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Relevant bibliographies by topics / Cycloalkanes

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Academic literature on the topic 'Cycloalkanes'

Author: Grafiati

Published: 4 June 2021

Last updated: 6 September 2023

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Journal articles on the topic "Cycloalkanes"

1

Herman, David C., Phillip M. Fedorak, and J. William Costerton. "Biodegradation of cycloalkane carboxylic acids in oil sand tailings." Canadian Journal of Microbiology 39, no. 6 (June 1, 1993): 576–80. http://dx.doi.org/10.1139/m93-083.

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The biodegradation of both an n-alkane and several carboxylated cycloalkanes was examined within tailings produced by the extraction of bitumen from the Athabasca oil sands. The carboxylated cycloalkanes examined were structurally similar to naphthenic acids that have been associated with the acute toxicity of oil sand tailings. The biodegradation potential of naphthenic acids was estimated by determining the biodegradation of both the carboxylated cycloalkanes and hexadecane in oil sand tailings. Carboxylated cycloalkanes were biodegraded within oil sand tailings, although compounds with meth

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Chen, Yubin, Bin Yuan, Chaomin Wang, Sihang Wang, Xianjun He, Caihong Wu, Xin Song, et al. "Online measurements of cycloalkanes based on NO⁺ chemical ionization in proton transfer reaction time-of-flight mass spectrometry (PTR-ToF-MS)." Atmospheric Measurement Techniques 15, no. 23 (December 2, 2022): 6935–47. http://dx.doi.org/10.5194/amt-15-6935-2022.

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Abstract. Cycloalkanes are important trace hydrocarbons existing in the atmosphere, and they are considered a major class of intermediate volatile organic compounds (IVOCs). Laboratory experiments showed that the yields of secondary organic aerosols (SOAs) from oxidation of cycloalkanes are higher than acyclic alkanes with the same carbon number. However, measurements of cycloalkanes in the atmosphere are still challenging at present. In this study, we show that online measurements of cycloalkanes can be achieved using proton transfer reaction time-of-flight mass spectrometry with NO+ chemical

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Wang, Jian, He Liu, Shiguang Fan, Shuai Wang, Guanjun Xu, Aijun Guo, and Zongxian Wang. "Dehydrogenation of Cycloalkanes over N-Doped Carbon-Supported Catalysts: The Effects of Active Component and Molecular Structure of the Substrate." Nanomaterials 11, no. 11 (October 26, 2021): 2846. http://dx.doi.org/10.3390/nano11112846.

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Efficient dehydrogenation of cycloalkanes under mild conditions is the key to large-scale application of cycloalkanes as a hydrogen storage medium. In this paper, a series of active metals loaded on nitrogen-doped carbon (M/CN, M = Pt, Pd, Ir, Rh, Au, Ru, Ag, Ni, Cu) were prepared to learn the role of active metals in cycloalkane dehydrogenation with cyclohexane as the model reactant. Only Pt/CN, Pd/CN, Rh/CN and Ir/CN can catalyze the dehydrogenation of cyclohexane under the set conditions. Among them, Pt/CN exhibited the best catalytic activity with the TOF value of 269.32 h−1 at 180 °C, fol

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4

Bogdanowicz-Szwed, Krystyna, та Michalina Kozicka. "Phase-Transfer Catalysed Alkylation of Enamines of some Cyclic β-Keto Carbothionic Acid Anilides with 1,2-Dibromoethane. Synthesis of Enamines of 1-Oxo-2-(3-phenyl tetrahydrothiazol-2-ylidene)-cycloalkanes". Zeitschrift für Naturforschung B 42, № 9 (1 вересня 1987): 1174–80. http://dx.doi.org/10.1515/znb-1987-0919.

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The alkylation of morpholine enam ines of 2-oxo-cycloalkane-1-carbothionic acid anilides (1-3) with 1,2-dibromoethane under phase-transfer catalytic conditions yields enam ines of 1-oxo-2-(3-phenyl-tetrahydrothiazol-2-ylidene)-cycloalkanes (4-6). Compounds 4-6 were hydrolysed to appropriate keto derivatives 8-10. The structure of obtained com pounds was established on the basis of IR. NM R and MS spectral data.

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Wang, Wei, Shaoying Sun, Fengan Han, Guangyi Li, Xianzhao Shao, and Ning Li. "Synthesis of Diesel and Jet Fuel Range Cycloalkanes with Cyclopentanone and Furfural." Catalysts 9, no. 11 (October 25, 2019): 886. http://dx.doi.org/10.3390/catal9110886.

