Relevant bibliographies by topics / Methyl cyanide

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Methyl cyanide'

Author: Grafiati
Published: 4 June 2021
Last updated: 16 February 2022

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Journal articles on the topic "Methyl cyanide"

1

Schneider, J., V. Bürger, and F. Arnold. "Methyl cyanide and hydrogen cyanide measurements in the lower stratosphere: Implications for methyl cyanide sources and sinks." Journal of Geophysical Research: Atmospheres 102, no. D21 (1997): 25501–6. http://dx.doi.org/10.1029/97jd02364.

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Chen, You-Sheng, and Jian-Hong Zhang. "2-Methyl-3-nitrobenzyl cyanide." Acta Crystallographica Section E Structure Reports Online 65, no. 4 (2009): o767. http://dx.doi.org/10.1107/s1600536809008484.

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Dechamps, Noémie, Robert Flammang, Michaël Boulvin, et al. "Ion—Molecule Reactions Involving Methyl Isocyanide and Methyl Cyanide." European Journal of Mass Spectrometry 13, no. 6 (2007): 385–95. http://dx.doi.org/10.1255/ejms.896.

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de Meester, P., S. S. C. Chu, and J. E. Johnson. "(E)-O-Methyl-p-nitrobenzohydroximoyl cyanide." Acta Crystallographica Section C Crystal Structure Communications 42, no. 11 (1986): 1656–57. http://dx.doi.org/10.1107/s0108270186091084.

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Rosero, V., P. Hofner, S. Kurtz, J. Bieging, and E. D. Araya. "METHYL CYANIDE OBSERVATIONS TOWARD MASSIVE PROTOSTARS." Astrophysical Journal Supplement Series 207, no. 1 (2013): 12. http://dx.doi.org/10.1088/0067-0049/207/1/12.

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Green, Sheldon. "Collisional excitation of interstellar methyl cyanide." Astrophysical Journal 309 (October 1986): 331. http://dx.doi.org/10.1086/164605.

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Abd-Ei-Aziz, Alaa S., Debbie A. Armstrong, Shelly Bernardin, and Harold M. Hutton. "Nucleophilic addition to di- and poly-iron arene complex cations." Canadian Journal of Chemistry 74, no. 11 (1996): 2073–82. http://dx.doi.org/10.1139/v96-236.

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Hydride and cyanide addition to a series of di- and polycyclopentadienyliron arene complex cations with etheric bridges is described. Reaction of the di-iron complexes with sodium borohydride resulted in the formation of a number of adducts.p-Methyl- and o,o-dimethylphenoxybenzene cyclopentadienyliron complexes were used as models in this study to allow for the characterization of the analagous di-iron complexes. The use of HH COSY and CH COSY NMR techniques enabled us to identify the isomeric nature of these adducts. The hydride addition results indicated that the etheric substituent had the
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Arnold, Donald R., Kimberly A. McManus, and Mary S. W. Chan. "Photochemical nucleophile–olefin combination, aromatic substitution (photo-NOCAS) reaction, Part 13. The scope and limitations of the reaction with cyanide anion as the nucleophile." Canadian Journal of Chemistry 75, no. 8 (1997): 1055–75. http://dx.doi.org/10.1139/v97-126.

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The scope of the photochemical nucleophile–olefin combination, aromatic substitution (photo-NOCAS) reaction has been extended to include cyanide anion as the nucleophile. Highest yields of adducts were obtained when the alkene or diene has an oxidation potential less than ca. 1.5 V (SCE). No adducts were obtained from 2-methylpropene (9), oxidation potential 2.6 V. Oxidation of cyanide anion, by the radical cation of the alkene or diene, can compete with the combination. With the alkenes, 2,3-dimethyl-2-butene (2) and 2-methyl-2-butene (10), both nitriles and isonitriles were obtained; isonitr
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Noland, Wayland E., Ryan J. Herzig, Abigail J. Engwall, Renee C. Jensen, and Kenneth J. Tritch. "Crystal structures of methyl 3,5-dibromo-4-cyanobenzoate and methyl 3,5-dibromo-4-isocyanobenzoate." Acta Crystallographica Section E Crystallographic Communications 74, no. 3 (2018): 345–48. http://dx.doi.org/10.1107/s2056989018002256.

