Tesis sobre el tema "Organosulfur"
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Haughey, Simon Anthony. "Chemoenzymatic synthesis of organosulfur compounds". Thesis, Queen's University Belfast, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.318731.
Texto completoKing, Alistair William Thomas. "Chemoenzymatic synthesis of chiral organosulfur compounds". Thesis, Queen's University Belfast, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.396118.
Texto completoChowdhury, Mohima Begum Roomi. "Unsaturated organosulfur chemistry : synthesis and applications". Thesis, University College London (University of London), 2018. http://discovery.ucl.ac.uk/10045805/.
Texto completoClass, Caleb Andrew. "Predicting organosulfur chemistry in fuel sources". Thesis, Massachusetts Institute of Technology, 2015. http://hdl.handle.net/1721.1/98155.
Texto completoCataloged from PDF version of thesis.
Includes bibliographical references.
Desulfurization of fossil fuels with supercritical water (SCW) has been the topic of many studies over the past few decades. This process does not require the use of any catalyst, eliminates the need for a hydrogen feed, and minimizes coke formation. Previous research has shown that it has the potential to be a viable commercial process, and recent experimental studies have proven that water acts as one hydrogen source for sulfur removal in this process. However, the exact desulfurization mechanism is largely unknown, as are many other reaction mechanisms involving sulfur compounds. Recent work has greatly expanded our ability to build comprehensive reaction mechanisms automatically for the decomposition of organic sulfur compounds using the automated Reaction Mechanism Generator (RMG). This thesis presents the implementation of this and other tools to investigate chemical processes relevant to our use of fuel sources containing sulfur compounds, and it shows some steps that have been taken to improve our predictions for these mechanisms and those that will be generated in the future. Previous investigations had focused on the pyrolysis of small sulfur compounds containing less than six heavy atoms, so RMG is first used to study the pyrolysis of t-butyl sulfide. A detailed reaction mechanism is then presented for the SCW desulfurization of hexyl sulfide. Comprehensive kinetic mechanisms for these larger molecules are likely to include thousands of reactions, so RMG builds this model in a systematic and unbiased way using a database of ab initio data. This database is expanded with potentially relevant thermochemical and kinetic parameters using transition state theory and quantum chemical calculations at the CBS-QB3 and CCSD(T)-F12 levels of theory. With these data, as well as previously calculated rates for hydrocarbon and sulfur kinetics, RMG is used to build a reaction mechanism for the conversion of hexyl sulfide to hydrogen sulfide, pentane, and carbon monoxide in the presence of SCW. This mechanism is validated with results from batch and flow reactor experiments, and predictions are accurate within a factor of two for reactant and major product concentrations. Analysis of the proposed mechanism shows that the molecular addition of water to the carbonsulfur double-bond in hexanethial is a key step in the SCW process, as this not only leads to the desulfurization of the compound, but also prevents the thioaldehyde from undergoing addition reactions with other hydrocarbons in a process that could eventually form coke. Thus, this work not only has implications in the SCW desulfurization process, but in the overall crude oil upgrading process as well. The calculated kinetic and thermochemical parameters are used to generate predictive reaction mechanisms for other processes relevant in fuel chemistry, such as the geological formation of oil and gas from kerogen. This not only allows us to model experimental work investigating the effect sulfur compounds have on the oil-to-gas process, but we also explore how these effects differ at geological conditions and timescales. And as the possible applications of RMG grow, the need for accurate parameters in mechanism generation become even more critical. A thermochemical database is generated for a wide variety of sulfur compounds using the highaccuracy CCSD(T)-F12/cc-pVTZ-F12 method, and this provides a basis for the investigation of organosulfur chemistry with tighter uncertainty.
by Caleb Andrew Class.
Ph. D.
Ramesha, A. R. "Organosulfur Reactions In Organic Synthesis With Tetrathiomolybdate". Thesis, Indian Institute of Science, 1994. http://hdl.handle.net/2005/107.
Texto completoShepherd, S. D. "Chemical and enzymatic synthesis of organosulfur compounds". Thesis, Anglia Ruskin University, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.396225.
Texto completoHendrickx, Ramon Adriaan Antonius Johannes Hendrickx. "Mechanistic studies of organosulfur oxidations by dimethyldioxirane". Thesis, University of York, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.399615.
