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Journal articles on the topic 'Dimethylsulfone'

Author: Grafiati

Published: 30 May 2022

Last updated: 31 May 2022

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1

Ghazoyan, Heghine H., and Shiraz A. Markaryan. "VOLUMETRIC PROPERTIES OF SOLUTIONS OF DIMETHYLSULFONE IN ETHANOL-WATER MIXTURE AT TEMPERATURES RANGE OF 298.15-323.15 K." IZVESTIYA VYSSHIKH UCHEBNYKH ZAVEDENIY KHIMIYA KHIMICHESKAYA TEKHNOLOGIYA 60, no. 7 (August 24, 2017): 27. http://dx.doi.org/10.6060/tcct.2017607.5564.

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This paper studies volumetric properties of ternary dimethylsulfone-ethanol-water systems. The biomedical and environmental significance for the fundamental investigations of aqueous solution of dimethylsulfone and influences of third component on volumetric behavior of this system arises from several reasons. In the global sulfur cycle dimethylsulfide is converted to dimethylsulfone leading to an annual atmospheric production of some million tones of dimethylsulfone, much of which would be deposited in rain and snow. In addition, dimethylsulfone has been extensively studied from a medical point of view. It was established that dimethylsulfone is contained in small amounts in human blood and urine. Also of interest is that methionine is transformed into dimethylsulfone in living organisms. In this work densities of solution of dimethylsulfone in ethanol-water mixtures with various compositions have been measured over available concentration range. As it is evident from experimental data, the increase in a temperature leads to the reduction of density. The apparent and partial molar volumes of solutions were determined over the 298.15–323.15K temperature range. As it follows from these data, the apparent molar volumes increase with increasing of temperature. The influence of ethanol on the volumetric behavior has been taken into account by changing the apparent molar volume compared with the apparent molar volume of the binary aqueous solutions of DMSO2. It is found also the effect of the amount of ethanol on the volumetric properties of these solutions. It is interesting that the effect of ethanol on the values of apparent molar volumes does not change monotone with increasing in quantity of ethanol in ethanol-water mixture. In dimethylsulfone+(ethanol-water) solutions the partial molar volume of dimethylsulfone increases when quantity of ethanol in ethanol-water mixture more than 0.5 molar fraction. The observed phenomena are explained by the presence of competition of intermolecular interactions. In the DMSO2-ethanol-water system the strongest interaction between ethanol and water molecules leads to the increase in partial molar volumes for DMSO2.For citation:Ghazoyan H.H., Markaryan S.A. Volumetric properties of solutions of dimethylsulfone in ethanol-water mixture at tempe-ratures range of 298.15-323.15 K. Izv. Vyssh. Uchebn. Zaved. Khim. Khim. Tekhnol. 2017. V. 60. N 7. P. 27-33.

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2

Legrand, L., A. Tranchant, R. Messina, F. Romain, and A. Lautie. "Raman Study of Aluminum Chloride−Dimethylsulfone Solutions." Inorganic Chemistry 35, no. 5 (January 1996): 1310–12. http://dx.doi.org/10.1021/ic941455q.

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3

Harvey, George R., and Russell F. Lang. "Dimethylsulfoxide and dimethylsulfone in the marine atmosphere." Geophysical Research Letters 13, no. 1 (January 1986): 49–51. http://dx.doi.org/10.1029/gl013i001p00049.

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4

Ramalho-Santos, João, Ricardo Negrão, and Maria da Conceição Pedroso de Lima. "Role of hydrophobic interactions in the fusion activity of influenza and sendai viruses towards model membranes." Bioscience Reports 14, no. 1 (February 1, 1994): 15–24. http://dx.doi.org/10.1007/bf01901634.

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We have studied the role of hydrophobic interactions in the fusion activity of two lipid enveloped viruses, influenza and Sendai. Using the fluorescent probe ANS (1-aminonaphtalene-8-sulfonate) we have shown that low-pH-dependent influenza virus activation involves a marked increase in the viral envelope hydrophobicity. The effect of dehydrating agents on the fusion activity of both viruses towards model lipid membranes was studied using a fluorescence dequenching assay. Dehydrating agents such as dimethylsulfoxide and dimethylsulfone greatly enhanced the initial rate of the fusion process, the effect of dimethylsulfone doubling that of dimethylsulfoxide. The effect of poly(ethylene glycol) on the fusion process was found to be dependent on the polymer concentration and molecular weight. In general, similar observations were made for both viruses. These results stress the importance of dehydration and hydrophobic interactions in the fusion activity of influenza and Sendai viruses, and show that these factors may be generally involved in membrane fusion events mediated by many other lipid enveloped viruses.

