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Artykuły w czasopismach na temat "Organosulfur"
Arisawa, Mieko, i Masahiko Yamaguchi. "Transition-metal-catalyzed synthesis of organosulfur compounds". Pure and Applied Chemistry 80, nr 5 (1.01.2008): 993–1003. http://dx.doi.org/10.1351/pac200880050993.
Pełny tekst źródłaQiu, Yichen, Yunchao Feng, Ashley C. Lindsay, Xianhai Zeng i Jonathan Sperry. "Synthesis of bio-based 2-thiothiophenes". Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences 379, nr 2209 (13.09.2021): 20200350. http://dx.doi.org/10.1098/rsta.2020.0350.
Pełny tekst źródłaChauvin, Jean-Philippe R., Zosia A. M. Zielinski i Derek A. Pratt. "Inspired by garlic: insights on the chemistry of sulfenic acids and the radical-trapping antioxidant activity of organosulfur compounds". Canadian Journal of Chemistry 94, nr 1 (styczeń 2016): 1–8. http://dx.doi.org/10.1139/cjc-2015-0438.
Pełny tekst źródłaShine, Henry J. "Researches in organosulfur chemistry by a non-organosulfur chemist". Sulfur reports 15, nr 3 (sierpień 1994): 381–93. http://dx.doi.org/10.1080/01961779408050635.
Pełny tekst źródłaDoddipatla, Srinivas, Chao He, Ralf I. Kaiser, Yuheng Luo, Rui Sun, Galiya R. Galimova, Alexander M. Mebel i Tom J. Millar. "A chemical dynamics study on the gas phase formation of thioformaldehyde (H2CS) and its thiohydroxycarbene isomer (HCSH)". Proceedings of the National Academy of Sciences 117, nr 37 (28.08.2020): 22712–19. http://dx.doi.org/10.1073/pnas.2004881117.
Pełny tekst źródłaArisawa, Mieko, i Masahiko Yamaguchi. "Rhodium-Catalyzed Synthesis of Organosulfur Compounds Involving S-S Bond Cleavage of Disulfides and Sulfur". Molecules 25, nr 16 (7.08.2020): 3595. http://dx.doi.org/10.3390/molecules25163595.
Pełny tekst źródłaEgbujor, Melford Chuka, Maria Petrosino, Karim Zuhra i Luciano Saso. "The Role of Organosulfur Compounds as Nrf2 Activators and Their Antioxidant Effects". Antioxidants 11, nr 7 (26.06.2022): 1255. http://dx.doi.org/10.3390/antiox11071255.
Pełny tekst źródłaYuen, Pong Kau, i Cheng Man Diana Lau. "New approach for assigning mean oxidation number of carbons to organonitrogen and organosulfur compounds". Chemistry Teacher International 4, nr 1 (8.10.2021): 1–13. http://dx.doi.org/10.1515/cti-2021-0015.
Pełny tekst źródłaNakahodo, Tsukasa, Midori O. Ishitsuka, Yuta Takano, Takahiro Tsuchiya, Takeshi Akasaka, M. Angeles Herranz, Nazario Martin, Dirk M. Guldi i Shigeru Nagase. "Organosulfur-Based Fullerene Materials". Phosphorus, Sulfur, and Silicon and the Related Elements 186, nr 5 (1.05.2011): 1308–11. http://dx.doi.org/10.1080/10426507.2010.523033.
Pełny tekst źródłaKiełbasiński, Piotr. "Biocatalysis in Organosulfur Chemistry". Phosphorus, Sulfur, and Silicon and the Related Elements 186, nr 5 (1.05.2011): 1104–18. http://dx.doi.org/10.1080/10426507.2010.541397.
Pełny tekst źródłaRozprawy doktorskie na temat "Organosulfur"
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.
Pełny tekst źródłaKing, 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.
Pełny tekst źródłaChowdhury, Mohima Begum Roomi. "Unsaturated organosulfur chemistry : synthesis and applications". Thesis, University College London (University of London), 2018. http://discovery.ucl.ac.uk/10045805/.
