Дисертації з теми "Gas-Phase Ion/Ion Reactions"
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Wilson, Paul Francis. "Experimental studies of gas-phase ion-molecule reactions." Thesis, University of Canterbury. Department of Science, 1994. http://hdl.handle.net/10092/8318.
Повний текст джерелаRoss, Charles William. "Gas phase ion - molecule reactions studied by Fourier transform ion cyclotron resonance mass spectrometry /." The Ohio State University, 1993. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487846885778077.
Повний текст джерелаYin, Winnie Weixin. "Fourier transform ion cyclotron resonance mass spectrometric study of gas-phase ion-molecule reactions /." The Ohio State University, 1993. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487847309051562.
Повний текст джерелаParry, A. J. "Studies of ions and ion-molecule reactions in the gas phase using mass spectrometry." Thesis, Swansea University, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.638416.
Повний текст джерелаVan, Orden Steven Lee. "Mechanistic investigations of gas phase ion-molecule reactions using Fourier transform ion cyclotron resonance mass spectrometry." Diss., The University of Arizona, 1993. http://hdl.handle.net/10150/186137.
Повний текст джерелаParker, Mariah L. "The Investigation of Oxidative Addition Reactions of Metal Complexes in Cross-Coupling Catalytic Cycles Based on a Unique Methodology of Coupled Ion/Ion-Ion/Molecule Reactions." VCU Scholars Compass, 2018. https://scholarscompass.vcu.edu/etd/5651.
Повний текст джерелаMahdi, A. M. "A mass spectrometric study of translational energy release in the reactions of gas phase cations." Thesis, University of Essex, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.379376.
Повний текст джерелаBeelen, Eric Stephan Edmond van. "Proton transfer and ligand exchange induced reactions in the gas phase." [S.l. : Amsterdam : s.n.] ; Universiteit van Amsterdam [Host], 2005. http://dare.uva.nl/document/18421.
Повний текст джерелаZhong, Meili. "Kinetics, potential energy surfaces, and structure-reactivity relationships of gas phase ion molecule reactions. /." May be available electronically:, 1997. http://proquest.umi.com/login?COPT=REJTPTU1MTUmSU5UPTAmVkVSPTI=&clientId=12498.
Повний текст джерелаHall, Robin Gibson. "The development of a quinquaquadrupole mass spectrometer : the study of ion-molecule reactions in the gas phase using multiple quadrupole instruments." Thesis, University of St Andrews, 1991. http://hdl.handle.net/10023/15506.
Повний текст джерелаPetrie, Simon Antony Hudson. "A selected-ion flow tube study of some gas-phase ion-molecule reactions of potential relevance to the chemistry of dense interstellar clouds." Thesis, University of Canterbury. Chemistry, 1991. http://hdl.handle.net/10092/7253.
Повний текст джерелаHayes, Roger Nicholas. "A study of some gas phase nucleophilic substitution reactions of carbon, silicon and boron by ion cyclotron resonance mass spectrometry /." Title page, table of contents and summary only, 1985. http://web4.library.adelaide.edu.au/theses/09PH/09phH418.pdf.
Повний текст джерелаSvilar, Ljubica. "Structural elucidation of secondary metabolites from Hypoxylon fragiforme, using high resolution mass spectrometry and gas-phase ion-molecule reactions." Paris 6, 2012. http://www.theses.fr/2012PA066468.
Повний текст джерелаLes champignons produisent une grande variété de composés/métabolites biologiquement actifs qui peuvent être utilisés à des fins médicinales et pharmaceutiques. Les mitorubrines, membres de la famille des azaphilones, constituent un ensemble particulièrement intéressant de métabolites secondaires, présentant une grande étendue d’activités biologiques (e. G. Antimicrobienne, antibactérienne, antipaludique). Ce travail présente le développement de plusieurs approches de spectrométrie de masse permettant de résoudre la diversité structurelle naturelle et la complexité des azaphilones extraits des champignons Hypoxylon fragiforme. La première partie de ce manuscrit est dédiée au développement et à la validation d’une méthodologie analytique impliquant la chromatographie liquide couplée à la spectrométrie de masse haute résolution pour la détection efficace et précise de traces d’azaphilones dans des extraits fongiques complexes. En outre, des expériences de spectrométrie de masse en mode tandem (par dissociation induite par collision, CID) et d'échange hydrogène/deutérium ont été effectuées pour élucider et caractériser les azaphilones et leurs analogues azotés chez Hypoxylon fragiforme. La deuxième partie est consacrée à l'application de ces différentes stratégies analytiques pour la caractérisation approfondie d'une nouvelle famille de métabolites secondaires dérivés des azaphilones, les mitorubramines. Enfin, ces différents métabolites secondaires ont été purifiés pour confirmer leur structure chimique par spectroscopie RMN
Betts, Nicholas B. "Laboratory studies of gas phase ion-neutral reaction rate constants relevant to the interstellar medium." Diss., Connect to online resource, 2006. http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqdiss&rft_dat=xri:pqdiss:1439438.