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5

Kim, Sangjae, Shota Kumeno, Kenta Kamebuchi, Kensuke Kuroda, and Masazumi Okido. "Effect of Li Ions on Al Electrodeposition from Dimethylsulfone." Journal of Surface Engineered Materials and Advanced Technology 08, no. 04 (2018): 110–25. http://dx.doi.org/10.4236/jsemat.2018.84010.

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6

Khibiev, Kh S., K. O. Omarova, and Sh Sh Khidirov. "Electrochemical synthesis of dimethylsulfone and methanesulfonic acid from dimethylsulfoxide." Russian Journal of Electrochemistry 46, no. 8 (August 2010): 960. http://dx.doi.org/10.1134/s1023193510080161.

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7

Gabrielyan, Liana S., Shiraz A. Markarian, and Hermann Weingärtner. "Dielectric spectroscopy of dimethylsulfone solutions in water and dimethylsulfoxide." Journal of Molecular Liquids 194 (June 2014): 37–40. http://dx.doi.org/10.1016/j.molliq.2014.01.013.

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8

Legrand, L., A. Tranchant, and R. Messina. "Behaviour of aluminium as anode in dimethylsulfone-based electrolytes." Electrochimica Acta 39, no. 10 (July 1994): 1427–31. http://dx.doi.org/10.1016/0013-4686(94)85054-2.

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9

Salama, Nahla N., Mohammed A. El Ries, Safaa Toubar, Maha Abd El Hamid, and Mohammed I. Walash. "Thermoanalytical Investigation of Some Sulfone-Containing Drugs." Journal of Analytical Methods in Chemistry 2012 (2012): 1–9. http://dx.doi.org/10.1155/2012/439082.

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The thermal behavior of some sulfone-containing drugs, namely, dapsone (DDS), dimethylsulfone (MSM), and topiramate (TOP) in drug substances, and products were investigated using different thermal techniques. These include thermogravimetry (TGA), derivative thermogravimetry (DTG), differential thermal analysis (DTA), and differential scanning calorimetry (DSC). The thermogravimetric data allowed the determination of the kinetic parameters: activation energy (Ea), frequency factor (A), and reaction order (n). The thermal degradation of dapsone and topiramate was followed a first-order kinetic behavior. The calculated data evidenced a zero-order kinetic for dimethylsulfone. The relative thermal stabilities of the studied drugs have been evaluated and follow the order DDS > TOP > MSM. The purity was determined using DSC for the studied compounds, in drug substances and products. The results were in agreement with the recommended pharmacopoeia and manufacturer methods. DSC curves obtained from the tablets suggest compatibility between the drugs, excipients and/or coformulated drugs. The fragmentation pathway of dapsone with mass spectrometry was taken as example, to correlate the thermal decomposition with the resulted MS-EI. The decomposition modes were investigated, and the possible fragmentation pathways were suggested by mass spectrometry.

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10

MIYAKE, Masao, Mizuki HIRATA, Hiroaki OKAMOTO, and Tetsuji HIRATO. "Electrodeposition of Aluminum Using Dimethylsulfone-based Baths in Dry Air." Journal of The Surface Finishing Society of Japan 70, no. 10 (October 1, 2019): 523–27. http://dx.doi.org/10.4139/sfj.70.523.

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11

Matsui, Isao, Satoshi Ono, Yorinobu Takigawa, Tokuteru Uesugi, and Kenji Higashi. "Fabrication of bulk nanocrystalline Al electrodeposited from a dimethylsulfone bath." Materials Science and Engineering: A 550 (July 2012): 363–66. http://dx.doi.org/10.1016/j.msea.2012.04.088.

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12

Wicht, Denyce K. "The reduced flavin-dependent monooxygenase SfnG converts dimethylsulfone to methanesulfinate." Archives of Biochemistry and Biophysics 604 (August 2016): 159–66. http://dx.doi.org/10.1016/j.abb.2016.07.001.

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13

OKAMOTO, Hiroaki, Masao MIYAKE, and Tetsuji HIRATO. "Influence of Water Content on Electrodeposition of Aluminum from Dimethylsulfone Baths." Journal of MMIJ 130, no. 2_3 (2014): 70–75. http://dx.doi.org/10.2473/journalofmmij.130.70.

