51. http://dx.doi.org/10.1515/znb-1993-0622.

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Transesterification or acylation method has been used for the preparation of three novel hydroxy-substituted aromatic aminoxyl esters 4, 5, and 8 from which three new spin-labelled azo compounds 10,13, and 14 have been synthesized.
6

Zhang, Yong-Kang, e Edward G. Janzen. "An EPR and MS Investigation of Hexa-Substituted Pyrrolidine-l-oxyl Aminoxyl Stable Radicals. Unexpectedly Large y-Hydrogen Splittings". Zeitschrift für Naturforschung B 50, n.º 10 (1 de outubro de 1995): 1531–36. http://dx.doi.org/10.1515/znb-1995-1017.

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The y-hydrogen hyperfine splitting constant (γ-H hfsc) for stable aminoxyl (nitroxide) spin labels such as 2,2,5,5-tetramethylpyrrolidine-1-oxyl and their derivatives is usually very small (<1.0 G) and not distinguished with EPR spectrometry. Surprisingly, large γ-H hfsc’s (≥2 .0 G) have been detected with EPR for the first time from ten 2-alkyl-2-phenyl-3,3,5,5- tetramethylpyrrolidine-1-oxyl stable aminoxyl radicals. It is discovered that γ-H hfsc’s are very sensitive to the size and the substitution pattern of 2-alkyl groups. When the 2-alkyl group is CH3 or CD3, γ-H hfsc’s are not resolved in the EPR spectra. But if the 2-alkyl group is C2H5, one γ-H hfsc is very large, equal to 4.72 G in C6H6. If the substituent is longer than C2H5, such as n-C3H7, n-C4H9, n-C5H11, n-C6H13 and CH2=CHCH2- substituents, the γ-H hfsc is slightly smaller, equal to 4.59 G. For secondary substituents such as sec-C4H9 and cyclo-C6H11 , the γ-H hfsc decreases to 2.00 G. Intermediate γ-H hfsc’s correspond to C6H5CH2 (3.18 G) or a tertiary alkyl group such as t-C4H9 (3.47 G). Variation of γ-H hfsc’s is based on the change of the pyrrolidine ring conformation which is a result of the 2-alkyl group influence. The structures of these aminoxyl radicals are characterized also with mass spectrometry. Possible MS fragmentation mechanisms are discussed.
7

Daro, Nathalie, Philippe Guionneau, Stéphane Golhen, Daniel Chasseau, Lahcène Ouahab e Jean-Pascal Sutter. "Aminoxyl radical substituted uranyl compounds". Inorganica Chimica Acta 326, n.º 1 (dezembro de 2001): 47–52. http://dx.doi.org/10.1016/s0020-1693(01)00593-x.

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8

Acton, Austin, Annette D. Allen, Andrei V. Fedorov, Huda Henry-Riyad e Thomas T. Tidwell. "Aminoxyl radical addition to arylketenes". Journal of Physical Organic Chemistry 19, n.º 12 (dezembro de 2006): 841–46. http://dx.doi.org/10.1002/poc.1036.

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9

Haire, D. Larry, Uwe M. Oehler, H. Duane Goldman, Robert L. Dudley e Edward G. Janzen. "The first 1H and 14N ENDOR spectra of an oxygen-centered radical adduct of DMPO-type nitrones". Canadian Journal of Chemistry 66, n.º 9 (1 de setembro de 1988): 2395–402. http://dx.doi.org/10.1139/v88-377.

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We report the first 1H and 14N electron nuclear double resonance (ENDOR) spectra of oxygen-centered radical adducts (i.e., derived from the addition of tert-butoxyl radicals) of 5,5-dimethyl-1-pyrroline-N-oxide (DMPO) as well as the related cyclic nitrones: 4-phenyl-5,5-dimethyl-1-pyrroline-N-oxide (4-Ph-DMPO) and 3,3,5,5-tetramethyl-1-pyrroline-N-oxide (M4PO). Features of the electron paramagnetic resonance (EPR) and ENDOR spectra of these cyclic (pyrrolidine) aminoxyl (nitroxide) species along with some deuterated analogues in liquid toluene solutions are highlighted. For instance, we found several long-range γ-H hyperfine splittings (HFS's) detectable by ENDOR that provide unique spectral signatures for these radical adducts. Conformational assignments of the pyrrolidine aminoxyl structures based upon the EPR and ENDOR findings are also discussed. Signs of the various hyperfine splittings (i.e., aN, [Formula: see text]) investigated by cross-relaxation intensity sequence patterns (CRISP) in the ENDOR spectra are also presented.
10