Повний текст джерелаSantos, Ivan. "Quantification of gas-phase ion-molecule reactions of complex organic compounds and a study of the factors involved in these determinations by Fourier transform ion cyclotron resonance mass spectrometry /." The Ohio State University, 1987. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487335992902583.
Повний текст джерелаLopes, Allan. "Réactions ion-molécule en phase gaz pour la chimie des ionosphères planétaires et des plasmas." Thesis, Université Paris-Saclay (ComUE), 2017. http://www.theses.fr/2017SACLS577/document.
Повний текст джерелаThis PhD project is focused on the experimental study of reactions of positive and negative ions for which we want to characterize the effect of different energies: internal energy of parents ions and/or collisional energy on the reactivity. There are two main goals. The first is to understand the reaction dynamics of the studied systems. The second one is to obtain data for modelisation of the chemistry in complex areas (ionosphere, plasmas...). Studied systems will concern the reactivity of excited cations CH₃⁺ with saturated and unsaturated hydrocarbons (alcane, alcene and alcyne from C1 to C4) as well as the reactivity of the C₃N⁻ anion with acetylene C₂H₂. Targets are chosen for theirs different chemical functions and interesting size for theoretical studies of Titan. We have studied the reactivity of these systems on the CERISES setup as a function of internal and collisional energies of the parent ions. C₃N⁻ anions are produced by dissociative electron attachment on BrC₃N. CH₃⁺ cations can be produced by two different methods. At the LCP, electronic impact on methane CH₄ produce CH₃⁺ cations with low internal energy whereas electronic impact on chloromethane CH₃Cl produce CH₃⁺ cations with more internal energy. This observation allowed us to prepare for the experiments at the SOLEIL synchrotron where CH₃⁺ cations are produced with controlled internal energy by photoionisation of CH₃ radicals produced in-situ by pyrolysis of nitromethane CH₃NO₂. Tuning of the photon energy between 9.8 and 15 eV allowed us to change the vibrational or electronic energy distribution of the CH₃⁺ cations. The development of a photoelectron detector fitted to the radical source enabled TPEPICO experiments (Threshold PhotoElectron PhotoIon Coincidence) where ions are extracted from the source in coincidence with threshold electrons which allow a total control of their energy.We saw that the internal energy of CH₃⁺ can have an important role on its reactivity by opening paths of reaction like sequential dissociation of products (seen in reactions with methane, propene…) or endothermic charge transfer (with methane and ethene) which is not efficiently enhanced by collisional energy. From the evolution of the absolute reaction cross section with the two different energies we discussed the mechanisms of formation of the observed products (decomposition of a complex or direct transfer). The reaction C₃N⁻ + C₂H₂ produce C₂H⁻, CN⁻ and C₅N⁻ anions in small quantities and only above collisional energy threshold which exclude their formation in cold atmosphere like Titan’s one unless there is processes leading to the production of C₃N⁻ with energy
Yahia, Marei Abdelrahim Mohamed. "Bio(molecular) control of selective ion transport, gas separation and catalytic enzyme-based reactions using functionalized membranes." Thesis, Montpellier, 2015. http://www.theses.fr/2015MONTS251/document.
