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Journal articles on the topic 'Sultone'

Author: Grafiati

Published: 4 June 2021

Last updated: 11 January 2025

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1

Bindu Nair. "Final Report On the Safety Assessment of Sodium Alpha-Olefin Sulfonates." International Journal of Toxicology 17, no. 5_suppl (1998): 39–65. http://dx.doi.org/10.1177/109158189801700504.

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Sodium C14-16 OlefinSulfonate, Sodium C12-14 Olefin Sulfonate, Sodium C 14-18 Olefin Sulfonate, and Sodium C16-18 Olefin Sulfonate are the Sodium α-Olefin Sulfonates used in cosmetics as surfactant-cleansing agents. The highest concentration reportedly is 16% in shampoos and bath and shower products. These ingredients are a mixture of long-chain sulfonate salts prepared by sulfonation of α-olefins of various carbon chain lengths noted as subscripts. In the manufacture of these ingredients, delta and gamma sultones may be produced. Sodium α-Olefin Sulfonates are poorly absorbed through normal s

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2

Mubarakova, Liliya R., та German K. Budnikov. "Determination of δ-hexadecansultone in sodium α-olefinesulphonates and liquid detergents using gas chromatography-mass spectrometry (GC/MS)". Industrial laboratory. Diagnostics of materials 85, № 7 (2019): 16–21. http://dx.doi.org/10.26896/1028-6861-2019-85-7-16-21.

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Sultones are cyclic esters of hydroxysulfonic acids, which are formed in the process of sulfonation of α-olefins with sulfur trioxide gas. More stable sultones may be present in the final product — an anionic surfactant — sodium α-olefin sulfonate (AOC-Na). AOC-Na is widely used in the production of household chemicals and cosmetic products, including liquid dishwashing detergents. Sultones are strong skin sensitizers, their level in AOC-Na should be strictly controlled and not exceed 5 ppm. Operational and strict control of the sultone content upon AOC-Na production allows timely adjustment a

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3

Gladkova, Elizaveta D., Arina A. Chepanova, Ekaterina S. Ilina, et al. "Discovery of Novel Sultone Fused Berberine Derivatives as Promising Tdp1 Inhibitors." Molecules 26, no. 7 (2021): 1945. http://dx.doi.org/10.3390/molecules26071945.

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A new type of berberine derivatives was obtained by the reaction of berberrubine with aliphatic sulfonyl chlorides. The new polycyclic compounds have a sultone ring condensed to C and D rings of a protoberberine core. The reaction conditions were developed to facilitate the formation of sultones with high yields without by-product formation. Thus, it was shown that the order of addition of reagents affects the composition of the reaction products: when sulfochlorides are added to berberrubine, their corresponding 9-O-sulfonates are predominantly formed; when berberrubine is added to pre-genera

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4

Roberts, D. W., and D. L. Williams. "Sultone chemistry." Tetrahedron 43, no. 6 (1987): 1027–62. http://dx.doi.org/10.1016/s0040-4020(01)90041-9.

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5

King, James Frederick, та Kishan Chand Khemani. "The mechanism of hydrolysis of 2-hydroxyethanesulfonyl chloride: the intermediacy of 1,2-oxathietane 2,2-dioxide (β-sultone)". Canadian Journal of Chemistry 67, № 12 (1989): 2162–72. http://dx.doi.org/10.1139/v89-336.

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The hydrolysis of 2-hydroxyethanesulfonyl chloride (1) has been investigated with the aid of kinetic and product analysis studies. The results are quantitatively consistent with the mechanism of hydrolysis shown in Scheme 1, the chief features of which are (a) formation of β-sultone (2) and its rapid further reaction (the major pathway), together with (b) a minor direct hydrolysis route. The kinetics of both the β β-sultone formation and the direct hydrolysis shows two terms, one first order in 1 alone, and the other first order in hydroxide as well; the rates of the first- and second-order re

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6

Köppen, M., O. Beyer, S. Wuttke, U. Lüning, and N. Stock. "Synthesis, functionalisation and post-synthetic modification of bismuth metal–organic frameworks." Dalton Transactions 46, no. 26 (2017): 8658–63. http://dx.doi.org/10.1039/c7dt01744h.

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7

Nurgalieva, S. M., T. A. Bispen, A. N. Il’in, D. D. Moldavskii, and E. A. Rozhkova. "Perfluoroethanesulfonyl fluoride: Preparation from sultone." Russian Journal of Applied Chemistry 80, no. 9 (2007): 1562–65. http://dx.doi.org/10.1134/s1070427207090224.