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14

Ling, Yong-Chien, Thomas J. Vickers, and Charles K. Mann. "Background Correction in Raman Spectroscopic Determination of Dimethylsulfone, Sulfate, and Bisulfate." Applied Spectroscopy 39, no. 3 (May 1985): 463–70. http://dx.doi.org/10.1366/0003702854248700.

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A study has been made to compare the effectiveness of thirteen methods of spectroscopic background correction in quantitative measurements. These include digital filters, least-squares fitting, and cross-correlation, as well as peak area and height measurements. Simulated data sets with varying S/N and degrees of background curvature were used. The results were compared with the results of corresponding treatments of Raman spectra of dimethyl sulfone, sulfate, and bisulfate. The range of variation of the simulated sets was greater than was possible with the experimental data, but where conditions were comparable, the agreement between them was good. This supports the conclusion that the simulations were valid. Best results were obtained by a least-squares fit with the use of simple polynomials to generate the background correction. Under the conditions employed, limits of detection were about 80 ppm for dimethyl sulfone and sulfate and 420 ppm for bisulfate.

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15

Legrand, L., A. Chaussé, and R. Messina. "Investigations on the Electroreduction of Titanium Chlorides in AlCl3‐Dimethylsulfone Electrolyte." Journal of The Electrochemical Society 145, no. 1 (January 1, 1998): 110–15. http://dx.doi.org/10.1149/1.1838221.

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16

Shiomi, Suguru, Masao Miyake, and Tetsuji Hirato. "Electrodeposition of Bright Al-Zr Alloy Coatings from Dimethylsulfone-Based Baths." Journal of The Electrochemical Society 159, no. 4 (2012): D225—D229. http://dx.doi.org/10.1149/2.079204jes.

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17

LEGRAND, L., A. TRANCHANT, and R. MESSINA. "ChemInform Abstract: Behavior of Aluminum as Anode in Dimethylsulfone-Based Electrolytes." ChemInform 25, no. 45 (August 18, 2010): no. http://dx.doi.org/10.1002/chin.199445008.

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18

Pereira-Ramos, Jean-Pierre, Richard Messina, and Jacques Perichon. "Electrochemical formation of LiAl alloy in molten dimethylsulfone at 150°C." Journal of Electroanalytical Chemistry and Interfacial Electrochemistry 209, no. 2 (September 1986): 283–96. http://dx.doi.org/10.1016/0022-0728(86)80554-x.

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19

Miyake, Masao, Hiroshi Motonami, Suguru Shiomi, and Tetsuji Hirato. "Electrodeposition of purified aluminum coatings from dimethylsulfone–AlCl3 electrolytes with trimethylamine hydrochloride." Surface and Coatings Technology 206, no. 19-20 (May 2012): 4225–29. http://dx.doi.org/10.1016/j.surfcoat.2012.04.027.

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20

Otsuki, Shujiro, Weihua Qian, Atsushi Ishihara, and Toshiaki Kabe. "Elucidation of dimethylsulfone metabolism in rat using a 35S radioisotope tracer method." Nutrition Research 22, no. 3 (March 2002): 313–22. http://dx.doi.org/10.1016/s0271-5317(01)00402-x.

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21

Jiang, T., M. J. Chollier Brym, G. Dubé, A. Lasia, and G. M. Brisard. "Studies on the AlCl3/dimethylsulfone (DMSO2) electrolytes for the aluminum deposition processes." Surface and Coatings Technology 201, no. 14 (April 2007): 6309–17. http://dx.doi.org/10.1016/j.surfcoat.2006.11.035.

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22

Legrand, L., A. Chausse, and R. Messina. "Investigations on the stability of titanium(II) species in AlCl3–dimethylsulfone electrolytes." Electrochimica Acta 46, no. 15 (April 2001): 2407–13. http://dx.doi.org/10.1016/s0013-4686(01)00435-2.

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23

SELVARAJ, S., A. DHANABALAN, J. S. A. AMAITHIRANI, and N. ARUMUGAM. "ChemInform Abstract: Condensation of Dimethylsulfone with Aromatic Aldehydes Using Phase- Transfer Catalysis." ChemInform 22, no. 47 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199147178.

