Academic literature on the topic 'ESR'

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Journal articles on the topic "ESR"

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Kajiwara, Atsushi. "Characterizations of radicals formed in radical polymerizations and transfer reactions by electron spin resonance spectroscopy." Pure and Applied Chemistry 90, no. 8 (August 28, 2018): 1237–54. http://dx.doi.org/10.1515/pac-2018-0401.

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Abstract Electron spin resonance (ESR, aka electron paramagnetic resonance, EPR) investigations have been conducted on radicals formed during radical polymerizations and provide a detailed characterization of the active radical species. Active propagating radicals can be observed during actual radical polymerizations by ESR/EPR. The chain lengths of the observed radicals were estimated by a combination of atom transfer radical polymerization (ATRP) and ESR/EPR. The structures of the chain end radicals were determined by analysis of the ESR/EPR spectra. An increase in the dihedral angles between terminal p-orbital of radical and Cβ–H bonds was observed with increasing chain lengths of methacrylate polymers. Radical transfer reactions were observed during radical polymerization of acrylates. A combination of ATRP and ESR/EPR clarified a 1,5-hydrogen shift mechanism of the radical transfer reactions using model adamantyl acrylate radicals. Penultimate unit effects were also observed. Time-resolved ESR/EPR (TR ESR) spectroscopy clarified the initiation processes of an alternating copolymerization of styrene with maleic anhydride and the copolymerization of styrene with 1,3-butadiene. Several unsolved problems in conventional radical polymerization processes have been clarified using combinations of ATRP with ESR/EPR and TR ESR. Characterization of the radicals in radical polymerizations using various ESR techniques would definitely provide interesting and useful information on conventional radical polymerizations.
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Dzuba, S., G. R. Hanson, K. P. Mishra, and H. Ohta. "Modern Developments in EPR/ESR Spectroscopy: Asia-Pacific EPR/ESR Symposium 2006, Novosibirsk, Russia." Applied Magnetic Resonance 33, no. 1-2 (March 2008): 1. http://dx.doi.org/10.1007/s00723-008-0079-7.

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Berliner, Lawrence J. "The evolution of biomedical EPR (ESR)." Biomedical Spectroscopy and Imaging 5, no. 1 (June 20, 2017): 5–26. http://dx.doi.org/10.3233/bsi-150128.

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Salikhov, Kev M. "2nd Asia-Pacific EPR/ESR Symposium." Applied Magnetic Resonance 19, no. 1 (May 2000): 1. http://dx.doi.org/10.1007/bf03162255.

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Yang, Ju-Hye, Jae-Myung Yoo, Won-Kyung Cho, and Jin Yeul Ma. "Ethanol Extract of Sanguisorbae Radix Inhibits Mast Cell Degranulation and Suppresses 2,4-Dinitrochlorobenzene-Induced Atopic Dermatitis-Like Skin Lesions." Mediators of Inflammation 2016 (2016): 1–8. http://dx.doi.org/10.1155/2016/2947390.

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Sanguisorbae Radix (SR) is well known as herbal medicine named “Zi-Yu” in Korea, which is the dried roots ofSanguisorba officinalisL. (Rosacease). We investigated the underlying mechanism on the inhibition of atopic dermatitis (AD) of an ethanol extract of SR (ESR) using 2,4-dinitrochlorobenzene- (DNCB-) induced AD mice model. Oral administration of ESR significantly suppressed DNCB-induced AD-like symptoms such as scratching behavior, ear thickness, epidermal thickness, and IgE levels. To investigate the effects of ESR treatment on degranulation of IgE/Ag-activated mouse bone marrow-derived mast cells (BMMCs), we measured the release ofβ-hexosaminidase (β-HEX, degranulation marker). ESR decreased the infiltration of eosinophils and mast cells into the AD skin lesions. Furthermore, ESR significantly inhibited degranulation of IgE/Ag-activated BMMCs. We have demonstrated that ESR decreased AD symptoms in mice and inhibits degranulation of IgE/Ag-activated mast cells. Our study suggests that ESR may serve as a potential therapeutic candidate for the treatment of AD symptoms.
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Almeras, Christophe, Benjamin Pradere, Vincent Estrade, and Paul Meria. "Endoscopic Papillary Abnormalities and Stone Recognition (EPSR) during Flexible Ureteroscopy: A Comprehensive Review." Journal of Clinical Medicine 10, no. 13 (June 29, 2021): 2888. http://dx.doi.org/10.3390/jcm10132888.