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8

Braden, Dale A., Gary L. Gard, and Heinz Oberhammer. "Trifluoroethylene Sultone: Structure and Chemistry." Zeitschrift f�r anorganische und allgemeine Chemie 621, no. 11 (1995): 1849–55. http://dx.doi.org/10.1002/zaac.19956211106.

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9

Khiratkar, Avinash Ganesh, Prashant Narayan Muskawar, and Pundlik Rambhau Bhagat. "Polymer-supported benzimidazolium based ionic liquid: an efficient and reusable Brønsted acid catalyst for Biginelli reaction." RSC Advances 6, no. 107 (2016): 105087–93. http://dx.doi.org/10.1039/c6ra23781a.

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A polymer-supported benzimidazolium based ionic liquid (PSBIL) was synthesized by reaction of poly(vinylbenzyl chloride) and benzimidazole followed by ring opening of 1,4-butane sultone and acidification with sulphuric acid.

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10

Muir, K. W., C. S. Rodger, D. G. Morris, and K. S. Ryder. "A Sultone Derived from Racemic Camphene." Acta Crystallographica Section C Crystal Structure Communications 54, no. 10 (1998): 1546–48. http://dx.doi.org/10.1107/s0108270198006179.

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11

Pustenko, Aleksandrs, and Raivis Žalubovskis. "Recent advances in sultone synthesis (microreview)." Chemistry of Heterocyclic Compounds 53, no. 12 (2017): 1283–85. http://dx.doi.org/10.1007/s10593-018-2208-z.

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12

Natus, G., and E. J. Goethals. "Sulfoalkylation of dimethylsulfoxide with propane sultone." Bulletin des Sociétés Chimiques Belges 74, no. 9-10 (2010): 450–52. http://dx.doi.org/10.1002/bscb.19650740908.

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13

Morimoto, Yoshiki, Hajime Kurihara та Takamasa Kinoshita. "Can α-sultone exist as a chemical species? First experimental implication for intermediacy of α-sultone". Chemical Communications, № 3 (2000): 189–90. http://dx.doi.org/10.1039/a909094k.

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14

Hryhoriv, Halyna V., Dmitry A. Lega, and Leonid A. Shemchuk. "1,2-Benzoxathiin-4(3H)-one 2,2-dioxide – an underinvestigated building block with a high synthetic and pharmacological potential: synthesis, chemical properties, biological activity." Journal of Organic and Pharmaceutical Chemistry 19, no. 2(74) (2021): 4–28. http://dx.doi.org/10.24959/ophcj.21.234271.

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Aim. To analyze the available literature data on the methods of synthesis, chemical transformations and the biological activity of derivatives containing a sultone core – 1,2-benzoxathiin-4(3H)-one 2,2-dioxide – and to show the possibilities of their further use in the construction of new molecular systems with attractive pharmacological properties. Results and discussion. The most widespread method for the synthesis of 1,2-benzoxathiin-4(3H)-one 2,2-dioxides is the cyclization of salicylic acid derivatives. The known chemical transformations of 1,2-benzoxathiin-4(3H)-one 2,2-dioxides deal wit

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15

Pires, Julie, Laure Timperman, Aurore Castets, et al. "Role of propane sultone as an additive to improve the performance of a lithium-rich cathode material at a high potential." RSC Advances 5, no. 52 (2015): 42088–94. http://dx.doi.org/10.1039/c5ra05650k.

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This study presents the use of 1,3-propane sultone (PS) as a protective additive for the Li-rich-NMCxLi<sub>2</sub>MnO<sub>3</sub>–(1 −x)LiMO<sub>2</sub>(x≫ 1; M = Ni, Co, Mn) cathode–electrolyte interface during cathode material activation and cycling at a high potential (5 Vvs.Li).

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16

Ziyaei Halimehjani, Azim, Petr Beier та Maryam Khalili Foumeshi. "Synthesis of Novel α,β-Unsaturated Sulfonic Acid Derivatives Containing Dithiocarbamate/Xanthate Groups by Ring Opening of an α,β-Unsaturated γ-Sultone". Synlett 31, № 10 (2020): 987–90. http://dx.doi.org/10.1055/s-0040-1707970.

