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Journal articles on the topic 'Dithionates'

Author: Grafiati

Published: 4 June 2021

Last updated: 31 July 2024

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1

Bogushevich, S. E., I. I. Ugolev, and A. K. Potapovich. "Investigation of dosimetric properties of barium and strontium dithionates." Journal of Applied Spectroscopy 65, no. 3 (1998): 385–89. http://dx.doi.org/10.1007/bf02675457.

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2

Lund, E., H. Gustafsson, M. Danilczuk, et al. "Formates and dithionates: sensitive EPR-dosimeter materials for radiation therapy." Applied Radiation and Isotopes 62, no. 2 (2005): 317–24. http://dx.doi.org/10.1016/j.apradiso.2004.08.015.

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3

Fawcett, John, Andrew W. G. Platt, and David R. Russell. "Synthesis, structure and properties of lanthanide dithionates and their triphenylphosphine oxide complexes." Inorganica Chimica Acta 274, no. 2 (1998): 177–83. http://dx.doi.org/10.1016/s0020-1693(97)06045-3.

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4

Gustafsson, H., M. Danilczuk, M. D. Sastry, A. Lund, and E. Lund. "Enhanced sensitivity of lithium dithionates doped with rhodium and nickel for EPR dosimetry." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 62, no. 1-3 (2005): 614–20. http://dx.doi.org/10.1016/j.saa.2005.01.024.

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5

Haussühl, S. "Elastic properties of the dithionates Na2S2O6 · 2 H2O, K2S2O6, Rb2S2O6, CaS2O6 · 4H2O and SrS2O6 · 4 H2O." Crystal Research and Technology 29, no. 1 (1994): 119–24. http://dx.doi.org/10.1002/crat.2170290126.

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6

Lulu, Mekdes, Bekele Lemma, and Asmare Melese. "Phosphorous Sorption Characteristics of Soils in Smallholding Land Use in Southern Ethiopia." Applied and Environmental Soil Science 2022 (October 26, 2022): 1–9. http://dx.doi.org/10.1155/2022/6319739.

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Purpose. This study evaluated the P sorption characteristics of soils under smallholding land use in Wolaita Zone, Southern Ethiopia. Methods. Soil samples (0–20 cm) were collected from each of the home garden, grazing land, cropland, and woodlot in three replications at two sites and analyzed for P sorption isotherm data and selected soil properties. Results. The P sorption data were generated by equilibration with P solutions and the data were fitted with the Freundlich model (r2 = 0.88–0.98, SE = 0.16–0.24) and Langmuir model (r2 = 0.81–0.98, SE = 0.45–1.71). The Langmuir P sorption maximum

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7

Harrison, William T. A., and M. John Plater. "An unexpected oxidation: NaK5Cl2(S2O6)2revisited." Acta Crystallographica Section E Crystallographic Communications 73, no. 2 (2017): 188–91. http://dx.doi.org/10.1107/s2056989017000494.

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The title compound, NaK5Cl2(S2O6)2[systematic name: sodium pentapotassium dichloride bis(dithionate)], arose as an unexpected product from an organic synthesis that used dithionite (S2O42−) ions as a reducing agent to destroy excess permanganate ions. Compared to the previous study [Stanley (1953).Acta Cryst.6, 187–196], the present tetragonal structure exhibits a root 2a× root 2a×csuper-cell due to subtle changes in the orientations of the dithionate anions. The structure can be visualized as a three-dimensional framework of [001] columns of alternatingtrans-NaO4Cl2and KO4Cl2octahedra cross-l

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8

Platt, Andrew W. G., John Fawcett, Robert S. Hughes, and David R. Russell. "Complexes of lanthanide dithionates 2. Electrospray mass spectrometry of Ln2(S2O6)3 and their Ph3PO complexes; the X-ray crystal structure of Pr2(S2O6)3(Ph3PO)6(H2O)6." Inorganica Chimica Acta 295, no. 2 (1999): 146–52. http://dx.doi.org/10.1016/s0020-1693(99)00344-8.

