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Relevant bibliographies by topics / NMR theory][High resolution NMR

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Academic literature on the topic 'NMR theory][High resolution NMR'

Author: Grafiati

Published: 4 June 2021

Last updated: 14 February 2022

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Journal articles on the topic "NMR theory][High resolution NMR"

1

Wong, Tuck C. "Book Reviews: High Resolution NMR: Theory and Chemical Applications." Applied Spectroscopy 54, no. 8 (August 2000): 279A. http://dx.doi.org/10.1366/0003702001950878.

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Alderman, Oliver L. G., Dinu Iuga, Andrew P. Howes, Kevin J. Pike, Diane Holland, and Ray Dupree. "Spectral assignments and NMR parameter–structure relationships in borates using high-resolution 11B NMR and density functional theory." Physical Chemistry Chemical Physics 15, no. 21 (2013): 8208. http://dx.doi.org/10.1039/c3cp50772f.

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Plainchont, Bertrand, Daisy Pitoux, Ghanem Hamdoun, Jean-Michel Ouvrard, Denis Merlet, Jonathan Farjon, and Nicolas Giraud. "Achieving high resolution and optimizing sensitivity in spatial frequency encoding NMR spectroscopy: from theory to practice." Physical Chemistry Chemical Physics 18, no. 33 (2016): 22827–39. http://dx.doi.org/10.1039/c6cp01054g.

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Plainchont, Bertrand, Daisy Pitoux, Ghanem Hamdoun, Jean-Michel Ouvrard, Denis Merlet, Jonathan Farjon, and Nicolas Giraud. "Correction: Achieving high resolution and optimizing sensitivity in spatial frequency encoding NMR spectroscopy: from theory to practice." Physical Chemistry Chemical Physics 18, no. 45 (2016): 31338. http://dx.doi.org/10.1039/c6cp90272c.

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Correction for ‘Achieving high resolution and optimizing sensitivity in spatial frequency encoding NMR spectroscopy: from theory to practice’ by Bertrand Plainchont et al., Phys. Chem. Chem. Phys., 2016, 18, 22827–22839.

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Roberts, John D. "Pople, Schneider, and Bernstein A truly seminal treatise of NMR." Canadian Journal of Chemistry 83, no. 9 (September 1, 2005): 1626–28. http://dx.doi.org/10.1139/v05-156.

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The appearance of the authoritative and comprehensive book, High-Resolution Nuclear Resonance Spectroscopy, by John A. Pople, William G. Schneider, and Harold J. Bernstein in 1959 came at just the right time for chemists and other scientists to develop a clear vision of the wide breadth of applications of this critical emerging field and, in addition, to have the opportunity to learn the underlying basic theory in substantial detail.Key words: Pople, Schneider, Bernstein, NMR theory, NMR applications.

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Pallister, Peter J., Igor L. Moudrakovski, and John A. Ripmeester. "High-field multinuclear solid-state nuclear magnetic resonance (NMR) and first principle calculations in MgSO4 polymorphs." Canadian Journal of Chemistry 89, no. 9 (September 2011): 1076–86. http://dx.doi.org/10.1139/v11-044.

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A combination of solid-state nuclear magnetic resonance (NMR) and first principles calculations was applied to obtain 17O, 25Mg, and 33S NMR parameters for two polymorphs of anhydrous magnesium sulfate. Working at the very high magnetic field of 21.14 T results in a dramatic improvement of resolution through a reduction of the effects of quadrupolar interactions and significant improvement in sensitivity. Experimental 25Mg and 33S spectra are dominated by quadrupolar interactions with quadrupolar parameters unique for each polymorph. In the case of 17O, there is a substantial contribution of the chemical shift anisotropy. The use of multiple-quantum magic-angle spinning (MQMAS) experiments allows the resolution of distinct oxygen species and assignment of signals in the experimental 17O spectrum. Chemical shielding constants and quadrupolar parameters for all three nuclei were calculated using plane wave pseudopotential density functional theory as implemented in the CASTEP computational package. The calculated NMR parameters are in very good agreement with the experimental results and help in signal assignment of the 17O spectrum. The results suggest applicability of such a combined computational and experimental solid-state NMR approach for the refinement of crystallographic data.