Повний текст джерелаDifferent research works have been described in this thesis. The research works can be summarized as the following. The first chapter deals with the identification of effective potent inhibitors for the human carbonic anhydrase I (hCAI) isozyme. Considering the pharmacological importance to find selective CA inhibitors (CAIs) and CA activators (CAAs), human carbonic anhydrase I (hCAI) has been subjected to a parallel screening of various constitutional dynamic libraries (CDL). In the second chapter, constitutional dynamic networks have been used in liquid and solid membrane systems as a carrier network for transporting lanthanides. The transport is based on the complexing ability of lanthanides metals (La+3, Lu+3, and Eu+3) with the functional polyether groups in the membrane materials. In the third chapter, the proposed approach consists in using supported ionic liquid membranes (SILMs) comprising two different carbonic anhydrase enzymes, the thermo-resistant SspCA enzyme and the Bovine-CA enzyme, which catalyze the reaction of reversible conversion of CO2 to bicarbonate, enhancing the driving force for CO2 transport. Membrane stability, CO2 and N2 permeability and (CO2/N2) ideal selectivity were determined for the membranes developed. In the fourth chapter, the research work consists in the synthesis and characterization of dense polymeric membranes for gas separation application. The gas permeability measurements for the synthesized polymeric membranes showed that the permeability of CO2 is higher than other used gases (N2 and CH4). In the last chapter, two different methods of PVDF membrane functionalization with a phosphotriesterase (PTE) enzyme have been developed to construct biocatalytic membrane reactor (BMR) for bioconversion and selective separation of paraoxon substrate. The first method employs reversible dispersion of magnetic nanoparticle immobilized with PTE using an external magnetic field on the surface of native PVDF membrane. On the contrary, the second method comprises chemical grafting of the PTE enzyme, after surface modification of the native PVDF membrane (DAMP-GA-Enzyme). Both methods of enzyme immobilization showed good efficiency and sensitivity towards the bioconversion of paraoxon substrate at different conditions applied in a biocatalytic membrane reactor (BMR).In general, the concepts developed in this thesis research work will help bring new tracks on the way to the development of a polymeric membrane for selective ion and gas separation but also for selective catalytic reaction under bio(molecular) control
Aldajaei, Jamal. "Determination of the factors that affect the gas-phase reactivity of metal-centered cyclopropanation catalysts and examination of the properties of their reaction products." VCU Scholars Compass, 2014. http://scholarscompass.vcu.edu/etd/3393.
Повний текст джерелаO'Hair, Richard Alfred John. "Studies in gas phase ion chemistry : a thesis presented for the degree of Doctor of Science in the Faculty of Science of the University of Adelaide /." Title page, table of contents and summary only, 2004. http://web4.library.adelaide.edu.au/theses/09SD/09sdo362.pdf.
Повний текст джерелаAttah, Isaac Kwame. "BINDING ENERGIES AND SOLVATION OF ORGANIC MOLECULAR IONS, REACTIONS OF TRANSITION METAL IONS WITH, AND PLASMA DISCHARGE IONIZATION OF MOLECULAR CLUSTERS." VCU Scholars Compass, 2013. http://scholarscompass.vcu.edu/etd/525.
Повний текст джерелаFirmino, Thiago Diamond Reis. "Reações de solvólise em fase gasosa do cátion +SiCl3: experimento e teoria." Universidade de São Paulo, 2010. http://www.teses.usp.br/teses/disponiveis/46/46132/tde-20072010-201222/.
Повний текст джерелаPolyhalogenated silicenium ions, X3Si+ (X = F, Cl), are common fragment ions in the mass spectra of polyhalogenated silanes obtained by electron ionization. These ions are powerful electrophiles and are believed to play a role in plasma enhanced corrosion processes and plasma enhanced chemical vapour deposition processes. In this dissertation, we present some new results on the gas-phase reactivity of the +SiCl3 ion with a number of simple n electron donor bases such as water, alcohols, ammonia, amines and some π electron donor bases. Ion-molecule reactions were characterized experimentally by Fourier transform ion cyclotron resonance mass spectrometry (FTICR) at pressures in the 10-8 Torr range. Reactions were followed as a function of trapping time of the ions in the cell of the spectrometer and this allowed for the identification of subsequent reactions of the primary product ions. The energy diagram and structure of the different silicenium ions were also characterized by computational chemistry using both ab initio and density functional theory methods in order to understand the mechanism of these reactions. +SiCl3 reacts rapidly in gas phase with various neutral substrates through processes similar to solvolysis in which the neutral substrate adds onto the silicenium ion followed by elimination of HCl. In some cases, complete solvolysis is observed with substitution of all three chlorine atoms. The calculations show that reactions proceed by initial addition of the electrophile onto the electron center of the neutral substrates giving rise to stable adducts. The transition state for these reactions involve a 1,3 hydrogen migration and the calculated energy for these transition states is less than the energy of the isolated reactants, a fact that is common to fast gas-phase ion-molecule reactions. Similar calculations for +CCl3 reveal similar solvolysis reactions to be energetically unfavourable, and in fact these reactions are not observed experimentally. Secondary reactions have been observed for the product ions ClnSi(OH)3-n+ (n = 1, 2 and 3), obtained from successive hydrolysis of +SiCl3, with the parent SiCl4 neutral. These secondary condensation reactions yield ionic species containing a siloxane type linkage (-Si-O-Si-). The theoretical calculations suggest that is that these secondary condensation reactions initially proceed via chloronium ion intermediate, R1-Cl+-R2 , followed by formal Cl transfer and rearrangement to a siloxane type structure.