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24

Kuma, Chisaki, Kana Sato, Isao Matsui, Yorinobu Takigawa, Tokuteru Uesugi, and Kenji Higashi. "Ductile electrodeposited Al from a dimethylsulfone bath with trace amounts of tin chloride." Materials Letters 244 (June 2019): 192–94. http://dx.doi.org/10.1016/j.matlet.2019.02.074.

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25

Hirsch, O., K. Weingarten, B. Blümich, and C. Jäger. "Comparative study of motions in dimethylsulfone by noise excitation and solid echo spectroscopy." Solid State Nuclear Magnetic Resonance 16, no. 3 (June 2000): 123–30. http://dx.doi.org/10.1016/s0926-2040(99)00066-1.

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26

Ghazoyan, Heghine H., and Shiraz A. Markarian. "Densities and thermochemical properties of dimethylsulfone in dimethylsulfoxide and dimethylsulfoxide/water equimolar mixture." Journal of Molecular Liquids 183 (July 2013): 85–88. http://dx.doi.org/10.1016/j.molliq.2013.04.010.

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27

Hirato, T., J. Fransaer, and J. P. Celis. "Electrolytic Codeposition of Silica Particles with Aluminum from AlCl[sub 3]-Dimethylsulfone Electrolytes." Journal of The Electrochemical Society 148, no. 4 (2001): C280. http://dx.doi.org/10.1149/1.1354616.

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28

Borodina, Elena, Donovan P. Kelly, Frederick A. Rainey, Naomi L. Ward-Rainey, and Ann P. Wood. "Dimethylsulfone as a growth substrate for novel methylotrophic species of Hyphomicrobium and Arthrobacter." Archives of Microbiology 173, no. 5-6 (May 5, 2000): 425–37. http://dx.doi.org/10.1007/s002030000165.

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29

MIYAKE, Masao, Yuki KUBO, and Tetsuji HIRATO. "Electrodeposition of Bright Al Coatings from Dimethylsulfone-AlCl3 Baths with the Addition of Tetraethylenepentamine." Journal of The Surface Finishing Society of Japan 64, no. 6 (2013): 364–67. http://dx.doi.org/10.4139/sfj.64.364.

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30

Kim, Sangjae, Naoya Matsunaga, Kensuke Kuroda, and Masazumi Okido. "Effect of [Al(DMSO2)3] 3+ Concentration on Al Electrodeposition from AlCl3/Dimethylsulfone Baths." Journal of Electrochemical Science and Technology 9, no. 1 (March 31, 2018): 69–77. http://dx.doi.org/10.33961/jecst.2018.9.1.69.

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31

Matsui, Isao, Yudai Hanaoka, Satoshi Ono, Yorinobu Takigawa, Tokuteru Uesugi, and Kenji Higashi. "Pre-electrodeposition process for improving tensile ductility of Al electrodeposited from a dimethylsulfone bath." Materials Letters 109 (October 2013): 229–32. http://dx.doi.org/10.1016/j.matlet.2013.07.103.

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32

Shao, Pengcheng P., Feng Ye, Prasun K. Chakravarty, James B. Herrington, Ge Dai, Randal M. Bugianesi, Rodolfo J. Haedo, et al. "Improved Cav2.2 Channel Inhibitors through a gem-Dimethylsulfone Bioisostere Replacement of a Labile Sulfonamide." ACS Medicinal Chemistry Letters 4, no. 11 (September 13, 2013): 1064–68. http://dx.doi.org/10.1021/ml4002612.

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33

Legrand, L., E. Chassaing, A. Chausse, and R. Messina. "RDE and impedance study of anodic dissolution of aluminium in organic AlCl3/dimethylsulfone electrolytes." Electrochimica Acta 43, no. 21-22 (July 1998): 3109–15. http://dx.doi.org/10.1016/s0013-4686(98)00065-6.

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34

Kuma, Chisaki, Kana Sato, Yudai Hanaoka, Isao Matsui, Yorinobu Takigawa, Tokuteru Uesugi, and Kenji Higashi. "Reduction of impurity contents in aluminum plates electrodeposited from a dimethylsulfone-aluminum chloride bath." Journal of Alloys and Compounds 783 (April 2019): 919–26. http://dx.doi.org/10.1016/j.jallcom.2018.12.355.

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35

Yanga, Chao-Chen, and Hsin-Yi Hsu. "Raman Spectroscopic Study of a New Type of Room Temperature ZnCl2-DMSO2 Molten Salts." Zeitschrift für Naturforschung A 65, no. 8-9 (September 1, 2010): 745–48. http://dx.doi.org/10.1515/zna-2010-8-917.

