Academic literature on the topic 'Electron para magnetic resonance'

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Journal articles on the topic "Electron para magnetic resonance"

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Paris, S., and E. Ilisca. "Electron−Nucleus Resonances and Magnetic Field Accelerations in the Ortho−Para H2Conversion." Journal of Physical Chemistry A 103, no. 25 (June 1999): 4964–68. http://dx.doi.org/10.1021/jp990040t.

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Qing Jin, Chang, Liu Kun Wang, and Yany An Liu. "Magnetic resonance experiments on undoped and doped poly(para-phenylene)." Synthetic Metals 49, no. 1-3 (August 1992): 261–65. http://dx.doi.org/10.1016/0379-6779(92)90098-4.

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Schaefer, Ted, Rudy Sebastian, and Frank E. Hruska. "1H nuclear magnetic resonance and molecular orbital studies of the internal rotational potential and electron delocalization in triphenylphosphine." Canadian Journal of Chemistry 71, no. 5 (May 1, 1993): 639–43. http://dx.doi.org/10.1139/v93-085.

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The 1H nuclear magnetic resonance spectral parameters are reported for triphenylphosphine as solutions in CS2/C6D12 and acetone-d6 at 300 K. The internal rotational potential opposing torsion about the P—C bond is computed by AMI and STO-3G MO methods. The computed potentials are used to calculate the average shielding of the para protons caused by the diamagnetic anisotropies of the neighbouring phenyl groups. The results are used to estimate the degree of electron delocalization from the lone pair on phosphorus. The extent of delocalization depends on the internal motions and comparisons are made with phenylphosphine. The maximum possible screening of the para protons in phenylphosphine is calculated as 0.19 ppm for a conformation in which the lone pair on phosphorus is oriented perpendicular to the aromatic plane. The intramolecular rotational potentials then yield 0.029 ppm as the shielding of the para protons in triphenylphosphine due to electron delocalization, just as found for the CS2/C6D12 solution after correction for diamagnetic anisotropy fields.
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Dunn, E. J., J. G. Purdon, R. A. B. Bannard, K. Albright, and E. Buncel. "Correlation of 31P nuclear magnetic resonance chemical shifts in aryl phosphinates with Hammett substituent constants: Inductive versus resonance interactions and relevance to pπ–dπ bonding." Canadian Journal of Chemistry 66, no. 12 (December 1, 1988): 3137–42. http://dx.doi.org/10.1139/v88-484.

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Substituent-induced chemical shifts and coupling constants in the 31P, 13C, and 1H nuclear magnetic resonance spectra of meta- and para-substituted phenyl dimethylphosphinates (1), methylphenylphosphinates (2), and diphenylphosphinates (3) have been determined in CDCl3 solvent. For all three series, a correlation of δ 31P with Hammett–Taft σ0 (or σ) constants is preferred over σ− on the basis of the correlation coefficient and standard deviations of the slope and intercept values. Electron-withdrawing substituents induce downfield shifts in δ 31P, in contrast to the inverse trends observed for structurally related series of oxyphosphorus acids and their derivatives. It is proposed that electron-withdrawing substituents act to deplete the electron density on the aryl oxygen, thereby weakening a pπ–dπ bonding interaction between the aryl oxygen and phosphorus. The resultants loss of d-orbital density on phosphorus causes a downfield shift in δ 31P in each of the phosphinate series. Phenyl substituents attached directly to phosphorus in series 2 and 3 increase the phosphoryl pπ–dπ back-bonding interactions, either through inductive or resonance effects, which leads to shielding of the phosphorus atom, overriding the anticipated downfield shift through inductive electron withdrawal of the phenyl substituents in series 2 and 3, relative to the methyls in series 1. Trends in Hammett ρ values for the plots of δ 31P and δ 13C versus σ0 and differences in the shielding of 13C and 1H nuclei of the methyl attached to phosphorus in series 1 and 2 suggest that the phenyl groups may interact in π bonding with the phosphorus atom through a resonance interaction.
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Ito, Akihiro, and Kazuyoshi Tanaka. "Macrocyclic oligoarylamine-based spin system." Pure and Applied Chemistry 82, no. 4 (March 17, 2010): 979–89. http://dx.doi.org/10.1351/pac-con-09-10-16.