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Venianakis, Themistoklis, Christina Oikonomaki, Michael G. Siskos, Panayiotis C. Varras, Alexandra Primikyri, Eleni Alexandri, and Ioannis P. Gerothanassis. "DFT Calculations of 1H- and 13C-NMR Chemical Shifts of Geometric Isomers of Conjugated Linoleic Acid (18:2 ω-7) and Model Compounds in Solution." Molecules 25, no. 16 (August 11, 2020): 3660. http://dx.doi.org/10.3390/molecules25163660.

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A density functional theory (DFT) study of the 1H- and 13C-NMR chemical shifts of the geometric isomers of 18:2 ω-7 conjugated linoleic acid (CLA) and nine model compounds is presented, using five functionals and two basis sets. The results are compared with available experimental data from solution high resolution nuclear magnetic resonance (NMR). The experimental 1H chemical shifts exhibit highly diagnostic resonances due to the olefinic protons of the conjugated double bonds. The “inside” olefinic protons of the conjugated double bonds are deshielded than those of the “outside” protons. Furthermore, in the cis/trans isomers, the signals of the cis bonds are more deshielded than those of the trans bonds. These regularities of the experimental 1H chemical shifts of the olefinic protons of the conjugated double bonds are reproduced very accurately for the lowest energy DFT optimized single conformer, for all functionals and basis sets used. The other low energy conformers have negligible effects on the computational 1H-NMR chemical shifts. We conclude that proton NMR chemical shifts are more discriminating than carbon, and DFT calculations can provide a valuable tool for (i) the accurate prediction of 1H-NMR chemical shifts even with less demanding functionals and basis sets; (ii) the unequivocal identification of geometric isomerism of CLAs that occur in nature, and (iii) to derive high resolution structures in solution.

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Monti, J. P., P. Gallice, A. Crevat, M. el Mehdi, C. Durand, and A. Murisasco. "Intra-erythrocytic sodium in uremic patients, as determined by "high-resolution" 23Na nuclear magnetic resonance." Clinical Chemistry 32, no. 1 (January 1, 1986): 104–7. http://dx.doi.org/10.1093/clinchem/32.1.104.

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Abstract The use of 23Na nuclear magnetic resonance with aqueous shift reagent has made it possible to determine intracellular sodium concentrations in living erythrocytes. We applied this technique to samples from 16 healthy subjects and 41 uremic patients. The results seem to show distinct populations among the latter. Classically, two different relaxation times are obtained for intracellular sodium in biological media, according to relaxation NMR theory. Some patients, however, exhibit abnormal results that cannot be accounted for by this theory.

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Ahmed, Raheel, Panayiotis C. Varras, Michael G. Siskos, Hina Siddiqui, M. Iqbal Choudhary, and Ioannis P. Gerothanassis. "NMR and Computational Studies as Analytical and High-Resolution Structural Tool for Complex Hydroperoxides and Diastereomeric Endo-Hydroperoxides of Fatty Acids in Solution-Exemplified by Methyl Linolenate." Molecules 25, no. 21 (October 23, 2020): 4902. http://dx.doi.org/10.3390/molecules25214902.

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A combination of selective 1D Total Correlation Spectroscopy (TOCSY) and 1H-13C Heteronuclear Multiple Bond Correlation (HMBC) NMR techniques has been employed for the identification of methyl linolenate primary oxidation products without the need for laborious isolation of the individual compounds. Complex hydroperoxides and diastereomeric endo-hydroperoxides were identified and quantified. Strongly deshielded C–O–O–H 1H-NMR resonances of diastereomeric endo-hydroperoxides in the region of 8.8 to 9.6 ppm were shown to be due to intramolecular hydrogen bonding interactions of the hydroperoxide proton with an oxygen atom of the five-member endo-peroxide ring. These strongly deshielded resonances were utilized as a new method to derive, for the first time, three-dimensional structures with an assignment of pairs of diastereomers in solution with the combined use of 1H-NMR chemical shifts, Density Functional Theory (DFT), and Our N-layered Integrated molecular Orbital and molecular Mechanics (ONIOM) calculations.

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Kanzari-Mnallah, Dorra, Med L. Efrit, Jiří Pavlíček, Frédéric Vellieux, Habib Boughzala, and Azaiez B. Akacha. "Synthesis, Conformational Analysis and Crystal Structure of New Thioxo, Oxo, Seleno Diastereomeric Cyclophosphamides Containing 1,3,2-dioxaphosphorinane." Current Organic Chemistry 23, no. 2 (April 23, 2019): 205–13. http://dx.doi.org/10.2174/1385272823666190213142748.