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In this study, Raman spectra of binary zinc chloride-dimethylsulfone (ZnCl2-DMSO2) melts have been measured. The intra-molecular vibrations of group and ionic species have been confirmed and discussed. From the Raman spectrum analysis and discussions, the equilibrium reaction equation about the complex ions forming in the ZnCl2-DMSO2 melt is submitted, such as n ZnCl2+n(n−2)(CH3)2SO2 ⇔ 2ZnCln2−n +(n−2) Zn[(CH3)2SO2]n2+, (n ≧ 3). However, the Raman spectra reveal that the ZnCl42− (375 cm−1) and ZnCl3 − (290 cm−1) complexes are the major ions for the 40 - 90 mol%ZnCl2 melts; furthermore, as the DMSO2 content is increased, the binary melt advantage the forming of Zn[(CH3)2SO2]n2+ complex ion and promote its transport characteristic

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36

Egorin, M. J., D. M. Rosen, R. Sridhara, L. Sensenbrenner, and M. Cottler-Fox. "Plasma concentrations and pharmacokinetics of dimethylsulfoxide and its metabolites in patients undergoing peripheral-blood stem-cell transplants." Journal of Clinical Oncology 16, no. 2 (February 1998): 610–15. http://dx.doi.org/10.1200/jco.1998.16.2.610.

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PURPOSE Dimethylsulfoxide (DMSO) is used to cryopreserve hematopoietic stem cells and is obligatorily infused into patients who receive stem-cell transplants. This study characterized the plasma concentrations and pharmacokinetics of DMSO and its metabolites in patients who underwent peripheral-blood stem-cell transplants. MATERIALS AND METHODS Plasma concentrations of DMSO, dimethylsulfone (DMSO2), and dimethylsulfide (DMSH2) were assessed in 10 patients who underwent autologous transplants with stem cells, cryopreserved in 10% DMSO (vol/vol). Blood was sampled at multiple times after the stem-cell infusion. Urine was pooled during the 24 hours postinfusion. DMSO, DMSO2, and DMSH2 were assayed simultaneously by gas chromatography. A one-compartment model with saturable elimination proved most suitable for fitting plasma DMSO concentration-versus-time data. RESULTS Stem-cell volumes infused ranged between 180 and 585 mL (254 to 824 mmol DMSO). Infusions lasted between 20 and 120 minutes. Peak plasma DMSO concentrations were 19.1 +/- 6.3 mmol/L (mean +/- SD). Pharmacokinetic parameters for volume of the central compartment (Vc), maximum velocity (Vmax), and Michaels-Menten constant (Km) were 37.3 +/- 17 L, 0.99 +/- 0.57 mmol/L/h, and 5.2 +/- 5.0 mmol/L, respectively. Plasma DMSO2 concentrations increased during the first 24 hours, plateaued at 4.4 +/- 1.2 mmol/L, and remained there until 48 hours (the last sample). DMSH2 concentrations were at steady-state by 5 minutes and remained between 3 and 5 mmol/L for 48 hours. Urinary excretion of DMSO and DMSO2 accounted for 44% +/- 4% and 4% +/- 1%, respectively, of the administered DMSO dose. Renal clearance of DMSO was 14.1 +/- 3.4 mL/min. CONCLUSION These data (1) document plasma concentrations of DMSO and metabolites in patients following peripheral-blood stem-cell transplants; (2) allow consideration of potential effects of these concentrations on stem-cell engraftment and drug-drug interactions; and (3) can facilitate a concentration-guided phase I trial of DMSO.

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37

Hanaoka, Yudai, Satoshi Ono, Isao Matsui, Yorinobu Takigawa, Tokuteru Uesugi, and Kenji Higashi. "Preparatory Electrodeposition Process for High Purity Bulk Aluminum." Advanced Materials Research 922 (May 2014): 237–41. http://dx.doi.org/10.4028/www.scientific.net/amr.922.237.

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Electrodeposition for Al from a dimethylsulfone (DMSO2) bath was consecutively performed, applying two types of current waveforms such as direct current and pulsed current, to investigate the effect of a current type on the preparatory electrodeposition (pre-electrodeposition) process. Electrodeposited Al from a DMSO2bath has a nanograined structure and high strength. However, the electrodeposits showed no plastic deformability due to the large amount of sulfur and chlorine which were incorporated into the electrodeposits as sulfide and chloride. Therefore, we obtained high purity Al from a DMSO2bath using pre-electrodeposition process, which could decrease sulfur and chlorine contents without using additives. The sulfur and chlorine contents of electrodeposits, obtained from a DMSO2bath applying both types current, both decreased to approximately 0.1 at.%. This result indicated that the waveforms made no difference in pre-electrodeposition process.