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Alternating meta- and para-phenylene-linked oligoarylamines are considered as promising molecular parts for the molecule-based electronics and/or spintronics due to their intriguing electronic and magnetic properties. From the magnetic viewpoint, a -meta-phenylene linker plays a crucial role in ensuring the effective ferromagnetic interaction, while para-phenylene linker plays an important part in stabilizing the spin-containing aminium radical cations. Of the meta–para and all-meta oligoarylamines prepared so far, the macrocyclic oligoarylamines are structurally defined, and therefore we can employ them as the component pieces to prepare the two- or three-dimensionally structured oligoarylamines. The spin electronic properties of polycationic species generated from two kinds of macrocyclic oligoarylamines, which will be able to be extended into the 2D multi-spin molecular systems, are described on the basis of the pulsed electron spin resonance (ESR) measurements.
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Schaefer, Ted, Rudy Sebastian, and Glenn H. Penner. "1H nuclear magnetic resonance spectral parameters of toluene. Implications for conformational analysis and isotope shifts." Canadian Journal of Chemistry 63, no. 10 (October 1, 1985): 2597–600. http://dx.doi.org/10.1139/v85-431.

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A precise analysis of the 1H nmr spectrum of toluene as a dilute solution in carbon disulfide yields a revised set of spectral parameters. The chemical shift of the para proton lies 12.6 ppb to low frequency of that of the ortho protons at 300 K. The ring proton chemical shifts are discussed and compared with 1H and 3H shifts observed in carbon tetrachloride. The long-range couplings between methyl and ring protons can be said to be quantitatively understood in terms of σ and σ–π electron transmitted mechanisms. The changes observed in these three couplings in phenylacetaldehyde can be quantitatively reproduced in terms of these mechanisms and also illustrate how these changes are direct measures of the conformational preferences in this molecule.
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Schaefer, Ted, Scott Kroeker, and David M. McKinnon. "1H and 13C nuclear magnetic resonance and molecular orbital studies of the internal rotational potential and of spin–spin coupling transmission in phenylallene." Canadian Journal of Chemistry 73, no. 9 (September 1, 1995): 1478–87. http://dx.doi.org/10.1139/v95-183.

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The 1H nuclear magnetic resonance spectra of phenylallene, diluted in acetone-d6 and benzene-d6, yield long-range coupling constants over as many as eight formal bonds between the ring and side-chain protons. These are discussed in terms of σ- and π-electron spin–spin coupling mechanisms, which are sensitive to the torsion angle between the allenyl and phenyl fragments. The torsion angle is assessed by means of molecular orbital computations of the internal rotational potential, whose height is calculated as 16.0 kJ/mol at the MP2/6-31G* level of correlation-gradient theory. Comparison with experimental and theoretical internal rotational potentials for styrene suggests that steric repulsions in the planar form of styrene amount to about 4 kJ/mol. In a field of 7.0 T, phenylallene is partially aligned, entailing a positive dipolar coupling constant between the methylene protons, from which absolute signs of the spin–spin coupling constants involving these protons can be inferred. Such coupling constants over seven and eight bonds, to the meta and para protons, are taken as being mediated by the extended π-electron system, providing a measure of π-electron contributions to coupling constants between meta protons and those in side chains (spin correlation). Some coupling constants between protons and 13C nuclei in the side chain, as well as between ring protons and these 13C nuclei, are also discussed in terms of spin coupling mechanisms. Solvent perturbations of one-bond proton–carbon coupling constants in the allenyl group do not follow the usual pattern in which an increase in polarity of the solvent is associated with an increase in the magnitude of the coupling constant. Keywords: 1H NMR, phenylallene; 1H NMR, long-range spin–spin coupling constants in phenylallene; phenylallene, internal rotational potential, molecular orbital computations; molecular orbital calculations, an internal rotational potential in phenylallene.
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Steel-Goodwin, Linda, Tasha L. Pravecek, and Alasdair J. Carmichael. "Trichloroethylene metabolism in vitro: an EPR/SPIN trapping study." Human & Experimental Toxicology 15, no. 11 (November 1996): 878–84. http://dx.doi.org/10.1177/096032719601501103.