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9

Rusanova, Julia A., Volodymyr N. Kokozay, Svitlana Petrusenko, and Nataliya Plyuta. "Synthesis and crystal structure of a solvated Co^III complex with 2-hydroxy-3-methoxybenzaldehyde thiosemicarbazone ligands." Acta Crystallographica Section E Crystallographic Communications 77, no. 11 (2021): 1130–34. http://dx.doi.org/10.1107/s2056989021010616.

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The title CoIII complex, bis[bis(2-hydroxy-3-methoxybenzaldehyde thiosemicarbazonato)cobalt(III)] dithionate–dimethylformamide–methanol (1/4/3), [Co(C9H10N3O2S)2]2(S2O6)·4C3H7NO·3CH3OH, with monodeprotonated 2-hydroxy-3-methoxybenzaldehyde thiosemicarbazone as ligands crystallizes in the space group P\overline{1}. The asymmetric unit consists of two mononuclear [CoL 2]+ cations, one dithionate anion (S2O6)2− as counter-anion and seven solvate molecules (four dimethylmethanamide and three methanol). Each CoIII ion has a moderately distorted octahedral S2N2O2 geometry. In the crystal, the compon

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10

Warneck, Peter. "The oxidation of sulfur(iv) by reaction with iron(iii): a critical review and data analysis." Physical Chemistry Chemical Physics 20, no. 6 (2018): 4020–37. http://dx.doi.org/10.1039/c7cp07584g.

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11

Ortiz-Rodríguez, Luis A., Sean J. Hoehn, Chris Acquah, Nadia Abbass, Lidia Waidmann, and Carlos E. Crespo-Hernández. "Femtosecond intersystem crossing to the reactive triplet state of the 2,6-dithiopurine skin cancer photosensitizer." Physical Chemistry Chemical Physics 23, no. 44 (2021): 25048–55. http://dx.doi.org/10.1039/d1cp04415j.

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This study elucidates the electronic relaxation mechanism leading to the population of the reactive triplet state in 2,6-dithiopurine; the most effective dithionated nucleobase skin cancer photosensitizer agent reported thus far.

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12

Kim, Yang, Brian W. Skelton та Allan H. White. "catena-Poly[[trans-bis(ethane-1,2-diamine-κ2N,N′)copper(II)]-μ-dithionato-κ2O:O′] andtrans-diaquabis(propane-1,3-diamine-κ2N,N′)copper(II) dithionate". Acta Crystallographica Section C Crystal Structure Communications 59, № 12 (2003): m546—m548. http://dx.doi.org/10.1107/s0108270103025447.

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13

Uzoho, Bethel, Nnaemeka Okoli, and Ugochi Ekwugha. "Impact of Texture on Sesquioxide Distribution in Southeastern Nigerian Soils." International Journal of Environment 8, no. 1 (2019): 43–58. http://dx.doi.org/10.3126/ije.v8i1.23148.

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Sesquioxides which play significant roles in soil classification and dominant soil properties vary in soils with particle size fractions. Using randomized complete block design, this study was conducted in the month of June 2018 to evaluate the impact of texture on sesquioxide distribution in humid rainforest soils of Southeastern Nigeria. Four mini-pedons were dug at four landscape positions (upslope, midslope, downslope and flat surface) and triplicate soil samples taken from 0-20, 20-40 and 40-60 cm depths, summing to total of 36 samples. Crystalline and amorphous Al, Fe, Mn and Si oxides w

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14

Qu, Bing, Lin Deng, Biao Deng, Kejie He, Bing Liao, and Shijun Su. "Oxidation kinetics of dithionate compound in the leaching process of manganese dioxide with manganese dithionate." Reaction Kinetics, Mechanisms and Catalysis 123, no. 2 (2017): 743–55. http://dx.doi.org/10.1007/s11144-017-1284-x.