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Thioxo, Oxo and Seleno diastereomeric cyclophosphamides containing 1,3,2- dioxaphosphorinane are prepared by a one-step chemical reaction. Their structural determination is carried out by means of Nuclear Magnetic Resonance NMR (31P, 1 H, 13C) and High-Resolution Mass Spectroscopy (HRMS). The conformational study of diastereomeric products is described. Density Functional Theory (DFT) calculations allowed the identification of preferred conformations. Experimental and calculated 31P, 13C, 1H NMR chemical shifts are compared. The molecular structure of the 2-Benzylamino-5-methyl-5- propyl-2-oxo-1,3,2-dioxaphosphorinane (3d) has been determined by means of crystal Xray diffraction methods.

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Dissertations / Theses on the topic "NMR theory][High resolution NMR"

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Davies, S. J. "Frequency-selective excitation and non-linear data processing in nuclear magnetic resonance." Thesis, University of Oxford, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.233510.

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McManus, Jamie. "Residual broadening in high-resolution NMR of quadrupolar nuclei in solids." Thesis, University of Exeter, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.367404.

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Vlassenbroek, Alain. "Radiation damping in High Resolution NMR." Doctoral thesis, Universite Libre de Bruxelles, 1993. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/212811.

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Laage, Ségolène. "High-resolution solid-state NMR for proteins." Lyon, Ecole normale supérieure, 2010. http://www.theses.fr/2010ENSL0583.

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La RMN a récemment prouvé son potentiel en biologie structurale. Cette thèse décrit les méthodes que nous avons développées pour l’étude de protéines par RMN du solide à haute résolution. Après une présentation des récents progrès du domaine, nous présentons les améliorations liées à l’utilisation de la rotation à l’angle magique à très haute vitesse, notamment les techniques de découplage hétéronucléaire et de polarisation croisée à basse puissance, appliquées aux cas de la Superoxide Dismutase (SOD) et de la protéine GB1. Nous détaillons ensuite les perspectives émergeant dans l’utilisation des couplages J, avec trois nouvelles séquences. La J-CHHC renseigne sur les distances entre protons, le bloc S3E améliore résolution et sensibilité en effectuant du découplage J, et l’INADEQUATE-S3E combine transfert de polarisation par couplage J et découplage J. Nous donnons enfin des perspectives de mesure de longues distances par l’exploitation des propriétés paramagnétiques de la Cu(II) SOD
Solid-state NMR recently proved its potential for structural biology. This thesis details metods we developed for high resolution NMR of nanocrystalline proteins. After an introductory presentation of the recent advances in solid-state NMR of bio-systems, we present the improvements we proposed in the ultra-fast magic-angle spinning regime, notably low-field heteronuclear decoupling and low-field cross-polarization. We demonstrate them with the study of the Superoxide Dismutase (SOD) and the protein GB1. We then focus on the perspectives arising for J-couplings in proteins by presenting three new sequences. The J-CHHC sequence probes 1H-1H distances encoded in 13C-13C correlation experiments. The S3E block improves resolution and sensitivity by performing J-decoupling, and the INADEQUATE-S3E combines J-based transfer of polarization and J-decoupling. We finally give perspectives to probe long-range structural constraints with data exploiting the paramagnetic properties of Cu(II)-SOD

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Cookson, Nikki Jade. "High-resolution NMR studies of nano-cages." Thesis, University of Leeds, 2016. http://etheses.whiterose.ac.uk/13745/.