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Trichloroethylene (TCE) was hypothesized to produce free radicals which could be detected using electron para magnetic resonance spectroscopy with the spin trap, PBN (α-phenyl tert-butyl nitrone). The free radicals detected following incubation of precision cut liver slices in media containing 10 mM PBN had hyperfine coupling constants aN=1.61 mT and aH=0.325 mT. There was a linear increase in free radicals detected in the bathing media when the headspace TCE concentration was increased from 2500- 10 000 p.p.m. The levels of conjugated dienes measured in the slices incubated in PBN supplemented media were less than slices exposed to TCE in incubation media without PBN. The PBN trap may act as a scavenger preventing the propagation of free radicals and inhibiting lipid peroxida tion. The experiments suggest that free radical formation by TCE leads to a concomitant increase in conjugated dienes in liver slices which may contribute to the pathological changes which occur in liver following TCE exposure.
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Budi Lelono, Eko, and Isnawati Isnawati. "PERANAN IPTEK NUKLIR DALAM EKSPLORASI HIDROKARBON." Jurnal Forum Nuklir 1, no. 2 (November 1, 2007): 79. http://dx.doi.org/10.17146/jfn.2007.1.2.3274.

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Perkembangan iptek nuklir berpengaruh terhadap teknik eksplorasi hidrokarbon, antara lain terbukti dengan adanya penggunaan isotop radioaktif untuk menentukan umur absolute batuan. Penentuan umur batuan yang pada awalnya menggunakan fosil penunjuk umur (baik mikro maupun makro-fosil) yang menghasilkan umur relatif batuan, belakangan ini diperkaya dengan metode perhitungan peluruhan mineral radioaktif untuk menentukan umur absolute batuan, sehingga posisi stratigrafi suatu lapisan batuan (batuan induk dan reservoir) dapat ditentukan dengan pasti. Sementara itu, aplikasi teknologi nuklir juga dipergunakan dalam survey sumur pemboran eksplorasi yang antara lain dikenal dengan Nuclear Magnetic Resonance (NMR) yang membantu ahli geologi dalam mengukur porositas dan permiabilitas secara langsung di lapangan, sehingga dapat memprediksi keberadaan hidrokarbon. Dari sisi sedimentologi, iptek nuklir juga diaplikasikan dalam laboratorium X Ray Diffraction (XRD Laboratory) untuk menentukan jenis mineral penyusun batuan dan laboratorium Scanning Electron Microscope (SEM Laboratory) untuk mengetahui porositas batuan. Kedua hal tersebut membantu ahli eksplorasi dalam menyusun manajemen reservoir.
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Kuvshinova, Elizaveta M., Olga V. Gornukhina, Alexander S. Semeikin, Irina A. Vershinina, and Sergey A. Syrbu. "COORDINATION PROPERTIES OF NITRO-SUBSTITUTED 5,15-DIPHENYL-3,7,13,17-TETRAMETHYL-2,8,12,18-TETRAETHYLPORPHYRIN WITH MANGANESE ACETATE IN PYRIDINE AND ACETIC ACID." IZVESTIYA VYSSHIKH UCHEBNYKH ZAVEDENII KHIMIYA KHIMICHESKAYA TEKHNOLOGIYA 63, no. 9 (August 4, 2020): 49–55. http://dx.doi.org/10.6060/ivkkt.20206309.6218.

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The synthesis of 5,15-diphenyl-3,7,13,17-tetramethyl-2,8,12,18-tetraethylporphyrin and its nitro substituted was carried out. Nitro groups are located in meso-positions of the tetrapyrrole macrocycle and (or) para-positions of the phenyl rings. The synthesized porphyrins are characterized by a set of modern research methods: electron absorption spectroscopy; IR and nuclear magnetic resonance spectroscopy 1H. The reactions of the formation of manganese complexes with nitro-substituted 5,15-diphenyl-3,7,13,17-tetramethyl-2,8,12,18-tetraethylporphyrin and their stability in organic solvents are studied. It was found that the rate of reactions of formation of manganese complexes in pyridine with the introduction of nitrogroups in 5,15-diphenyl-3,7,13,17-tetramethyl-2,8,12,18-tetraethylporphine grows as the degree of deformation of the tetrapyrrole macrocycle increases. Obviously, in this case, not only the stretching of NH bonds, due to the presence of electron-withdrawing substituents (NO2) in the para positions of the phenyl rings, makes a decisive contribution to the energy of the transition state, but also the increase in the basicity of tertiary nitrogen atoms, which form strong bonds in the transition state with a solvated cation of salt. In acetic acid, the macrocycle deformation effect leads to a decrease in the reaction rate, which is due to the specific solvation of the porphine reaction center by acetic acid molecules. It was found that steric distortions of the planar structure of porphyrins have relatively little effect on the kinetic parameters of the solvoprotolytic dissociation of manganese complexes of 5,15-diphenyl-3,7,13,17-tetramethyl-2,8,12,18-tetraethylporphyrin and its nitro-substituted ones. This is probably due to the fact that the coordination of the manganese cation results in a more planar structure of the porphyrin macrocycle. The decrease in the dissociation reaction rate with an increase in the number of nitrogroups in 5,15-diphenyl-3,7,13,17-tetramethyl-2,8,12,18-tetraethylporphyrine is due to the influence of the negative inductive effect of nitrogroups, which reduces the effective charge in the macrocycle on nitrogen atoms that are attacked by a solvated proton.
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Dissertations / Theses on the topic "Electron para magnetic resonance"

