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1

Almagro-Gómez, Carmen María, José Ginés Hernández-Cifre, and Joaquín Ángel Ortuño. "Real-Time Potentiometric Monitoring of Tetrachloroaurate(III) with an Ion-Selective Electrode and Its Applications to HAuCl4 Iodide-Catalyzed Reduction by Hydroxylamine." Chemosensors 12, no. 6 (2024): 95. http://dx.doi.org/10.3390/chemosensors12060095.

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Ion-selective electrodes for tetrachloroaurate(III) have been developed for potentiometric monitoring of the reduction reaction of tetrachloroaurate(III). Three different plasticized polyvinyl chloride membranes containing tridodecymethylammonium chloride as an anion exchanger were investigated. These membranes differ in the plasticizer used, either 2-nitrophenyl octyl ether (NPOE) or tricresyl phosphate (TCP) or bis-(2-ethylhexyl) sebacate (DOS). The potentiometric response of the electrodes to the tetrachloroaurate(III) concentration was studied by two methods. In the first method, commonly
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2

Jones, P. G., D. Jentsch, and E. Schwarzmann. "Trichlorosulfonium(IV) tetrachloroaurate(III)." Acta Crystallographica Section C Crystal Structure Communications 44, no. 2 (1988): 210–12. http://dx.doi.org/10.1107/s0108270187009533.

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3

Freire Erdbrügger, C., P. G. Jones, R. Schelbach, E. Schwarzmann, and G. M. Sheldrick. "Tetrachlorophosphonium(V) tetrachloroaurate(III)." Acta Crystallographica Section C Crystal Structure Communications 43, no. 10 (1987): 1857–59. http://dx.doi.org/10.1107/s0108270187089856.

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4

Jones, P. G., R. Schelbach, and E. Schwarzmann. "Thallium(I) tetrachloroaurate(III)." Acta Crystallographica Section C Crystal Structure Communications 43, no. 9 (1987): 1674–75. http://dx.doi.org/10.1107/s0108270187090619.

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5

Jones, P. G., R. Schelbach, and E. Schwarzmann. "Trichloroselenonium(IV) tetrachloroaurate(III)." Acta Crystallographica Section C Crystal Structure Communications 43, no. 4 (1987): 607–9. http://dx.doi.org/10.1107/s0108270187094824.

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6

Jones, P. G., R. Hohbein, and E. Schwarzmann. "Anhydrous sodium tetrachloroaurate(III)." Acta Crystallographica Section C Crystal Structure Communications 44, no. 7 (1988): 1164–66. http://dx.doi.org/10.1107/s0108270188002756.

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7

Preut, H., B. Fischer, and B. Lippert. "9-Ethylguaninium tetrachloroaurate(III) hydrate." Acta Crystallographica Section C Crystal Structure Communications 46, no. 6 (1990): 1115–17. http://dx.doi.org/10.1107/s010827019000124x.

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8

Zhang, Xiang-Pei, Guang Yang, and Seik Weng Ng. "4,4′-Bipyridinium tetrachloroaurate(III) chloride." Acta Crystallographica Section E Structure Reports Online 62, no. 9 (2006): m2018—m2020. http://dx.doi.org/10.1107/s1600536806029199.

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9

Gidd, Anna N., Madhukar D. Bhand, and Gavisiddappa S. Gokavi. "Tetrachloroaurate(III) oxidation of thallium(I)." Transition Metal Chemistry 20, no. 4 (1995): 367–68. http://dx.doi.org/10.1007/bf00139131.

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10

Schröder, Uwe, Rainer Richter, Jürgen Hartung, Ulrich Abram, and Lothar Beyer. "Substituierte 1,2,4-Thiadiazolium-dichloroaurate(I) und -tetra- chloroaurate(III) als Reaktionsprodukte von N-Thiocarbamoyl- benzamidinen mit TetrachIorogold(III)-Verbindungen / Substituted 1,2,4-Thiadiazolium dichloroaurates(I) and -tetrachloroaurates(III) as Products o f the Reaction o f N -Thiocarbam oyl-benzamidines with Tetrachlorogold(III) Compounds." Zeitschrift für Naturforschung B 52, no. 5 (1997): 620–28. http://dx.doi.org/10.1515/znb-1997-0513.