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Diesel and jet fuel range cycloalkanes were obtained in ~84.8% overall carbon yield with cyclopentanone and furfural, which can be produced from hemicellulose. Firstly, 2,5-bis(furan-2-ylmethyl)-cyclopentanone was prepared by the aldol condensation/hydrogenation reaction of cyclopentanone and furfural under solid base and selective hydrogenation catalyst. Over the optimized catalyst (Pd/C-CaO), 98.5% carbon yield of 2,5-bis(furan-2-ylmethyl)-cyclopentanone was acquired at 423 K. Subsequently, the 2,5-bis(furan-2-ylmethyl)-cyclopentanone was further hydrodeoxygenated over the M/H-ZSM-5(Pd, Pt a

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Staudt, Svenja, Edyta Burda, Carolin Giese, Christina A. Müller, Jan Marienhagen, Ulrich Schwaneberg, Werner Hummel, Karlheinz Drauz, and Harald Gröger. "Direct Oxidation of Cycloalkanes to Cycloalkanones with Oxygen in Water." Angewandte Chemie International Edition 52, no. 8 (January 21, 2013): 2359–63. http://dx.doi.org/10.1002/anie.201204464.

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Shen, Hai M., Xiong Wang, A. Bing Guo, Long Zhang, and Yuan B. She. "Catalytic oxidation of cycloalkanes by porphyrin cobalt(II) through efficient utilization of oxidation intermediates." Journal of Porphyrins and Phthalocyanines 24, no. 10 (September 29, 2020): 1166–73. http://dx.doi.org/10.1142/s1088424620500303.

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The catalytic oxidation of cycloalkanes using molecular oxygen employing porphyrin cobalt(II) as catalyst was enhanced through use of cycloalkyl hydroperoxides, which are the primary intermediates in oxidation of cycloalkanes, as additional oxidants to further oxidize cycloalkanes in the presence of porphyrin copper(II), especially for cyclohexane, for which the selectivity was enhanced from 88.6 to 97.2% to the KA oil; at the same time, the conversion of cyclohexane was enhanced from 3.88 to 4.41%. The enhanced efficiency and selectivity were mainly attributed to the avoided autoxidation of c

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Silva, Letícia B., Felipe S. Stefanello, Sarah C. Feitosa, Clarissa P. Frizzo, Marcos A. P. Martins, Nilo Zanatta, Bernardo A. Iglesias, and Helio G. Bonacorso. "Novel 7-(1H-pyrrol-1-yl)spiro[chromeno[4,3-b]quinoline-6,1′-cycloalkanes]: synthesis, cross-coupling reactions, and photophysical properties." New Journal of Chemistry 45, no. 8 (2021): 4061–70. http://dx.doi.org/10.1039/d0nj05740a.

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This paper covers the synthesis of a series of eleven examples of new 7-(1H-pyrrol-1-yl)spiro[chromeno[4,3-b]quinoline-6,1′-cycloalkanes] (3), where cycloalkanes are cyclopentane, cyclohexane, and cycloheptane.

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Wackett, Lawrence P. "Cycloalkanes and bacteria." Environmental Microbiology 16, no. 1 (January 2014): 333–34. http://dx.doi.org/10.1111/1462-2920.12336.

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Geraghty, Niall W. A., and John J. Hannan. "Functionalisation of cycloalkanes: the photomediated reaction of cycloalkanes with alkynes." Tetrahedron Letters 42, no. 18 (April 2001): 3211–13. http://dx.doi.org/10.1016/s0040-4039(01)00390-2.

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Dissertations / Theses on the topic "Cycloalkanes"

1

Warburton, Elizabeth Jean. "The metabolism of cycloalkanes by different species of Xanthobacter." Thesis, Nottingham Trent University, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.329184.

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Shirley, Neil John. "Synthesis of compounds of natural and unnatural origin by intramolecular alkylations." Title page, contents and summary only, 1987. http://web4.library.adelaide.edu.au/theses/09PH/09phs558.pdf.

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Parkinson, Nigel Christopher. "Nucleoside and nucleotide analogues containing fluorine." Thesis, Durham University, 1993. http://etheses.dur.ac.uk/5639/.