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Introduction: The increasing efficiency of the different lasers and the improved performance of endoscopic devices have led to smaller stone fragments that impact the accuracy of microscopic evaluation (morphological and infrared). Before the stone destruction, the urologist has the opportunity to analyze the stone and the papillary abnormalities endoscopically (endoscopic papillary recognition (EPR) and endoscopic stone recognition (ESR)). Our objective was to evaluate the value for those endoscopic descriptions. Methods: The MEDLINE and EMBASE databases were searched in February 2021 for studies on endoscopic papillary recognition and endoscopic stone recognition. Results: If the ESR provided information concerning the main crystallization process, EPR provided information concerning the origin of the lithogenesis and its severity. Despite many actual limitations, those complementary descriptions could support the preventive care of the stone formers in improving the diagnosis of the lithogenesis mechanism and in identifying high-risk stone formers. Conclusion: Until the development of an Artificial Intelligence recognition, the endourologist has to learn EPSR to minimize the distortion effect of the new lasers on the stone analysis and to improve care efficiency of the stone formers patients.
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Wang, Bin, Junkai Lai, Mimi Liu, Feifei Jin, Yifei Peng, and Chen Yao. "Electronic Source Data Transcription for Electronic Case Report Forms in China: Validation of the Electronic Source Record Tool in a Real-world Ophthalmology Study." JMIR Formative Research 6, no. 12 (December 16, 2022): e43229. http://dx.doi.org/10.2196/43229.

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Background As researchers are increasingly interested in real-world studies (RWSs), improving data collection efficiency and data quality has become an important challenge. An electronic source (eSource) generally includes direct capture, collection, and storage of electronic data to simplify clinical research. It can improve data quality and patient safety and reduce clinical trial costs. Although there are already large projects on eSource technology, there is a lack of experience in using eSource technology to implement RWSs. Our team designed and developed an eSource record (ESR) system in China. In a preliminary prospective study, we selected a cosmetic medical device project to evaluate ESR software’s effect on data collection and transcription. As the previous case verification was simple, we plan to choose more complicated ophthalmology projects to further evaluate the ESR. Objective We aimed to evaluate the data transcription efficiency and quality of ESR software in retrospective studies to verify the feasibility of using eSource as an alternative to traditional manual transcription of data in RWS projects. Methods The approved ophthalmic femtosecond laser project was used for ESR case validation. This study compared the efficiency and quality of data transcription between the eSource method using ESR software and the traditional clinical research model of manually transcribing the data. Usability refers to the quality of a user’s experience when interacting with products or systems including websites, software, devices, or applications. To evaluate the system availability of ESR, we used the System Usability Scale (SUS). The questionnaire consisted of the following 2 parts: participant information and SUS evaluation of the electronic medical record (EMR), electronic data capture (EDC), and ESR systems. By accessing log data from the EDC system previously used by the research project, all the time spent from the beginning to the end of the study could be counted. Results In terms of transcription time cost per field, the eSource method can reduce the time cost by 81.8% (11.2/13.7). Compared with traditional manual data transcription, the eSource method has higher data transcription quality (correct entry rate of 2356/2400, 98.17% vs 47,991/51,424, 93.32%). A total of 15 questionnaires were received with a response rate of 100%. In terms of usability, the average overall SUS scores of the EMR, EDC, and ESR systems were 50.3 (SD 21.9), 51.5 (SD 14.2), and 63.0 (SD 11.3; contract research organization experts: 69.5, SD 11.5; clinicians: 59.8, SD 10.2), respectively. The Cronbach α for the SUS items of the EMR, EDC, and ESR systems were 0.591 (95% CI −0.012 to 0.903), 0.588 (95% CI −0.288 to 0.951), and 0.785 (95% CI 0.576-0.916), respectively. Conclusions In real-world ophthalmology studies, the eSource approach based on the ESR system can replace the traditional clinical research model that relies on the manual transcription of data.
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Ulusoy, Ü., and F. Apaydín. "ESR studies and ESR dating of quartz." Applied Radiation and Isotopes 47, no. 11-12 (November 1996): 1405–7. http://dx.doi.org/10.1016/s0969-8043(96)00251-5.