Park, Sung Chul, Jung-Ho Lee, Ji-Yeon Hwang, Oh-Seok Kwon, Lijuan Liao, Dong-Chan Oh, Ki-Bong Oh e Jongheon Shin. "Ochraceopetalin, a Mixed-Biogenetic Salt of Polyketide and Amino Acid Origins from a Marine-Derived Aspergillus ochraceopetaliformis Fungus". Marine Drugs 19, n.º 8 (26 de julho de 2021): 413. http://dx.doi.org/10.3390/md19080413.

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Ochraceopetalin (1), a mixed-biogenetic salt compound and its component 2 were isolated from the culture broths of a marine-derived fungus, Aspergillus ochraceopetaliformis. Based on combined spectroscopic and chemical analyses, the structure of 1 was determined to be a sulfonated diphenylether-aminol-amino acid ester guanidinium salt of an unprecedented structural class, while 2 was determined to be the corresponding sulfonated diphenylether. Ochraceopetaguanidine (3), the other guanidine-bearing aminol amino acid ester component, was also prepared and structurally elucidated. Compound 1 exhibited significant cytotoxicity against K562 and A549 cells.
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Artigos de revistas

Teses / dissertações sobre o assunto "Aminojíl":

1

Plotěná, Michaela. "Fázová separace v systému aminojíl-biopolymer". Master's thesis, Vysoké učení technické v Brně. Fakulta chemická, 2017. http://www.nusl.cz/ntk/nusl-316185.

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The aim of this diploma thesis was to study the structure and to evaluate the properties of the hydrogel prepared by the interaction of the aminolclay with the biopolymer. Representatives of the biopolymers were selected from low to medium molecular weight sodium hyaluronate and sodium polystyrenesulfonate. On the basis of the experiments carried out, it was found that phase separation takes place only when the aminolclay interacts with medium molecular weight hyaluronan (MMW). In the experimental part, analyzes of this sample were carried out in order to determine the formation of phase-separated hydrogel by influencing the solution by ionic strength, investigation of hydrogel extinction in various organic solvents, stability of hydrogel under extreme temperature conditions, the effect of storage on its degradation, etc. Viscoelastic properties were experimentally proven by rheology and thermal analysis detected binding water. Inhibition of microorganisms was confirmed by antibacterial diffusion assays. All experiments were carried out for the use of the Aj-HyA hydrogel (MMW) in the field of medical applications, specifically for the modern method of wet wound healing of the skin.
2

Jančík, Procházková Anna. "Fluorescenční spektroskopie ve výzkumu aminojílů". Master's thesis, Vysoké učení technické v Brně. Fakulta chemická, 2017. http://www.nusl.cz/ntk/nusl-316156.

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Aminoclay belongs to a large group of organic modified materials based on clays. These materials could find many potential practical applications and, in particular, may be used as a matrix with the ability of the organisation and stabilisation of incorporated substances. The utilisation of aminoclay in the field of medical applications seems highly prospective, but there is the need to visualise the clay system and the processes within it. This essay deals with the issue of aminoclay visualisation by means of fluorescent spectroscopy. Through fluorescent spectroscopy, aminoclay was discovered to be autofluorescent. The autofluorescence of aminoclay is not usable in practical applications because of the low fluorescence intensity. This is the reason for the research into other possibilities for modifications of the internal structure of aminoclay by europium ions. These ions in chelated form are able to be fluorescent and modifications of the external structure are possible by electrostatic implementation of fluorescent dyes. Characterisation of the prepared complexes was provided by spectrofluorimetry and fluorescent microscopy for the purpose of evaluation of the practical application of aminoclay.
3

Dušek, Jakub. "Vlastnosti komplexů aminojílu a biologicky aktivních látek". Master's thesis, Vysoké učení technické v Brně. Fakulta chemická, 2020. http://www.nusl.cz/ntk/nusl-414180.