Kingston, R. G. "Charge-permutation reactions of gas-phase ions." Thesis, Swansea University, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.637801.
Повний текст джерелаGROVER, RENAUD. "Etude des reactions ion/molecule en phase gazeuse des melanges silane/ammoniac et silane/phosphine par spectrometrie de masse ft-icr. Etude comparee a la spectrometrie itms au moyen de plans d'experiences." Nice, 1998. http://www.theses.fr/1998NICE5242.
Повний текст джерелаBissonnette, Martine C. "Ion/radical and ion/molecule complexes and ion structure assignments in the gas phase." Thesis, University of Ottawa (Canada), 1991. http://hdl.handle.net/10393/7731.
Повний текст джерелаEichinger, Peter Charles Hans. "Negative ion rearrangements in the gas phase." Title page, contents and abstract only, 1991. http://web4.library.adelaide.edu.au/theses/09PH/09phe298.pdf.
Повний текст джерелаCumeras, Olmeda Raquel. "Micro Ion Mobility Spectrometry for Gas-phase Detection." Doctoral thesis, Universitat Autònoma de Barcelona, 2013. http://hdl.handle.net/10803/131286.
Повний текст джерелаIn an ideal world, we might be able to rapidly detect and classify any type of chemical and biological that is found in low concentrations, using instruments of small size and easy implementation. Is in that scenario where the Ion mobility spectrometry (IMS) appeared. It is a technique of measurement and analysis, where ionized analytes are separated by mobility differences under electric field in a flow of neutral gas or air at ambient pressure and temperature. The advantages of IMS include compactness and portability of instrumentation, short separation time (milliseconds scale), and low detection limits, and allow a wide range of applications. In this sense, an intense research effort has been focused towards miniaturization from the available IMS’s devices to the micro high-Field Asymmetric waveform Ion Mobility Spectrometers (FAIMS). This thesis presents the first developments and technological contributions to the FAIMS at IMB-CNM (CSIC). Particularly, this work is dedicated to the simulation, design, and fabrication of a micro planar FAIMS (p-FAIMS) for security applications. The work is organized in five chapters divided in two sections. The first section consists of three chapters. Chapter one is introductory, and on Chapter two introduces the lector to the actual state-of-the-art of the Ion Mobility Spectrometry in general and in particular for the micro high-Field Asymmetric waveform Ion Mobility Spectrometry. Chapter three described the modeling of a planar type of FAIMS for different electric fields and flow conditions. The second section consists of two chapters. Chapter four provides a summary of the different designs and materials considered for the p-FAIMS implementation: Glass-Si-Glass and PCB-PMMA-PCB structures; the technological tasks done for each one and the solving strategies that have leaded to it. UV photoionization has been the chosen as ionization method for safety reasons in all cases. It also presents the characterization with toluene of the new low-cost p-FAIMS prototype fabricated in the IMB-CNM. Chapter five provides a summary of the feasibility study of an online-monitoring of an analgesic drug (remifentanil) in patients breath under anesthesia. A commercial Ion Mobility Spectrometer is used for this medical application in collaboration with the KIST-Europe and the Chirurgische Universitätsklinik from Homburg (Germany).
Kullman, Michael John. "Computional chemistry studies of gas-phase ion structures." Thesis, Wichita State University, 2012. http://hdl.handle.net/10057/5412.
Повний текст джерелаThesis (M.S.)--Wichita State University, College of Liberal Arts and Sciences, Dept. of Chemistry
Ochran, Richard Acquaah. "Experimental and theoretical studies of unimolecular reactions of gas phase cluster ions." Thesis, University of Ottawa (Canada), 2002. http://hdl.handle.net/10393/6141.