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Kameya, Hiromi. "ESR (Electron Spin Resonance)." Nippon Shokuhin Kagaku Kogaku Kaishi 60, no. 4 (2013): 198. http://dx.doi.org/10.3136/nskkk.60.198.

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McLaughlin (INVITED), W. L. "ESR Dosimetry." Radiation Protection Dosimetry 47, no. 1-4 (May 1, 1993): 255–62. http://dx.doi.org/10.1093/oxfordjournals.rpd.a081745.

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Dissertations / Theses on the topic "ESR"

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Emi, Keiji. "Microscopic Environmental Studies on Solute-solvent Interaction by Using Pulsed ESR and CW-ESR." Kyoto University, 1998. http://hdl.handle.net/2433/182386.

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Kyoto University (京都大学)
0048
新制・課程博士
博士(人間・環境学)
甲第7506号
人博第46号
10||156(吉田南総合図書館)
新制||人||11(附属図書館)
UT51-98-U173
京都大学大学院人間・環境学研究科人間・環境学専攻
(主査)教授 山内 淳, 教授 堀 智孝, 助教授 田村 類
学位規則第4条第1項該当
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Kirui, Joseph Kiprono. "ESR study of DMTM(TCNQ)₂." Thesis, University of British Columbia, 1990. http://hdl.handle.net/2429/29191.

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The ESR g-value and susceptibility measurements for DMTM(TCNQ)₂ have been studied as a function of angle made by crystal with magnetic field and temperature. The angular dependence of g-value is fitted to g² = α+βcos2θ - γsin2θ for three orthogonal directions of crystal rotation. The principal g-values are close to those expected for TCNQ compounds: g₁ = 2.0034, g₂ = 2.0030, g₃ = 2.0024. The susceptibility as a function of temperature agrees with bulk susceptibility measurements except that the maximum position occurs at about 30 K. The results of Oostra et al. for bulk susceptibility showed a maximum at around 50 K. The phase transition reported by Visser et al. at 272 K is observed in the ESR data as a 15% decrease in susceptibility. The linewidth is remarkably anisotropic typical of TCNQ salts. The phase transition study is done for two orientations of the crystal with the magnet field. In one of the orientations the linewidth narrows from 0.15 to 0.11 gauss and in the other it narrows from 0.24 to 0.18 gauss. In the former case there is a growth of a second line due to the twinned stack; transformation twinning takes place at the phase transition. A small level-crossing interaction is inferred from the change in relative intensities of the lines near the crossover.
Science, Faculty of
Physics and Astronomy, Department of
Graduate
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Wilson, Peter John. "Electrochemical ESR of modified electrodes." Thesis, Imperial College London, 1989. http://hdl.handle.net/10044/1/47717.

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Maj, Stanislaw Paul. "ESR studies of organo-halide radicals." Thesis, University of Leicester, 1985. http://hdl.handle.net/2381/33795.

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Exposure of a range of dilute solutions of halogenobenzenes in fluoro-trichloromethane to 60Co y-rays at 77 K gave the corresponding cations characterised by their ESR spectra. The approximate spin-densities on the halogens were greater than predicted by comparison with neutral x-bromo radicals and increased from ca, 8% for PhF+ to 23% for PhCl+, 30% for PhBr+ and 46% for PhI+ In accord with the fall in the ionization potential for this series of halogen. For PhBr+, replacement of para hydrogen by Br, OH and SH gave a steady fall in spin-density on Br reflecting increasing n delocallsation onto the para substituent. Evidence for dimer cation formation in concentrated solutions is presented. The major species obtained from benzyl chloride suggested a preferred conformation with the chlorine close to, but not in, the plane of the benzene ring, with a significant barrier for the in-plane site, in contrast with benzyl bromide with strong hyperfine coupling to bromine [Chapters 3, 4 and 9]. Exposure of dilute solutions of Me2C(Br)C(Br)Me2 In CD3OD and MeTHF to 60Co y-rays at 77 K gave the radical Me2CC(Br)Me2. From changes in the e.s.r. spectrum of this radical, it is deduced that the stable structure is asymmetric, but that the rate of migration of bromine between the two equivalent sites becomes fast on the e.s.r. time-scale at ca. 100-1 [Chapter 6]. Evidence is given for the 1,2-intramolecular proton shift in the interconversion of isobutyl to tert-butyl radicals. The parent material was dissolved in a variety of matrices and exposed to 60Co y-rays at 77 K. The reaction was observed using an in-cavity Proportional, Integral and Differential (PID) temperature control system [Chapter 5]. A single crystal of ethyl iodide was grown and irradiated at 77 K with a a 60Co y-ray source. The spectra were orientation dependent but it was not possible to determine the principal g-values and the elements of the hyperfine tensor [Chapter 7]. 1-Bromo adamantane was dissolved in a variety of deuterated matrices and exposed to 60Co y-rays at 77 K. No firm conclusions can be drawn regarding the single proton coupling of ca. 65 G to the bromine. Exposure of dilute solutions of m-dinitrobenzene or s-trinitrobenzene in methyltetrahydrofuran to 60Co y-rays at 77 K gave two species at 77 K. One, favoured at low doses, had features characteristic of mono-anions with the unpaired electron localized on one nitro-group. At high 7-ray doses a second species with triplet state characteristics grew at the expense of the first. The average separation between the two unpaired electrons was estimated to be 5-6 A.
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Rowland, Ian J. "Halogen 6* radicals : an ESR study." Thesis, University of Leicester, 1988. http://hdl.handle.net/2381/33878.