Texto completoMurray, Jane. "Selective oxidation of organosulfur substrates by hydrogen peroxide". Thesis, University of York, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.428461.
Texto completoSavoie, Paul R. "Preparation, chemistry, and characterization of hypervalent organosulfur fluorides". Thesis, State University of New York at Albany, 2015. http://pqdtopen.proquest.com/#viewpdf?dispub=3739734.
Texto completoSince the discovery of the pentafluorosulfanyl (SF5) group around the 1960s, progress in exploring the chemistry of aliphatic SF 5-containing compounds stagnated because of a lack of efficient synthetic methods. More recent developments in the preparations of SF5-containing compounds afforded easier access to these compounds, and sparked great interest in exploring their chemistry. Chapter 1 discusses the development of efficient methods used to prepare SF5-containing aliphatic compounds.
This dissertation investigates the combination of steric and polar effects of pentafluorosulfanylation on aliphatic molecules. Chapter 2 discusses the synthesis and chemistry of aliphatic aldehydes and aldimines containing the SF5 group in the 2-position. The aldehydes undergo many of the common chemical transformations of aliphatic aldehydes, affording a variety of SF5-containing compounds. The large C–S bond dipole helps direct additions to the carbonyl group in a manner consistent with the Cornforth hypothesis, resulting in highly diastereoselective nucleophilic additions. Similarly, the synthesis of SF5-containing SF5β-lactams by [2+2] cycloadditions of 2-pentafluorosulfanylaldimines with azidoketene proceeds with high diastereofacial selectivity. The SF5 β-lactams formed by this reaction may lead to a greater variety of diastereoselectively-prepared amino acid compounds for study in peptides, the preparation of new antibacterial compounds, and the design of novel SF5 β-lactamase inhibitors.
Chapter 3 discusses the structural studies of some synthesized pentafluorosulfanylated molecules to help further elucidate the steric and polar effects of pentafluorosulfanylation on aliphatic compounds. Coupling constant analyses determined the local molecular structure near the SF5 group and revealed that the unexpected diastereotopic resonances in 1H NMR spectra were the result of partial insertion of a hydrogen atom between two equatorial fluorine atoms, thus “locking” the conformation of the alkyl chain near the SF5 group. Computational experiments confirmed the experimentally-determined S–C–C–O dihedral angle of 85° observed in the alcohols formed by nucleophilic addition to the aldehyde carbonyl group of 2-pentafluorosulfanyl aldehydes. Computation of the reaction profile for the [2+2] cycloaddition of 2-pentafluorosulfanylaldimines with azidoketene revealed a difference in the reaction barriers leading to the two diastereomeric pairs of products of about 4.1 kcal/mol. Formation of the 1,2-lk,lk products is favored over the formation of the other possible products.
Brooks, Andrew C. "The preparation of organosulfur derived electron transfer salts". Thesis, Nottingham Trent University, 2009. http://irep.ntu.ac.uk/id/eprint/284/.
Texto completoTakada, Hiroya. "Novel Asymmetric Reactions of Organosulfur and Organoselenium Compounds". Kyoto University, 1999. http://hdl.handle.net/2433/181822.
Texto completoSerapian, Stefano. "Simulating self-assembly of organosulfur species on gold nanoparticles". Thesis, Imperial College London, 2013. http://hdl.handle.net/10044/1/24839.
Texto completoOgunlaja, Adeniyi Sunday. "Oxidative desulfurization of fuel oils-catalytic oxidation and adsorptive removal of organosulfur compounds". Thesis, Rhodes University, 2014. http://hdl.handle.net/10962/d1013152.
Texto completoASHBY, MICHAEL THOMAS. "THE NATURE OF ORGANOSULFUR LONE PAIR ORBITAL INTERACTIONS WITH TRANSITION METAL D-ORBITALS". Diss., The University of Arizona, 1986. http://hdl.handle.net/10150/183814.
Texto completoChauvin, Jean-Philippe. "Elucidation of the Various Mechanisms of Antioxidant Activity of Organosulfur Compounds". Thesis, Université d'Ottawa / University of Ottawa, 2019. http://hdl.handle.net/10393/39675.