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This paper builds on previous research of aminoclay complexes in undergraduate studies. Theoretical part deals with study of current problems of aminoclay complexes with bioactive substances and the choice of substances for complexing with aminoclay. The experimental part consists of preparation of aminoclay complexes with selected bioactive agents at various concentrations. Verification of binding of bioactive agents to the aminoclay matrix was performed by Elemental Analysis (EA) and Fourier-transform infrared spectroscopy (FT-IR). For finding of the bound amount of bioactive substance were used the Ultra Performance Liquid Chromatography (UPLC®) and analysis of the cytotoxic properties of the formed complexes by used by the MTT assay. The main motivation of this study is to create new complexes with improved characteristics that would replace existing forms of substances used in pharmaceutical and biomedical applications.
4

Grice, I. Darren, e n/a. "Some New Aspects of Radical Trapping Using an Aminoxyl Radical Trap". Griffith University. School of Science, 1993. http://www4.gu.edu.au:8080/adt-root/public/adt-QGU20050915.150556.

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An investigation of the initiation mechanism in the free radical copolymerisation of acrylonitrile and vinyl acetate using the aminoxyl radical trapping technique, employing 1,1 ,3,3-tetramethyl-2,3-dihydro- 1 Hisoindol-2-yloxyl is reported. Based upon the experimental results, the mechanism of initiation is suggested as proceeding via the 'free monomer' mechanism. Additionally, the effect of Lewis acids on the initiation mechanism is reported. A study of the addition of phosphorus-centred radicals to alkenes and phenylacetylene, utilising the aminoxyl radical trapping technique is reported. The results indicate a decreased rate of addition by both diphenylphosphinyl and dimethoxyphosphinyl radicals to cyclic versus acyclic alkenes. In contrast to cyclic alkenes, both these phosphorus-centred radicals add readily to the triple bond of phenylacetylene. The stereochemistry of the addition of diphenyiphosphinyl and dimethoxyphosphinyl radicals and of the aminoxyl trap is discussed. The stereochemistry of the addition of benzoyloxyl radicals to a conformationally rigid alkene, trans-a2-octalin is reported. Attempts to examine the initiation mechanism in the free radical copolymerisation of styrene/maleic anhydride and of styrene/tetracyanoethylene utilising the aminoxyl radical trapping technique are described. Also described are attempts to synthesise some new phosphorus radical initiators.
5

Sampler, Edward Phillip. "Some aspects of the chemistry of cyclic aminol ethers". Thesis, Loughborough University, 2001. https://dspace.lboro.ac.uk/2134/16586.

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This thesis has been divided into three main sections. The first chapter contains a review of calixarene chemistry, in particular that relating to calix[4)resorcinarenes. Results and discussion are compiled in chapters two through seven and experimental details are provided in chapter eight. Chapters two and three contain results and discussion relating to the novel synthesis of the first example of an enantiomerically pure axially chiral resorcinarene derivative. Chapter two outlines the key step in the reaction sequence, that being the tetramethylation of diastereomerically pure tetrakis(3,4-dihydro-2H-1,3- benzoxazine)calix[4)resorcinarene derivatives. Chapter three describes the subsequent synthetic sequence developed to fragment 3,4-dihydro-2H-1,3- benzoxazines with a view to removing the a-methylbenzylamine chiral auxiliary, which was used to set up the observed axial chirality of the resorcinarene. The sequence incorporates a novel modified Eschweiler-Clarke reaction whereby refluxing the required tetrakis(3,4-dihydro-2H-1 ,3-benzoxazine)calix[4)resorcinarene derivative in aqueous formic acid resulted in reductive ring opening, furnishing the N-methylated analogue. Chapter four describes work on functionalising the 'lower rim' of resorcinarene macrocycles with a view to forming derivatives with a pendant functional group that could be manipulated further to support the newly formed axially chiral resorcinarene derivatives onto solid supports. Chapter five contains prelfminary investigations into the use of axially chiral resorcinarene derivatives as chiral ligands in the enantioselective addition of diethylzinc to benzaldehyde. Chapter six contains results of investigations into the mechanism of the 'RetroMannich' reaction, whereby an amine exchange reaction is observed when refluxing a dihydro-1,3-benzoxazine or Mannich base in a high boiling amine such as morpholine. Evidence has been provided that the reaction proceeds via an o-quinone methide intermediate. Chapter seven describes investigations into the generality of the modified EschweilerClarke reductive ring opening methodology whereby refluxing a formic acid solution of a cyclic aminol ether results in the formation of N,N-dialkyl derivatives via reductive ring opening. It was found that the procedure was general for compounds without sUbstituents at the two position. A second reaction protocol was developed for compounds with substituents at the two position, utilising a combination of sodium cyanoborohydride and chlorotrimethylsilane in acetonitrile to furnish the desired N,Ndialkyl derivatives in excellent yield. Finally, chapter eight contains full experimental details for the synthetic studies carried out in the preceding chapters.
6

Borozdina, Yulia B. [Verfasser]. "Aminoxyl radicals - pure organic materials with tunable magnetic and sensing properties / Yulia B. Borozdina". Mainz : Universitätsbibliothek Mainz, 2012. http://d-nb.info/1023189488/34.