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Abstract The reactions of N-diethylaminothiocarbonyl-benzamidines Et2N-C(S)-N=C(NHR)-Ph (1: R = Ph, 2: R = C3H7, 3: R = H) with gold(III) compounds were studied. Treatment of 1 and 2 with equivalent amounts of tetrachlorogold acid gives 2,3-substituted 5-diethylamino-1,2,4- thiadiazoliumdichloroaurates(I) (1a, 2a). With tetrachlorogold acid in excess 1 yields 2,3-diphenyl- 5-diethylamino-l,2,4-thiadiazolium-tetrachloroaurate(III) 1b. With 3 and Na[AuCl4] bis(3-phenyl-5- diethylamino-1,2,4-thiadiazolium)-chloride-tetrachloroaurate(III) 3b is produced. The structures of la, 2a and 3b were invest
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11

Shachter, A. M., E. B. Fleischer, and R. C. Haltiwanger. "The structure of (5,10,15,20-tetraphenylporphinato)gold(III) tetrachloroaurate(III)." Acta Crystallographica Section C Crystal Structure Communications 43, no. 10 (1987): 1876–78. http://dx.doi.org/10.1107/s0108270187089789.

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12

Jones, P. G., A. Olbrich, R. Schelbach, and E. Schwarzmann. "Bis(triphenylarsine oxide)hydrogen(I) tetrachloroaurate(III)." Acta Crystallographica Section C Crystal Structure Communications 44, no. 12 (1988): 2201–2. http://dx.doi.org/10.1107/s0108270188008947.

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13

Nockemann, Peter, Kristof Van Hecke, Luc Van Meervelt, and Koen Binnemans. "Bis{2-[(2-hydroxyethyl)iminomethyl]phenolato}gold(III) tetrachloroaurate(III)." Acta Crystallographica Section E Structure Reports Online 63, no. 2 (2007): m402—m404. http://dx.doi.org/10.1107/s1600536806055358.

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14

Pormohammad, Ali, and Raymond J. Turner. "Silver Antibacterial Synergism Activities with Eight Other Metal(loid)-Based Antimicrobials against Escherichia coli, Pseudomonas aeruginosa, and Staphylococcus aureus." Antibiotics 9, no. 12 (2020): 853. http://dx.doi.org/10.3390/antibiotics9120853.

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The present study surveys potential antibacterial synergism effects of silver nitrate with eight other metal or metalloid-based antimicrobials (MBAs), including silver nitrate, copper (II) sulfate, gallium (III) nitrate, nickel sulfate, hydrogen tetrachloroaurate (III) trihydrate (gold), aluminum sulfate, sodium selenite, potassium tellurite, and zinc sulfate. Bacteriostatic and bactericidal susceptibility testing explored antibacterial synergism potency of 5760 combinations of MBAs against three bacteria (Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus) in three different medi
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15

Cohen, Larissa R., Laura A. Peña, Anton J. Seidl, Janet M. Olsen, Jennifer Wekselbaum, and Patrick E. Hoggard. "The photocatalytic decomposition of chloroform by tetrachloroaurate(III)." Monatshefte für Chemie - Chemical Monthly 140, no. 10 (2009): 1159–65. http://dx.doi.org/10.1007/s00706-009-0175-x.

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16

Nirmala, N. Baby, and P. Vani P. Vani. "Oxidation of L-Tyrosine by Tetrachloroaurate(III) – a Kinetic Study." International Journal of Scientific Research 2, no. 4 (2012): 25–27. http://dx.doi.org/10.15373/22778179/apr2013/11.

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17

Schneider, Wolfgang, Andreas Bauer, and Hubert Schmidbaur. "[(N, N’, N”-Tricyclohexyl)-N”- cyclohexylcarbamoylguanidinium] Tetrachloroaurate(III) as a Product of the Reaction of Dicyclohexylcarbo- diimide with HAuCl4 . aq." Zeitschrift für Naturforschung B 52, no. 9 (1997): 1152–54. http://dx.doi.org/10.1515/znb-1997-0922.

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Reaction of tetrachloroauric(III) acid hydrate with dicyclohexylcarbodiimide (dcc) in dichloromethane in the presence of equimolar amounts of triethylamine leads to a complex reaction mixture. One of the components was shown by X-ray crystallography to be [(N, N’, N”-tricyclohexyl)- N”-cyclohexylcarbamoylguanidinium] tetrachloroaurate( III) (1) which contains as a cation the addition product of dcc with the corresponding urea.
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18

Neal, Sabine, Samuel Orefuwa, Atiya Overton, Richard Staples, and Ahmed Mohamed. "Synthesis of Diazonium Tetrachloroaurate(III) Precursors for Surface Grafting." Inorganics 1, no. 1 (2013): 70–84. http://dx.doi.org/10.3390/inorganics1010070.