Texto completoNicolau, Manterola Felipe. "Hydrocarbon and insecticide induction of Beauveria bassiana catalysis of organosulfur compounds". Diss., University of Iowa, 2016. https://ir.uiowa.edu/etd/3151.
Texto completoLow, Kam-hung y 魯錦鴻. "Synthesis, structural characterization and applications of homoleptic organosulfur and organoselenium metal polymers". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2009. http://hub.hku.hk/bib/B43703859.
Texto completoLachance, Russell Philip. "Oxidation and hydrolysis reactions in supercritical water : chlorinated hydrocarbons and organosulfur compounds". Thesis, Massachusetts Institute of Technology, 1995. http://hdl.handle.net/1721.1/33533.
Texto completoSmith, Muneerah. "An investigation into the anti-cancer mechanism of garlic-related organosulfur compounds". Master's thesis, University of Cape Town, 2014. http://hdl.handle.net/11427/12795.
Texto completoCrushed garlic contains organosulfur compounds (OSC), which are reported to have cancer chemotherapeutic properties both in vitro and in vivo. A library of 15 organosulfur analogues were obtained as mechanistic probes in WHCO1 oesophageal cancer cells. Structure-activity studies showed a positive correlation between the anti-proliferative-IC50 of disulfides and the relative stability of their anion leaving groups, as assessed through resonance and quantified by predictive pKa-values.
Jin, Peng. "Mechanism of Corrosion by Naphthenic Acids and Organosulfur Compounds at High Temperatures". Ohio University / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1384872234.
Texto completoFuruta, Satoru. "Synthetic Studies on Organofluorine Compounds through Oxidative Desulfurization -Fluorination of Organosulfur Compounds". Kyoto University, 2000. http://hdl.handle.net/2433/151524.
Texto completoDeCoste, Jared B. "Nucleophilic chemistry of faujasite X zeolites with isocyanates, organosulfur esters, and epoxides". Diss., Online access via UMI:, 2009.
Buscar texto completoLow, Kam-hung. "Synthesis, structural characterization and applications of homoleptic organosulfur and organoselenium metal polymers". Click to view the E-thesis via HKUTO, 2009. http://sunzi.lib.hku.hk/hkuto/record/B43703859.
Texto completoLorance, Edward Donald. "Synthetic and computational studies on organosulfur radical cations and alpha-metalated sulfides". Diss., The University of Arizona, 2000. http://hdl.handle.net/10150/284212.
Texto completoTieman, Tamara L. "A Helium Discharge Detector for the Determination of Organosulfur and Phosphorus Compounds". W&M ScholarWorks, 1992. https://scholarworks.wm.edu/etd/1539625734.
Texto completoOtsuka, Shinya. "Studies on Catalytic Transformations of Organosulfur Compounds via C-S Bond Cleavage". Kyoto University, 2019. http://hdl.handle.net/2433/242625.
Texto completoUhm, Hae Won. "Reaction of some chelating thioesters with chlorotris (triphenylphosphine) rhodium (I) : a model of the initial stages of hydrodesulfurization". Thesis, McGill University, 1986. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=65413.
Texto completoPETSOM, AMORN. "SYNTHETIC AND MECHANISTIC STUDIES ON THE ELECTROOXIDATION OF ORGANIC THIOETHERS". Diss., The University of Arizona, 1987. http://hdl.handle.net/10150/184178.
Texto completoWebb, Jared A. "A Comparative Study of Anaerobic Digestion Processes for Sewage Sludge". Thesis, Virginia Tech, 2006. http://hdl.handle.net/10919/41131.
Texto completoMaster of Science
Morris, Stephen Arthur. "The oxidative-addition to some organosulfur compounds to bis (ð5-cyclopentadienyl) titanium (II) dicarbonyl /". Thesis, McGill University, 1987. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=75828.
Texto completoZecchini, M. "Synthesis of new substituted organosulfur donors for the preparation of conductive and multifunctional materials". Thesis, Nottingham Trent University, 2015. http://irep.ntu.ac.uk/id/eprint/27926/.
Texto completoSvarovsky, Serge A. "Structure, stability and reactivity of small organic sulfinic and sulfonic acids toxicological implications ; Role of charge transfer complexes in oxidation cleavage of benzpinacols by iron (III) trispenanthroline /". Morgantown, W. Va. : [West Virginia University Libraries], 2000. http://etd.wvu.edu/templates/showETD.cfm?recnum=1231.