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7

Peiter, Andréia. "Desenvolvimento de sistema integrado para degradação de agrotóxicos e geração de energia". Universidade Estadual do Oeste do Parana, 2015. http://tede.unioeste.br:8080/tede/handle/tede/1812.

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Made available in DSpace on 2017-07-10T18:01:54Z (GMT). No. of bitstreams: 1 Andreia Peiter.pdf: 1366062 bytes, checksum: e0b82884da5c768cb61affcb50cffecf (MD5) Previous issue date: 2015-07-27
According on the demand for processes that minimize the environmental impact generated by waste, efficient systems that make possible the degradation of these compounds and allow its use as an alternative source for renewable energy generation are increasingly required. The increasing food production to meet the needs of the world population has encouraged the use of agrochemicals in order to ensure productivity in crops. The use of insecticides is increasing to control pests and herbicides for weed control, because there is a lack of effective control that includes new production strategies. Techniques such as crop rotation, no-till system introduction and use of green pesticides (natural insecticides) provide a more sustainable agriculture and reduce impacts to the environment. In this context, this work presents an alternative development of an integrated system for remediation of environments contaminated with simultaneous generation of electricity. The materials were prepared from reagents and accessible metals, which reduce costs and contribute to a clean process, without the addition of organic additives. Due to the high oxidizing potential of hydroxyl radicals generated by the pair electron-hole (e+ + h+) in the semiconductors, was possible to degrade the organic compounds used in the system. The results showed that the generation of current in an area of 6,9 cm2 was 193,37 uA in potassium hydrogen phthalate degradation, using Cu/CuO electrode as a photocatalyst. The Aminol® and Connect® pesticides have been degraded at a percentage of 54,46% and 21,02%, respectively, after 1 hour and 30 minutes in the system, under ultraviolet radiation. The degradation of organic contaminants and simultaneous power generation of energy in integrated system provides a self-sustaining form of wastewater treatment and energy recovery, being possible its use on a large scale.
Em função da demanda por processos que minimizem os impactos ambientais gerados por resíduos, sistemas eficientes que possibilitem a degradação desses compostos e permitam sua utilização como fonte alternativa para geração de energia renovável são cada vez mais requeridos. A crescente produção de alimentos para suprir as necessidades da população mundial tem incentivado o emprego de agroquímicos com o objetivo de assegurar a produtividade nas lavouras. Cada vez mais aumenta o uso de inseticidas para o controle de pragas e herbicidas para o controle de ervas daninhas, pois há carência de um controle efetivo que inclua novas estratégias de produção. Técnicas como rotação de cultura, introdução do sistema de plantio direto e utilização de inseticidas verdes (inseticidas naturais) propiciam uma agricultura mais sustentável e reduzem os impactos causados ao ambiente. Nesse contexto, o presente trabalho apresenta uma alternativa de desenvolvimento de um sistema integrado para remediação de ambientes contaminados com geração simultânea de energia elétrica. Os materiais foram preparados a partir de reagentes e metais acessíveis, os quais reduzem os custos e contribuem para um processo mais limpo, sem a ação de aditivos orgânicos. Devido ao alto potencial oxidante dos radicais hidroxila gerados por meio do par elétron-lacuna (e- + h+) em semicondutores, foi possível degradar os compostos orgânicos utilizados no sistema. Os resultados mostraram que a geração de corrente em uma área de 6,9 cm2 foi de 193,37 µA na degradação do padrão hidrogenoftalato de potássio, utilizando eletrodo de Cu/CuO como fotocatalisador. Os agrotóxicos Aminol 806® e Connect® foram degradados com percentual de 54,46% e 21,02%, respectivamente, após 1 hora e 30 minutos no sistema, sob radiação ultravioleta. A degradação de contaminantes orgânicos e simultânea geração de energia no sistema integrado prevê uma forma autossustentável de tratamento de efluentes e recuperação de energia, sendo possível sua utilização em grande escala.
8

LIN, SU-MI, e 林素密. "The synthesis of aminol, thiol and amine organogermanium derivatives". Thesis, 1991. http://ndltd.ncl.edu.tw/handle/56576218877712612862.