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The main objective of the study was to characterise, by electron spin resonance (ESR) spectroscopy, novel halogen containing a* radicals. These species are formed by ?-irradiation in a variety of halogen containing systems at liquid nitrogen temperatures. In Chapter One, a brief description of the first halogen a* radical to be identified, the Vx centre in potassium chloride (C12.-), is given in order to illustrate the general magnetic properties of the species. The dependence of these properties on the host matrix is also described. Accepted radiation damage mechanisms are presented with particular reference to dihalogen a* radicals. Some theoretical aspects of the ESR experiment is discussed in Chapter Two which explains briefly some of the phenomena encountered in the study. Sample preparation and analysis are also mentioned. Chapter Three describes the characteristics of the simplest halogen containing a* radical: the hydrogen halide radical anion. Hydrogen fluoride, hydrogen chloride, hydrogen bromide and hydrogen iodide radical anions isolated in a variety of host matrices are reported. The large matrix dependence of their magnetic parameters is explained in terms of intermolecular hydrogen bonding to the halogen. Attention is focused on nitrogen-halogen a* radicals in Chapter Four, where they are shown to be radiolytically formed in ammonium halides, mono, di and trialkylammonium iodides and monoalkylammonium bromides. Alkylamanium chloride radicals could not be identified. Chapter Five primarily explores the effect of the halide counter ion on the solid-state radiolysis of some tetraalkylammonium, trialkylsulphonium and trialkylsulphoxonium cations. During the course of the investigation, sulphur-halogen a* radicals are identified in the trialkylsulphonium salts after annealing. The last chapter investigates the factors which determine the type of species formed following electron capture by carbon halogen bonds. Both adducts and a* radicals are characterised and with particular reference to the specific example of iodoacetamide, consideration is given to the factors influencing their stability.
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Bakker, M. G. "ESR studies on some naphthalene derivatives." Thesis, University of Canterbury. Chemistry, 1985. http://hdl.handle.net/10092/8639.

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ESR Spectroscopy has been used to study conformational interconversion and addivity relationships in a number of series of naphthalene derivatives. Oscillation of the alkyl rings in 1,2,3,6,7,8-hexahydropyrene ions, and the ions of the related 5, 6 and 7 membered ring compounds has been studied. The temperature dependance of the ESR spectra have been used to assign the coupling constants. The aromatic ring coupling constants in the asymmetric compounds have been assigned on the basis of an additivity relationship. The ESR spectra of a number of methylnaphthalene anions have been recorded and analysed to give the coupling constants. Improved additivity relationships for both the proton and methyl coupling constants have been determined. The temperature dependence of the spectrum of 1,2,3,4-tetramethylnaphthalene has been analysed. In terms of an interconversion between a tight and loose ion pair. The ESR spectra of a number of methylnaphthalene cations have been generated using AlCl₃/SO₂ and their spectra recorded and analysed. For those methylnaphthalenes which did not have methyl substituents in the 1 and 4 or 1 and 5 positions, a series of compounds with g=2.008 were recorded. Evidence is presented to show that these compounds are methyl derivatives of naphtho [1,8-cd]-1,2 dithiole. An additivity relationship for the proton coupling constants of these compounds has also been found. ESR spectra from the methylperylenes formed in the Scholl Condensation of the methylnaphthalene cations were also observed and analysed Changes in the ESR spectra of 1,8-dimethylnaphthalene and octamethylnaphthalene were ascribed to the effect of hindered rotation of the methyl groups. Coupling constants for the ESR spectra of tetracyclopentanaphthalene have been determined.
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Davidson, Iain G. "ESR studies on γ-irradiated foods." Thesis, University of Aberdeen, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.327924.