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15

Yang, Lin, Cheng Wang, Lu Yao, Wenju Jiang, Xia Jiang, and Jianjun Li. "Removal of manganous dithionate (MnS2O6) with MnO2 from the desulfurization manganese slurry." RSC Advances 10, no. 3 (2020): 1430–38. http://dx.doi.org/10.1039/c9ra09810k.

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The manganous dithionate by-product of the desulfurized slurry could be oxidized with MnO<sub>2</sub> without any impurity. σ-MnO<sub>2</sub> showed the best activity due to its high surface area and expose much more surface-active oxygen.

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16

Greatrex, Robert, and Duncan C. Munro. "Complex Formation by Dithionate(V) Ion†." Journal of Chemical Research, no. 3 (1997): 94–95. http://dx.doi.org/10.1039/a605479j.

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17

Baran, M. P., O. A. Bugay, S. P. Kolesnik, et al. "Barium dithionate as an EPR dosemeter." Radiation Protection Dosimetry 120, no. 1-4 (2006): 202–4. http://dx.doi.org/10.1093/rpd/nci531.

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18

Frank, Walter, Thomas Stetzer та Ludwig Heck. "Darstellung und Kristallstruktur von [(NH3)5Rh(H7O4)Rh(NH3)5](S2O6)2,5 · H2O (1). Ein gemischtes Aquopentamminrhodium(III)-hydroxopentamminrhodium(III)- dithionat mit einer neuartigen μ-H7O4-Struktureinheit / Preparation and Crystal Structure of [(NH3)5Rh(H7O4)Rh(NH3)5](S2O6)2,5 · H2O (1). A Mixed Aquopentaamminerhodium(III)-hydroxopentaamminerhodium(III) Dithionate with a Novel μ-H7O4 Structural Unit". Zeitschrift für Naturforschung B 43, № 2 (1988): 189–95. http://dx.doi.org/10.1515/znb-1988-0210.

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The title compound 1 can be obtained from an aqueous solution of aquopentaammine rhodium(III) dithionate and hydroxopentaammine rhodium(III) dithionate. The crystal structure has been determined from single crystal X-ray diffraction data and refined to R = 0.035 for 4390 unique reflections. Crystal data: monoclinic, space group P21/c, a = 1300.9(5) pm. b = 1472.3(6) pm. c = 1478.8(9) pm, β = 106.20(4)°, Z = 4.In the crystal dinuclear rhodium cations with point group symmetry 1 (C1) are found. A central μ-H3O2-bridge is formed by strong hydrogen bonding between aquo and hydroxo ligands; this br

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19

Burrow, Robert A., and Rafael Duarte. "Hydrogen bond nets in dithionate metal salt crystals." Acta Crystallographica Section A Foundations and Advances 75, a1 (2019): a332. http://dx.doi.org/10.1107/s0108767319096764.

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20

de Matos Gomes, E. "Crystal structures of strontium and lead dithionate tetrahydrate." Acta Crystallographica Section B Structural Science 47, no. 1 (1991): 12–17. http://dx.doi.org/10.1107/s0108768190010412.

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21

Onischuk, V. A., J. de Boer, A. I. Levon, et al. "RESPONSE OF ALANINE AND BARIUM DITHIONATE EPR DOSIMETERS." Health Physics 98, no. 2 (2010): 412–16. http://dx.doi.org/10.1097/01.hp.0000346704.78283.2b.

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22

Donlevy, TM, LR Gahan, TW Hambley, et al. "Synthesis, X-Ray Crystal Structure and Magnetic Studies of a Biscopper(II) Complex of a C-Spiro Binucleating Linear Octadentate Ligand." Australian Journal of Chemistry 43, no. 8 (1990): 1407. http://dx.doi.org/10.1071/ch9901407.