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The title crystals, C9H5Br2NO2, are the first reported 2,6-dihalophenyl cyanide–isocyanide pair that have neither three- nor two-dimensional isomorphism. Both crystals contain contacts between the carbonyl O atom and a Br atom. In the crystal of the cyanide,R22(10) inversion dimers form based on C[triple-bond]N...Br contacts, a common packing feature in this series of crystals. In the isocyanide, the corresponding N[triple-bond]C...Br contacts are not observed. Instead, the isocyano C atom forms contacts with the methoxy C atom. RNC was refined as a two-component pseudo-merohedral twin.
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French, Richard C., Peter T. Kujawski, and Gerald R. Leather. "Effect of Various Flavor-Related Compounds on Germination of Curly Dock Seed (Rumex crispus) and Curly Dock Rust (Uromyces rumicis)." Weed Science 34, no. 3 (1986): 398–402. http://dx.doi.org/10.1017/s0043174500067060.

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Chemicals that stimulate germination of curly dock seed (Rumex crispus L. # RUMCR) and urediniospores of curly dock rust [Uromyces rumicis Schum. (Wint.)], an obligate parasite of this weed, were studied and compared. Methyl salicylate, benzyl cyanide, and benzonitrile were the best stimulators of germination of curly dock seed. The compounds tested were most effective at concentrations ranging from 250 to 1000 μl/L. A 500 μl/L concentration of methyl salicylate caused 99% of the curly dock seed to germinate. Exposure to volatiles from 10 μl methyl salicylate or octyl cyanide for 16 to 24 h wa
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Dissertations / Theses on the topic "Methyl cyanide"

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Hajsaleh, Jamal Y. (Jamal Yousef). "An Experimental Study of Collision Broadening of some Excited Rotational States of the Bending Vibration of Methyl Cyanide." Thesis, University of North Texas, 1993. https://digital.library.unt.edu/ark:/67531/metadc278369/.

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A double modulation microwave spectrometer is used to evaluate the linewidth parameters for some excited rotational components in the bending vibration v_8 of 13CH3 13C 15N and 13CH3C15N isotopomers of methyl cyanide. The linewidth parameters for self-broadening of the ΔJ=2←1 rotational components for the ground v_8 , 1v_8, and the 2v_8 vibrations were determined over a pressure range of 1 to 13 mtorr and at a temperature of 300 K. The double modulation technique is used to explore the high eighth derivative of the line shape profile of the spectral line. This technique proved to give good sig
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Tam, Hungsze. "Microwave Spectra of ¹³C Isotopic Species of Methyl Cyanide in the Ground, v₈=1 and v₈=2 Vibrational States." Thesis, North Texas State University, 1988. https://digital.library.unt.edu/ark:/67531/metadc332039/.

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The problem of the quadrupole interaction occurring in a vibrating-rotating C₃v symmetric top molecule has been studied in detail. The quadrupole interaction has been treated as another perturbation term to a general frequency expression accounting for the vibrating-rotating interaction of the molecule so that a complete frequency formula is obtained for both interactions, and from which hyperfine spectral components are predicted and measured. The hyperfine transitions in the ground, and v₈=1 and v₈=2 excited vibrational states of the ¹³C isotopes of methyl cyanide have been investigated in t
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Andersson, Johan. "Odour Communication in Pieris Butterflies." Doctoral thesis, KTH, Chemistry, 2004. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-3699.

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Davies, Gillian Mary. "Degradation of cyanide and metal cyanides using fungi." Thesis, University of Oxford, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.393787.

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Al-Share, Mohammad A. (Mohammad Abdel). "Anomalous Behavior in the Rotational Spectra of the v₈=2 and the v₈=3 Vibrations for the ¹³C and ¹⁵N Tagged Isotopes of the CH₃CN Molecule in the Frequency Range 17-95 GHz." Thesis, University of North Texas, 1990. https://digital.library.unt.edu/ark:/67531/metadc330976/.

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The rotational microwave spectra of the three isotopes (^13CH_3^12C^15N, ^12CH_3^13C^15N, and ^13CH_3^13C^15N) of the methyl cyanide molecule in the v_8=3, v_8=2, v_7=1 and v_4=1 vibrational energy levels for the rotational components 1£J£5 (for a range of frequency 17-95 GHz.) were experimentally and theoretically examined. Rotational components in each vibration were measured to determine the mutual interactions in each vibration between any of the vibrational levels investigated. The method of isotopic substitution was employed for internal tuning of each vibrational level by single and do
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Murtazina, Rushana. "Pheromone production in the butterfly Pieris napi L." Doctoral thesis, KTH, Organisk kemi, 2014. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-142551.

