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Journal articles on the topic '8-Hydroxyquinoline-5-Sulfonic Acid'

Author: Grafiati

Published: 4 June 2021

Last updated: 18 February 2022

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1

Sureshkumar, B., Y. Sheena Mary, Y. Shyma Mary, and S. Suma. "Spectroscopic and DFT investigations of 8-hydroxy quinoline-5-sulfonic acid-5-chloro-8-hydroxyquinoline cocrystal." Chemical Papers 75, no. 7 (March 13, 2021): 3387–99. http://dx.doi.org/10.1007/s11696-021-01579-x.

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2

Korn, Maria das Graças Andrade, Adriana Costa Ferreira, Leonardo Sena Gomes Teixeira, and Antonio Celso Spínola Costa. "Spectrophotometric Determination of Zinc Using 7-(4-Nitrophenylazo)-8-Hydroxyquinoline-5-Sulfonic Acid." Journal of the Brazilian Chemical Society 10, no. 1 (January 1999): 46–50. http://dx.doi.org/10.1590/s0103-50531999000100008.

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3

Muegge, Brian D., Sean Brooks, and Mark M. Richter. "Electrochemiluminescence of Tris(8-hydroxyquinoline-5-sulfonic acid)aluminum(III) in Aqueous Solution." Analytical Chemistry 75, no. 5 (March 2003): 1102–5. http://dx.doi.org/10.1021/ac026152p.

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4

Singru, R. N., and W. B. Gurnule. "Thermogravimetric study of 8-hydroxyquinoline 5-sulfonic acid–melamine–formaldehyde terpolymer resins-II." Journal of Thermal Analysis and Calorimetry 100, no. 3 (February 7, 2010): 1027–36. http://dx.doi.org/10.1007/s10973-010-0672-5.

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5

KAWAKUBO, Susumu, Shuji YAMAMOTO, Masaaki IWATSUKI, and Tsutomu FUKASAWA. "Fluorometric determination of aluminium in acid and water samples with 8-hydroxyquinoline-5-sulfonic acid." Bunseki kagaku 41, no. 5 (1992): T65—T71. http://dx.doi.org/10.2116/bunsekikagaku.41.5_t65.

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6

Soroka, Krystyna, Rathnapala S. Vithanage, Denise A. Phillips, Brian Walker, and Purnendu K. Dasgupta. "Fluorescence properties of metal complexes of 8-hydroxyquinoline-5-sulfonic acid and chromatographic applications." Analytical Chemistry 59, no. 4 (February 15, 1987): 629–36. http://dx.doi.org/10.1021/ac00131a019.

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7

Hafez, Mohamed B., and M. Tarek M. Zaki. "Application of 8-hydroxyquinoline-5-sulfonic acid in the spectrophotometric determination of some lanthanides." Microchemical Journal 34, no. 3 (December 1986): 258–61. http://dx.doi.org/10.1016/0026-265x(86)90118-9.

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8

Phillips, Denise A., Krystyna Soroka, Rathnapala S. Vithanage, and Purnendu K. Dasgupta. "Enhancement and quenching of fluorescence of metal chelates of 8-hydroxyquinoline-5-sulfonic acid." Mikrochimica Acta 88, no. 3-4 (May 1986): 207–20. http://dx.doi.org/10.1007/bf01196613.

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9

Xian, Zhang, Wang Hong, and Zhang Hua-shan. "Spectrofluorimetric determination of magnesium (II) with 7-(8-Hydroxy-3, 6-disulfonaphthylazo)-8-hydroxyquinoline-5-sulfonic acid." Wuhan University Journal of Natural Sciences 6, no. 4 (December 2001): 831–35. http://dx.doi.org/10.1007/bf02850913.

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10

Sharifian, Majid, Narges Ashraf, Mohammad Hossein Arbab Zavar, Mahmoud Chamsaz, and Fahimeh Afzali. "Microneedle Copper (II) Selective Electrode based on Polypyrrole Doped with 8-Hydroxyquinoline-5-Sulfonic Acid." Journal of The Electrochemical Society 162, no. 3 (December 18, 2014): B57—B61. http://dx.doi.org/10.1149/2.0371503jes.