Повний текст джерелаFaull, Peter Allen. "Exploring gas-phase protein conformations by ion mobility-mass spectrometry." Thesis, University of Edinburgh, 2009. http://hdl.handle.net/1842/3851.
Повний текст джерелаHarland, Peter W. "Studies of gas phase electron, ion and atom collision processes." Thesis, University of Edinburgh, 1995. http://hdl.handle.net/1842/14990.
Повний текст джерелаJones, Chad A. "Ion Structure and Energetics in the Gas Phase Characterized Using Fourier Transfom Ion Cyclotron Resonance Mass Spectrometry." BYU ScholarsArchive, 2014. https://scholarsarchive.byu.edu/etd/4253.
Повний текст джерелаNewson, Karl Adrian. "The properties of gas-phase multiply charged ions." Thesis, University College London (University of London), 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.324990.
Повний текст джерелаVillano, Stephanie M. "Gas-phase negative ion chemistry: Photoelectron spectroscopy, reactivity, and thermochemical studies." Connect to online resource, 2008. http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqdiss&rft_dat=xri:pqdiss:3337158.
Повний текст джерелаLiu, Hao. "Understanding two-phase reaction processes in electrodes for Li-ion batteries." Thesis, University of Cambridge, 2015. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.709262.
Повний текст джерелаSelbe, Tyler J. "Applications of aluminosilicate and zincosilicate materials: aqueous phase ion exchange and gas phase adsorption." Diss., Kansas State University, 2010. http://hdl.handle.net/2097/7057.
Повний текст джерелаDepartment of Chemical Engineering
Jennifer L. Anthony
Zeolites and zeolite-like materials have well-ordered structures and pores creating varying capacities for molecules based upon size, functional groups, polarity, and intermolecular forces making the materials useful for molecular sensing as well for molecules that are considered hazardous at very low concentrations with reproducible results because of these properties. This study will identify and characterize applications for zeolite and zeolite-like materials in gas and liquid phases based upon the dominating physical and chemical properties of the materials. The properties of interest include liquid phase ion exchange capacities, selectivities, gas/vapor phase adsorption capacity, and initial adsorption uptake rate. Zincosilicates have similar framework structures to aluminosilicate zeolites; however, they have distinct advantages over traditional zeolites. Zincosilicates typically have a higher ion density, lack “cages” in their structure which leads to all the cations being accessible for ion exchange, and have the ability to form three-membered rings which lead to large void spaces in their structure. These features lead to high capture capacities for divalent heavy metal mercury ions. In this work, the potential to use zincosilicates as ion exchangers such as VPI-7, VPI-9 and VPI-10 is presented. Results have shown that zincosilicates have capture capacities greater than traditional zeolites, even greater than those that have been synthesized with functional groups intended to increase metal sorption capacities. The selectivity coefficients in a binary ion exchange system were successfully modeled using the Gibbs-Donnan selectivity model. The selectivities for the zincosilicates were Pb>Na>Hg>K>Ca. Zeolites are also able to adsorb chemical species and therefore can be used as the recognition element in sensing devices. The sorption capacity of 2-chloroethyl ethyl sulfide, dimethyl methanephosphonate, ethanol, and n-butanethiol were examined with zeolites 13X, 4A, MCM-41, VPI-7, VPI-9, and ZSM-5. The zeolites selected provided very different framework composition, countercation, and surface area features for determining the most significant properties in adsorption. Zeolite 13X had the highest equilibrium and initial uptake rate for most compounds tested, whereas the low surface area zincosilicates, VPI-7 and VPI-9, had the lowest capacity. Based on these results, a piezoelectric device with an array of zeolites can be successfully employed as a sensor.
Gill, Andrew Christopher. "An investigation of the structure of ions in the gas phase by tandem mass spectrometry." Thesis, University of Warwick, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.340095.
Повний текст джерелаWalker, Nicholas R. "Gas-phase studies of multiply-charged transition metal complexes." Thesis, University of Sussex, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.299030.
Повний текст джерелаAnupriya, Anupriya. "Gas Phase Structure Characterization Using Fourier Transform Ion Cyclotron Resonance Mass Spectrometry." BYU ScholarsArchive, 2016. https://scholarsarchive.byu.edu/etd/6447.