Pełny tekst źródłaClass, Caleb Andrew. "Predicting organosulfur chemistry in fuel sources". Thesis, Massachusetts Institute of Technology, 2015. http://hdl.handle.net/1721.1/98155.
Pełny tekst źródłaCataloged 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.
Pełny tekst źródłaShepherd, 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.
Pełny tekst źródłaHendrickx, 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.
Pełny tekst źródłaMurray, 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.
Pełny tekst źródłaSavoie, 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.
Pełny tekst źródłaSince 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/.
Pełny tekst źródłaKsiążki na temat "Organosulfur"
Organosulfur chemistry. Oxford: Oxford University Press, 1995.
Znajdź pełny tekst źródłaB, Page Philip C., red. Organosulfur chemistry. Berlin: Springer, 1999.
Znajdź pełny tekst źródłaCremlyn, R. J. W. An introduction to organosulfur chemistry. Chichester: Wiley, 1996.
Znajdź pełny tekst źródłaPage, Philip C. B., red. Organosulfur Chemistry I. Berlin, Heidelberg: Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/3-540-48956-8.
Pełny tekst źródłaPage, Philip C. B., red. Organosulfur Chemistry II. Berlin, Heidelberg: Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/3-540-48986-x.
Pełny tekst źródłaSaul, Patai, i Rappoport Zvi, red. The Chemistry of sulphur-containing functional groups. Chichester [England]: Wiley, 1993.
Znajdź pełny tekst źródłaIstván, Hargittai. The structure of volatile sulphur compounds. Dordrecht, Holland: D. Reidel, 1985.
Znajdź pełny tekst źródłaI, Gusarʹ N., i Fokin A. V, red. Sulʹfenilkhloridy. Moskva: "Nauka", 1989.
Znajdź pełny tekst źródłaInternational Symposium on Organic Sulfur Chemistry (13th 1988 Odense, Denmark). Developments in the organic chemistry of sulfur: Proceedings of the XIII International Symposium on the Organic Chemistry of Sulfur, 7-12 August, 1988, Odense, Denmark. New York: Gordon and Breach, 1989.
Znajdź pełny tekst źródłaA, Maletina E., Roman V. K i Volʹpin M. E, red. Kremnekislorodnye soedinenii͡a︡ nemetallov: Proizvodnye kisloroda i sery. Novosibirsk: "Nauka," Sibirskoe otd-nie, 1991.
Znajdź pełny tekst źródłaCzęści książek na temat "Organosulfur"
Furka, Árpád. "Organosulfur Compounds". W SpringerBriefs in Molecular Science, 69–80. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-06004-6_5.
Pełny tekst źródłaMikołajczyk, Marian, i Jozef Drabowicz. "Chiral Organosulfur Compounds". W Topics in Stereochemistry, 333–468. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470147221.ch5.
Pełny tekst źródłaLea, Michael A. "Organosulfur Compounds and Cancer". W Advances in Experimental Medicine and Biology, 147–54. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4613-0399-2_12.
Pełny tekst źródłaBischoff, Karyn. "Glucosinolates and Organosulfur Compounds". W Nutraceuticals in Veterinary Medicine, 113–19. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-04624-8_9.
Pełny tekst źródłaRauchfuss, T. B. "With Organosulfur Anions [RS]-". W Inorganic Reactions and Methods, 109–15. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145203.ch85.
Pełny tekst źródłaZhao, Ming Ming, Shi Hang Xiong, Guan Ding Zhao i Hua Yu. "Organosulfur Compounds in Food". W Handbook of Dietary Phytochemicals, 1–21. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-1745-3_41-1.
Pełny tekst źródłaZhao, Ming Ming, Shi Hang Xiong, Guan Ding Zhao i Hua Yu. "Organosulfur Compounds in Food". W Handbook of Dietary Phytochemicals, 1741–61. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-15-4148-3_41.