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The work contained in this thesis is divided into four sections detailing the formation of (diethoxyphosphinyl)difluoromethylene substituted cycloalkanes and alkenes and their chemistry, as well as the syntheses of purine and pyrimidine substituted polyfluoroethers:(i) The methodology for the introduction of the (diethoxyphosphinyl)difluoromethylene group was studied and extended, with specific reference to cyclic systems. The group was successfully introduced into cyclic alkenes with (diethoxyphosphinyl)difluoro- methylene zinc bromide and saturated systems with (diethoxyphosphinyl)difluorome

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Gray, Gary. "The oxidation of cycloalkanes using dioxygen catalysed by homogeneous and supported metalloporphyrins." Thesis, University of York, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.245972.

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Budkina, Darya S. "Ultrafast photophysical and photochemical dynamics of polyhalogenated alkanes, cycloalkanes, and transition metal complexes." Bowling Green State University / OhioLINK, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1553686775405944.

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Navasero, Neenah. "Synthetic routes to non-symmetric tropones." Thesis, McGill University, 2006. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=101647.

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The synthesis of substituted non-symmetric tropones has proven to be a considerable synthetic challenge. Particularly, a 3,4,6-tnsubstituted tropone which is required for the total synthesis of CP-225,917 is currently being undertaken by our group.<br>Two approaches towards the synthesis of substituted tropones are presented. Both utilize linear diene precursors which are closed to 7-membered cycloheptene rings via ring closing metathesis. In the first method, linear precursors are synthesized by addition of nucleophilic substituents to carbonyl groups to form alcohol groups. After forming the

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McCleary, Michelle Angela, and n/a. "Synthetic and Structural Studies on the Novel Formation of Bicyclo[n.2.0]alkan-1-ols." Griffith University. School of Science, 2004. http://www4.gu.edu.au:8080/adt-root/public/adt-QGU20040520.143342.

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Reaction of phenyl vinyl sulfoxide with the lithium enolates of simple ketones of varying ring size (cyclopentanone, cycloheptanone and cyclooctanone) under controlled cyclisation conditions followed by subsequent oxidation resulted in the formation of the bicyclo[n.2.0]alkan-1-ols 253-255, 262, 263, 265, 268 and 269 in conjunction with alkylated species 256, 257, 264, 266 and 267. The ratio of bicyclo[n.2.0]alkan-1-ols to alkylated ketone formation observed was dependent on a number of factors including the variation of enolate reactivity between the different ring sizes, conversion of phenyl

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McCleary, Michelle Angela. "Synthetic and Structural Studies on the Novel Formation of Bicyclo[n.2.0]alkan-1-ols." Thesis, Griffith University, 2004. http://hdl.handle.net/10072/366615.

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Reaction of phenyl vinyl sulfoxide with the lithium enolates of simple ketones of varying ring size (cyclopentanone, cycloheptanone and cyclooctanone) under controlled cyclisation conditions followed by subsequent oxidation resulted in the formation of the bicyclo[n.2.0]alkan-1-ols 253-255, 262, 263, 265, 268 and 269 in conjunction with alkylated species 256, 257, 264, 266 and 267. The ratio of bicyclo[n.2.0]alkan-1-ols to alkylated ketone formation observed was dependent on a number of factors including the variation of enolate reactivity between the different ring sizes, conversion of phenyl

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Rogers, Bruce. "Approaches to cyclobutane containing cage compounds." Thesis, University of Nottingham, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.299584.

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Skibiński, Maciej. "Effect of gem-difluorination on the conformation of selected hydrocarbon systems." Thesis, University of St Andrews, 2014. http://hdl.handle.net/10023/7058.

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Owing to its unique electronic properties, the CF₂ group has the potential to affect the conformation and polarity of molecules. The Introduction provides an overview of the conformational effects induced by the incorporation of fluorine into hydrocarbons, e.g. gauche effect, 1,3-C,F bond repulsion and angle deviation in organofluorine compounds. A summary of synthetic strategies for the introduction of the gem-difluoride motif into organic molecules is also presented. In order to explore the conformational impact of the CF₂ group in alicyclic hydrocarbon systems, cyclododecane was employed as

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Books on the topic "Cycloalkanes"

1

Patai, Saul, and Zvi Rappoport, eds. Alkanes and Cycloalkanes (1992). Chichester, UK: John Wiley & Sons, Ltd, 1992. http://dx.doi.org/10.1002/0470034378.

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Saul, Patai, and Rappoport Zvi, eds. The Chemistry of alkanes and cycloalkanes. Chichester: Wiley, 1992.

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3

Moosavi, Sayed Mojtaba. Base-catalysed ring opening reactions of cycloalkanols. Manchester: Universityof Manchester, 1996.

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4

Drăguțan, Valerian. Catalytic polymerization of cycloolefins: Ionic, Ziegler-Natta and ring-opening metathesis polymerization. Amsterdam: Elsevier Science, 2000.