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11

Shiota, Akinobu, and Tooru Kuwamoto. "High-performance liquid chromatography-fluorometric determination of Sn(IV) with 8-hydroxyquinoline-5-sulfonic acid." Reactive Polymers 17, no. 1 (April 1992): 134–35. http://dx.doi.org/10.1016/0923-1137(92)90633-d.

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12

Rojas-Romo, Carlos, and Verónica Arancibia. "A Comparative Study of 8-Hydroxyquinoline and 8-Hydroxyquinoline-5-sulfonic Acid for Antimony(III) Determination by AdSV. Substituent Effect on Sensitivity II." Electroanalysis 27, no. 5 (March 9, 2015): 1262–67. http://dx.doi.org/10.1002/elan.201400616.

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13

Das, Asim Kumar. "Study of Equilibria and Kinetics of the Interactions of Iron(III) with 8-Hydroxyquinoline and 8-Hydroxyquinoline-5-sulfonic Acid in HClO4–NaClO4Media." Bulletin of the Chemical Society of Japan 65, no. 8 (August 1992): 2205–10. http://dx.doi.org/10.1246/bcsj.65.2205.

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14

Le Bahers, Tangui, Carlo Adamo, and Ilaria Ciofini. "Theoretical determination of the pKas of the 8-hydroxyquinoline-5-sulfonic acid: A DFT based approach." Chemical Physics Letters 472, no. 1-3 (April 2009): 30–34. http://dx.doi.org/10.1016/j.cplett.2009.02.072.

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15

Lucy, Charles A., and Liwen Ye. "Displacement post-column detection reagents based on the fluorescent magnesium 8-hydroxyquinoline-5-sulfonic acid complex." Journal of Chromatography A 671, no. 1-2 (June 1994): 121–29. http://dx.doi.org/10.1016/0021-9673(94)80230-0.

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16

Arbuthnot, Diane, Xiao-jun Wang, and E. T. Knobbe. "Spectroscopic study of 8-hydroxyquinoline-5-sulfonic-acid-doped sol-gel transition metal ion optrode materials." Journal of Non-Crystalline Solids 178 (November 1994): 52–57. http://dx.doi.org/10.1016/0022-3093(94)90264-x.

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17

Shvoeva, O. P., V. P. Dedkova, and A. A. Grechnikov. "Color reactions of vanadium(V) with 8-hydroxyquinoline-5-sulfonic acid and ascorbic acid on PANV–AV-17 disks." Journal of Analytical Chemistry 72, no. 7 (July 2017): 734–38. http://dx.doi.org/10.1134/s1061934817070115.

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18

HUANG, Hu, Yoshifumi ASAI, Masaaki HIROHATA, Masaaki NAKAMURA, and Fumiaki KAI. "Coordination selectivity in oxovandium(IV) Complex with 7-(3,5-dihalo-2-pyridylazo)-8-hydroxyquinoline-5-sulfonic acid." NIPPON KAGAKU KAISHI, no. 12 (1990): 1348–54. http://dx.doi.org/10.1246/nikkashi.1990.1348.

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19

Brunetti, Barbara, and Elio Desimoni. "A New Voltammetric Sensor Based on a Glassy Carbon Electrode Modified with 8-Hydroxyquinoline-5-sulfonic Acid." Electroanalysis 23, no. 5 (March 16, 2011): 1116–22. http://dx.doi.org/10.1002/elan.201000601.

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20

Mane, V. D., N. J. Wahane, and W. B. Gurnule. "Copolymer resin. VII. 8-hydroxyquinoline-5-sulfonic acid-thiourea-formaldehyde copolymer resins and their ion-exchange properties." Journal of Applied Polymer Science 111, no. 6 (January 2009): 3039–49. http://dx.doi.org/10.1002/app.29369.

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21

Balasubramani, K., P. Thomas, G. Bocelli, and A. Cantoni. "Synthesis and crystal structure of mercury(II) chloride–ferron (7-iodo-8-hydroxyquinoline-5-sulfonic acid) adduct." Journal of Coordination Chemistry 58, no. 18 (December 15, 2005): 1689–94. http://dx.doi.org/10.1080/00958970500239674.