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Aphrodisiac and anti-aphrodisiac pheromone production and composition in the green-veined white butterfly Pieris napi L. were investigated. Aphrodisiac pheromone biosynthesis had different time constraints in butterflies from the diapausing and directly developing generations. Effects of stable isotope incorporation in adult butterfly pheromone, in the nectar and flower volatiles of  host plants from labeled substrates were measured by solid phase microextraction and gas chromatography–mass spectrometry. A method to fertilize plants with stable isotopes was developed and found to be an effecti
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Le, Breton Michael Robert. "Airborne measurements of trace gases using a Chemical Ionisation Mass Spectrometer (CIMS) onboard the FAAM BAe-146 research aircraft." Thesis, University of Manchester, 2013. https://www.research.manchester.ac.uk/portal/en/theses/airborne-measurements-of-trace-gases-using-a-chemical-ionisation-mass-spectrometer-cims-onboard-the-faam-bae146-research-aircraft(84308915-6dae-46d8-acb6-f189683e3e6d).html.

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A chemical ionisation mass spectrometer (CIMS) was developed and utilised for measurements onboard the Facility for Atmospheric Airborne Measurements (FAAM) BAe-146 aircraft. The I- ionisation scheme was implemented to detect nitric acid (HNO3), formic acid (HC(O)OH), hydrogen cyanide (HCN) and dinitrogen pentoxide (N2O5) simultaneously at a sampling frequency of 1 Hz. Sensitivities ranged from 35±6 ion counts pptv-1 s-1 for HC(O)OH to 4±0.9 ion counts pptv-1 s-1 for HCN and limits of detection from 37 ppt for HNO3 and 5 ppt for HCN. Trace gas concentrations of species such as HC(O)OH are curr
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Kotdawala, Rasesh R. "Adsorption studies of hazardous air pollutants in microporous adsorbents using statistical mechanical and molecular simulation techniques." Worcester, Mass. : Worcester Polytechnic Institute, 2007. http://www.wpi.edu/Pubs/ETD/Available/etd-050407-112429/.

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Dissertation (Ph.D.) -- Worcester Polytechnic Institute.<br>Keywords: Activated carbons; Hydrogen cyanide; Methyl ethyl ketone; Adsorption; Mercury; Monte-Carlo; Solvents; Molecular simulations; Zeolites; Water; Methanol; Nanopores. Includes bibliographical references (leaves 147-150).
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Wood, Andrew John. "Mixed-metal complexes incorporating redox-active cyanomanganese ligands." Thesis, University of Bristol, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.311404.

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Cairns, Andrew B. "Mechanical and configurational degeneracy in transition metal cyanide materials." Thesis, University of Oxford, 2015. https://ora.ox.ac.uk/objects/uuid:49948a4e-4fde-403b-aef8-301227893856.

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Molecular framework materials - materials constructed like atomic scaffolding where anionic polyatomic linkers join cationic metal nodes - have great currency in contemporary functional material design. In this thesis the structures and properties of transition metal cyanides are investigated, focusing on the impact of mechanical and configurational degeneracy. These related phenomena give rise to materials with unusual and extreme negative mechanical responses on the one hand, and exotic structural states on the other. The mechanical response of primary interest here is negative linear compre
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Books on the topic "Methyl cyanide"

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Occupational Medicine and Hygiene Laboratory. Hydrogen cyanide in air: Laboratory method using an ion-selective electrode. Health and Safety Executive, 1990.

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2

Pohlandt-Watson, C. A revised ion-chromatographic method for the determination of free cyanide. Council for Mineral Technology, 1986.

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Pohlandt-Watson, C. A simplified flow-injection method for the determination of free cyanide in process solutions. Council for Mineral Technology, 1986.

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Pohlandt-Watson, C. The determination, by ion-interaction chromatography, of sulphur species in cyanide solutions, laboratory method no. 16/30. Council for Mineral Technology, 1988.

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K, Palmer S. A., ed. Metal/cyanide-containing wastes: Treatment technologies. Noyes Data Corp., 1988.

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Breton, M. A., T. J. Nunno, D. M. Sullivan, and N. F. Surprenant. Metal Cyanide-Containing Wastes: Treatment Technologies (Pollution Technology Review). Noyes Pubns, 1988.