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This thesis concerns the NMR investigations of supramolecular metallo-nanocages as hosts for host-guest chemistry. The research is based on metallo-nanocages constructed from cyclotriveratrylene (CTV)-derivatives The host-guest interaction between the [Pd6(L1)8]⋅12(BF4) stella octangula cage and sodium alkyl sulfate guests have been characterised by 1H 1 D, DOSY and 2-D ROESY NMR and ESI-MS. The host-guest stoichiometry was determined at 1:2 by Job’s plot analysis. The shorter the length of the guest’s alkyl tail, the more tightly bound it was to the host cage. The self-assembly and self-sorting of the [Pd6(L1)8]⋅12(BF4) stella octangula cage were also investigated. d6-DMSO competed with the L1 ligand for the palladium(II) cation. The rate of self-sorting of the [Pd6(L1)8]⋅12(BF4) stella octangula cage was found to be affected by concentration, with lower concentrations resulting in cage systems that self-sorted in to homochiral cages at a faster rate. The novel FL1 ligand was characterised by 1H and 19F NMR spectroscopy in d6 DMSO and d3 MeCN and was used to produce stella octangula cage assemblies. The self-assembly of this system in d6 DMSO was observed and found to require an excess of palladium to form. This FL1 system was also investigated for host-guest interactions with sodium dodecyl sulfate (SDS). It formed a system that exhibited weaker binding than L1. The FL1 ligand formed quantitative cages in d3 MeCN. This system was characterised by 1H and 19F NMR spectroscopy, 2-D ROESY NMR, ESI-MS and X-ray crystallography. The L1 and FL1 ligands were used to form cryptophanes with [1,3 bis(diphenylphosphino)propane] in d6 DMSO, d3 MeCN and d3 MeNO2. These were characterised by 1H, 19F, 31P NMR spectroscopy, 2-D ROESY NMR, ESI-MS and X-ray crystallography. Both ligands showed a strong preference for anti cryptophane isomers in solution, although a small amount of syn isomer was observed in the L1 systems. The syn isomer was predominant species in the solid state.

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Thornton, John Stephen. "Instrumentation for low cost, high resolution NMR imaging." Thesis, University of Manchester, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.358563.

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Dowell, Nicholas G. "Further developments in high-resolution quadrupolar NMR spectroscopy." Thesis, University of Exeter, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.407274.

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Salager, Elodie. "High-resolution solid-state NMR for powder crystallography." Lyon, Ecole normale supérieure, 2010. http://www.theses.fr/2010ENSL0592.

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La connaissance de la structure tridimensionnelle d’un composé solide est essentielle pour la compréhension de ses propriétés et le développement de nouveaux matériaux. La diffraction des rayons X est communément utilisée pour déterminer la structure des composés monocristallins. La caractérisation structurale de composés sous forme de poudre présente plus de difficulté. En particulier, beaucoup de composés ne peuvent pas être obtenus sous forme de monocristaux ; et les composés hautement polymorphiques (tels que la plupart des médicaments) doivent être caractérisés « tels quels » afin de limiter les risques de modification structurale. Cette thèse présente de nouvelles méthodes de cristallographie de poudre par résonance magnétique nucléaire (RMN) du solide à haute résolution, i. E. La détermination de la structure, en abondance isotopique naturelle, de composés en poudre par RMN. Dans une première partie, le cas complexe de la résolution des spectres proton est abordé. Les possibilités offertes par la dernière génération de sondes RMN sont explorées et de nouvelles méthodes de découplage sont proposées. Dans la deuxième partie, des protocoles de détermination structurale sont développés. Ces derniers s’appuient sur la forte dépendance des paramètres RMN avec les détails de la structure cristalline, et profitent de la haute résolution accessible en RMN du solide pour les protons et les carbones. Ces techniques sont appliquées à un composé test, le thymol, et démontrent le potentiel de la RMN du solide pour la résolution de la structure cristalline de composés en poudre
Knowledge of the three-dimensional structure is an invaluable element for the understanding of the properties of solid materials and towards the development of new materials. While single-crystal X-ray diffraction is established as the best tool to characterise monocrystalline samples, the experimental determination of the structure of polycrystalline powders remains a challenging domain. Many crystalline solids cannot be prepared as single crystals and must be characterized in the powder form. Other compounds are highly subject to polymorphism, and there is a need for structural determination techniques that minimize the risk of structural change during the characterisation. The problem is particularly relevant in the case of drug powders, which need to be accurately characterized in their active pharmaceutical form. This thesis presents new developments relating to powder nuclear magnetic resonance (NMR) crystallography, i. E. Structure determination of powdered samples using high-resolution solid-state NMR at natural isotopic abundance. The first part of the thesis concentrates on the challenging case of protons and illustrates the opportunities offered by the latest generation of commercial NMR probes and new decoupling methods. Protocols are proposed in the second part, which benefit of the high-resolution solid-state NMR spectra accessible for protons and carbons and which make use of the strong dependence of the NMR parameters on crystalline structure details. These techniques are successfully applied to a model compound, thymol, and demonstrate the potential of solid-state NMR for structural determination of powdered compounds

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Kervern, Gwendal. "High-resolution solid-state NMR of paramagnetic molecules." Lyon, École normale supérieure (sciences), 2008. http://www.theses.fr/2008ENSL0483.

