Relevant bibliographies by topics / Hexachloro-1

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

Academic literature on the topic 'Hexachloro-1'

Author: Grafiati
Published: 4 June 2021
Last updated: 8 February 2022

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Journal articles on the topic "Hexachloro-1"

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Jelínek, T., J. Fábry, L. Hummel, K. Malý, and V. Petříček. "Structure of tetramethylammonium 7,8,9,10,11,12-hexachloro-1,2,3,4,5,6-hexahydro-1-carba-closo-dodecaborate(1–)." Acta Crystallographica Section C Crystal Structure Communications 47, no. 5 (1991): 993–95. http://dx.doi.org/10.1107/s0108270190009210.

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Lock, Edward A., Iona S. Pratt, and John Ishmael. "Hexachloro-1, 3-butadiene-induced hydropic change in mouse liver." Journal of Applied Toxicology 5, no. 2 (1985): 74–79. http://dx.doi.org/10.1002/jat.2550050207.

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Apblett, Allen, Tristram Chivers, James F. Fait, and Rainer Vollmerhaus. "Negative hyperconjugation in hexachloro-3-cyclopentenylaminosulphenyl halides: Preparation and X-ray structure of C5Cl6NSBr and synthesis of C5Cl6NS+AsF6−." Canadian Journal of Chemistry 69, no. 6 (1991): 1022–27. http://dx.doi.org/10.1139/v91-150.

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The reaction of hexachlorocyclopentadiene with (NSCl)3 at 65 °C in the absence of a solvent produced hexachloro-3-cyclopentenylidenaminosulfenyl chloride, C5Cl6NSCl, in good yield. The derivatives C5Cl6NSX(X = Br, I, C5Cl6N, NPr2i, Ph) were prepared by treatment of C5Cl6NSCl with Me3SiBr, Me3SiI, Ph3Sb, iPr2NH, and Ph2Hg, respectively. The crystal structure of C5Cl6NSBr was determined by X-ray crystallography. Crystals of C5Cl6NSBr are triclinic, space group [Formula: see text] with a = 9.626(2), b = 9.810(2), c = 13.736(2) Å, α = 79.68(1), β = 88.62(1), γ = 74.73(1)°, Z = 4, final R and Rw va
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Herberhold, Max, Christine Dörnhöfer, and Ulf Thewalt. "Ferrocen-1,1′-dithiolato- und -diselenato-Derivate des Hexachlor-cyclotriphosphazens / Ferrocene-1,1′-dithiolato and -diselenato Derivatives of Hexachloro-cyclotriphosphazene." Zeitschrift für Naturforschung B 45, no. 6 (1990): 741–46. http://dx.doi.org/10.1515/znb-1990-0603.

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The three pairs of geminal chloro substituents in hexachloro-cyclotriphosphazene, N3P3Cl6, are stepwise replaced by chelating ferrocene-1,1′-dichalcogenato groups, [Fe(C5H4E)2.]2-, to give the spiro-cyclotriphosphazenes N3P3Cl6-2n[(EC5H4)2Fe]n (n = 1, 2, 3; E = S (a), Se (b)). The molecular structure of P,P′-bis(ferrocene-1,1′-dithiolato)-P″-dichlorocyclotriphosphazene, N3P3Cl,[(SC5H4)2Fe]2(2a) has been determined.
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AVDEENKO, A. P., and A. L. YUSINA. "ChemInform Abstract: Some Reactions of 4-Arylsulfonylimino-2,3,5,5,6,6-hexachloro-2- cyclohexen-1-ones." ChemInform 25, no. 31 (2010): no. http://dx.doi.org/10.1002/chin.199431115.

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Balde, L., R. Julien, and G. Morgant. "Crystal structure of 5-azoniaoctane-1,8-diammonium hexachloro tellurate(IV)-hydrogen chloride (1/1), (TeCl6)(C7N3H21) · HCl." Zeitschrift für Kristallographie - New Crystal Structures 216, no. 1-4 (2001): 239–40. http://dx.doi.org/10.1524/ncrs.2001.216.14.239.

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Kirby, Gordon M., and Peter H. Bach. "Enhanced Hexachloro-1:3-butadiene Nephrotoxicity in Rats with a Preexisting Adriamycin-Induced Nephrotic Syndrome." Toxicologic Pathology 23, no. 3 (1995): 303–12. http://dx.doi.org/10.1177/019262339502300307.

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Oesch, Franz, and C. Roland Wolf. "Properties of the microsomal and cytosolic glutathione transferases involved in hexachloro-1:3-butadiene conjugation." Biochemical Pharmacology 38, no. 2 (1989): 353–59. http://dx.doi.org/10.1016/0006-2952(89)90049-x.