Texto completoReese, Raymond Scott. "Self-assembled monolayers of organosulfur compounds on gold incorporating terminal conjugated arenes, redox active probes, and oligonucleotides /". Digital version accessible at:, 1998. http://wwwlib.umi.com/cr/utexas/main.
Texto completoChiu, Winnie Wai Hang. "Metal complexes with sulfur and selenium donor ligands /". View abstract or full-text, 2009. http://library.ust.hk/cgi/db/thesis.pl?CHEM%202009%20CHIU.
Texto completoRyan, M. Dominic (Michael Dominic). "Organopolychalcogenides, new bond energy results and synthesis via the first selenium transfer reagent". Thesis, McGill University, 1988. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=75753.
Texto completoExisting organoselenium bond energy data were also reevaluated and erroneous assumptions discovered. New bond energy estimates were made via a new procedure. It was concluded that the selenium-selenium bond is also stronger than the selenium-carbon of aliphatic diselenides.
The above results led to the conclusion that loss of molecular dichalcogen from molecules such as disulfides or diselenides is favored over the stepwise loss of a single chalcogen by about 40 Kcal/mol. Loss of molecular diselenium from dibenzyl diselenide is reported. The average carbon-selenium bond energy of the latter is calculated to be only 27 Kcal/mol.
The preparation of 2-thiatriselenides (RSeSSeR) and 2,3-dithiatetraselenides (RSeSSSeR) has been achieved from selenosilanes. The products were characterized by $ sp{77}$Se NMR and the trends of chemical shifts were analyzed.
The preparation of the first selenium transfer reagents, including the first unsymmetrical chalcogen transfer reagent, is reported. Their use to effect the synthesis of 2-selenatrisulfides (RSSeSR) is also reported. Low temperature $ sp{77}$Se NMR was used to elucidate the reaction mechanism and characterize several intermediates such as selenuranes, selenonium ions and azole selenides. In addition, 2,3-diselenatetrasulfides (RSSeSeSR) were characterized by $ sp{77}$Se NMR.
Chen, Xiangke. "Vibrational Sum Frequency Generation Studies of Biological and Atmospheric Relevant Interfaces: Lipids, Organosulfur Species and Interfacial Water Structure". The Ohio State University, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=osu1282061999.
Texto completoInami, Tasuku. "Studies on Nickel-Catalyzed Reactions via Alkyne Insertion into Carbon-Sulfur Bonds". 京都大学 (Kyoto University), 2015. http://hdl.handle.net/2433/199274.
Texto completoAtkinson, Sarah Jane y n/a. "Studies in Dendritic Scaffolds and Surface Functionalisation for Applications in Nanoscience". Griffith University. School of Biomolecular and Physical Sciences, 2007. http://www4.gu.edu.au:8080/adt-root/public/adt-QGU20071122.124705.
Texto completoAtkinson, Sarah Jane. "Studies in Dendritic Scaffolds and Surface Functionalisation for Applications in Nanoscience". Thesis, Griffith University, 2007. http://hdl.handle.net/10072/366865.
Texto completoThesis (PhD Doctorate)
Doctor of Philosophy (PhD)
School of Biomolecular and Physical Sciences
Full Text
Souza, Frederico Bernardes de. "Síntese e funcionalização de compostos organoenxofre: sulfóxidos, sulfetos e N-sulfinil iminas". Universidade de São Paulo, 2017. http://www.teses.usp.br/teses/disponiveis/9/9138/tde-19102017-155658/.
Texto completoIn this work we promote the synthesis of α-substituted vinylic sulfoxides through the Suzuki-Miyaura cross coupling reaction. Also the synthesis of unpublished enynic sulfoxides was made, by the addition of the nucleophile in the β-sulfoxide carbon. These compounds were susceptible to additive Pummerer rearragement reaction and thus generated a small library of compounds. One of these aldehydes synthesized was used in the formation reaction of a propargyl imine, with consequent CuAAC reaction, forming triazol imines. Other aryl imines were synthesized, undergoing a reduction step, in order to obtain the free amine, so that the cyclization reaction was carried out with the aid of an electrophilic agent. Another class of organosulfur compound was synthesized, the N-sulfinyl imine, which after the Sonogashira cross-coupling reaction, with consequent removal of a protecting group and formation of the heterocyclic ring, N-sulfinyl imine triazolic compounds were obtained.