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19

Kiriyama, H., N. Matsushita, and Y. Yamagata. "Structures of diguanidinium tetrachloropalladate(II) and guanidinium tetrachloroaurate(III)." Acta Crystallographica Section C Crystal Structure Communications 42, no. 3 (1986): 277–80. http://dx.doi.org/10.1107/s010827018609649x.

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20

Sen Gupta, Kalyan Kali, Sankar Das, and Shipra Sen Gupta. "Kinetics of the oxidation of sulphite by tetrachloroaurate(III)." Transition Metal Chemistry 13, no. 4 (1988): 261–63. http://dx.doi.org/10.1007/bf01025669.

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21

Makotchenko, E. V., I. A. Baidina, and D. Yu Naumov. "Synthesis and crystal structure of tris(ethylenediamine)cobalt(III) bis(tetrachloroaurate(III)) chloride." Journal of Structural Chemistry 47, no. 3 (2006): 499–503. http://dx.doi.org/10.1007/s10947-006-0328-2.

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22

Soni, Vimal, and Raj N. Mehrotra. "Mechanism of the oxidation of hydrazoic acid by tetrachloroaurate(III) ion." Transition Metal Chemistry 33, no. 3 (2008): 367–76. http://dx.doi.org/10.1007/s11243-007-9052-9.

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23

Sen Gupta, Kalyan K., Ankan Sanyal, and Pratik K. Sen. "Kinetics of the oxidation of nitrous acid by tetrachloroaurate(III) inHCl." Transition Metal Chemistry 19, no. 5 (1994): 534–38. http://dx.doi.org/10.1007/bf00136369.

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24

Sen, Pratik K., A. B. Bilkis, and Kalyan K. Sen Gupta. "Kinetics and mechanism of the oxidation of glycolaldehyde by tetrachloroaurate(III)." International Journal of Chemical Kinetics 30, no. 9 (1998): 613–19. http://dx.doi.org/10.1002/(sici)1097-4601(1998)30:9<613::aid-kin2>3.0.co;2-v.

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25

Maeda, Ichiro, and Takehiko Tsuruta. "Microbial Gold Biosortion and Biomineralization from Aqueous HAuCl4 Solution." Minerals 10, no. 3 (2020): 285. http://dx.doi.org/10.3390/min10030285.

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The removal of gold (III) from aqueous systems using biosorption and biomineralization by microbial cells was investigated. High levels of gold (III) were removed from a hydrogen tetrachloroaurate (III) solution for 72 h by microbial species, including bacteria, fungi and yeasts. Previously, we reported that the amounts of gold (III) removed through biosorption by gram-positive bacteria, fungi, and yeasts was lower than that by gram-negative bacteria. Candida krusei was able to remove large amounts of gold (III) through biosorption and biomineralization. Interestingly, more gold was removed by
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26

Ramos, Manuel, Karina Castillo, Domingo A. Ferrer, Rurik J. Farias, Sergio Flores, and Russell R. Chianelli. "Microwave-Assisted Synthesis Core-Fe3O4 Shell-Au Cubic Nanoparticles." ISRN Nanotechnology 2011 (October 26, 2011): 1–3. http://dx.doi.org/10.5402/2011/893879.

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Core-Shell (Fe3O4/Au) nanoparticles were synthesized using iron II chloride tetrahydrate (FeCl2H2O) and potassium tetrachloroaurate III (AuCl4K) precursors under microwave-assisted conditions. Products were analyzed using field emission gun electron microscope in transmission and scanning modes; energy disperse X-ray spectroscopy performed during STEM measurements indicated a signal for gold K and M signals at 9 keV and 13 keV, respectively, confirming Au atoms at nanoparticle's perimeter and Fe-L signal at 8 keV to be at the center.
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27

Kavokina, Stella, Anton Osipov, Vlad Samyshkin, et al. "Laser Fabrication of Gold–sp-Carbon Films." Condensed Matter 8, no. 4 (2023): 96. http://dx.doi.org/10.3390/condmat8040096.