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Souza, Pedro Victor Brondino Duarte de. "Desenvolvimento de um subsistema non-real-time para o gerenciamento de dispositivos periféricos e desenvolvimento de interfaces gráficas." Universidade de São Paulo, 2016. http://www.teses.usp.br/teses/disponiveis/76/76132/tde-21102016-140615/.

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Ressonância Magnética (RM) é uma técnica bastante versátil, pois é utilizada em muitas áreas de pesquisa, como biologia, física, química, engenharia e medicina. Apesar disso, constitui-se uma desvantagem o alto custo do equipamento e suas restrições físicas para alguns experimentos. Para reduzir essas desvantagens, o grupo de pesquisadores do CIERMag está desenvolvendo um equipamento de RMN multipropósito e, para complementá-lo, este trabalho vem desenvolver um subsistema non-real-time que gerencia os dispositivos periféricos de um experimento. Foi proposta uma rede de dispositivos que é controlada por um Raspberry Pi como elemento central, o qual está conectado ao terminal computadorizado do sistema através de uma rede local (Local Area Network - LAN) via Ethernet e conectado aos dispositivos periféricos via Serial Peripheral Interface (SPI). Com o objetivo de ser possível gerenciar qualquer tipo de dispositivo, foi desenvolvido um conjunto de parâmetros baseado no Transducer Electronic Data Sheet (TEDS), definido no padrão IEEE 1451, de modo que cada dispositivo, normalmente um transdutor, possui seu próprio. Foram elaboradas duas interfaces de software: uma desenvolvida em Python e a outra uma interface web HTML. Ambas as interfaces possuem as mesmas funcionalidades: editor e gerenciador de TEDS, visualização gráfica de medidas dos sensores e interface para os atuadores.
Magnetic Resonance (MR) is a very versatile technique, since it is used in many research areas such as biology, physics, chemistry, engineering and medicine. Despite this, the cost of the equipment and its physical restrictions in some experiments constitute a serious drawback. To minimize these problems, the CIERMag research team is developing multipurpose MR equipment and, to complement this equipment, this work develops a non-real-time subsystem that manages the peripheral devices of the experiment. It was proposed a network of devices controlled by a Raspberry Pi as its central element, which is connected to the terminal computer of the system. The protocol adopted for this was Ethernet via Local Area Network (LAN); communication with peripheral transducers was performed with the Serial Peripheral Interface (SPI). With the objective to be able to manage any type of device, we created parameter sets based on Transducer Electronic Data Sheet (TEDS), defined in the IEEE 1451 standard, so each device, normally a transducer, has its own parameter set. We created two software interfaces: one developed with Python and the other is a HTML web interface. Both have the same functionalities: a TEDS editor and manager, a graphical visualization of sensor measurements and also an actuator interface.
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Murakami, Nayara Saty. "Processamento e caracterização do gel Magic-f com raios-x, espectroscopia por RMN e EPR e espectrofotometria UV/Vis." Universidade Tecnológica Federal do Paraná, 2017. http://repositorio.utfpr.edu.br/jspui/handle/1/2642.