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9

Steinmaß, Holger [Verfasser]. "Anellierte 2-Phenylchinoline als Vorstufen entsprechender Aminoxyl-Radikale zur fluorimetrischen Detektion von Stickstoffmonoxid / vorgelegt von Holger Steinmaß". 2009. http://d-nb.info/993624243/34.

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Livros sobre o assunto "Aminojíl":

1

Janzen, E. G., e J. R. Bolton. International Symposium: Spin Trapping and Aminoxyl Radical Chemistry, Parts I & II. Routledge, 1990.

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Capítulos de livros sobre o assunto "Aminojíl":

1

Zhdanov, R. I. "The Toxicity of Aminoxyl Radicals". In Bioactive Spin Labels, 429–38. Berlin, Heidelberg: Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-642-48724-8_17.

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2

Janzen, Edward G., e Rheal A. Towner. "Aminoxyl Radicals as MRI Contrast Agents". In Bioactive Spin Labels, 573–83. Berlin, Heidelberg: Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-642-48724-8_24.

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3

Zhdanov, R. I., A. M. Komarov e L. P. Kayushin. "Aminoxyl Spin Labels in Clinical Analysis". In Bioactive Spin Labels, 585–610. Berlin, Heidelberg: Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-642-48724-8_25.

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4

Iwamura, Hiizu, e Katsuya Inoue. "Magnetic Ordering in Metal Coordination Complexes with Aminoxyl Radicals". In Magnetism: Molecules to Materials, 61–108. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2003. http://dx.doi.org/10.1002/9783527620548.ch2a.

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5

Bottle, S. E., W. K. Busfield, I. D. Grice, K. Heiland, I. D. Jenkins, W. Meutermans e M. Monteiro. "Some Recent Developments in the Aminoxyl Radical Trapping Technique". In Progress in Pacific Polymer Science 3, 85–97. Berlin, Heidelberg: Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-78759-1_7.

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6

Berliner, Lawrence J. "Compilation of Hyperfine Splittings andg-Factors for Aminoxyl (Nitroxide) Radicals". In Multifrequency Electron Paramagnetic Resonance, 287–96. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527672431.ch5.

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7

Pardasani, R. T., e P. Pardasani. "Magnetic properties of gold(I) complex containing aminoxyl radical-substituted phosphine ligand". In Magnetic Properties of Paramagnetic Compounds, 1109–10. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_620.

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Pardasani, R. T., e P. Pardasani. "Magnetic properties of gold(I) complex containing aminoxyl radical-substituted phosphine ligand". In Magnetic Properties of Paramagnetic Compounds, 1111–12. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_621.

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9

Zhang, J., D. Liu e Y. Chen. "1.9 Oxygen-Centered Radicals". In Free Radicals: Fundamentals and Applications in Organic Synthesis 1. Stuttgart: Georg Thieme Verlag KG, 2021. http://dx.doi.org/10.1055/sos-sd-234-00177.

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AbstractOxygen-centered radicals (R1O•) are reactive intermediates in organic synthesis, with versatile synthetic utilities in processes such as hydrogen-atom transfer (HAT), β-fragmentation, radical addition to unsaturated carbon–carbon bonds, and rearrangement reactions. In this review, we focus on recent advances in the generation and transformation of oxygen-centered radicals, including (alkyl-, α-oxo-, aryl-) carboxyl, alkoxyl, aminoxyl, phenoxyl, and vinyloxyl radicals, and compare the reactivity of oxygen-centered radicals under traditional reaction conditions with their reactivity under visible-light-induced reaction conditions.
10

Tidwell, T. T. "-Aroyloxyamines by Aminoxyl Radical Addition to Monoarylketenes". In Three Carbon-Heteroatom Bonds: Thio-, Seleno-, and Tellurocarboxylic Acids and Derivatives; Imidic Acids and Derivatives; Ortho Acid Derivatives, 1. Georg Thieme Verlag KG, 2006. http://dx.doi.org/10.1055/sos-sd-023-00417.

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Trabalhos de conferências sobre o assunto "Aminojíl":

1

Komaromi, Istvan, e Jean M. J. Tronchet. "The planarity 〈--〉 pyramidality at the radical center of the small aminoxyl radicals. An ab initio (SCF,MP2) study". In The first European conference on computational chemistry (E.C.C.C.1). AIP, 1995. http://dx.doi.org/10.1063/1.47647.

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