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We develop a method for the laser synthesis and deposition of carbon–gold films formed by a net of linear sp-carbon chains and stabilized by gold nanoparticles. The originality of the method is in the simultaneous production of carbon chains and gold nanoparticles due to the laser fragmentation of the amorphous carbon and hydrogen tetrachloroaurate (III) or chloroauric acid. We study how surface resistivity alters the effect of the obtained films via the illumination in the visible spectral range.
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28

Canovese, Luciano, Lucio Cattalini, Michele Tomaselli, and Martin L. Tobe. "Reactivity of heterocyclic nitrogen donors in systems containing the tetrachloroaurate(III) anion." Journal of the Chemical Society, Dalton Transactions, no. 2 (1991): 307. http://dx.doi.org/10.1039/dt9910000307.

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29

Streszewski, Bartłomiej, Wiktor Jaworski, Konrad Szaciłowski, and Krzysztof Pacławski. "Kinetics and Mechanism of Redox Reaction between Tetrachloroaurate(III) Ions and Hydrazine." International Journal of Chemical Kinetics 46, no. 6 (2014): 328–37. http://dx.doi.org/10.1002/kin.20850.

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30

Pratik, K. Sen, R. Samaddar Purabi, Das Debasmita, and Das Kaushik. "Kinetics and mechanism of the oxidation of ethane diol and butane-2,3-diol by tetrachloroaurate(III) in acetate buffer medium." Journal of Indian Chemical Society Vol. 84, May 2007 (2007): 462–67. https://doi.org/10.5281/zenodo.5819939.

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Department of Chemistry, Jadavpur University, Kolkata-700 032, India <em>E-mail</em> : senpk@yahoo.com <em>Manuscript received 4 December 2006, accepted 22 March 2007</em> The reductivities of ethane diol and butane-2,3-diol towards tetrachloroaurate(III) in acetate buffer medium have been studied. The reaction is of first order with respect to the oxidant but of complex order with respect to the substrate. The reaction is inhibited by both H<sup>+</sup> and Cl<sup>-</sup> ions. A decrease in the dielectric constant of the medium diminishes the rate. Different thermodynamic parameters have bee
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31

Shi, Ren-xin, Yun-kui Liu, and Zhen-yuan Xu. "Sodium tetrachloroaurate(III) dihydrate-catalyzed efficient synthesis of 1,5-benzodiazepine and quinoxaline derivatives." Journal of Zhejiang University SCIENCE B 11, no. 2 (2010): 102–8. http://dx.doi.org/10.1631/jzus.b0900288.

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32

Suwalsky, Mario, Pamela Zambenedetti, Emilio Carpené, et al. "Effects of chronic treatment with sodium tetrachloroaurate(III) in mice and membrane models." Journal of Inorganic Biochemistry 98, no. 12 (2004): 2080–86. http://dx.doi.org/10.1016/j.jinorgbio.2004.09.015.

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33

Soni, Vimal, R. S. Sindal, and Raj N. Mehrotra. "Kinetics and mechanism of the oxidation of oxalic acid by tetrachloroaurate(III) ion." Inorganica Chimica Acta 360, no. 10 (2007): 3141–48. http://dx.doi.org/10.1016/j.ica.2007.03.006.

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34

Ishikawa, Atsushi, Yukari Ito, Keizo Horiuchi, Tetsuo Asaji, and Daiyu Nakamura. "Chlorine nuclear quadrupole resonances and motion of pyridinium ions in pyridinium tetrachloroaurate(III)." Journal of Molecular Structure 192, no. 3-4 (1989): 221–27. http://dx.doi.org/10.1016/0022-2860(89)85042-2.

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35

Shaikjee, Ahmed, Demetrius C. Levendis, Helder M. Marques, and Richard Mampa. "A gold(III) complex and a tetrachloroaurate salt of the neuroepileptic drug gabapentin." Inorganic Chemistry Communications 14, no. 4 (2011): 534–38. http://dx.doi.org/10.1016/j.inoche.2011.01.017.

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36

Berglund, Johan, and Lars I. Elding. "Kinetics and Mechanism for Reduction of Tetrachloroaurate(III), trans-Dicyanodichloraurate(III), and trans-Dicyanodibromoaurate(III) by Sulfite and Hydrogen Sulfite." Inorganic Chemistry 34, no. 2 (1995): 513–19. http://dx.doi.org/10.1021/ic00106a013.