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Chapter 1 discusses the history, applications and effects (both beneficial and hazardous) of food irradiation and the techniques developed to detect irradiated foods. The basic radiation chemistry of major food components is reviewed. The preparation of 3,5-dimethyl-4-nitrosopyridine-1-oxide (DMNPO) and its dichloro- and dibromo- derivatives is described. Spin trapping of a variety of free radicals by DMNPO showed it to be an efficient trap for carbon-centred radicals but it did not form stable adducts with oxygen-centred radicals at room temperature as had been previously reported. The esr spectra were complicated by couplings arising from the hydrogens and nitrogen of the trap. The dichloro- and dibromo-analogues gave simpler spectra but were much more difficult to isolate. The effects of ionising radiation on spices and the methods used to detect these effects are reviewed. The measurement of free radical concentrations by esr spectroscopy was examined as a dosimetric method of identifying γ-irradiated spices. This proved to be impracticable because of the relatively rapid decay of the radicals and the variation in base-line radical concentrations. The short lived free radicals produced by irradiation were found to arise from the oleoresins. Identification of these radicals was attempted by irradiating the oleoresins and their major components, followed by spin trapping. In some cases, hydrogen abstraction gave the same radicals as those produced by irradiation. Separation of the spin adducts, formed from oleoresin components, by reverse phase HPLC is also described. Irradiation of food is known to cause destruction of vitamins. However, the processes involved are not fully understood. The solid state radiation chemistry of vitamins was investigated by spin trapping and esr spectroscopy. Irradiation of bones produces stable free radicals with characteristic esr spectra. It was shown that measurement of free radical concentrations in irradiated bones by esr spectroscopy could provide a dosimetric technique as the radical concentrations were stable and proportional to the applied dose.
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Kanschat, Peter. "ESR und spinabhängige Rekombination in mikrokristallinem Silizium." [S.l. : s.n.], 2000. http://deposit.ddb.de/cgi-bin/dokserv?idn=962370657.

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Moll, Klaus-Peter. "Mobilität von ESR-Spinsonden nach epikutaner Applikation." [S.l.] : [s.n.], 2004. http://deposit.ddb.de/cgi-bin/dokserv?idn=972617426.

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Mamat, Che Rozid. "Director disorder in liquid crystals : ESR investigations." Thesis, University of Southampton, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.442855.

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Books on the topic "ESR"

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Berliner, Lawrence J., ed. In Vivo EPR (ESR). Boston, MA: Springer US, 2003. http://dx.doi.org/10.1007/978-1-4615-0061-2.

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Shukla, Ashutosh Kumar, ed. EMR/ESR/EPR Spectroscopy for Characterization of Nanomaterials. New Delhi: Springer India, 2017. http://dx.doi.org/10.1007/978-81-322-3655-9.

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Y, Grinberg Oleg, and Berliner Lawrence J, eds. Very high frequency (VHF) ESR/EPR. New York: Kluwer Academic/Plenum Publishers, 2004.

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Grinberg, Oleg Y., and Lawrence J. Berliner, eds. Very High Frequency (VHF) ESR/EPR. Boston, MA: Springer US, 2004. http://dx.doi.org/10.1007/978-1-4757-4379-1.

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J, Berliner Lawrence, ed. In vivo EPR (ESR): Theory and application. New York: Kluwer Academic/Plenum Publishers, 2003.

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Berliner, Lawrence J. In Vivo EPR (ESR): Theory and Application. Boston, MA: Springer US, 2003.

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Grün, Rainer. Die ESR-Altersbestimmungsmethode. Berlin, Heidelberg: Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-95569-3.