Pełny tekst źródłaSagdic, Osman, i Fatih Tornuk. "Antimicrobial Properties of Organosulfur Compounds". W Dietary Phytochemicals and Microbes, 127–56. Dordrecht: Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-94-007-3926-0_4.
Pełny tekst źródłaTowl, A. D. C. "In Hydrolyses of Organosulfur Compounds". W Inorganic Reactions and Methods, 186. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145159.ch122.
Pełny tekst źródłaWhite, Curt M., L. J. Douglas, R. R. Anderson, C. E. Schmidt i R. J. Gray. "Organosulfur Constituents in Rasa Coal". W Geochemistry of Sulfur in Fossil Fuels, 261–86. Washington, DC: American Chemical Society, 1990. http://dx.doi.org/10.1021/bk-1990-0429.ch016.
Pełny tekst źródłaStreszczenia konferencji na temat "Organosulfur"
Matzka, Marco, Marianna Lucio, Basem Kanawati, Eric Quirico, Lydie Bonal, Stefan Loehle i Philippe Schmitt-Kopplin. "Profiling of magnesium organosulfur chemistry in meteorites". W Goldschmidt2021. France: European Association of Geochemistry, 2021. http://dx.doi.org/10.7185/gold2021.4692.
Pełny tekst źródłaRahman, Ramees K., Abhijeet G. Raj i Salisu Ibrahim. "Formation of Mercaptans and Organosulfur Species in Claus Process". W Abu Dhabi International Petroleum Exhibition & Conference. Society of Petroleum Engineers, 2017. http://dx.doi.org/10.2118/188255-ms.
Pełny tekst źródłaHsu, C. W., David P. Baldwin, Chung-Lin Liao i Cheuk Yiu Ng. "Nonresonant two-photon pulsed field ionization studies of organosulfur molecules and radicals". W OE/LASE '94, redaktor John W. Hepburn. SPIE, 1994. http://dx.doi.org/10.1117/12.178108.
Pełny tekst źródłaAhillah, Nurul, Sri Rahayu Lestari i Abdul Gofur. "Single bulb garlic organosulfur compounds in inhibiting angiotensin-converting enzyme (ACE) as hypertension therapeutic strategies: An in silico study". W INTERNATIONAL CONFERENCE ON LIFE SCIENCES AND TECHNOLOGY (ICoLiST 2020). AIP Publishing, 2021. http://dx.doi.org/10.1063/5.0052658.
Pełny tekst źródłaSa'adah, Nur Alfi Maghfirotus, Bella Aulia, Dimas Nur Ramadhani, Maria Dwi Cahyani, Muhammad Mauludi Zulkifli, Siti Nur Arifah, Mochammad Fitri Atho'illah, Sri Rahayu Lestari i Abdul Gofur. "In silico study of potential organosulfur and flavonoids compounds in garlic (Allium sativum L.) as inhibitor of α-glucosidase enzyme". W THE 4TH INTERNATIONAL CONFERENCE ON LIFE SCIENCE AND TECHNOLOGY (ICoLiST). AIP Publishing, 2023. http://dx.doi.org/10.1063/5.0113522.
Pełny tekst źródłaSumei, Li, Shi Quan, Zhang Hongan, Xu Tianwu, Chen Xianfei i Ji Hong. "Characteristics and Significances of Organosulfur Compounds in Typical Saline Lacustrine Oils From Bohai Bay Basin Identified by ESI FT-ICR MS". W 29th International Meeting on Organic Geochemistry. European Association of Geoscientists & Engineers, 2019. http://dx.doi.org/10.3997/2214-4609.201902795.
Pełny tekst źródłaSundararajan, Desikan, i Abdul-Majeed Azad. "Development of Logistic Fuel Desulfurizers Endowed With Nanoartifacts". W ASME 2008 6th International Conference on Fuel Cell Science, Engineering and Technology. ASMEDC, 2008. http://dx.doi.org/10.1115/fuelcell2008-65138.