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Cette thèse porte sur la RMN haute résolution de composés paramagnétiques solides. Elle présente de nouvelles méthodes permettant d'obtenir de tels spectres, ainsi que l'exploitation des spectres ainsi obtenus pour la caractérisation structurale de complexes paramagnétiques. Nous avons dans un premier temps développé des méthodes qui permettent de surmonter les difficultés liées au paramagnétisme. Ces méthodes inclues du transfert d'aimantation par recouplage dipolaire, l'adaptation d'impulsions adiabatiques pour les solides en rotation à très haute vitesse et la compréhension des phénomènes mis en cause dans leur efficacité. Nous présentons ensuite l'exploitation des données ainsi obtenues. Notamment pour la caractérisation de la structure électronique d'un catalyseur à base de fer à haut spin, la démonstration de l'absence de relaxation dite "de Curie" dans les solides ainsi que le développement d'un nouvel outil de cristallographie par RMN de poudres
This thesis is about high-resolution solid-state NMR of paramagnetic molecules. It exposes new methods to obtain high-resolution NMR spectra of paramagnetic solids. These methods gave us access to the structural information born by the electronic paramagnetism. In the first part, we propose new tools to overcome the difficulties associated with NMR of paramagnetic solids. These methods include proton to carbon magnetization transfer via dipolar recoupling, the use of adiabatic pulses with paramagnetic solids rotating at high MAS speeds, the development of a theory for a better understanding of the physics of such pulses. The second part exposes the interpretation of the high quality spectra obtained throught those methods. We characterized the electronic structure of high-spin iron (II) catalyst, we tackled the absence of the so-called "Curie relaxation" mechanism in the solid-state an we developed a new tool for crystallography thanks to proton NMR of paramagnetic powedrs

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Odedra, Smita. "Some novel developments in high-resolution NMR spectroscopy." Thesis, University of Glasgow, 2014. http://theses.gla.ac.uk/5772/.

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The radiofrequency (rf) pulses used in NMR are subject to a number of imperfections, such as those resulting from the inhomogeneity of the rf field or an offset of the transmitter frequency from exact resonance. In spin-echo experiments, these imperfections yield spectra with reduced signal intensity and distorted phase. Composite pulses, which have tailored bandwidth properties with respect to experimental frequency parameters such as the rf field strength or resonance offset, offer a route to improving the amplitude of the spin-echo signal. However, the symmetry of the pulse sequence must be carefully considered to prevent the introduction of phase errors into the spin-echo signal. Here, composite pulses will be studied as a means to improving one of the most common techniques for 1H background suppression in MAS NMR, the ”Depth” sequence. Novel composite 180° pulses will be presented for this application and verified experimentally. The composite pulse Depth experiment yields spectra with improved amplitude of the 1H signals of interest, while successfully maintaining good suppression of background signals. Novel families of dual-compensated 180° composite pulses for I = 1/2 will also be designed for use in NMR spin-echo experiments. These pulses are capable of simultaneously compensating for resonance offset and rf inhomogeneity problems. Crucially, unlike many composite pulses that have been presented before, these new pulses have the correct symmetry properties to form a spin echo without phase distortion. Composite pulses have found wide usage in solution-state NMR, and although in principle the same pulses can be applied in solid-state NMR experiments, complications can arise under magic angle spinning (MAS). The effects of MAS on composite pulse performance will be explored both through computer simulations and 31P experiments. Finally, on a different theme, we will investigate spin-locking of half-integer quadrupolar nuclei in solids. Spin-locking is an important feature of many NMR experiments, yet the complex behaviour observed for quadrupolar nuclei is not fully understood. Using the theoretical model introduced by Ashbrook and Wimperis, we will investigate the far off-resonance case of spinlocking for I = 3/2 and I = 5/2 nuclei.

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Books on the topic "NMR theory][High resolution NMR"

1

Becker, Edwin D. High resolution NMR: Theory and chemical applications. 3rd ed. San Diego, CA: Academic Press, 2000.

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Evans, Myron W. Developing the theory of optical ESR and NMR for ultra high resolution investigations of proteins and other complex materials. Ithaca, N.Y: Cornell Theory Center, Cornell University, 1990.

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Chandrakumar, Narayanan. Modern techniques in high-resolution FT-NMR. New York: Springer-Verlag, 1987.