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Este trabalho teve como objetivo realizar o processamento do gel polimérico MAGICf, irradiá-lo e caracterizá-lo com quatro métodos de leitura, uma vez que a dosimetria com gel polimérico é uma área promissora no âmbito de controle de qualidade dos tratamentos radioterápicos, pois permite a avaliação de dose tridimensionalmente. Os métodos para caracterização do gel MAGIC-f foram: Tomografia Computadorizada (TC), espectroscopia de Ressonância Magnética Nuclear (RMN), Ressonância Paramagnética Eletrônica (EPR) e espectrofotometria UV/Vis. Para a caracterização por esse último método, foi feita uma nova formulação do gel MAGIC-f adicionando fluoresceína. Os resultados da caracterização desse gel dosimétrico com tomografia computadorizada e EPR não foram satisfatórios, porém com a espectroscopia de RMN obteve-se bons resultados, assim como com a espectrofotometria UV/Vis. A nova formulação do gel para a caracterização com espectrofotometria mostrou-se ser um método inovador e bastante promissor para essa área.
This work aimed to perform the processing of the MAGIC-f polymeric gel, to irradiate it and to characterize it with four methods of reading, since the dosimetry with polymeric gel is a promising area within the scope of quality control of the radiotherapeutic treatments, because it allows dose evaluation three-dimensional. The methods for characterization of the MAGIC-f gel were: Computed Tomography (CT), Nuclear Resonance Magnetic (NMR) and Electron Paramagnetic Resonance (EPR) spectroscopy, and UV/Vis spectrophotometry. For characterization with this last method, a new MAGIC-f gel formulation was made adding fluorescein. The results of the characterization of this dosimetric gel with computed tomography and EPR were not satisfactory, but with NMR spectroscopy satisfactory results were obtained as well as UV / Vis spectrophotometry. The new gel formulation for characterization with UV / Vis spectrophotometry has proved to be an innovative and very promising method for this area.
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Allsopp, Richard Antony. "Electron spin resonance studies of magnetic defects in solids." Thesis, University of Oxford, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.253301.

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Fong, Kin Chung. "High Sensitivity Electron Spin Resonance by Magnetic Resonance Force Microscopy at Low Temperature." The Ohio State University, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=osu1228338129.

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Elbahrawy, Mohammed. "High field electron magnetic resonance in complex correlated spin systems." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2010. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-39380.

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In this thesis we used ESR to investigate magnetic properties of low D vandium and copper oxides in which small quantum spins are arranged in 1D chains and 2D layers. The thesis covers five different low dimensional spin systems. They turned out to be experimental reliazation of some of the most intersiting theoritical models in the field of quantum magnetism.
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Bingham, Stephen John. "Magnetic circular dichroism and electron paramagnetic resonance of transition ions." Thesis, University of East Anglia, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.357179.

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Hunter, David M. "Studies of electron transfer in plastocyanins by nuclear magnetic resonance." Thesis, University of Newcastle Upon Tyne, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.270171.

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Crook, Nigel Paul. "The application of quantitative environmental magnetic measurements to sedimentary systems." Thesis, Manchester Metropolitan University, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.248812.

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Caldwell, Joshua D. "Investigation of electron-nuclear spin interactions in two-dimensional electron systems via magnetoresistively detected magnetic resonance." [Gainesville, Fla.] : University of Florida, 2004. http://purl.fcla.edu/fcla/etd/UFE0008397.

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Oprea, Corneliu I. "Density Functional Response Theory with Applications to Electron and Nuclear Magnetic Resonance." Doctoral thesis, Stockholm, : Bioteknologi, Kungliga Tekniska högskolan, 2007. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-4367.

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Books on the topic "Electron para magnetic resonance"

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T, Navrot͡s︡kiĭ V., and Sabad E. P, eds. Resonance phenomena in electron-atom collisions. Berlin: Springer-Verlag, 1992.

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Transition ion electron paramagnetic resonance. Oxford: Clarendon Press, 1990.

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Magnetic atoms and molecules. New York: Dover Publications, 1989.

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Ivano, Bertini, and Luchinat C. 1952-, eds. Nuclear and electron relaxation: The magnetic nucleus-unpaired electron coupling in solution. Weinheim: VCH, 1991.

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Banci, Lucia. Nuclear and electron relaxation: The magnetic nucleus-unpaired electron coupling in solution. New York: VCH, 1991.

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Yokoyama, Hidekatsu. EPR imaging and its in vivo application. Hauppauge, NY: Nova Science Publishers, 2009.

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Strutz, Thomas. High magnetic field electron spin-lattice relaxation in a diluted magnetic semiconductor: CdMnTe. Konstanz: Hartung-Gorre Verlag, 1991.

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Bingham, Stephen John. Magnetic and circular dichroism and electron paramagentic resonance of transition ions. Norwich: University of East Anglia, 1993.

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Poole, Charles P. Electron spin resonance: A comprehensive treatise on experimental techniques. Mineola, N.Y: Dover Publications, 1996.