Pełny tekst źródłaApitz Castro, R., E. Ledezma, A. Jorquera i M. K. Jain. "REVERSIBLE BLOCKADE OF PLATELET ACTIVATION DURING CARDIO-PUIMONAR BYPASS IN DOGS AFTER IV ADMINISTRATION OF AJOENE". W XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644820.
Pełny tekst źródłaSalimi, Hamidreza, Maryam Namdar Zanganeh, Sven McCarthy, Lucian Pirlea, Jurriaan Nortier, Dario Frigo, Haitham Balushi, Mustafa Lawati i Mohamed Yarabi. "A Quantitative and Predictive Reservoir-Souring Approach to Assess Reservoir-Souring Risk During Waterflood Development". W SPE Conference at Oman Petroleum & Energy Show. SPE, 2022. http://dx.doi.org/10.2118/200087-ms.
Pełny tekst źródłaHosseini, S. H., S. Poetz, B. Horsfield, H. Wilkes, O. Kavak i M. N. Yalçın. "Insights into Aromatic Organosulphur Compounds in Solid Bitumen and Heavy Oils from Southeast Turkey". W 29th International Meeting on Organic Geochemistry. European Association of Geoscientists & Engineers, 2019. http://dx.doi.org/10.3997/2214-4609.201902836.
Pełny tekst źródłaRaporty organizacyjne na temat "Organosulfur"
Ternay, Andrew L., i Jr. Organosulfur Compounds as ChemDefense Agents - Mustard. Fort Belvoir, VA: Defense Technical Information Center, wrzesień 2001. http://dx.doi.org/10.21236/ada409740.
Pełny tekst źródłaHsu, Chia-Wei. Photodissociation and photoionization of organosulfur radicals. Office of Scientific and Technical Information (OSTI), maj 1994. http://dx.doi.org/10.2172/10190413.
Pełny tekst źródłaRuscic, B., i J. Berkowitz. Photoionization studies of organosulfur transient species. Office of Scientific and Technical Information (OSTI), marzec 1994. http://dx.doi.org/10.2172/10132759.
Pełny tekst źródłaWoods, Nina Tani. Characterization of organosulfur monolayer formation at gold electrodes. Office of Scientific and Technical Information (OSTI), sierpień 1996. http://dx.doi.org/10.2172/383576.
Pełny tekst źródłaCheung, Yu San. Single- and multi-photon ionization studies of organosulfur species. Office of Scientific and Technical Information (OSTI), luty 1999. http://dx.doi.org/10.2172/350831.
Pełny tekst źródłaPurdy, R. F., B. Ward i J. E. Lepo. Microbial extraction of sulfur from model coal organosulfur compounds. Office of Scientific and Technical Information (OSTI), grudzień 1991. http://dx.doi.org/10.2172/10175584.
Pełny tekst źródłaKilbane, J. J. II. Microbial strain improvement for organosulfur removal from coal. [Rhodococcus rhodochrous]. Office of Scientific and Technical Information (OSTI), styczeń 1991. http://dx.doi.org/10.2172/5792238.
Pełny tekst źródłaEliel, Ernest L. Neighboring Group Participation in Solvolysis of Organosulfur and Related Compounds. Fort Belvoir, VA: Defense Technical Information Center, sierpień 1985. http://dx.doi.org/10.21236/ada161458.
Pełny tekst źródłaKilbane, J. J. II. Microbial strain improvement for organosulfur removal from coal. Technical report, September 1--November 30, 1991. Office of Scientific and Technical Information (OSTI), grudzień 1991. http://dx.doi.org/10.2172/10122904.
Pełny tekst źródłaKilbane, J. J. II, i K. Ho. Microbial strain improvement for organosulfur removal from coal. Technical report, December 1, 1992--February 28, 1993. Office of Scientific and Technical Information (OSTI), maj 1993. http://dx.doi.org/10.2172/10149989.
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