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22

Jiang, Feng Jun, and Wei Dong Xue. "Preparation of Tris(8-Hydroxyquinoline-5-Sulfonic Acid) Iron(III) Complex and Photocatalytic Property of Surface Modified TiO₂." Advanced Materials Research 399-401 (November 2011): 1481–86. http://dx.doi.org/10.4028/www.scientific.net/amr.399-401.1481.

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Tris(8-hydroxyquinoline-5-sulfonic acid) iron(III) complex (Fe(HQS)3) was prepared and characterized by elemental analysis, infrared, nuclear magnetic resonance and Raman spectrum. The results indicated that the Fe atom was located at the center of the Fe(HQS)3complex and the sulfonic groups did not present in the quinoline three-coordinate structure. The TGA analysis result showed that the three ligands were thermally stable within wide temperature range (364 °C, 512 °C, 628 °C,). According to XRD and UV-vis data, the nano-TiO2prepared by hydrothermal method was mainly in the form of anatase and brookite, and the Fe(HQS)3complex had single crystal structure. Neither Fe(HQS)3nor nano-TiO2has observable photocatalytic activity according to the result of our methyl orange degrading experiment. The Fe(HQS)3-TiO2complex, however, demonstrated strong spectral response and photocatalytic activity under visible light.

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23

Lu, Yongguang, Wei Cheng, Xiangru Meng, and Hongwei Hou. "Synthesis, crystal structures and fluorescent properties of two new 7-iodo-8-hydroxyquinoline-5-sulfonic acid-containing polymers." Journal of Molecular Structure 875, no. 1-3 (March 2008): 183–88. http://dx.doi.org/10.1016/j.molstruc.2007.04.027.

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24

Swaile, David F., and Michael J. Sepaniak. "Determination of metal ions by capillary zone electrophoresis with on-column chelation using 8-hydroxyquinoline-5-sulfonic acid." Analytical Chemistry 63, no. 2 (January 15, 1991): 179–84. http://dx.doi.org/10.1021/ac00002a017.

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25

Lü, Xiaodan, Jing Yang, Yuqin Fu, Qianqian Liu, Bin Qi, Changli Lü, and Zhongmin Su. "White light emission from Mn2 +doped ZnS nanocrystals through the surface chelating of 8-hydroxyquinoline-5-sulfonic acid." Nanotechnology 21, no. 11 (February 22, 2010): 115702. http://dx.doi.org/10.1088/0957-4484/21/11/115702.

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26

Le Bahers, Tangui, Carlo Adamo, and Ilaria Ciofini. "Photophysical Properties of 8-Hydroxyquinoline-5-sulfonic Acid as a Function of the pH: A TD-DFT Investigation." Journal of Physical Chemistry A 114, no. 18 (May 13, 2010): 5932–39. http://dx.doi.org/10.1021/jp1014498.

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27

BALASUBRAMANI, Kasthuri, Packianathan Thomas MUTHIAH, Gabrielle BOCELLI, and Andrea CANTONI. "Synthesis and Crystal Structure of Mercury(II) Bromide-Ferron (7-iodo-8-hydroxyquinoline-5-sulfonic acid) Adduct Monohydrate." Analytical Sciences: X-ray Structure Analysis Online 23 (2007): x129—x130. http://dx.doi.org/10.2116/analscix.23.x129.

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28

Martínez-Gómez, Ana Isabel, Sergio Martínez-Rodríguez, Joaquín Pozo-Dengra, Davide Tessaro, Stefano Servi, Josefa María Clemente-Jiménez, Felipe Rodríguez-Vico, and Francisco Javier Las Heras-Vázquez. "Potential Application of N-Carbamoyl-β-Alanine Amidohydrolase from Agrobacterium tumefaciens C58 for β-Amino Acid Production." Applied and Environmental Microbiology 75, no. 2 (November 14, 2008): 514–20. http://dx.doi.org/10.1128/aem.01128-08.