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Kutter, Christoph. Pulsed electron paramagnetic resonance in high magnetic fields using far infrared lasers. Konstanz: Hartung-Gorre, 1995.

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Book chapters on the topic "Electron para magnetic resonance"

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Slichter, Charles P. "Electron Spin Resonance." In Principles of Magnetic Resonance, 503–54. Berlin, Heidelberg: Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-662-09441-9_11.

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Wertz, John E., and James R. Bolton. "Energy-level Splitting in Zero Magnetic Field. The Triplet State." In Electron Spin Resonance, 223–57. Dordrecht: Springer Netherlands, 1986. http://dx.doi.org/10.1007/978-94-009-4075-8_10.

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Maurel, V., and S. Gambarelli. "EPR of Short-Lived Magnetic Species." In Electron Paramagnetic Resonance Spectroscopy, 283–312. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-39668-8_10.

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Azarkh, Mykhailo, and Malte Drescher. "Long-Range Distance Constraints in Biomacromolecules by a Combined Approach of Site-Directed Spin Labeling and Double Electron–Electron Resonance (DEER) Spectroscopy." In Modern Magnetic Resonance, 1–18. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-28275-6_109-1.

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Azarkh, Mykhailo, and Malte Drescher. "Long-Range Distance Constraints in Biomacromolecules by a Combined Approach of Site-Directed Spin Labeling and Double Electron–Electron Resonance (DEER) Spectroscopy." In Modern Magnetic Resonance, 1013–30. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-28388-3_109.

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Belorizky, E., and P. H. Fries. "Characterising Contrast Agents for Magnetic Resonance Imaging." In Electron Paramagnetic Resonance Spectroscopy, 313–49. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-39668-8_11.

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Misra, Sushil K. "Single-Molecule Magnets and Magnetic Quantum Tunneling." In Multifrequency Electron Paramagnetic Resonance, 845–74. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2011. http://dx.doi.org/10.1002/9783527633531.ch21.

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Menard, David, and Robert Barklie. "Electron Paramagnetic and Ferromagnetic Resonance." In Handbook of Magnetism and Magnetic Materials, 1–35. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-63101-7_25-1.

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Prisner, Thomas, and Mark J. Prandolini. "Dynamic Nuclear Polarization (DNP) at High Magnetic Fields." In Multifrequency Electron Paramagnetic Resonance, 921–46. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2011. http://dx.doi.org/10.1002/9783527633531.ch24.

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Eaton, Sandra S., and Gareth R. Eaton. "High Magnetic Fields and High Frequencies." In Handbook of Electron Spin Resonance, 345–70. New York, NY: Springer New York, 1999. http://dx.doi.org/10.1007/978-1-4612-1486-1_11.

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Conference papers on the topic "Electron para magnetic resonance"

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Daughton, David R., Masaki Yamaguchi, Li Li, Jing Han, and Katsuya Inoue. "Photomixer-based THz electron magnetic resonance measurements." In 2016 41st International Conference on Infrared, Millimeter, and Terahertz waves (IRMMW-THz). IEEE, 2016. http://dx.doi.org/10.1109/irmmw-thz.2016.7758376.

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Yordanov, N. D. "Electron Magnetic Resonance of Disordered Systems (EMARDIS – 91)." In International Workshop on Electron Magnetic Resonance of Disordered Systems (EMARDIS-91). WORLD SCIENTIFIC, 1991. http://dx.doi.org/10.1142/9789814538749.

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Cates, Gordon D. "Laser-polarized Noble Gases for Magnetic Resonance Imaging." In SPIN 2002: 15th International Spin Physics Symposium and Workshop on Polarized Electron Sources and Polarimeters. AIP, 2003. http://dx.doi.org/10.1063/1.1607133.

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Chernyshov, N. N., A. V. Belousov, I. N. Gvozdevskiy, N. I. Slipchenko, Khansaa A. Ghazi, and M. A. F. Alkhawaldeh. "Spin Resonance in a Semiconductor Structure in Quantizing Magnetic Field." In 2019 International Seminar on Electron Devices Design and Production (SED). IEEE, 2019. http://dx.doi.org/10.1109/sed.2019.8798465.

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Shalashov, A. G., P. A. Bagryansky, E. D. Gospodchikov, A. L. Solomakhin, and D. V. Yakovlev. "Theory of electron cyclotron resonance startup in the gas dynamic trap." In OPEN MAGNETIC SYSTEMS FOR PLASMA CONFINEMENT (OS2016): Proceedings of the 11th International Conference on Open Magnetic Systems for Plasma Confinement. Author(s), 2016. http://dx.doi.org/10.1063/1.4964164.