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Rappoport, Zvi, and Saul Patai. The Chemistry of Alkanes And Cycloalkanes. John Wiley & Sons Inc, 2006.

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6

Dragutan, Ileana, and Valerian Dragutan. Polymers From Cycloolefins. CRC, 2008.

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7

Hoffmann, Reinhard W. Dehydrobenzene and Cycloalkynes. Elsevier Science & Technology Books, 2012.

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8

Wang, Zhandong. Experimental and Kinetic Modeling Study of Cyclohexane and Its Mono-alkylated Derivatives Combustion. Springer, 2018.

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9

Wang, Zhandong. Experimental and Kinetic Modeling Study of Cyclohexane and Its Mono-alkylated Derivatives Combustion. Springer, 2019.

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10

Dragutan, V., and R. Streck. Catalytic Polymerization of Cycloolefins: Ionic, Ziegler-Natta and Ring-Opening Metathesis Polymerization. Elsevier Science & Technology Books, 2000.

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Book chapters on the topic "Cycloalkanes"

1

Vollhardt, Peter, and Neil Schore. "Cycloalkanes." In Organic Chemistry, 218–85. New York: Macmillan Learning, 2014. http://dx.doi.org/10.1007/978-1-319-19197-9_4.

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2

Petrov, Alexander A. "Cycloalkanes (Naphthenes)." In Petroleum Hydrocarbons, 68–137. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-71737-6_4.

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Ahluwalia, V. K., and Renu Aggarwal. "Conformations of Cycloalkanes." In Alicyclic Chemistry, 63–88. Cham: Springer Nature Switzerland, 2023. http://dx.doi.org/10.1007/978-3-031-36068-8_8.

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Ahluwalia, V. K., and Renu Aggarwal. "Properties of Cycloalkanes." In Alicyclic Chemistry, 17–25. Cham: Springer Nature Switzerland, 2023. http://dx.doi.org/10.1007/978-3-031-36068-8_4.

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Ahluwalia, V. K., and Renu Aggarwal. "Nomenclature of Cycloalkanes." In Alicyclic Chemistry, 3–6. Cham: Springer Nature Switzerland, 2023. http://dx.doi.org/10.1007/978-3-031-36068-8_2.

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Ahluwalia, V. K., and Renu Aggarwal. "Synthesis of Cycloalkanes." In Alicyclic Chemistry, 7–15. Cham: Springer Nature Switzerland, 2023. http://dx.doi.org/10.1007/978-3-031-36068-8_3.

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Bährle-Rapp, Marina. "C9–16 Alkanes/Cycloalkanes." In Springer Lexikon Kosmetik und Körperpflege, 84. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_1540.

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Bährle-Rapp, Marina. "C11–15 Alkanes/Cycloalkanes." In Springer Lexikon Kosmetik und Körperpflege, 84. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_1541.

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Rasmussen, Kjeld. "Applications: Alkanes and cycloalkanes." In Lecture Notes in Chemistry, 119–30. Berlin, Heidelberg: Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/978-3-642-45591-9_10.

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Davies, A. G. "17.3.2 Radical cations of other cycloalkanes." In Phosphorus-Centered Radicals, Radicals Centered on Other Heteroatoms, Organic Radical Ions. Part 2, 223–36. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-87641-0_24.

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Conference papers on the topic "Cycloalkanes"

1

Otto, Jessica, Evan Davison, and Randy Maglinao. "Synthesis of Cycloalkanes from Lignocellulosic Platform." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/qbeo2379.

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Abstract: Catalytic hydrodeoxygenation of biooil is instrumental in producing sustainable aviation fuels, specifically cycloalkanes, from lignocellulosic materials. Cycloalkanes typically have higher energy densities, lower freeze points and higher flash points than conventional jet fuel. In our study, we compared hydrodeoxygenation of p-cresol using Pd/C and tandem hydrogenation-dehydration using Pd/C for hydrogenation and heteropolyacid on alumina catalyst for dehydration. All of the hydrodeoxygenation and hydrogenation trials were ran at 250°C and 600 psi of hydrogen gas while dehydration t

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Haoer, R. S., K. A. Atan, A. M. Khalaf, and R. Hasni. "Eccentric connectivity index of unicyclic graphs with application to cycloalkanes." In 2015 International Conference on Research and Education in Mathematics (ICREM7). IEEE, 2015. http://dx.doi.org/10.1109/icrem.2015.7357055.