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ABSTRACT An N-carbamoyl-β-alanine amidohydrolase of industrial interest from Agrobacterium tumefaciens C58 (βcarAt) has been characterized. βcarAt is most active at 30°C and pH 8.0 with N-carbamoyl-β-alanine as a substrate. The purified enzyme is completely inactivated by the metal-chelating agent 8-hydroxyquinoline-5-sulfonic acid (HQSA), and activity is restored by the addition of divalent metal ions, such as Mn2+, Ni2+, and Co2+. The native enzyme is a homodimer with a molecular mass of 90 kDa from pH 5.5 to 9.0. The enzyme has a broad substrate spectrum and hydrolyzes nonsubstituted N-carbamoyl-α-, -β-, -γ-, and -δ-amino acids, with the greatest catalytic efficiency for N-carbamoyl-β-alanine. βcarAt also recognizes substrate analogues substituted with sulfonic and phosphonic acid groups to produce the β-amino acids taurine and ciliatine, respectively. βcarAt is able to produce monosubstituted β2- and β3-amino acids, showing better catalytic efficiency (k cat/Km ) for the production of the former. For both types of monosubstituted substrates, the enzyme hydrolyzes N-carbamoyl-β-amino acids with a short aliphatic side chain better than those with aromatic rings. These properties make βcarAt an outstanding candidate for application in the biotechnology industry.

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29

Khalid, Mohd, Ayaz Hassan, Ana M. B. Honorato, Frank N. Crespilho, and Hamilton Varela. "8-Hydroxyquinoline-5-sulfonic acid on reduced graphene oxide layers as a metal-free electrode material for supercapacitor applications." Journal of Electroanalytical Chemistry 847 (August 2019): 113193. http://dx.doi.org/10.1016/j.jelechem.2019.113193.

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30

Ünak, P., D. Özdemir, and T. Ünak. "Stability constants of uranium(VI) and thorium(IV) complexes formed with 8-hydroxyquinoline and its 5-sulfonic acid derivative." Journal of Radioanalytical and Nuclear Chemistry Letters 186, no. 4 (March 1994): 325–32. http://dx.doi.org/10.1007/bf02162616.

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31

Rodríguez-Rodríguez, Cristina, José Manuel Amigo, Jordi Coello, and Santiago Maspoch. "An Introduction to Multivariate Curve Resolution-Alternating Least Squares: Spectrophotometric Study of the Acid–Base Equilibria of 8-Hydroxyquinoline-5-sulfonic Acid." Journal of Chemical Education 84, no. 7 (July 2007): 1190. http://dx.doi.org/10.1021/ed084p1190.

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32

Conelly-Espinosa, Patricia, and David Morales-Morales. "[Pd(HQS)2] (HQS=8-hydroxyquinoline-5-sulfonic acid) a highly efficient catalyst for Suzuki–Miyaura cross couplings in water." Inorganica Chimica Acta 363, no. 6 (April 2010): 1311–15. http://dx.doi.org/10.1016/j.ica.2009.12.038.

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33

Jourquin, G., M. C. Mahedero, S. Paredes, J. C. Vire, and J. M. Kauffmann. "Fluorimetric determination of tin and organotin compounds in hydroorganic and micellar media in the presence of 8-hydroxyquinoline-5-sulfonic acid." Journal of Pharmaceutical and Biomedical Analysis 14, no. 8-10 (June 1996): 967–75. http://dx.doi.org/10.1016/s0731-7085(96)01795-5.

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34

Ye, Liwen, Jennifer E. Wong, and Charles A. Lucy. "Determination of Aminopolycarboxylate Ligands Using 8-Hydroxyquinoline-5-sulfonic Acid-Based Ternary Complexes in Capillary Zone Electrophoresis with Laser-Induced Fluorescence." Analytical Chemistry 69, no. 10 (May 1997): 1837–43. http://dx.doi.org/10.1021/ac9610321.

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35

Salinas, F., A. Mumrñoz de la Peña, and M. S. Duran. "Determination of Aluminium with 8-Hydroxyquinoline-5-Sulfonic Acid in Presence of A Cationic Surfactant by First and Second Derivative Synchronous Fluorimetry." Analytical Letters 21, no. 8 (August 1988): 1457–68. http://dx.doi.org/10.1080/00032718808059876.

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36

Abbasi, S. A., P. C. Nipaney, and R. Soni. "Environmental Status of Cobalt and Its Microdetermination With 7-Nitroso-8-Hydroxyquinoline-5-Sulfonic Acid In Waters, Aquatic Weeds and Animal Tissues." Analytical Letters 22, no. 1 (January 1989): 225–35. http://dx.doi.org/10.1080/00032718908051196.

