Relevant bibliographies by topics / Thiodiethanol

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Academic literature on the topic 'Thiodiethanol'

Author: Grafiati
Published: 10 March 2023

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Journal articles on the topic "Thiodiethanol"

1

Zhang, Yousheng, Suning Wang, Craig Bridges, and John E. Greedan. "Co(II) and Mn(II) complexes of 2,2'-thiodiethanol: [CoII(2,2'-thiodiethanol)2Cl2] and [Mn(2,2'-thiodiethanol)Cl2]n." Canadian Journal of Chemistry 78, no. 10 (October 1, 2000): 1289–94. http://dx.doi.org/10.1139/v00-132.

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[Co(2,2'-thiodiethanol)2Cl2] (1) and [Mn(2,2'-thiodiethanol)Cl2]n (2), have been synthesized and characterized structurally. Compound 1 is a six-coordinate, mononuclear Co(II) complex. The mononuclear units in the crystal lattice of 1 are linked together through intermolecular hydrogen bonds between hydroxy and chloride groups to form a three-dimensional array. Compound 2 consists of six-coordinate Mn(II) units that are linked by covalently bound 2,2'-thiodiethanol and chloride ligands to form an alternating one-dimensional chain, which is further linked together by inter-chain hydrogen bonds to form a two-dimensional sheet. Antiferromagnetic exchange is present in compound 2.Key words: cobalt, manganese, 2,2'-thiodiethanol, structure, magnetism.
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Zhang, Yousheng, Suning Wang, Craig Bridges, and John E. Greedan. "Co(II) and Mn(II) comple×es of 2,2'-thiodiethanol: [CoII(2,2'-thiodiethanol)2Cl2] and [Mn(2,2'-thiodiethanol)Cl2]n." Canadian Journal of Chemistry 78, no. 10 (2000): 1289–94. http://dx.doi.org/10.1139/cjc-78-10-1289.

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3

Kangas, Michael, Adreanna Ernest, Rachel Lukowicz, Andres Mora, Anais Quossi, Marco Perez, Nathan Kyes, and Andrea Holmes. "The Identification of Seven Chemical Warfare Mimics Using a Colorimetric Array." Sensors 18, no. 12 (December 6, 2018): 4291. http://dx.doi.org/10.3390/s18124291.

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Chemical warfare agents pose significant threats in the 21st century, especially for armed forces. A colorimetric detection array was developed to identify warfare mimics, including mustard gas and nerve agents. In total, 188 sensors were screened to determine the best sensor performance, in order to identify warfare mimics 2-chloro ethyl ethylsulfide, 2-2′-thiodiethanol, trifluoroacetic acid, methylphosphonic acid, dimethylphosphite, diethylcyanophosphonate, and diethyl (methylthiomethyl)phosphonate. The highest loadings in the principle component analysis (PCA) plots were used to identify the sensors that were most effective in analyzing the RGB data to classify the warfare mimics. The dataset was reduced to only twelve sensors, and PCA results gave comparable results as the large data did, demonstrating that only twelve sensors are needed to classify the warfare mimics.
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4

Lydon, John D., and Richard C. Thompson. "Reduction of peroxotitanium(IV) by iodide, thiodiethanol, thioxane, and thiourea in acidic solution." Inorganic Chemistry 25, no. 20 (September 1986): 3694–97. http://dx.doi.org/10.1021/ic00240a035.

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5

Bossle, P. C., S. F. Hallowell, D. J. Reutter, and E. W. Sarver. "Analysis of 2,2′-thiodiethanol in aqueous matrices by liquid chromatography with electrochemical detection." Journal of Chromatography A 330 (January 1985): 388–91. http://dx.doi.org/10.1016/s0021-9673(01)82000-8.

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6

Mohan, Hari, and J. P. Mittal. "Electron transfer reactions in aqueous solutions of 2,2′-thiodiethanol: A pulse radiolysis study." International Journal of Radiation Applications and Instrumentation. Part C. Radiation Physics and Chemistry 38, no. 1 (January 1991): 45–50. http://dx.doi.org/10.1016/1359-0197(91)90043-2.

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7

Staudt, Thorsten, Marion C. Lang, Rebecca Medda, Johann Engelhardt, and Stefan W. Hell. "2,2′-Thiodiethanol: A new water soluble mounting medium for high resolution optical microscopy." Microscopy Research and Technique 70, no. 1 (2006): 1–9. http://dx.doi.org/10.1002/jemt.20396.

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8

Aoyagi, Yuka, Ryosuke Kawakami, Hisayuki Osanai, Terumasa Hibi, and Tomomi Nemoto. "A Rapid Optical Clearing Protocol Using 2,2′-Thiodiethanol for Microscopic Observation of Fixed Mouse Brain." PLOS ONE 10, no. 1 (January 29, 2015): e0116280. http://dx.doi.org/10.1371/journal.pone.0116280.

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9

Kawashima, Hideki. "Production of [(2-Hydroxyethyl)thio] acetic Acid from Thiodiglycol (2,2′-Thiodiethanol) by Resting Cells ofCandida rugosaIFO 1364." Bioscience, Biotechnology, and Biochemistry 59, no. 5 (January 1995): 934–35. http://dx.doi.org/10.1271/bbb.59.934.

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10

Borowicz, Marcin, Joanna Paciorek-Sadowska, Jacek Lubczak, and Bogusław Czupryński. "Biodegradable, Flame-Retardant, and Bio-Based Rigid Polyurethane/Polyisocyanurate Foams for Thermal Insulation Application." Polymers 11, no. 11 (November 5, 2019): 1816. http://dx.doi.org/10.3390/polym11111816.

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This article raised the issue of studies on the use of new bio-polyol based on white mustard seed oil and 2,2’-thiodiethanol (3-thiapentane-1,5-diol) for the synthesis of rigid polyurethane/polyisocyanurate (RPU/PIR) foams. For this purpose, new formulations of polyurethane materials were prepared. Formulations contained bio-polyol content from 0 to 0.4 chemical equivalents of hydroxyl groups. An industrial flame retardant, tri(2-chloro-1-methylethyl) phosphate (Antiblaze TCMP), was added to half of the formulations. Basic foaming process parameters and functional properties, such as apparent density, compressive strength, brittleness, absorbability and water absorption, aging resistance, thermal conductivity coefficient λ, structure of materials, and flammability were examined. The susceptibility of the foams to biodegradation in soil was also examined. The increase in the bio-polyol content caused a slight increase in processing times. Also, it was noted that the use of bio-polyol had a positive effect on the functional properties of obtained RPU/PIR foams. Foams modified by bio-polyol based on mustard seed oil showed lower apparent density, brittleness, compressive strength, and absorbability and water absorption, as well as thermal conductivity, compared to the reference (unmodified) foams. Furthermore, the obtained materials were more resistant to aging and more susceptible to biodegradation.
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Book chapters on the topic "Thiodiethanol"

1

Pardasani, R. T., and P. Pardasani. "Magnetic properties manganese(II) complex of 2,2′-thiodiethanol." In Magnetic Properties of Paramagnetic Compounds, 629–30. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54228-6_350.

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van Lierop, Ben, Laurence Castle, Alexandre Feigenbaum, and Achim Boenke. "Thiodiethanol bis(3-(3,5-di-tert-butyl-4-hydroxyphenyl) propionate)." In Spectra for the Identification of Additives in Food Packaging, 480–84. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-5222-8_95.

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Journal articles
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