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Panaye, A., J. P. Doucet, E. Feuilleaubois, and S. Rahali El Azzouzi. "Neuromimetic approach to 13C NMR shifts prediction for methyl substituted cycloalkanes." In The first European conference on computational chemistry (E.C.C.C.1). AIP, 1995. http://dx.doi.org/10.1063/1.47784.

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Beteringhe, Adrian, and Ion Sima. "A new chemometric tool to predict the boiling points of some cycloalkanes." In 2016 8th International Conference on Electronics, Computers and Artificial Intelligence (ECAI). IEEE, 2016. http://dx.doi.org/10.1109/ecai.2016.7861154.

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"Renewable jet fuel range cycloalkanes from integrated catalytic processes of lignocellulosic biomass." In 2015 ASABE International Meeting. American Society of Agricultural and Biological Engineers, 2015. http://dx.doi.org/10.13031/aim.20152189641.

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Bellan, Josette R., and Panayotis Kourdis. "A Unified Reduction of Elementary Kinetic Mechanisms for n-Alkanes, Highly-Branched Alkanes and Cycloalkanes." In 55th AIAA Aerospace Sciences Meeting. Reston, Virginia: American Institute of Aeronautics and Astronautics, 2017. http://dx.doi.org/10.2514/6.2017-0834.

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Matveev, S. S., D. V. Idrisov, and A. S. Semenikhin. "LAMINAR BURNING VELOCITY OF INDIVIDUAL HYDROCARBONS AND KEROSENE SURROGATES." In 9TH INTERNATIONAL SYMPOSIUM ON NONEQUILIBRIUM PROCESSES, PLASMA, COMBUSTION, AND ATMOSPHERIC PHENOMENA. TORUS PRESS, 2020. http://dx.doi.org/10.30826/nepcap9a-25.

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Surrogate fuel blends are often used in laboratory experiments and in combustion modeling to reproduce important characteristics of real transportation fuels. Fuel surrogates usually consist of a few class-representative hydrocarbons such as normal and branched alkanes, aromatics, and cycloalkanes. The complexity of a particular blend depends on the number of combustion properties (targets) taken into account. Most often, binary [1] and ternary blends were suggested as kerosene surrogates; yet, in some cases, a single species, n-decane [2], was used to make comparison with kerosene combustion

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Carpani, Giovanna, Ilaria Pietrini, Massimiliano Baric, Francesca D'Ambrosi, Carlo Alberto Cova, Jahanzaib Akhtar, and Melania Buffagni. "Bioremediation of Cutting Pits by Autochtonous Bacteria-Fungi Consortia." In Abu Dhabi International Petroleum Exhibition & Conference. SPE, 2021. http://dx.doi.org/10.2118/207921-ms.

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Abstract The aim of this work is to verify the potential of a consortium of autochthonous bacteria and fungi, isolated from samples of contaminated soils and water collected in a site containing cutting pits muds, in order to evaluate enhancing in biodegradation of hydrocarbons content. This innovative technique would take advantage of the synergistic effect of bacteria and fungi. In addition, this technique would allow to avoid the introduction of commercial allochthonous microflora for soil remediation and the use of chemical products for tool cleaning. Samples retrieved from a production si

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Dagaut, P., A. Mze´-Ahmed, K. Hadj-Ali, and P. Die´vart. "Synthetic Jet Fuel Combustion: Experimental and Kinetic Modeling Study." In ASME 2011 Turbo Expo: Turbine Technical Conference and Exposition. ASMEDC, 2011. http://dx.doi.org/10.1115/gt2011-45234.

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Fischer-Tropsch liquid fuels synthesized from syngas, also called synthetic paraffinic jet fuel (SPK), can be used to replace conventional petroleum-derived fuels in jet engines. Whereas currently syngas is mostly produced from coal of natural gas, its production from biomass has been reported. These synthetic liquid fuels contain a very high fraction of iso-alkanes, while conventional jet fuels contain large fractions of n-alkanes, cycloalkanes (naphtenes), and aromatics. In that contest, a jet-stirred reactor (JSR) was used to study the kinetics of oxidation of a 100% SPK and a 50/50 SPK/Jet

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Masmui, Neneng Windayani, Ferli Septi Irwansyah, and Efa Nur Asyiah. "Making Augmented Reality Learning Media In Conformation of Alkane and Cycloalkane Concepts." In 2019 IEEE 5th International Conference on Wireless and Telematics (ICWT). IEEE, 2019. http://dx.doi.org/10.1109/icwt47785.2019.8978227.

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