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Reaction of the binucleating ligand 5,5-bis(4-amino-2-thiabutyl)-3,7- dithianonane-1,9-diamine (L1) with a copper(II) salt in aqueous solution, and in the presence of lithium dithionate, results in the isolation of a dark blue crystalline solid identified as [Cu2(L1)](S2O6)2.4H2O. Crystals of the complex are triclinic, space group Pī , a 8.227(2), b 13.103(3), c 16.423(4) Ǻ, α 68.68(2), β 86.68(2), γ 75.50(2)°, Z 2, R 0.026 (5039 F). The structure consists of two copper(II) atoms each of which is coordinated through two thioether and two primary amine atoms. The two copper sites are linked thr

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23

Gomes, E. de Matos, J. Ortega, J. Etxebarria, F. J. Zúñiga, and T. Breczewski. "The crystal structure and optical activity of potassium dithionate,." Journal of Physics: Condensed Matter 8, no. 12 (1996): 2063–71. http://dx.doi.org/10.1088/0953-8984/8/12/018.

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24

Schindler, Manon, Nicolas Couvrat, Yohann Cartigny, Clément Brandel, and Gérard Coquerel. "Synthesis and Characterization of Sodium Dithionate and its Dihydrate." Chemical Engineering & Technology 42, no. 7 (2019): 1446–51. http://dx.doi.org/10.1002/ceat.201800705.

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25

Rumyantsev, V. V., S. A. Fedorov, K. V. Gumennyk, and A. Ye Rybalka. "GYROTROPY FEATURES OF AN IMPERFECT OPTICALLY ACTIVE 1D PHOTONIC ORIENTATIONALLY DISORDERED CRYSTAL." Journal of Applied Spectroscopy 89, no. 3 (2022): 354–59. http://dx.doi.org/10.47612/0514-7506-2022-89-3-354-359.

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The paper is devoted to gyrotropic characteristics of a non-ideal 1D photonic crystal with an arbitrary number of sublattices (of which one is the optically active potassium dithionate K2S2O6) and to their variation due to a random layer substitution in the K2S2O6 sublattice by modeling impurity layers of an orientationally disordered molecular crystal. We adopt a microscopic approach to study the specific (per unit volume) light polarization plane rotation angle in the exciton spectrum region and perform the numerical calculation of the superlattice optical activity dependence on concentratio

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26

Danilczuk, M., H. Gustafsson, M. D. Sastry, E. Lund, and A. Lund. "Ammonium dithionate—A new material for highly sensitive EPR dosimetry." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 69, no. 1 (2008): 18–21. http://dx.doi.org/10.1016/j.saa.2007.03.001.

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27

Bogushevich, S. E., та I. I. Ugolev. "Analysis of the EPR spectrum of γ-irradiated barium dithionate". Journal of Applied Spectroscopy 71, № 6 (2004): 794–98. http://dx.doi.org/10.1007/s10812-005-0004-x.

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28

Baran, N. P., V. M. Maksimenko, V. V. Teslenko та A. A. Bugay. "EPR spectra of γ-irradiated hydrated barium dithionate single crystals". Journal of Applied Spectroscopy 75, № 1 (2008): 15–20. http://dx.doi.org/10.1007/s10812-008-9017-6.

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29

Pollum, Marvin, Minh Lam, Steffen Jockusch, and Carlos E. Crespo-Hernández. "Dithionated Nucleobases as Effective Photodynamic Agents against Human Epidermoid Carcinoma Cells." ChemMedChem 13, no. 10 (2018): 1044–50. http://dx.doi.org/10.1002/cmdc.201800148.

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30

Bernhardt, PV, TW Hambley, and GA Lawrance. "Crystal Structures of [H4L](ClO4)4.6H2O And [Zn(H2L)(S2O6)2].4H2O (L = 6,13-Dimethyl-1,4,8,11-tetraazacyclotetradecane-6,13-diamine)." Australian Journal of Chemistry 43, no. 4 (1990): 699. http://dx.doi.org/10.1071/ch9900699.