Maclellan, Paul William. "Asymmetric synthesis of tertiary thiols by lithiation of thiocarbamates". Thesis, University of Manchester, 2011. https://www.research.manchester.ac.uk/portal/en/theses/asymmetric-synthesis-of-tertiary-thiols-by-lithiation-of-thiocarbamates(ee91a5d1-63ba-458b-87bc-fd32e7c27b96).html.
Texto completoHitchcock, Jessica Kaari. "The immunomodulatory effects of the garlic organosulfur compounds allicin and Z-ajoene in an in vitro murine model of LPS-induced inflammation". Master's thesis, University of Cape Town, 2015. http://hdl.handle.net/11427/15735.
Texto completoBattin, Erin E. "The role of metal coord[i]nation in the inhibition of iron(ii)- and copper(i)-mediated DNA damage by organoselenium and organosulfur compounds". Connect to this title online, 2008. http://etd.lib.clemson.edu/documents/1219862989/.
Texto completoDannenberg, Carl A. Verfasser], Carsten [Akademischer Betreuer] [Bolm y Dieter [Akademischer Betreuer] Enders. "Method development for the synthesis of organosulfur compounds and their functionalization by C–H activation and reductive borylation / Carl A. Dannenberg ; Carsten Bolm, Dieter Enders". Aachen : Universitätsbibliothek der RWTH Aachen, 2017. http://d-nb.info/1156924286/34.
Texto completoUlivi, Paola <1975>. "Activity and mechanisms of action of novel organosulfur derivatives of the HDAC inhibitor Valproic Acid in human experimental models of non-small-cell lung cancer". Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2014. http://amsdottorato.unibo.it/6310/.
Texto completoGomes, Sónia Maria. "Catalytic oxidation of organic compounds : a sustainable approach". Doctoral thesis, Universidade de Aveiro, 2014. http://hdl.handle.net/10773/14892.
Texto completoOne of the biggest challenges for organic chemistry researchers is the development of catalytic systems able to selectively oxidize organic compounds, under mild and environmental sustainable conditions. In fact, this is a transformation which nature operates with an extraordinary ability but is of remarkable difficulty for both academia and industry. Metalloporphyrins, as biomimetic models of cytochromes P450, are thus catalysts with great potential. After the first introductory chapter, where the above-mentioned concepts are fully discussed, some general features of porphyrin properties, synthetic methodologies and reactivity are presented in Chapter 2 of this dissertation. The synthetic routes to all the Mn(III) and Fe(III) porphyrins used as catalysts during the work are also discribed in this chapter. Chapter 3 is dedicated to the application of Mn(III) and Fe(III) metalloporphyrin complexes on the oxidative catalysis of organosulfur compounds (sulfides, benzothiophenes, dibenzothiophenes and 1,3-di-hydrobenzothiophenes) by hydrogen peroxide. Besides revealing a high efficient approach for the obtention of the corresponding sulfones, the use of mild and nontoxic conditions turns this approach environmentally safe. The potentiality of the developed methodology only can be fully recognized through the heterogenization of porphyrin complexes in a solid support. So, in chapter 4 the immobilization strategies of tetrapyrrolic macrocycles onto Merrifield resin and silica supports are presented. Three heterogeneous metalloporphyrin-based materials were prepared and the results of catalytic assays with thioanisole as substrate and H2O2 as oxidant put in evidence the efficiency and recyclability of two of them. The catalytic experiments with metalloporphyrins were extended to other substrate classes, namely benzofurans and naphtoquinones, and the results are described and discussed in Chapters 5 and 6, respectively. Despite the complexity of the products obtained, the preferential oxidation route in both cases seems to involve first an epoxidation. Finally, the efficiency of two non-porphyrinic catalysts, namely a manganese polyoxometalate and graphene oxide (tested under homogeneous and heterogeneous conditions, respectively), was also evaluated in sulfoxidation processes by hydrogen peroxide, being the results described in Chapter 7. Graphene 3D oxide, whose catalytic performance was evaluated for the first time, demonstrates to be efficient and recyclable in the oxidation of thioanisole. The last chapter includes some general conclusions and future perspectives for the developed work.