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38

Shu, Min-Fong, Hsin-Yi Hsu, and Chao-Chen Yang. "Physical Properties Of A New Type Of Molten Electrolytes, Zncl2-Dmso2." Zeitschrift für Naturforschung A 58, no. 7-8 (August 1, 2003): 451–56. http://dx.doi.org/10.1515/zna-2003-7-811.

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In the present work some physical properties of binary zinc chloride-dimethylsulfone (ZnCl2- DMSO2) melts were investigated; the phase diagram was determined by Differential Scanning Calorimeter (DSC) and Thermogravimetric Analyzer (TGA) analyses; the electric conductivity was measured using a direct-current computerized method. The conductivities of the melts increased with increasing temperature and DMSO2 content. There was a maximum of the conductivity at 40 mol% ZnCl2; the conductivity was 0.00423 S/cm at 110 ◦C. The density of all the melts decreased with increasing temperature and DMSO2 contents. The equivalent conductivities were given by Λ =κMmix/ρ, where Mmix is the mean equivalent weight. These equivalent conductivities were fitted by the Arrhenius equation, where the activation energies were 25.2, 34.6, 44.5, 53.7 kJ/mol for 40, 50, 60, 70 mol% ZnCl2, respectively.

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39

Yang, Chao-Chen, and Min-Fong Shu. "Preparation of Perpendicular GdFeCo Magnetic Thin Films with Pulse Electrodeposition Technique Utilizing Molten Salt as Electrolyte." Zeitschrift für Naturforschung A 62, no. 12 (December 1, 2007): 761–68. http://dx.doi.org/10.1515/zna-2007-1215.

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We have utilized ZnCl2-dimethylsulfone (DMSO2) as the electrolyte with added GdCl3, FeCl2, and CoCl2, for electrodepositing a perpendicular GdFeCo magnetic thin film. The reaction at the electrode surface and the electrical conductivity of the ionic substance at different ionic concentrations were studied by cyclic voltammetry and a computerized direct current method. Moreover, the electrodeposition of the GdFeCo thin film was determined by a pulse potential method. Relation between the composition of the deposited thin film and control parameters including applied potentials was determined by EDS analysis. An amorphous structure and the thickness of the thin film were obtained by TEM analysis. Its roughness and uniformity were determined by AFM analysis. Meanwhile, a perpendicular magnetic property and pinning magnetic domain of the thin film were analyzed from results of AGM and MFM.

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40

KANEKO, Yoshikazu. "Phosphorescencemetry and Acid-Base Reactions of Vanadium Oxides in Molten Bisulfate, Dimethylsulfone and Some Solvents." Denki Kagaku oyobi Kogyo Butsuri Kagaku 62, no. 6 (June 5, 1994): 508–12. http://dx.doi.org/10.5796/electrochemistry.62.508.

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41

Pereira‐Ramos, J. P., R. Messina, and J. Perichon. "Electrochemical Formation of Vanadium Pentoxide Bronzes M x V 2 O 5 in Molten Dimethylsulfone." Journal of The Electrochemical Society 135, no. 12 (December 1, 1988): 3050–57. http://dx.doi.org/10.1149/1.2095486.

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42

Akhmedov, M. A., K. O. Ibragimova, and Sh Sh Khidirov. "Comparative Evaluation of Dimethylsulfoxide and Dimethylsulfone Adsorption on a Smooth Platinum Electrode in Acidic Environment." Russian Journal of Electrochemistry 56, no. 5 (May 2020): 396–404. http://dx.doi.org/10.1134/s1023193520040023.

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43

Li, Xiaolong, Youer Deng, Zhiying Zhao, Yachun Liu, Chao Zhang, and Zaihui Fu. "A green catalyst-free concomitant air oxidation of DMSO and cumene to form methylsulfonylmethane (dimethylsulfone)." Journal of Sulfur Chemistry 43, no. 2 (October 5, 2021): 132–43. http://dx.doi.org/10.1080/17415993.2021.1982943.