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Chandrakumar, Narayanan. Modern techniques in high-resolution FT-NMR. New York: Springer-Verlag, 1987.

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Chandrakumar, Narayanan, and Sankaran Subramanian. Modern Techniques in High-Resolution FT-NMR. New York, NY: Springer New York, 1987. http://dx.doi.org/10.1007/978-1-4612-4626-8.

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Quantum description of high-resolution NMR in liquids. Oxford: Clarendon, 1988.

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Quantum description of high resolution NMR in liquids. Oxford: Clarendon Press, 1988.

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Goldman, M. Quantum description of high-resolution NMR in liquids. Oxford: Clarendon Press, 1988.

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Spin choreography: Basic steps in high resolution NMR. Oxford: Spektrum, 1997.

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Engelhardt, Günter. High-resolution solid-state NMR of silicates and zeolites. Chichester [West Sussex]: Wiley, 1987.

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Book chapters on the topic "NMR theory][High resolution NMR"

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Chandrakumar, Narayanan, and Sankaran Subramanian. "Introduction and General Theory." In Modern Techniques in High-Resolution FT-NMR, 1–32. New York, NY: Springer New York, 1987. http://dx.doi.org/10.1007/978-1-4612-4626-8_1.

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Axenrod, Theodore. "High Resolution NMR Spectroscopy in Liquids and Solids." In Physical Methods on Biological Membranes and Their Model Systems, 5–25. Boston, MA: Springer US, 1985. http://dx.doi.org/10.1007/978-1-4684-7538-8_2.

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Brown, Larry R. "Conformational Studies of Membrane Proteins by High-Resolution NMR." In Physical Methods on Biological Membranes and Their Model Systems, 135–40. Boston, MA: Springer US, 1985. http://dx.doi.org/10.1007/978-1-4684-7538-8_10.

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Merbach, André E., and J. W. Akitt. "High Resolution Variable Pressure NMR for Chemical Kinetics." In High Pressure NMR, 189–232. Berlin, Heidelberg: Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-75926-0_5.

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Demas, Vasiliki, John M. Franck, Jeffrey A. Reimer, and Alexander Pines. "High-Resolution NMR in Inhomogeneous Fields." In Single-Sided NMR, 143–64. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-16307-4_6.

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Prestegard, J. H. "High Resolution NMR of Biomolecules." In High Magnetic Fields, 426–34. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/3-540-45649-x_18.

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Massiot, Dominique. "High-Resolution Solid-State NMR." In High Magnetic Fields, 435–53. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/3-540-45649-x_19.

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van de Velde, Fred, and Harry S. Rollema. "High Resolution NMR of Carrageenans." In Modern Magnetic Resonance, 1605–10. Dordrecht: Springer Netherlands, 2008. http://dx.doi.org/10.1007/1-4020-3910-7_178.

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Kenwright, A. M. "High-Resolution NMR and ROMP." In Ring Opening Metathesis Polymerisation and Related Chemistry, 57–67. Dordrecht: Springer Netherlands, 2002. http://dx.doi.org/10.1007/978-94-010-0373-5_5.

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Frye, J. S. "High-Resolution NMR of Solids." In NMR: Principles and Applications to Biomedical Research, 79–98. New York, NY: Springer New York, 1990. http://dx.doi.org/10.1007/978-1-4612-3300-8_4.

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Conference papers on the topic "NMR theory][High resolution NMR"

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Bowden, T. T., and J. H. Pearson. "The Effect of Fuel Composition Upon Combustion Performance in a Rolls Royce Tyne Combustor." In ASME 1985 International Gas Turbine Conference and Exhibit. American Society of Mechanical Engineers, 1985. http://dx.doi.org/10.1115/85-gt-39.

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The combustion performance of a wide range of fuel types has been examined utilizing a single combustor from a Rolls-Royce Tyne gas-turbine engine. The results provide further evidence to suggest that fuel total hydrogen content provides a better indication of fuel combustion perfomance than does aromatic content. However, an even better prediction of fuel combustion performance is given by smoke point, although the acknowledged imprecision of the smoke point test does militate against its use as a primary specification requirement. Analysis of certain fuels by 13C NMR and low resolution mass spectroscopy demonstrates that it is those fuels with high concentrations of polycyclic aromatics whose combustion performance in terms of flame radiation and exhaust emissions, is underpredicted by fuel total hydrogen content. There are indications that low concentrations of high molecular weight polycyclic aromatics may substantially impair combustion performance.