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37

Nakajima, Akira, Emiko Matsuda, Yuto Ueda, and Kunihiko Tajima. "ESR analysis of the oxidation reactions of phosphorus-containing nitrone-type spin traps with gold(III) ion." Canadian Journal of Chemistry 88, no. 6 (2010): 556–62. http://dx.doi.org/10.1139/v10-033.

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Phosphorus-containing cyclic nitrones, such as DEPMPO, CYPMPO, and DPPMPO, were oxidized by hydrogen tetrachloroaurate(III) to DEPMPOX, CYPMPOX, and DPPMPOX with the precipitation of Au(0). The reaction was depressed by the addition of chloride or hydroxide ions. The peculiar pH dependency was observed in DEPMPOX, CYPMPOX, and DPPMPOX formation, which should be caused by the diethoxyphosphoryl group in DEPMPO, the 1,3-propoxy cyclophosphoryl group in CYPMPO, and the diphenylphosphinoyl group in DPPMPO. The oxidation of the nitrones proceeded through the ligand exchange of Cl– in AuCl4– with &g
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38

Sulaeman, Uyi, Richo Dwi Permadi, Alfa Marcorius, Hartiwi Diastuti, Anung Riapanitra, and Shu Yin. "The Surface Modification of Ag3PO4 using Tetrachloroaurate(III) and Metallic Au for Enhanced Photocatalytic Activity." Bulletin of Chemical Reaction Engineering & Catalysis 16, no. 4 (2021): 707–15. http://dx.doi.org/10.9767/bcrec.16.4.10863.707-715.

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The improvement of Ag3PO4 photocatalytic activity was successful by incorporating tetrachloroaurate(III) (AuCl4−) and metallic Au on the surface of Ag3PO4. The photocatalysts were synthesized using the coprecipitation and chemisorption method. Coprecipitation of Ag3PO4 was carried out under ethanol-water solution using the starting material of AgNO3 and Na2HPO4.12H2O. AuCl4− ion and metallic Au were incorporated on the surface of Ag3PO4 using a chemisorption method under auric acid solution. The photocatalysts were characterized using XRD, DRS, SEM, and XPS. The AuCl4− ion and metallic Au were
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39

Soni, Vimal, R. S. Sindal, and Raj N. Mehrotra. "Kinetics of oxidation of l-histidine by tetrachloroaurate(III) ion in perchloric acid solution." Polyhedron 24, no. 10 (2005): 1167–74. http://dx.doi.org/10.1016/j.poly.2005.03.057.

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40

Palgrave, Robert G., and Ivan P. Parkin. "Aerosol Assisted Chemical Vapor Deposition of Gold and Nanocomposite Thin Films from Hydrogen Tetrachloroaurate(III)." Chemistry of Materials 19, no. 19 (2007): 4639–47. http://dx.doi.org/10.1021/cm0629006.

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41

Holt, Katherin B, Genevieve Sabin, Richard G Compton, John S Foord, and Frank Marken. "Reduction of Tetrachloroaurate(III) at Boron-Doped Diamond Electrodes: Gold Deposition Versus Gold Colloid Formation." Electroanalysis 14, no. 12 (2002): 797. http://dx.doi.org/10.1002/1521-4109(200206)14:12<797::aid-elan797>3.0.co;2-m.

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42

Sakamoto, Takeru, Noriko Yamauchi, Takumu Takase, Mone Kimura, Kohsuke Gonda, and Yoshio Kobayashi. "Synthesis of Single Nanometer-Sized Au Nanoparticles Coated with Silica Toward X-Ray Contrast Agent." Solid State Phenomena 354 (December 20, 2023): 119–28. http://dx.doi.org/10.4028/p-5loba0.

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In this study, we proposed a method for fabricating diagnostic imaging nanoparticles composed of Au nanoparticles and silica shells (Au/SiO2). The proposed method consisted of two steps. The first step was the synthesis of Au nanoparticles. In sodium hydroxide (NaOH) solution, hydrogen tetrachloroaurate (III) trihydrate was reduced with tetrakis(hydroxymethyl)phosphonium chloride to synthesize Au nanoparticles with a diameter of 1.7 ± 0.3 nm. The Au nanoparticles were then coated with silica in the following step. The silica coating was achieved via a sol–gel reaction of tetraethyl orthosilica
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43

Vicente, Jose, Maria-Teresa Chicote, Maria D. Bermudez, et al. "Synthesis of mixed diarylgold(III) complexes. Crystal structure of cis-[2-(phenylazo)phenyl][2-{(dimethylamino)methyl}phenyl]gold(III) tetrachloroaurate." Journal of Organometallic Chemistry 310, no. 3 (1986): 401–9. http://dx.doi.org/10.1016/0022-328x(86)80201-7.