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44

Ledyard, KM, and JWH Dacey. "Dimethylsulfide production from dimethylsulfonio-propionate by a marine bacterium." Marine Ecology Progress Series 110 (1994): 95–103. http://dx.doi.org/10.3354/meps110095.

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45

Abou-ElWafa, Ghada S. E., Mohamed Shaaban, Khaled A. Shaaban, Mohamed E. E. El-Naggar, and Hartmut Laatsch. "Three New Unsaturated Fatty Acids from the Marine Green Alga Ulva fasciata Delile." Zeitschrift für Naturforschung B 64, no. 10 (October 1, 2009): 1199–207. http://dx.doi.org/10.1515/znb-2009-1014.

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From the dichloromethane extract of the marine green alga Ulva fasciata Delile, collected from the Mediterranean coast of Egypt, three new fatty acids, namely, (E)-11-oxo-octadeca-12-enoic acid (1a), (E)-11-hydroxy-octadeca-12-enoic acid (2a) and 6-hydroxy-oct-7-enoic acid (3a) together with cholesterol were isolated. Analysis of the unpolar part of the extract using GC-MS detected the existence of further ten compounds, namely, dimethylsulfoxide, dimethylsulfone, phenylacetamide, 6,10,14-trimethyl-pentadecan-2-one, 8-heptadecene, dodecane, tridecane, 4-oxo-pentanoic acid, hexadecanoic acid, and the naturally new 1,1ʹ-bicyclohexyl. Structures of the isolated compounds 1a - 3a were confirmed by spectroscopic analyses including mass spectra (EI-MS, HR/ESIMS), 1D and 2D NMR experiments, and by the synthetic conversion into their corresponding methyl esters 1b - 3b. The algal extract and its components were comparatively examined against several pathogenic microorganisms, and brine shrimps for cytotoxicity.

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46

Yang, Chao-Chen, and Min-Fong Shu. "Electrodeposition of Magnetic Films of Co-Zn in ZnCl2-DMSO2-CoCl2 Molten Salt Electrolytes." Zeitschrift für Naturforschung A 60, no. 11-12 (December 1, 2005): 853–60. http://dx.doi.org/10.1515/zna-2005-11-1215.

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Abstract:

The electrodeposition of magnetic films of Co-Zn in zinc chloride-dimethylsulfone (ZnCl2- DMSO2) molten salt electrolytes with added CoCl2 has been studied. The phase diagram of ZnCl2- DMSO2 molten salts was determined by differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). Various compositions of alloys with different deposition potentials on the electrode surface have been studied by cyclic voltammetry. Either the constant potential method or the pulse potential method of plating can be used for electrodepositing Co-Zn thin films. The surface morphologies and magnetic properties have been studied. It has been shown that compact needle-type Co-Zn thin films are obtained at a constant potential of −0.1 V. Compact and uniform Co-Zn thin films are obtained by pulse electrodeposition. The magnetic properties of these films show higher coercive forces (Hc) and smoother domains than those obtained by the constant potential method.

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Zhu, Lei, J. M. Nicovich, and P. H. Wine. "Temperature-dependent kinetics studies of aqueous phase reactions of SO4− radicals with dimethylsulfoxide, dimethylsulfone, and methanesulfonate." Journal of Photochemistry and Photobiology A: Chemistry 157, no. 2-3 (May 2003): 311–19. http://dx.doi.org/10.1016/s1010-6030(03)00064-9.

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PEREIRARAMOS, J., R. MESSINA, and J. PERICHON. "A kinetic study of electrochemical lithium insertion into vanadium pentoxide in molten dimethylsulfone at 150°C." Solid State Ionics 40-41 (August 1990): 974–77. http://dx.doi.org/10.1016/0167-2738(90)90166-o.

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Zhu, Lei, J. Michael Nicovich, and Paul H. Wine. "Temperature-dependent kinetics studies of aqueous phase reactions of hydroxyl radicals with dimethylsulfoxide, dimethylsulfone, and methanesulfonate." Aquatic Sciences - Research Across Boundaries 65, no. 4 (December 1, 2003): 425–35. http://dx.doi.org/10.1007/s00027-003-0673-6.

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Miyake, Masao, Seiya Tajikara, and Tetsuji Hirato. "Fabrication of TiAl3 coating on TiAl-based alloy by Al electrodeposition from dimethylsulfone bath and subsequent annealing." Surface and Coatings Technology 205, no. 21-22 (August 2011): 5141–46. http://dx.doi.org/10.1016/j.surfcoat.2011.05.019.

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