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Coppola, Silvia, and Franco Valenza. Inhalation injury in the ICU. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199600830.003.0107.

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Inhalation injury represents one of the most serious associated injuries complicating the care of thermally-injured patient. It can result in severe respiratory failure and acute respiratory distress syndrome (ARDS) by three mechanisms—thermal or chemical injury, and impairment of systemic oxygen supply. Thermal injury can cause erythema, ulceration, and progressive, life-threatening oedema, particularly of the upper airways. Chemical injury is due to irritants or cytotoxic compounds, and depends on the material burned, the temperature of the fire, and the amount of oxygen present in the fire
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O'Brien, James. The Scientific Sherlock Holmes. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199794966.001.0001.

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One of the most popular and widely known characters in all of fiction, Sherlock Holmes has an enduring appeal based largely on his uncanny ability to make the most remarkable deductions from the most mundane facts. The very first words that Sherlock Holmes ever says to Dr. Watson are, "How are you? You have been in Afghanistan, I perceive." Watson responds, "How on earth did you know that?" And so a crime-solving legend is born. In The Scientific Sherlock Holmes, James O'Brien provides an in-depth look at Holmes's use of science in his investigations. Indeed, one reason for Holmes's appeal is
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Book chapters on the topic "Methyl cyanide"

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Rodrigues, Marco Antônio Siqueira, Luciano Marder, Andréa Moura Bernardes, and Jane Zoppas Ferreira. "Electrodialysis Treatment of Metal-Cyanide Complexes." In Electrodialysis and Water Reuse. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-40249-4_11.

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Dunbar, Kim R., and Robert A. Heintz. "Chemistry of Transition Metal Cyanide Compounds: Modern Perspectives." In Progress in Inorganic Chemistry. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470166468.ch4.

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Ferbinteanu, Marilena, Fanica Cimpoesu, and Stefania Tanase. "Metal-Organic Frameworks with d–f Cyanide Bridges: Structural Diversity, Bonding Regime, and Magnetism." In Lanthanide Metal-Organic Frameworks. Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/430_2014_156.

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Sebastian, Joby, and Darbha Srinivas. "Double-Metal Cyanide Catalyst Design in CO2/Epoxide Copolymerization." In Sustainable Polymers from Biomass. Wiley-VCH Verlag GmbH & Co. KGaA, 2017. http://dx.doi.org/10.1002/9783527340200.ch13.

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Peters, John W. "6. Carbon Monoxide and Cyanide Ligands in the Active Site of [FeFe]-Hydrogenases." In Metal-Carbon Bonds in Enzymes and Cofactors. Royal Society of Chemistry, 2009. http://dx.doi.org/10.1039/9781847559333-00179.

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Sosa-Torres, Martha E., and Peter M. H. Kroneck. "10. Interaction of Cyanide with Enzymes Containing Vanadium, Manganese, Non-Heme Iron, and Zinc." In Metal-Carbon Bonds in Enzymes and Cofactors. Royal Society of Chemistry, 2009. http://dx.doi.org/10.1039/9781847559333-00363.

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Zhang, Yan, Qian Li, Xiaoliang Liu, et al. "Mechanism of Intensifying Cyanide Leaching of Gold from a Calcine by the Pretreatment of Acid or Alkali Washing." In Rare Metal Technology 2017. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-51085-9_15.

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Atanasov, Mihail, and Peter Comba. "Magnetic Anisotropy in Cyanide Complexes of First Row Transition Metal Ions." In Structure and Function. Springer Netherlands, 2009. http://dx.doi.org/10.1007/978-90-481-2888-4_3.

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Lukey, Grant C., and Jannie S. J. van Deventer. "Fundamental Developments in Understanding the Interactions Between Metal Cyanides and Functional Polymers." In Fundamentals and Applications of Anion Separations. Springer US, 2004. http://dx.doi.org/10.1007/978-1-4419-8973-4_12.

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Barrezueta-Delgado, Erika, Naysha Blas-Trujillo, Yaneth Vasquez-Olivera, Carlos Raymundo, Nestor Mamani-Macedo, and Javier M. Moguerza. "A Cyanide Tailings Management Method Using Pseudomonas Fluorescens to Improve Conventional Treatments for Progressive Closure at Small Gold Mines." In Advances in Intelligent Systems and Computing. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-50791-6_42.