Повний текст джерелаChen, Yuping. "Ion-molecule clustering studies in the gas phase and solution phase by electrospray mass spectrometry." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape2/PQDD_0026/MQ51314.pdf.
Повний текст джерелаAshman, A. S. "Laser spectroscopy of molecular ions in an Ion Cyclotron Resonance apparatus." Thesis, University of Reading, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.234408.
Повний текст джерелаSirois, Martin. "The assignment of gas phase ion structures and fragmentation mechanisms by mass spectrometry." Thesis, University of Ottawa (Canada), 1992. http://hdl.handle.net/10393/10954.
Повний текст джерелаBertier, Paul. "Study of solvated molecular ion stability in the gas-phase : cooling and irradiation." Thesis, Lyon, 2017. http://www.theses.fr/2017LYSE1207/document.
Повний текст джерелаRadiation can damage our biological environment, but it can also be beneficial under certain controlled conditions. Initial action at microscopic scale consists of electronic excitation in molecules. The redistribution of this excitation energy to the environment is the primary process to be understood to describe the radiation effect on biomolecular system. Isolated molecular clusters in gas-phase are a promising model system to study the molecular interaction under radiation.The first part of this work describes the construction and the validation of a beamline which can produce bunches of cold molecular cluster ions to be injected in the RIKEN cryogenic electrostatic (RICE} storage ring. The beamline is composed of an electrospray ion source, a quadrupole mass filter, ion guides and an acceleration tube; with the main part being a cryogenic ion trap cool down to SK. The cold ion bunches, in which the ions have been mass selected and accelerated to 20keV, was probed with a laser. The beamline was successfully taken into operation and a measurement of the methylene blue action spectrum in gas-phase was carried out. The second part of this work rely on experiment realized with the dispositif d'irradiation d'agrégats moléculaires (DIAM-IPNL}. The COINTOF-VMI method allows the measurement of the velocity distributions of evaporated molecules from a cluster after high velocity collisions with an argon atom. The velocity distribution measured for mixed clusters protonated pyridine and water has two components: a low velocity part which corresponds to the evaporation of a water molecule after energy redistribution in the cluster, and a high velocity part in which the molecule is evaporated before total energy redistribution. Comparison with the distribution calculated by statistic molecular dynamic simulation shows that the low velocity part can be interpreted as the contribution of two possible excitations induced by collision: excitation on protonated pyridine and excitation on a water molecule
Hopper, Jonathan T. S. "Studying protein-ligand complexes in the gas-phase using ion mobility-mass spectrometry." Thesis, University of Nottingham, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.576159.
Повний текст джерелаLuo, Zhaohui. "GC/FT-ICR Mass Spectral Analysis of Complex Mixtures: A Multidimensional Approach for Online Gas Phase Basicity Measurements." Fogler Library, University of Maine, 2006. http://www.library.umaine.edu/theses/pdf/LuoZX2006.pdf.
Повний текст джерелаRicketts, Claire Louise. "The reactions of gas phase doubly-charged ions with neutral molecules of relevance to planetary ionospheres." Thesis, University of London, 2005. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.497500.
Повний текст джерелаOdeneye, Michael Adetunji. "Infrared photodissociation of gas phase ions : single photon and multiphoton events." Thesis, University of Sussex, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.311414.
Повний текст джерелаMcCullough, Bryan John. "Development of an ion mobility mass spectrometer to study gas phase conformations of biomolecules." Thesis, University of Edinburgh, 2007. http://hdl.handle.net/1842/15325.
Повний текст джерелаRidal, Jeffrey J. "An analysis of the gas phase (benzyl radical)(+) ion populations generated from simple aromatic molecules." Thesis, University of Ottawa (Canada), 1987. http://hdl.handle.net/10393/5324.
Повний текст джерелаFagiani, Matias Ruben [Verfasser]. "Cryogenetic ion vibrational spectroscopy of gas-phase clusters : Structure, Anharmonicity and Fluxionality / Matias Ruben Fagiani." Berlin : Freie Universität Berlin, 2017. http://d-nb.info/113162937X/34.
Повний текст джерелаUechi, Guy Takeo. "Infrared photophysics of gas phase ions in a Fourier transform ion cyclotron resonance mass spectrometer." Case Western Reserve University School of Graduate Studies / OhioLINK, 1993. http://rave.ohiolink.edu/etdc/view?acc_num=case1056650065.
Повний текст джерела