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HILL, S., A. KOVALEV, M. M. MOLA, C. PALASSIS, Z. Q. MAO, Y. MAENO, and J. S. QUALLS. "ELECTRON MAGNETIC RESONANCE FERMI SURFACE IMAGING: APPLICATIONS TO ORGANIC CONDUCTORS AND Sr2RuO4." In Physical Phenomena at High Magnetic Fields - IV. WORLD SCIENTIFIC, 2002. http://dx.doi.org/10.1142/9789812777805_0049.

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ZVYAGIN, S. A., G. CAO, L. C. BRUNEL, and J. CROW. "ELECTRON-SPIN RESONANCE EVIDENCE OF THE QUANTUM SPIN GAP IN THE LiCu2O2." In Physical Phenomena at High Magnetic Fields - IV. WORLD SCIENTIFIC, 2002. http://dx.doi.org/10.1142/9789812777805_0126.

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Song, Suk-Ho, Takahito Ono, and Masayoshi Esashi. "Microprobe Integrated with Single-Electron Transistor for Magnetic Resonance Force Microscopy." In TRANSDUCERS 2007 - 2007 International Solid-State Sensors, Actuators and Microsystems Conference. IEEE, 2007. http://dx.doi.org/10.1109/sensor.2007.4300491.

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Kalmykova, T. V., A. A. Vakula, S. V. Nedukh, S. I. Tarapov, A. G. Belous, and O. Yelenich. "Simulation of the electron magnetic resonance peak shape for Fe3O4 nanopowder." In 2016 9th International Kharkiv Symposium on Physics and Engineering of Microwaves, Millimeter and Submillimeter Waves (MSMW). IEEE, 2016. http://dx.doi.org/10.1109/msmw.2016.7538090.

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Murugesan, R., Murali C. Krishna, and P. Alli. "Adaptive Fuzzy Control Approach for Enhancement of Electron Magnetic Resonance Tomograms." In International Conference on Computational Intelligence and Multimedia Applications (ICCIMA 2007). IEEE, 2007. http://dx.doi.org/10.1109/iccima.2007.210.

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Reports on the topic "Electron para magnetic resonance"

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Van Willigen, H. Magnetic resonance studies of photo-induced electron transfer reactions. Office of Scientific and Technical Information (OSTI), January 1992. http://dx.doi.org/10.2172/5710499.

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van Willigen, H. Magnetic resonance studies of photo-induced electron transfer reactions. Office of Scientific and Technical Information (OSTI), November 1992. http://dx.doi.org/10.2172/6889113.

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van Willigen, H. Magnetic resonance studies of photo-induced electron transfer reactions. Office of Scientific and Technical Information (OSTI), December 1990. http://dx.doi.org/10.2172/6286127.

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van Willigen, H. Magnetic resonance studies of photo-induced electron transfer reactions. Final report, June 1, 1990--May 31, 1993. Office of Scientific and Technical Information (OSTI), November 1992. http://dx.doi.org/10.2172/10142337.

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Van Willigen, H. Magnetic resonance studies of photo-induced electron transfer reactions. Progress report, June 1, 1991--May 31, 1992. Office of Scientific and Technical Information (OSTI), January 1992. http://dx.doi.org/10.2172/10126713.

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Scott, J. Robert. Characterization of the Iron-Sulfur Clusters in Xanthine Dehydrogenase Using Electron Paramagnetic Resonance Spectroscopy and Magnetic Coupling Interactions. Office of Scientific and Technical Information (OSTI), February 2004. http://dx.doi.org/10.2172/826759.

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Doetschman, D. C., R. C. Mehlenbacher, and O. Ito. A study of coal extraction with electron paramagnetic resonance (EPR) and proton nuclear magnetic resonance relaxation techniques. Quarterly technical progress report, April 1, 1993--June 30, 1993. Office of Scientific and Technical Information (OSTI), September 1993. http://dx.doi.org/10.2172/10180889.

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van Willigen, H. Magnetic resonance studies of photoinduced electron transfer in homogeneous and heterogeneous media. Progress report, June 1, 1993--May 31, 1994. Office of Scientific and Technical Information (OSTI), January 1994. http://dx.doi.org/10.2172/10147924.

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