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An efficient method is disclosed for the synthesis of novel α,β-unsaturated sulfonic acid derivatives containing dithiocarbamate/xanthate groups through ring opening of an α,β-unsaturated γ-sultone with dithiocarbamic acid salts or xanthates prepared in situ. Treatment of the primary products with hydrochloric acid afforded the corresponding β-chloro-γ-(dithiocarbamato)propanesulfonic acids in excellent yields.

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17

Yamamura, E., H. Hirono, and M. Takeuchi. "The micronucleus assay with 1,3-propane sultone." Mutation Research/Environmental Mutagenesis and Related Subjects 292, no. 3 (1993): 303. http://dx.doi.org/10.1016/0165-1161(93)90133-k.

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18

Morimoto, Yoshiki, Hajime Kurihara та Takamasa Kinoshita. "ChemInform Abstract: Can α-Sultone Exist as a Chemical Species? First Experimental Implication for Intermediacy of α-Sultone." ChemInform 31, № 18 (2010): no. http://dx.doi.org/10.1002/chin.200018088.

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19

Yoon, Sa Rang, and Soon Ki Jeong. "Effects of Organic Additives on Electrochemical Properties of SiO_x Electrodes in Lithium Secondary Batteries." Applied Mechanics and Materials 835 (May 2016): 121–25. http://dx.doi.org/10.4028/www.scientific.net/amm.835.121.

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Electrochemical reactions occurring at a SiOx electrode were investigated to gain insight about the effects of film-forming additives, such as vinylene carbonate (VC), ethylene sulfite (ES) and 1,3-propane sultone (PS), on the formation of a solid electrolyte interface (SEI) on the SiOx electrode. The SEI formed in the presence of PS was found to have the smallest resistance, resulting in low irreversible capacity and good cycle performance.

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20

Singh, C., and A. P. Shamsherry. "Propane sultone mutagenesis in relation to treatment conditions." CYTOLOGIA 50, no. 3 (1985): 603–10. http://dx.doi.org/10.1508/cytologia.50.603.

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21

Brown, D. S., H. Heaney, and K. G. Mason. "The structure of a five-membered cyclic sultone." Acta Crystallographica Section C Crystal Structure Communications 43, no. 9 (1987): 1800–1802. http://dx.doi.org/10.1107/s0108270187090127.

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22

TAKADA, Daisuke, Hiroshi SUEMUNE, and Kiyoshi SAKAI. "Sultone formation from .ALPHA.-hydroxycyclopentanones and alkanesulfonyl chloride." CHEMICAL & PHARMACEUTICAL BULLETIN 38, no. 1 (1990): 234–35. http://dx.doi.org/10.1248/cpb.38.234.

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23

Antkowiak, Róża, Wiesłlaw Z. Antkowiak, and Karol Bruzik. "The structure of sultone formed in reychler's reaction." Tetrahedron 45, no. 23 (1989): 7515–22. http://dx.doi.org/10.1016/s0040-4020(01)89214-0.

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24

Singh, C., and B. L. Kaul. "Caffeine potentiation of propane sultone mutagenesis in barley." Mutation Research Letters 144, no. 4 (1985): 239–42. http://dx.doi.org/10.1016/0165-7992(85)90057-0.

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25

Liang, T. C., та V. Caluya. "Sultone-Assisted Inactivation of α-Chymotrypsin by Hydroxylamine". Bioorganic Chemistry 22, № 3 (1994): 268–75. http://dx.doi.org/10.1006/bioo.1994.1020.

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26

MUIR, K. W., C. S. RODGER, D. G. MORRIS, and K. S. RYDER. "ChemInform Abstract: A Sultone Derived from Racemic Camphene." ChemInform 30, no. 7 (2010): no. http://dx.doi.org/10.1002/chin.199907030.

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27

Lobaton, Esther, Maria-Jose Camarasa, and Sonsoles Velazquez. "ChemInform Abstract: An Efficient Synthesis of 3′-Spiro Sultone Nucleosides Functionalized on the Sultone Moiety via Pd-Catalyzed Cross-Coupling Reaction." ChemInform 31, no. 49 (2000): no. http://dx.doi.org/10.1002/chin.200049207.

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28

Singh, C. "Toxicity mutability relationship of 1,3-propane-sultone in barley." CYTOLOGIA 55, no. 3 (1990): 479–82. http://dx.doi.org/10.1508/cytologia.55.479.

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29

Wolckenhauer, Scott A., A. Sloan Devlin та J. Du Bois. "δ-Sultone Formation Through Rh-Catalyzed C−H Insertion". Organic Letters 9, № 21 (2007): 4363–66. http://dx.doi.org/10.1021/ol701950d.