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The substituted macrocycle 6,13-dimethyl-1,4,8,11- tetraazacyclotetradecane-6,13-diamine (L) can be crystallized as the perchlorate salt or the zinc dithionate complex. The crystal structures of [H4L](ClO4)4.6H2O (1) and [Zn(H2L)(S2O6)2].4H2O (2) have been determined by X-ray diffraction methods and refined to a residual of 0.058 for 1926 independent observed reflections for (1) and 0.022 for 2122 independent reflections for (2). The crystals of (1) are monoclinic, P21/c, a 10.657(2), b 12.466(7), c 12.216(3)Ǻ, β 96.73(2)° and those of (2) are monoclinic, P21/c, a 8.521(1), b 12.990(1), c 12.7

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31

Pu, Pengyan, Lin Yang, Lu Yao, Xia Jiang, and Wenju Jiang. "The Formation of Manganous Dithionate in the Manganese Oxide Flue Gas Desulfurization." Recent Innovations in Chemical Engineering (Formerly Recent Patents on Chemical Engineering) 12, no. 4 (2019): 287–95. http://dx.doi.org/10.2174/2405520412666190821102847.

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Background & Objective: The Manganous Dithionate (MnS2O6, MD) was formed during the flue gas desulfurization process over manganese ore slurry, which impeded the following valuable using of the desulfurized lixivium. In this study, the MD formation and restraint in the desulfurization process using manganese was carefully investigated. Methods & Results: Different type of manganese oxides/carbonate was used for the flue gas desulfurization, and the MD formation with the process was detected to obtain the basic information of the MD formation and restraint. The MD was directly formed by

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32

Katagiri, Akira, and Takaharu Matsubara. "Electro‐Oxidation of Sulfite to Dithionate in the Presence of Copper Ion." Journal of The Electrochemical Society 135, no. 7 (1988): 1709–14. http://dx.doi.org/10.1149/1.2096102.

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33

Bogushevich, S. E., V. N. Makatun, A. K. Potapovich, I. I. Ugolev, and I. A. Shingel'. "Investigation of thermal decomposition of barium dithionate by EPR and IR spectroscopy." Journal of Applied Spectroscopy 53, no. 5 (1990): 1201–5. http://dx.doi.org/10.1007/bf00938138.

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34

Brown, SJ, SKC Kok, PA Lay, and AF Masters. "Electrochemical Behavior of Bis[pentane-2,4-dithionato(1-)]iron(II), Fe(sacsac)2, and Dicarbonylbis[pentane-2,4-dithionato(1-)]iron(II), Fe(sacsac)2(CO)2." Australian Journal of Chemistry 42, no. 11 (1989): 1839. http://dx.doi.org/10.1071/ch9891839.

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The redox behaviours of Fe(sacsac)2 and Fe( sacsac )2(CO)2 in chloroform are reported ( sacsac - = C5H7S2- = dithioacetylacetonate anion = pentane-2,4-dithionate anion). Fe( sacsac )2 is reversibly reduced to [Fe( sacsac )2]-, but no other redox processes are observed within the solvent limits. Fe( sacsac )2(CO)2 undergoes a reversible one-electron reduction followed by rapid loss of carbon monoxide to generate [Fe( sacsac )2]-. The oxidation of Fe( sacsac )2(CO)2 results in the oxidation of a dithioacetylacetonate ligand to the 3,5-dimethyl-1,2-dithiolium cation and the formation of a previou

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35

Scerba, Michael T., Maxime A. Siegler, and Nigel H. Greig. "Thionation of Aminophthalimide Hindered Carbonyl Groups and Application to the Synthesis of 3,6′-Dithionated Pomalidomides." Synlett 32, no. 09 (2021): 917–22. http://dx.doi.org/10.1055/s-0040-1720460.