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Conference papers on the topic "Methyl cyanide"

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McMillan, James, Frank De Lucia, and Christopher Neese. "THE COMPLETE, TEMPERATURE RESOLVED SPECTRUM OF METHYL CYANIDE BETWEEN 200 AND 277 GHZ." In 71st International Symposium on Molecular Spectroscopy. University of Illinois at Urbana-Champaign, 2016. http://dx.doi.org/10.15278/isms.2016.th06.

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Manteca-Diego, C., J. Domenech, and G. Domenech-Manteca. "Synthesis and Applications of Methyl Cyanide Addition Compound of Boron Trichloride, Donor-Aceptor Bonding." In FRONTIERS OF FUNDAMENTAL PHYSICS: Eighth International Symposium FFP8. AIP, 2007. http://dx.doi.org/10.1063/1.2737029.

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Farquharson, Stuart, Alan Gift, Paul Maksymiuk, Frank E. Inscore, and Wayne W. Smith. "pH dependence of methyl phosphonic acid, dipicolinic acid, and cyanide by surface-enhanced Raman spectroscopy." In Optical Technologies for Industrial, Environmental, and Biological Sensing, edited by Arthur J. Sedlacek III, Richard Colton, and Tuan Vo-Dinh. SPIE, 2004. http://dx.doi.org/10.1117/12.510626.

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Schwaab, G. W. "TuFIR: self-broadening measurements on methyl cyanide in the frequency range from 770 GHz to 1300 GHz." In 15th International Conference on Infrared and Millimeter Waves. SPIE, 1990. http://dx.doi.org/10.1117/12.2301652.

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Manteca-Diego, Consolación, Jezabel Doménech, and Gumer F. Doménech-Manteca. "Spectroscopy Study (IR, 1HNMR, 13C-NMR, MS) of Methyl Cyanide Addition Compound of Boron Trichloride. Donor-Aceptor Bonding and Applications." In FRONTIERS OF FUNDAMENTAL PHYSICS: Eighth International Symposium FFP8. AIP, 2007. http://dx.doi.org/10.1063/1.2737009.

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Müller, Holger, Robert Sams, Isabelle Kleiner, et al. "ROTATIONAL SPECTROSCOPY AS A TOOL TO INVESTIGATE INTERACTIONS BETWEEN VIBRATIONAL POLYADS IN SYMMETRIC TOP MOLECULES: LOW-LYING STATES v8 ≤ 2 OF METHYL CYANIDE." In 70th International Symposium on Molecular Spectroscopy. University of Illinois at Urbana-Champaign, 2015. http://dx.doi.org/10.15278/isms.2015.fb04.

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Dent, M. H., and W. R. Williamson. "Cyanide Plating with Closed Loop Recovery." In Annual Aerospace/Airline Plating and Metal Finishing Forum and Exposition. SAE International, 1985. http://dx.doi.org/10.4271/850707.

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Herlacher, Martin F., and F. Robert McGregor. "Photozone Destruction of Cyanide Waste at Tinker AFB (Pilot Plant Results)." In Annual Aerospace/Airline Plating and Metal Finishing Forum and Exposition. SAE International, 1987. http://dx.doi.org/10.4271/870746.

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Reichmann, L., and L. Dobson. "360. Development of an Automated, Pyridine-Free Method for Aerosol Cyanide Compounds and Hydrogen Cyanide Vapor." In AIHce 2000. AIHA, 2000. http://dx.doi.org/10.3320/1.2763710.

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Aiba, Akihiro, Kazumi Kawamura, and Masashi Kumagai. "Novel Cyanide Free Electroless Au Plating for the Reliable Joint Between Ni-P/Au and Sn-Ag-Cu Based Lead Free Solder." In ASME 2005 Pacific Rim Technical Conference and Exhibition on Integration and Packaging of MEMS, NEMS, and Electronic Systems collocated with the ASME 2005 Heat Transfer Summer Conference. ASMEDC, 2005. http://dx.doi.org/10.1115/ipack2005-73079.

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Novel cyanide free electroless Au plating with an excellent bath stability and the reliable joint with solder was developed. Although the Au plating solution was based on sulfurous acid, the solution’s stability turned out to be excellent by the effective complexing force of the novel additives. The bath stood working without any precipitations for more than 3 metal turnovers. Since the displacement reaction between Ni-P and Au took place in the mild and the uniform way by the aid of the additives involved, resulting in the uniform and the fine grain structure of the plated film, almost no pin
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