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Die ESR-Altersbestimmungsmethode. Berlin: Springer-Verlag, 1989.

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M, Ikeya, Miki T, and International Symposium on ESR Dating,, eds. ESR dating and dosimetry. Tokyo: Ionics, 1985.

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Grün, Rainer. Beiträge zur ESR-Datierung. Köln, Federal Republic of Germany: Geologisches Institut der Universität zu Köln, Bibliothek, 1985.

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Book chapters on the topic "ESR"

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Dinse, Klaus-Peter, and Gunnar Jeschke. "EPR-ESR-EMR, an Ongoing Success Story." In Methods in Physical Chemistry, 159–89. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527636839.ch5.

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Mehlhorn, Heinz. "ESR." In Encyclopedia of Parasitology, 958. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-43978-4_3853.

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Mehlhorn, Heinz. "ESR." In Encyclopedia of Parasitology, 1. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-27769-6_3853-1.

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Gooch, Jan W. "ESR." In Encyclopedic Dictionary of Polymers, 274. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_4510.

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Berliner, Lawrence J., and Harold M. Swartz. "Introduction to in Vivo EPR." In In Vivo EPR (ESR), 1–20. Boston, MA: Springer US, 2003. http://dx.doi.org/10.1007/978-1-4615-0061-2_1.

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Gallez, Bernard. "Packaging of Paramagnetic Materials in Oximetry and Other Applications." In In Vivo EPR (ESR), 259–84. Boston, MA: Springer US, 2003. http://dx.doi.org/10.1007/978-1-4615-0061-2_10.

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Timmins, Graham S., and Ke Jian Liu. "Spin Trapping in Vivo: Facts and Artifacts." In In Vivo EPR (ESR), 285–308. Boston, MA: Springer US, 2003. http://dx.doi.org/10.1007/978-1-4615-0061-2_11.

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Mason, Ronald P., and Maria B. Kadiiska. "Ex Vivo Detection of Free Radical Metabolites of Toxic Chemicals and Drugs by Spin Trapping." In In Vivo EPR (ESR), 309–23. Boston, MA: Springer US, 2003. http://dx.doi.org/10.1007/978-1-4615-0061-2_12.

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Komarov, Andrei M. "Chemistry and Biology of Nitric Oxide." In In Vivo EPR (ESR), 325–79. Boston, MA: Springer US, 2003. http://dx.doi.org/10.1007/978-1-4615-0061-2_13.

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Fujii, Hirotada, and Lawrence J. Berliner. "In Vivo and in Vitro Detection of NO by EPR." In In Vivo EPR (ESR), 381–402. Boston, MA: Springer US, 2003. http://dx.doi.org/10.1007/978-1-4615-0061-2_14.

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Conference papers on the topic "ESR"

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Berliner, L. J., H. Fujii, and X. Wan. "In-vivo ESR and EPR imaging." In Proceedings of the Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE, 1988. http://dx.doi.org/10.1109/iembs.1988.94576.

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White, Christopher J., Colin T. Elliott, and James R. White. "Micro-electron spin resonance (ESR/EPR) spectroscopy." In SPIE Defense, Security, and Sensing, edited by Mark A. Druy, Christopher D. Brown, and Richard A. Crocombe. SPIE, 2010. http://dx.doi.org/10.1117/12.849682.

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Baffa, Oswaldo. "ESR Dosimetry." In MEDICAL PHYSICS: Eighth Mexican Symposium on Medical Physics. AIP, 2004. http://dx.doi.org/10.1063/1.1811817.

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Karpovich, I. A., L. V. Cvirko, V. B. Odzhaev, V. N. Popok, I. I. Azarko, A. D. Tarasevitch, and V. P. Tolstykh. "Superheterodyne ESR-spectrometer." In 1999 9th International Crimean Microwave Conference 'Microwave and Telecommunication Technology'. Conference Proceedings. IEEE, 1999. http://dx.doi.org/10.1109/crmico.1999.815264.

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Metter, K., FL Dumoulin, KE Grund, and G. Farin. "Zwischen EMR und ESD: Endoskopische Submukosaresektion (ESR) zur optimierten en bloc Resektion kolorektaler Läsionen bis 50 mm." In Viszeralmedizin 2019. Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-1695571.