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Ketchersid, Mary L., Frederick W. Plapp, and Morris G. Merkle. "Sorghum (Sorghum bicolor) Seed Safeners as Insecticide Synergists." Weed Science 33, no. 6 (1985): 774–78. http://dx.doi.org/10.1017/s0043174500083338.

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Certain oximes, including cyometrinil [(Z)-α-(cyanomethoxy)iminobenzeneacetonitrile], CGA-92194 [N-(1,3-dioxolan-2-yl-methoxy)-iminobenzeneacetonitrile], 2-pyridinealdoxime-O-benzyl ether (PA-B), and 2-pyridinealdoxime-O-phenethyl ether (PA-PE), which are known to protect sorghum from chloroacetanilide herbicides, increased the toxicity of the insecticide propoxur (o-isopropoxyphenyl-methyl carbamate) to a resistant strain of housefly (Musca domesticaL.). Flurazole [5-thiazolecarboxylic acid, benzyl ester, 2-chloro-4-(trifluoromethyl)], a nonoxime protectant for grain sorghum, had less effect
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Golinske, Dirk, and Jürgen Voss. "Electroreduction of Organic Compounds, 35. Quantum Chemical Calculations of Reaction Pathways for the Cathodic Dehalogenation of Chlorodibenzofurans and Oligochlorobenzenes." Zeitschrift für Naturforschung B 60, no. 7 (2005): 780–86. http://dx.doi.org/10.1515/znb-2005-0714.

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Quantum chemical (DFT) calculations on the course of the electroreductive carboxylation of chloroarenes were performed. An explanation for the extraordinary behaviour of 2- chlorodibenzofuran (2) as compared with the corresponding 1-chloro, 3-chloro and 4-chloro derivatives was sought for and was found in the particular reaction coordinate of 2 and in the SOMO spin density distributions of the four isomers. In the same way, the regioselectivity in the formation of dicarboxylic acids from hexachloro- and 1,2,4,5-tetrachlorobenzene was investigated by DFT-MO calculations and was shown to be due
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Dissertations / Theses on the topic "Hexachloro-1"

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au, D. James@murdoch edu, and Donny Lawrence James. "Biochemical Dechlorination of Hexachloro-1,3-butadiene." Murdoch University, 2010. http://wwwlib.murdoch.edu.au/adt/browse/view/adt-MU20100216.212048.

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Hexachloro-1,3-butadiene (HCBD) is a toxic aliphatic chlorinated hydrocarbon which is widely used as a fungicide, herbicide and heat transformer fluid. HCBD is resistant to microbial degradation and, therefore, persists in aquatic and soil environments worldwide. In this thesis, the ability of non-specific bacteria from various sources to dechlorinate HCBD in the presence of either acetate or lactate (as an electron donor) and cyanocobalamin (as an electron shuttle) under different conditions was investigated. Cultivating specific populations to reduce cyanocobalamin as a method to increase HC
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Book chapters on the topic "Hexachloro-1"

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Winkelmann, J. "Diffusion of hexachloro-benzene (1); carbon dioxide (2)." In Gases in Gases, Liquids and their Mixtures. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-49718-9_120.

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Gartland, Kevin P. R., F. W. Bonner, and J. K. Nicholson. "Application of 1H NMR Urinalysis to the Examination of Nephrotoxic Lesions Induced by Mercuric Chloride, Hexachloro-1, 3-Butadiene, and Propyleneimine." In Nephrotoxicity. Springer US, 1989. http://dx.doi.org/10.1007/978-1-4757-2040-2_79.

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Yang, Raymond S. H. "Hexachloro-1,3-Butadiene: Toxicology, Metabolism, and Mechanisms of Toxicity." In Reviews of Environmental Contamination and Toxicology. Springer New York, 1988. http://dx.doi.org/10.1007/978-1-4612-3770-9_4.

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Jordanov, Svetomir Hadzi. "How to Remediate Pollution with Mercury and Hexachloro-Cyclohexane Residues in a Chemical Plant." In Methods and Techniques for Cleaning-up Contaminated Sites. Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-6875-1_9.

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Conference papers on the topic "Hexachloro-1"

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Yeh, W. C., R. Ishihara, S. Morishita, and M. Matsumura. "Low-Temperature Chemical-Vapor-Deposition of Silicon-Nitride Film from Hexachloro-Disilane and Hydrazine." In 1995 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 1995. http://dx.doi.org/10.7567/ssdm.1995.pa-1-4.

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You might also be interested in the extended bibliographies on the topic 'Hexachloro-1' for particular source types:
Journal articles
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