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AbstractHerein, we present a new one-pot procedure for the 3,6′-dithionation of pomalidomide derivatives in which the key 3-position sulfur atom is preferentially installed at the desired (but sterically congested) carbonyl of the aminophthalimide system and with regiochemistry distinct from Lawesson’s Reagent thionation methods. When heated in 1,4-dioxane with P4S10–pyridine complex, pomalidomides are smoothly and reproducibly converted into their 3,6′-dithionated analogues in roughly 30% isolated yield and at various scales. While detrimental to the desired 3,6′-type outcome when employing L

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36

Andersen, Peter, Eva Bang, H. Nevala, et al. "The Crystal Structure of Tris{di-mu-hydroxotetraamminechromium(III)}chromium(III) Dithionate Tetrahydrate." Acta Chemica Scandinavica 40a (1986): 476–78. http://dx.doi.org/10.3891/acta.chem.scand.40a-0476.

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37

Harris, Pernille, and Pauli Kofod. "A methyl-coordinated RhIIIion in methylpentaamminerhodium(III)–chloropentaamminerhodium(III)–dithionate (0.73/2.27/3)." Acta Crystallographica Section E Structure Reports Online 58, no. 8 (2002): m460—m462. http://dx.doi.org/10.1107/s1600536802013466.

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38

Badri, Babiker. "Spectrophotometric determination of sulphite, sulphate and dithionate in the presence of each other." Analyst 113, no. 2 (1988): 351. http://dx.doi.org/10.1039/an9881300351.

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39

Bogushevich, S. E., I. I. Ugolev, and A. K. Potapovich. "Production of SO 3 − ion-radicals in barium dithionate exposed to ionizing radiation." Journal of Applied Spectroscopy 63, no. 2 (1996): 207–11. http://dx.doi.org/10.1007/bf02606727.

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40

Boyd, Peter D. W., Clifton E. F. Rickard, and Kingsley J. Cavell. "[Bis(diphenylphosphino)alkane](pentane-2,4-dithionato) complexes of nickel(II)." Acta Crystallographica Section C Crystal Structure Communications 56, no. 1 (2000): e16-e18. http://dx.doi.org/10.1107/s0108270199016078.

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41

Rahim, Shermin, and John Milne. "Studies on the interaction of selenite and selenium with sulphur donors. Part 4. Thiosulfate." Canadian Journal of Chemistry 74, no. 5 (1996): 753–59. http://dx.doi.org/10.1139/v96-082.

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Raman and Se-77 NMR spectroscopy confirm that when selenous acid is reduced by thiosulfate in water selenopentathionate and tetrathionate are formed.[Formula: see text]Depending upon the stoichiometry and pH, two isomers of the selenopentathionate ion, O- and S-bonded, are formed. Insufficiently acid solutions cause decomposition to selenium and tetrathionate ion.[Formula: see text]Fresh solutions prepared from crystalline sodium selenopentathionate and water undergo slow decompositon. NMR and Raman spectra show the presence of both the O-bonded and S-bonded linkage isomers. The O-bonded isome

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42

Lay, PA, AF Masters, and CD Wasiowych. "The Reactions of Electrogenerated [Ni(sacsac)2]-: Biomimetic Chemistry Related to Nickel Enzymes." Australian Journal of Chemistry 48, no. 4 (1995): 835. http://dx.doi.org/10.1071/ch9950835.

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The electrochemical reduction of [Ni( sacsac )2] ( sacsac = C5H7S2- = pentane-2,4-dithionate) has been investigated by cyclic voltammetry and controlled-potential electrolysis in acetone/tetra- butylammonium tetrafluoroborate (0.1 M). The reactions of the reduction product(s) with CO, CO2, CH3I, C12H25SH, light and water have been surveyed. At a scan rate of 100 mV s-1, [Ni( sacsac )2] (0.5 mM ) undergoes a quasi-reversible one-electron reduction (∆ Ep = 88 mV) at -1.543 V (v. Fc+/0) and an irreversible four-electron oxidation at +0.635 V. The oxidation generates the 3,5-dimethyl-1,2-dithioliu

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43

Yamaguchi, Hiroshi, Shigehito Sato, Seiji Watanabe, and Hiroshi Naito. "Pre-embarkment Prognostication for Acute Paraquat Poisoning." Human & Experimental Toxicology 9, no. 6 (1990): 381–84. http://dx.doi.org/10.1177/096032719000900604.