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30

Craig, Donald C., and John D. Stevens. "Isolation of a sultone as an unusual acetolysis product." Carbohydrate Research 346, no. 6 (2011): 854–57. http://dx.doi.org/10.1016/j.carres.2011.01.035.

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31

Zhang, Qimeng, Zhixing Wang, Xinhai Li, et al. "Comparative study of 1,3-propane sultone, prop-1-ene-1,3-sultone and ethylene sulfate as film-forming additives for sodium ion batteries." Journal of Power Sources 541 (September 2022): 231726. http://dx.doi.org/10.1016/j.jpowsour.2022.231726.

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32

Wang, Song, and Chengcheng Tian. "Polyvinylpolypyrrolidone Supported Brønsted Acidic Catalyst for Esterification." International Journal of Polymer Science 2016 (2016): 1–7. http://dx.doi.org/10.1155/2016/8104838.

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A polyvinylpolypyrrolidone (PVPP) supported Brønsted acidic catalyst ([PVPP-BS]HSO4) was prepared by coupling SO3H-functionalized polyvinylpolypyrrolidone with H2SO4in this work. After the characterization through FT-IR, FESEM, TG, BET, and elemental analysis, it was found that 1,4-butane sultone (BS) and sulfuric acid reacted with PVPP and were immobilized on PVPP surface. The prepared[PVPP-BS]HSO4catalyst shows high catalytic activity for a series of esterification reactions and could be separated from the reacted mixture easily. Moreover, this catalyst could be recycled and reused for six t

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33

Lakouraj, Moslem Mansour, Nazanin Bagheri, and Vahid Hasantabar. "Synthesis and Application of Nanocrystalline-Cellulose-Supported Acid Ionic Liquid Catalyst in Pechmann Reaction." International Journal of Carbohydrate Chemistry 2013 (October 29, 2013): 1–8. http://dx.doi.org/10.1155/2013/452580.

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Nanocrystalline-cellulose-supported acidic ionic liquid carrying SO3H functional group was prepared using nanocrystalline cellulose, imidazole and 1,4-butane sultone as the source chemicals. The prepared nanocrystalline-cellulose-supported ionic liquid catalyst was characterized by AFM and SEM and its catalytic activity in the reaction of resorcinol with ethyl acetoacetate was tested in a solvent-free condition. The effects of reaction time, reaction temperature, and the ratio of catalyst on the conversion of resorcinol were investigated. A variety of coumarin derivatives were obtained in good

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34

YAMAGUCHI, Kentaro, Zenzo TAMURA, and Masako MAEDA. "Molecular Structure of Bromophenol Blue Having a .GAMMA.-Sultone Ring." Analytical Sciences 13, no. 6 (1997): 1057–58. http://dx.doi.org/10.2116/analsci.13.1057.

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35

Singh, C., and A. P. Shamsherry. "Impact of seed moisture on efficiency of propane sultone mutagenesis." CYTOLOGIA 53, no. 2 (1988): 269–73. http://dx.doi.org/10.1508/cytologia.53.269.

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36

Bakker, Bert H., та Hans Cerfontain. "Sulfonation of alkenes with sulfur trioxide; stereospecific β-sultone formation". Tetrahedron Letters 28, № 15 (1987): 1699–702. http://dx.doi.org/10.1016/s0040-4039(00)95398-x.

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37

Adamczyk, Maciej, and Sushil Rege. "Microwave assisted sulfopropylation of N-heterocycles using 1,3-propane sultone." Tetrahedron Letters 39, no. 52 (1998): 9587–88. http://dx.doi.org/10.1016/s0040-4039(98)02301-6.

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38

Forohar, Farhad, та Darryl D. DesMarteau. "Synthesis and reactions of the β-sultone of perfluorovinylsulfonyl fluoride". Journal of Fluorine Chemistry 66, № 2 (1994): 101–4. http://dx.doi.org/10.1016/0022-1139(93)03003-5.

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39

Sudarma, I. M., R. Hidayati, and M. G. Darmayanti. "SYNTHESIS OF NEW FUSED RING SULTONE FROM EUGENOL AND ITS DERIVATIVES." Rasayan Journal of Chemistry 13, no. 02 (2020): 1193–98. http://dx.doi.org/10.31788/rjc.2020.1325358.