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37

Wang, Ying, Chengyong Wang, Abraham Warshawsky, and Brian Berkowitz. "8-Hydroxyquinoline-5-sulfonic Acid (HQS) Impregnated on Lewatit MP 600 for Cadmium Complexation: Implication of Solvent Impregnated Resins for Water Remediation." Separation Science and Technology 38, no. 1 (January 3, 2003): 149–63. http://dx.doi.org/10.1081/ss-120016703.

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38

Li, Qi, Xiangyang Liu, Meng Zhuang, Xu Wang, and Hua Cui. "Cobalt(ii)-8-hydroxyquinoline-5-sulfonic acid complex/N-(4-aminobutyl)-N-ethylisoluminol/reduced graphene hybrids as nanocatalytic reaction platforms for chemiluminescence." RSC Advances 7, no. 59 (2017): 37261–67. http://dx.doi.org/10.1039/c7ra06327j.

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39

Ignatova, Milena, Nevena Manolova, Iliya Rashkov, Nadya Markova, Rositsa Kukeva, Radostina Stoyanova, Ani Georgieva, and Reneta Toshkova. "8-Hydroxyquinoline-5-Sulfonic Acid-Containing Poly(Vinyl Alcohol)/Chitosan Electrospun Materials and Their Cu2+ and Fe3+ Complexes: Preparation, Antibacterial, Antifungal and Antitumor Activities." Polymers 13, no. 16 (August 12, 2021): 2690. http://dx.doi.org/10.3390/polym13162690.

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Novel poly(vinyl alcohol) (PVA)/chitosan (Ch)-based fibrous materials containing an ionizable model drug, 8-hydroxyquinoline-5-sulfonic acid (SQ), were successfully fabricated by electrospinning. Complexes between the components of the crosslinked PVA/Ch/SQ mats and Cu2+ and Fe3+ ions were formed. The coordination of these ions in the mats was examined by electron paramagnetic resonance spectroscopy (EPR). The microbiological screening against S. aureus and C. albicans revealed that both the incorporation of SQ in the mats and the complexation with Cu2+ and Fe3+ imparted to these materials antibacterial and antifungal activities. Moreover, the SQ-containing mats and their complexes displayed good cytotoxicity against human cervical HeLa tumor cells. The most prominent was the cytotoxicity of the Cu2+ complex of the mats. The combined antibacterial, antifungal and in vitro antitumor activities render these novel materials promising candidates for wound dressing applications and for application in the local treatment of cervical tumors.

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40

Shvoeva, O. P., V. P. Dedkova, and S. B. Savvin. "Sensitivity and selectivity of the reaction of vanadium(V) with 4-(2-Pyridylazo)resorcinol on a solid support containing anion-exchange groups and modified with 8-hydroxyquinoline or 8-hydroxyquinoline-5-sulfonic acid." Journal of Analytical Chemistry 55, no. 1 (January 2000): 21–24. http://dx.doi.org/10.1007/bf02757626.

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41

Zhang, Jing, Xiaojing Yong, Dongyan Zhao, and Qiuyi Shi. "Accurate Quantification of Two Key Time Points Used in the Determination of Hydroxyl Polyaluminum Species by Ferron Timed Spectrophotometry." Journal of AOAC INTERNATIONAL 98, no. 1 (January 1, 2015): 225–29. http://dx.doi.org/10.5740/jaoacint.14-073.

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Abstract The content of mononuclear Al (Ala%) changed with its determination time (ta) under different dosages of Ferron (7-iodo-8-hydroxyquinoline-5-sulfonic acid, [Ferron]), and the change of Ala% with [Ferron] at different ta was systematically investigated for the firsttime. Thus, the most appropriate ta was found with the optimal [Ferron]. Also, the judgment of the platform (flat or level portion) of the complete reaction on the absorption-time curve determined in the hydroxyl polyaluminum solution by Ferron timed spectrophotometry (Ferron assay) was first digitized. The time point (tb) of complete reaction between the medium polyaluminum (Alb)and Ferron reagent depended on the reaction extent, and time could not be used only to judge. Thus, the tb was accurately determined and reduced to half of original, which improved the experiment efficiency significantly. The Ferron assay was completely optimized.