Um dos maiores desafios para os investigadores da área da química orgânica prende-se com o desenvolvimento de sistemas catalíticos capazes de promover, mesmo sob condições moderadas e ambientalmente sustentáveis, a oxidação selectiva de compostos orgânicos. Esta é uma transformação que a natureza realiza de uma forma extraordinária mas que se reveste de tremenda dificuldade tanto no meio académico como a nível industrial. As metaloporfirinas, consideradas modelos biomiméticos do citocromo P450, revestem-se por isso de um enorme potencial em catálise. Assim, nesta dissertação, após o primeiro capítulo introdutório, onde os conceitos mencionados acima são apresentados, no capítulo 2 são abordados alguns dos principais aspectos relativos às propriedades, síntese e reactividade das porfirinas. São ainda descritas neste capítulo as rotas sintéticas para todas as metaloporfirinas de Mn(III) e de Fe(III) usadas durante o trabalho. O capítulo 3 reporta-se à aplicação de complexos metaloporfirínicos de Mn(III) e de Fe(III) na catálise oxidativa de compostos organosulfurados (sulfuretos, benzotiofenos, dibenzotiofenos e 1,3-di-hidrobenzotiofenos) pelo peróxido de hidrogénio. Para além de se revelar uma metodologia altamente eficiente para a obtenção das correspondentes sulfonas, o uso de condições moderadas e atóxicas, torna esta abordagem segura para o meio ambiente. A potencialidade da metodologia desenvolvida só pode ser amplamente reconhecida através da heterogeneização do complexo porfirínico num suporte sólido. Desta forma, no capitulo 4 são apresentadas as estratégias de imobilização de diferentes macrociclos tetrapirrólicos na resina de Merrifield e na sílica funcionalizada. Foram preparados três materiais baseados em metaloporfirinas e os resultados dos ensaios catalíticos envolvendo o tioanisol como substrato e como oxidante o H2O2 colocam em evidência a eficiência e a reciclabilidade de dois deles. Os ensaios catalíticos com metaloporfirinas foram alargados a outras classes de substratos, nomeadamente os benzofuranos e as naftoquinonas, cujos resultados se apresentam nos capítulos 5 e 6, respectivamente. Apesar da complexidade de produtos obtida, a preferencial via de oxidação parece envolver, em ambos os casos, em primeiro lugar uma epoxidação. Finalmente, foi ainda avaliada a eficiência de dois catalisadores não porfirínicos, nomeadamente um polioxometalato e um óxido de grafeno (testados em condições homogéneas e heterogéneas respectivamente) em processos de sulfoxidação pelo peróxido de hidrogénio, cujos resultados se descrevem no capitulo 7. O último capítulo inclui as conclusões gerais e algumas perspectivas futuras para o trabalho desenvolvido.
Halpern, Melissa Dale. "The in vivo and in vitro effects of diethyldithiocarbamate on autoimmune New Zealand Black/White F₁ hybrid, MRL/Mp-lpr/lpr and related and normal murine strains". Diss., The University of Arizona, 1989. http://hdl.handle.net/10150/184940.
Texto completoZhu, Lei. "Aqueous phase reaction kinetics of organic sulfur compounds of atmospheric interest". Diss., Available online, Georgia Institute of Technology, 2004:, 2004. http://etd.gatech.edu/theses/available/etd-11172004-142820/unrestricted/zhu%5Flei%5F200412%5Fphd.pdf.
Texto completoDavis, Douglas, Committee Member ; Huey, Greg, Committee Member ; Nenes, Athanasios, Committee Member ; Weber, Rodney, Committee Member ; Whetten, Robert, Committee Member ; Wine, Paul H., Committee Chair. Includes bibliographical references.
Yin, Fangdong Seinfeld John H. "Atmospheric photooxidation of organosulphur compounds /". Diss., Pasadena, Calif. : California Institute of Technology, 1990. http://resolver.caltech.edu/CaltechETD:etd-11192007-092214.
Texto completoMonin, Guillaume. "Stabilisation chimique des électrolytes polymères pour pile à combustible". Phd thesis, Université de Grenoble, 2012. http://tel.archives-ouvertes.fr/tel-00728176.
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