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40

Barabanov, V. G., T. A. Bispen, V. V. Kornilov, D. D. Moldavskii, A. S. Odinokov та I. M. Fenichev. "Improvement of procedures for preparing Tetrafluoroethane-β-sultone and fluorocarbonyldifluoromethanesulfonyl fluoride". Russian Journal of Applied Chemistry 87, № 5 (2014): 619–23. http://dx.doi.org/10.1134/s1070427214050140.

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41

Liu, Lun-Zu, Li Tian, Guo-Yan Xu, and Yong Ye. "1,3-Dipolar Cycloaddition Reactionsof Nitrones to Prop-1-ene-1,3-sultone." Synthesis 2003, no. 09 (2003): 1329–34. http://dx.doi.org/10.1055/s-2003-40201.

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42

Jung, Hyun Min, Seong-Hyo Park, Jongho Jeon, et al. "Fluoropropane sultone as an SEI-forming additive that outperforms vinylene carbonate." Journal of Materials Chemistry A 1, no. 38 (2013): 11975. http://dx.doi.org/10.1039/c3ta12580g.

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43

Bakker, Bert H., та Hans Cerfontain. "Sulfonation of alkenes with sulfur trioxide; reversible stereospecific β-sultone formation". Tetrahedron Letters 30, № 40 (1989): 5451–54. http://dx.doi.org/10.1016/s0040-4039(01)80591-8.

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44

Lee, Albert W. M., W. H. Chan, L. S. Jiang та K. W. Poon. "Synthesis and Diels–Alder reactions of α,β-unsaturated γ-sultone". Chemical Communications, № 6 (1997): 611–12. http://dx.doi.org/10.1039/a700656j.

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45

Raikow, R. B., J. P. OKunewick, M. J. Buffo, and D. L. Kociban. "Effect of propane sultone pretreatment on Friend virus leukemogenesis in mice." Experientia 41, no. 5 (1985): 664–66. http://dx.doi.org/10.1007/bf02007709.

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46

Duarte-Peña, Lorena, Héctor Magaña, and Emilio Bucio. "Catheters with Dual-Antimicrobial Properties by Gamma Radiation-Induced Grafting." Pharmaceutics 15, no. 3 (2023): 960. http://dx.doi.org/10.3390/pharmaceutics15030960.

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Dual antimicrobial materials that have a combination of antimicrobial and antifouling properties were developed. They were developed through modification using gamma radiation of poly (vinyl chloride) (PVC) catheters with 4-vinyl pyridine (4VP) and subsequent functionalization with 1,3-propane sultone (PS). These materials were characterized by infrared spectroscopy, thermogravimetric analysis, swelling tests, and contact angle to determine their surface characteristics. In addition, the capacity of the materials to deliver ciprofloxacin, inhibit bacterial growth, decrease bacterial and protei

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47

Jeżewska, Anna. "Determination of Propane-1,3-sultone in Workplace Air for Occupational Exposure Assessment." International Journal of Environmental Research and Public Health 17, no. 4 (2020): 1414. http://dx.doi.org/10.3390/ijerph17041414.

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Propane-1,3-sultone (PS) is an alkylating substance used in the production of polymers, fungicides, insecticides, dyes, and detergents. It is absorbed into the human body by inhalation, digestion, and through the skin; it is also a possible carcinogen. Occupational exposure to this substance may occur on industrial or laboratory contact. In Poland, the maximum allowable concentration (MAC) for PS in workplace air is 7 µg/m3. The paper presents a method for determination of PS in workplace air using a gas chromatograph coupled with a mass spectrometer (GC-MS). Air containing PS is passed throug

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48

Benbrahim-Tallaa, Lamia, Béatrice Lauby-Secretan, Dana Loomis, et al. "Carcinogenicity of perfluorooctanoic acid, tetrafluoroethylene, dichloromethane, 1,2-dichloropropane, and 1,3-propane sultone." Lancet Oncology 15, no. 9 (2014): 924–25. http://dx.doi.org/10.1016/s1470-2045(14)70316-x.

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49

Adamczyk, Maciej, and Sushil Rege. "ChemInform Abstract: Microwave-Assisted Sulfopropylation of N-Heterocycles Using 1,3-Propane Sultone." ChemInform 30, no. 12 (2010): no. http://dx.doi.org/10.1002/chin.199912069.

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50

MATSULEVICH, ZH V., A. V. BORISOV та I. V. BODRIKOV. "ChemInform Abstract: Reagents for the Selective Sulfonation of Styrene to β-Sultone." ChemInform 26, № 34 (2010): no. http://dx.doi.org/10.1002/chin.199534136.

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