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1 In order to assess which laboratory parameters could be related to the prognosis of patients with acute paraquat poisoning, we reviewed the medical records of 160 patients who had ingested paraquat in an attempt at suicide. 2 Serum creatinine and potassium concentrations, arterial blood bicarbonate and base excess levels, arterial blood pH, volume of paraquat ingested and the strength of the urinary paraquat qualitative test (sodium dithionate colour reaction) on admission in the surviving patients were significantly different from those of the patients who died within 48 h of ingestion. 3 T

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44

Jones, Alison M., and Roger Knowles. "Sulfide alleviation of acetylene inhibition of nitrous oxide reduction by Flexibacter Canadensis." Canadian Journal of Microbiology 38, no. 2 (1992): 143–48. http://dx.doi.org/10.1139/m92-023.

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The role of sulfide in the relief of acetylene inhibition of nitrous oxide reduction by Flexibacter canadensis was studied. In this organism, the reversal of acetylene inhibition of nitrous oxide reduction is correlated with a 90% decrease in the dissolved sulfide concentration. The fate of this sulfide is not known, since there was no concomitant increase in acid-soluble sulfide and volatile sulfur compounds were not detectable by flame photometric gas chromatography. Of the other sulfur-containing compounds tested (sulfate, sulfite, thiosulfate, cysteine, methionine, dithionite, dithionate,

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45

Eizadi-Mood, Nastaran, Shadi Haddad, Parisa Mirmoghtadaei, Razieh Mahvari, and Rokhsareh Meamar. "Rare fatal poisoning through dermal exposure to paraquat." SAGE Open Medical Case Reports 10 (January 2022): 2050313X2211396. http://dx.doi.org/10.1177/2050313x221139621.

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Paraquat skin contact occurs less frequently and is rarely fatal. This article reports a case of a 45-year-old man who presented with dysphagia, respiratory distress and grade two, and third skin burns focusing on the upper body after accidental exposure to paraquat. He was admitted to the hospital 6 days after the first contact. The urine sodium dithionate test was strongly positive. The O2 saturation at admission was 52%, which reached 91% with a bag valve mask. Rising blood liver enzymes, urea, creatinine, and respiratory acidosis in the venous blood gas analysis were observed in the lab da

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Kalsbeek, Nicoline, Sine Larsen, Béla Kazinczy, et al. "Crystal Structure of Tri-mu-hydroxobis[(1,4,7-trimethyl-1,4,7-triazacyclononane)chromium(III)] Dithionate Tetrahydrate." Acta Chemica Scandinavica 53 (1999): 149–54. http://dx.doi.org/10.3891/acta.chem.scand.53-0149.

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Lente, Gábor, and István Fábián. "Effect of Dissolved Oxygen on the Oxidation of Dithionate Ion. Extremely Unusual Kinetic Traces." Inorganic Chemistry 43, no. 13 (2004): 4019–25. http://dx.doi.org/10.1021/ic0499087.

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Petrie, Lloyd M., M. Emmelyn Jakel, Richard L. Brandvig, and Joseph G. Kroening. "Ion chromatography of sulfur dioxide, sulfate ion, and dithionate ion in aqueous mineral leachates." Analytical Chemistry 65, no. 7 (1993): 952–55. http://dx.doi.org/10.1021/ac00055a020.

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Brandt, Christian, and Rudi Van Eldik. "The formation of dithionate during the iron(III)-catalysed autoxidation of sulfur(IV)-oxides." Atmospheric Environment 31, no. 24 (1997): 4247–49. http://dx.doi.org/10.1016/s1352-2310(97)00284-7.

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He, Ke-jie, Shi-jun Su, Sang-lan Ding, and Wei-yi Sun. "Formation characteristics of dithionate and sulfate ions in the pyrolusite leaching process with SO2." Reaction Kinetics, Mechanisms and Catalysis 123, no. 2 (2018): 757–70. http://dx.doi.org/10.1007/s11144-018-1365-5.

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