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44

Pratik, K. Sen, Sarkar Anirban, Maiti Krishnendu, and Pal Biswajit. "Reduction of gold(III) by malonate in acetate buffer : Mechanism of the rate processes." Journal of Indian Chemical Society 93, Mar 2016 (2016): 321–26. https://doi.org/10.5281/zenodo.5639042.

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Department of Chemistry, Jadavpur University, Kolkata-700 032, India <em>E-mail </em>: senpk@yahoo.com Department of Chemistry, St. Paul&rsquo;s Cathedral Mission College, 33/1, Raja Rammohan Roy Sarani, Kolkata-700 009, India <em>E-mail </em>: palbiswajit@yahoo.com <em>Manuscript received 08 June 2015, accepted 26 November 2015</em> The kinetics of reduction of tetrachloroaurate(III) by sodium malonate has been spectrophotometrically studied in acetic acid-sodium acetate buffer in the pH range 4.20&ndash;4.83. The reaction is of first order with respect to AuIII but of complex order with resp
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45

Santosa, Sri Juari, Philip Anggo Krisbiantoro, Mustika Yuniarti, Kustomo, and Soerja Koesnarpardi. "Magnetically separable humic acid-functionalized magnetite for reductive adsorption of tetrachloroaurate(III) ion in aqueous solution." Environmental Nanotechnology, Monitoring & Management 15 (May 2021): 100454. http://dx.doi.org/10.1016/j.enmm.2021.100454.

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46

Pal, Biswajit, Pratik K. Sen, and Kalyan K. Sen Gupta. "Reactivity of alkanols and aryl alcohols towards tetrachloroaurate(III) in sodium acetate-acetic acid buffer medium." Journal of Physical Organic Chemistry 14, no. 5 (2001): 284–94. http://dx.doi.org/10.1002/poc.361.

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47

Lee, Ming-Ting, Tamana Ahmed та Michael E. Friedman. "Inhibition of Hydrolytig Enzymes by Gold Compounds I. β-Glucuronidase and Acid Phosphatase by Sodium Tetrachloroaurate (III) and Potassium Tetrabromoaurate (III)". Journal of Enzyme Inhibition 3, № 1 (1989): 23–33. http://dx.doi.org/10.3109/14756368909030361.

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48

Sun, Lingling, Min Li, Fei Li, Fuchun Wang, Xiangfeng Liang, and Qinghui Shou. "Solution-Phase Synthesis of KCl Nanocrystals Templated by PEO-PPO-PEO Triblock Copolymers Micelles." Polymers 16, no. 7 (2024): 982. http://dx.doi.org/10.3390/polym16070982.

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The current work introduces the synthesis of inorganic salt nano/micro-crystals during the reduction of hydrogen tetrachloroaurate(III) by Pluronic triblock copolymers (P123, PEO20–PPO70–PEO20). The morphologies and component were confirmed using an electron microscope with an electronic differential system (EDS), and the crystal structures were determined with X-ray diffraction (XRD). The morphologies highly depend on the concentrations of Pluronic and pH values. The mean size of the nanocrystal and hollow micro-crystal were controlled typically in the range of 32–150 nm (side length) and 1.4
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49

Hsu, Shih-Jen, and Ivan J. B. Lin. "Synthesis of Gold Nanosheets through Thermolysis of Mixtures of Long Chain 1-Alkylimidazole and Hydrogen Tetrachloroaurate(III)." Journal of the Chinese Chemical Society 56, no. 1 (2009): 98–106. http://dx.doi.org/10.1002/jccs.200900014.

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Hassan, S. "Nitron tetrachloroaurate(III) electrodes with poly(vinyl chloride) and liquid membranes for the selective determination of gold." Talanta 38, no. 5 (1991): 561–66. http://dx.doi.org/10.1016/0039-9140(91)80181-x.

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