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Fleury, M., J. Tabary, M. Locatelli, and J.-P. Martin. "A High Resolution NMR Logging Tool – Concept Validation." In EAGE Conference on Exploring the Synergies between Surface and Borehole Geoscience - Petrophysics meets Geophysics. European Association of Geoscientists & Engineers, 2000. http://dx.doi.org/10.3997/2214-4609-pdb.19.b13.

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Gardeniers, J. G. E., J. Bart, A. J. Kolkman, A. J. de Vries, J. W. G. Janssen, P. J. M. van Bentum, K. A. M. Ampt, S. S. Wijmenga, and A. P. M. Kentgens. "Microfluidic high-resolution NMR chip for biological fluids." In TRANSDUCERS 2009 - 2009 International Solid-State Sensors, Actuators and Microsystems Conference. IEEE, 2009. http://dx.doi.org/10.1109/sensor.2009.5285775.

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Gu, I. Y. H., M. Billeter, M. R. Sharafy, V. A. Sorkhabi, J. Fredriksson, and D. K. Staykova. "Parameter estimation of multidimensional NMR signals based on high-resolution subband analysis of 2D NMR projections." In ICASSP 2009 - 2009 IEEE International Conference on Acoustics, Speech and Signal Processing. IEEE, 2009. http://dx.doi.org/10.1109/icassp.2009.4959629.

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Feeney, James. "Development of high resolution NMR spectroscopy as a structural tool." In SPIE Institutes for Advanced Optical Technologies 9, edited by Robert Bud and Susan E. Cozzens. SPIE, 1992. http://dx.doi.org/10.1117/12.2283718.

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Baxan, N., A. Rengle, A. Briguet, L. Fakri-Bouchet, J.-F. Chateaux, G. Pasquet, and P. Morin. "High-Resolution 1H NMR Micro spectroscopy using an Implantable Micro-coil." In 13th IEEE International Conference on Electronics, Circuits and Systems. IEEE, 2006. http://dx.doi.org/10.1109/icecs.2006.379799.

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Jiang, Dezhi, Haibo Chen, Zhong Chen, and Zhenyao Zheng. "The Digital Field-Frequency Lock System of High-Resolution NMR Spectrometer." In 2010 International Conference on Electrical and Control Engineering (ICECE). IEEE, 2010. http://dx.doi.org/10.1109/icece.2010.574.

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Bernier, P., Z. Belahmer, F. Rachdi, M. Ribet, J. Reichenbach, L. Firlej, C. Goze, G. Zimmer, and M. Mehring. "Intercalation in C/sub 60/: High resolution /sub13/C NMR results." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.834660.

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Ming Li, Kevin M. Keener, and Brian E. Farkas. "Frying Oil Studied by High Resolution NMR 1H and 13C spectra." In 2003, Las Vegas, NV July 27-30, 2003. St. Joseph, MI: American Society of Agricultural and Biological Engineers, 2003. http://dx.doi.org/10.13031/2013.14195.

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BOWMAN, ROBERT C., JOSEPH W. REITER, SON-JONG HWANG, CHUL KIM, and HOURIA KABBOUR. "CHARACTERIZATION OF COMPLEX METAL HYDRIDES BY HIGH-RESOLUTION SOLID STATE NMR SPECTROSCOPY." In Proceedings of the International Symposium. WORLD SCIENTIFIC, 2009. http://dx.doi.org/10.1142/9789812838025_0018.

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Reports on the topic "NMR theory][High resolution NMR"

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Gann, Sheryl Lee. High-Resolution NMR of Quadrupolar Nuclei in the Solid State. Office of Scientific and Technical Information (OSTI), November 1995. http://dx.doi.org/10.2172/6371.

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Schneider, E. Applications of high resolution NMR to geochemistry: crystalline, glass, and molten silicates. Office of Scientific and Technical Information (OSTI), November 1985. http://dx.doi.org/10.2172/6246018.

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ALAM, TODD M. Quantitative Analysis of Microstructure in Polysiloxanes Using High Resolution Si29 NMR Spectroscopy: Investigation of Lot Variability in the LVM97 and HVM97 PDMS/PDPS Copolymers. Office of Scientific and Technical Information (OSTI), November 2002. http://dx.doi.org/10.2172/805875.

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