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42

Vavsari, Vaezeh Fathi, Ghodsi Mohammadi Ziarani, Saeed Balalaie, Arezoo Latifi, Mehdi Karimi, and Alireza Badiei. "New functionalized 8-hydroxyquinoline-5-sulfonic acid mesoporous silica (HQS-SBA-15) as an efficient catalyst for the synthesis of 2-thiohydantoin derivatives." Tetrahedron 72, no. 35 (September 2016): 5420–26. http://dx.doi.org/10.1016/j.tet.2016.07.034.

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43

Huang, Shih-Yi, and Shiuh-Jen Jiang. "8-Hydroxyquinoline-5-sulfonic acid as the modifier for the determination of trace elements in cereals by slurry sampling electrothermal vaporization ICP-MS." Analytical Methods 2, no. 9 (2010): 1310. http://dx.doi.org/10.1039/c0ay00367k.

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44

Zhang, Jing, Yijin Ren, Fang Chang, and Qiuyi Shi. "Determination Time of the Mononuclear Aluminum Species in the Hydroxyl Polyaluminum Solution by Ferron (7-iodine-8-hydroxyquinoline-5-sulfonic Acid)-Timed Spectrometry." Spectroscopy Letters 48, no. 5 (December 13, 2014): 359–66. http://dx.doi.org/10.1080/00387010.2014.883543.

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45

Shijo, Yoshio, Atsuko Saitoh, and Kazuyoshi Suzuki. "Separation of Al(III), Cu(II), Ga(III), and Fe(III) as 8-Hydroxyquinoline-5-sulfonic Acid Complexes by High-performance Liquid Chromatography." Chemistry Letters 18, no. 2 (February 1989): 181–84. http://dx.doi.org/10.1246/cl.1989.181.

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46

Hamdi, Najwa, Federica Proietto, Hédi Ben Amor, Alessandro Galia, Rosalinda Inguanta, Salah Ammar, Abdellatif Gadri, and Onofrio Scialdone. "Effective Removal and Mineralization of 8‐Hydroxyquinoline‐5‐sulfonic Acid through a Pressurized Electro‐Fenton‐like Process with Ni−Cu−Al Layered Double Hydroxide." ChemElectroChem 7, no. 11 (June 2, 2020): 2457–65. http://dx.doi.org/10.1002/celc.202000463.

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47

Kutluay, Sinan. "Excellent adsorptive performance of novel magnetic nano-adsorbent functionalized with 8-hydroxyquinoline-5-sulfonic acid for the removal of volatile organic compounds (BTX) vapors." Fuel 287 (March 2021): 119691. http://dx.doi.org/10.1016/j.fuel.2020.119691.

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48

Huang, Hu, Fumiaki Kai, Tomoko Shoda, and Masaaki Nakamura. "COORDINATION SELECTIVITIES IN IRON(II) AND VANADIUM(V) COMPLEXES WITH THE MULTIDENTATE LIGANDS, 7-[(3,5-DIHALO-2-PYRIDYL)AZO]-8-HYDROXYQUINOLINE-5-SULFONIC ACID." Journal of Coordination Chemistry 28, no. 2 (April 1993): 155–66. http://dx.doi.org/10.1080/00958979308035155.

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49

Huang, Hu, Fumiaki Kai, Yoshifumi Asai, Masaaki Hirohata, and Masaaki Nakamura. "Synthesis, Crystal Structure, and Property of Novel Tetranuclear Nickel(II) Complex with Multidentate Ligand 7-[(3,5-Dichloro-2-pyridyl)azo]-8-hydroxyquinoline-5-sulfonic Acid." Bulletin of the Chemical Society of Japan 64, no. 8 (August 1991): 2464–69. http://dx.doi.org/10.1246/bcsj.64.2464.

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50

Swaile, David F., and Michael E. Sepaniak. "Determination of metal ions by capillary zone electrophoresis with on-column chelation using 8-hydroxyquinoline-5-sulfonic acid [Erratum to document cited in CA114(2):16689q]." Analytical Chemistry 63, no. 8 (April 15, 1991): 848. http://dx.doi.org/10.1021/ac00008a025.

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