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Earle, Keith A., and Jack H. Freed. "ESR spectrometer at 250 GHz." In SPIE's 1995 International Symposium on Optical Science, Engineering, and Instrumentation, edited by Mohammed N. Afsar. SPIE, 1995. http://dx.doi.org/10.1117/12.224225.

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Hong, S., L. Kang, and J. Shin. "Development of Electroslag Remelting (ESR) Simulator to Predict Chemical Reaction During the ESR Process." In 8th International Congress on the Science and Technology of Steelmaking. AIST, 2022. http://dx.doi.org/10.33313/531/040.

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Grund, KE, P. Aepli, FL Dumoulin, R. Frei, K. Metter, and G. Farin. "Wichtige, aber bislang vernachlässigte Parameter bei EPE, EMR und ESD und die Rolle der Endoskopischen Submukosa Resektion (ESR)." In DGVS Digital: BEST OF DGVS. © Georg Thieme Verlag KG, 2020. http://dx.doi.org/10.1055/s-0040-1716293.

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Krzyminiewski, Ryszard, Bernadeta Dobosz, Grzegorz Schroeder, and Joanna Kurczewska. "ESR for Controlling Magnetite Nanoparticles Focusing." In The 3rd World Congress on New Technologies. Avestia Publishing, 2017. http://dx.doi.org/10.11159/icnfa17.134.

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Shibata, T., T. Takahashi, J. Taira, and T. Kure. "Superalloy 706 Large Forgings by ESR." In Superalloys. TMS, 2001. http://dx.doi.org/10.7449/2001/superalloys_2001_161_172.

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Reports on the topic "ESR"

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Marx, Daniel, C. Montag, JS Berg, J. Kewsich, Y. Lii, V. Ptitsyn, S. Tepikian, et al. Task Force Report: ESR Linear Lattice Design. Office of Scientific and Technical Information (OSTI), December 2021. http://dx.doi.org/10.2172/1837215.

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Berg, J., B. Gamage, H. Lovelace III, D. Marx, C. Montag, S. Peggs, V. Ptitsyn, G. Robert-Demolaize, and D. Xu. Synchronizing ESR and HSR for collisions at IP6 and IP8. Office of Scientific and Technical Information (OSTI), September 2022. http://dx.doi.org/10.2172/1889642.

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Podobedov, Boris, and Daniel Marx. ESR Magnet vibrational specifications for dynamic orbit stability at the IP. Office of Scientific and Technical Information (OSTI), September 2021. http://dx.doi.org/10.2172/1823635.

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Reyes, Ricardo A. Study of EPR/ESR Dosimetry in Fingernails as a Method for Assessing Dose of Victims of Radiological Accidents/Incidents. Fort Belvoir, VA: Defense Technical Information Center, May 2008. http://dx.doi.org/10.21236/ad1013777.

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Tang, Jau, S. N. Dikshit, and J. R. Norris. Study of one-dimensional electron hopping and its effects on ESR line shape. Office of Scientific and Technical Information (OSTI), August 1997. http://dx.doi.org/10.2172/516029.

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Ffield, Amy. Regional Stratification and Shear of the Various Streams Feeding the Philippine Straits - ESR Component. Fort Belvoir, VA: Defense Technical Information Center, September 2008. http://dx.doi.org/10.21236/ada533697.

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Field, Amy F. Regional Stratification and Shear of the Various Streams Feeding the Philippine Straits - ESR Component. Fort Belvoir, VA: Defense Technical Information Center, September 2006. http://dx.doi.org/10.21236/ada631416.

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Ffield, Amy. Regional Stratification and Shear of the Various Streams Feeding the Philippine Straits - ESR Component. Fort Belvoir, VA: Defense Technical Information Center, September 2007. http://dx.doi.org/10.21236/ada573076.

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Hickey, Charles F., Thomas Jr., Anctil Timothy S., and Albert A. Comparison of Ballistic Performance of a Split Heat of ESR and VAR 4340 Steel. Fort Belvoir, VA: Defense Technical Information Center, July 1985. http://dx.doi.org/10.21236/ada160924.

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Peppers, Larry G., and Vincent L. Trujillo. LANL Response to SRS Requirement G-ESR-G-00035 Item 11 Bed Temperature Requirements, Revision 4. Office of Scientific and Technical Information (OSTI), June 2013. http://dx.doi.org/10.2172/1084515.

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