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Journal articles on the topic 'Silver(I) catalyzed oxidation'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Chhajed, Ravisha, Sanyogita Sharma, Rakshit Ameta, and Pinki B. Punjabi. "Silver(I) Catalyzed Photochemical Oxidation of Methylene Blue and Safranine-O by Peroxydisulphate: A Green Chemical Approach." International Journal of Photochemistry 2014 (September 30, 2014): 1–6. http://dx.doi.org/10.1155/2014/232475.

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In the present investigation, a comparative study of silver(I) catalysed photochemical oxidation of methylene blue (MB) and safranine-O (SO) by peroxydisulphate has been reported. The effect of different parameters, such as pH, concentration of peroxydisulphate, silver nitrate, and light intensity, on the reaction rate has been observed. The progress of the photochemical oxidation was monitored spectrophotometrically. The optimum conditions for photochemical oxidation were achieved. The dyes were completely oxidized and degraded into CO2 and H2O. A tentative mechanism for silver(I) catalyzed p

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2

Chakraborty, Debashis, and Rima Das. "Silver Nitrate Catalyzed Oxidation of Sulfides." Synthesis 2011, no. 02 (2010): 277–80. http://dx.doi.org/10.1055/s-0030-1258331.

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3

Arpitha, M. K. "STUDY OF CATALYTIC POTENCY OF GREEN SYNTHESIZED SILVER DOPED CuO NANOPARTICLES WITH OXIDATION OF SERTRALINE HYDROCHLORIDE BY CHLORAMINE-T: A KINETIC AND MECHANISTIC INVESTIGATION." RASAYAN Journal of Chemistry 18, no. 01 (2025): 240–53. https://doi.org/10.31788/rjc.2025.1819110.

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In this study, the concentration was on the catalyzed potency of green synthesized silver-doped copper oxide nanoparticles, and the oxidation of sertraline hydrochloride was performed in an aqueous acid medium using chloramine-T. Sustainable CuO nanoparticles doped with silver were synthesized using sol-gel. Utilizing scanning electron microscopy (SEM), ultraviolet-visible light (UV) analysis, and X-ray diffraction (XRD) to characterize the nanoparticles served to validate their successful production. With regard to [CAT], both catalyzed and uncatalyzed reactions follow first-order kinetics. E

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4

Thomas, John W., and Jay E. Taylor. "High temperature–pressure aqueous oxidations. IV. A kinetic study of the oxidation and enolization of cyclohexanone in the presence of catalytic metal ions." Canadian Journal of Chemistry 67, no. 1 (1989): 165–70. http://dx.doi.org/10.1139/v89-027.

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The aqueous high pressure–temperature oxidation of cyclohexanone was found to be strongly catalyzed by silver, iron(III), and copper ions but not by aluminum, cobalt, manganese(II), or nickel ions. The reactivities of the catalytic ions were inhibited by the acidic oxidation products. Accordingly, initial reaction velocities were determined and used to correlate the kinetic data. A detailed kinetic study of copper ion catalysis has shown that in the presence of that ion the reaction was first order in cyclohexanone, one-half order in copper ion, and zero order in oxygen. The rate of enolizatio

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5

Das, Rima, and Debashis Chakraborty. "ChemInform Abstract: Silver Nitrate Catalyzed Oxidation of Sulfides." ChemInform 42, no. 21 (2011): no. http://dx.doi.org/10.1002/chin.201121087.

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6

Wu, Hao, Yi-Chun Wang, Andrey Shatskiy, et al. "Modular synthesis of 3-substituted isocoumarins via silver-catalyzed aerobic oxidation/6-endo heterocyclization of ortho-alkynylbenzaldehydes." Organic & Biomolecular Chemistry 19, no. 30 (2021): 6657–64. http://dx.doi.org/10.1039/d1ob01065d.

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A method involving silver-catalyzed aerobic oxidation/6-endo heterocyclization of ortho-alkynylbenzaldehydes to yield 3-substituted isocoumarins is described. Mechanistic studies suggest the involvement of a free-radical pathway.

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7

Liu, Mingxin, Haining Wang, Huiying Zeng, and Chao-Jun Li. "Silver(I) as a widely applicable, homogeneous catalyst for aerobic oxidation of aldehydes toward carboxylic acids in water—“silver mirror”: From stoichiometric to catalytic." Science Advances 1, no. 2 (2015): e1500020. http://dx.doi.org/10.1126/sciadv.1500020.

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The first example of a homogeneous silver(I)-catalyzed aerobic oxidation of aldehydes in water is reported. More than 50 examples of different aliphatic and aromatic aldehydes, including natural products, were tested, and all of them successfully underwent aerobic oxidation to give the corresponding carboxylic acids in extremely high yields. The reaction conditions are very mild and greener, requiring only a very low silver(I) catalyst loading, using atmospheric oxygen as the oxidant and water as the solvent, and allowing gram-scale oxidation with only 2 mg of our catalyst. Chromatography is c

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8

Ye, Yingjie, Yi Guo, Yuan Yue, et al. "Colorimetric sensing of copper ions based on the anti-aggregation of unmodified silver nanoparticles in the presence of 1,4-dithiothreitol." Analytical Methods 7, no. 2 (2015): 566–72. http://dx.doi.org/10.1039/c4ay02359e.

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9

Grigoreva, Anna, Ekaterina Kolobova, Ekaterina Pakrieva, et al. "Supported Silver Nanoparticles as Catalysts for Liquid-Phase Betulin Oxidation." Nanomaterials 11, no. 2 (2021): 469. http://dx.doi.org/10.3390/nano11020469.

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Herein, it has been shown that betulin can be transformed into its biologically active oxo-derivatives (betulone, betulinic and betulonic aldehydes) by liquid-phase oxidation over supported silver catalysts under mild conditions. In order to identify the main factors determining the catalytic behavior of nanosilver catalysts in betulin oxidation, silver was deposited on various alumina supports (γ-alumina and boehmite) using deposition–precipitation with NaOH and incipient wetness impregnation methods, followed by treatment in H2 or O2. Silver catalysts and the corresponding supports were char

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10

Uchiyama, G., and S. Fujine. "Destruction of butyraldehyde isomers using silver catalyzed electrochemical oxidation." Journal of Radioanalytical and Nuclear Chemistry 230, no. 1-2 (1998): 105–9. http://dx.doi.org/10.1007/bf02387454.

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11

Schade, Oliver R., Abhijeet Gaur, Anna Zimina, Erisa Saraçi, and Jan-Dierk Grunwaldt. "Mechanistic insights into the selective oxidation of 5-(hydroxymethyl)furfural over silver-based catalysts." Catalysis Science & Technology 10, no. 15 (2020): 5036–47. http://dx.doi.org/10.1039/d0cy00878h.

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Silver-catalyzed oxidation of 5-(hydroxymethyl)furfural (HMF) to 5-hydroxymethyl-2-furancarboxylic acid (HFCA) was investigated using in situ X-ray absorption spectroscopy under reaction conditions over Ag/ZrO<sub>2</sub> and Ag/TiO<sub>2</sub> catalysts.

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12

Vijay, Devra. "Kinetics and mechanism of silver(I) catalyzed oxidation of alanine by cerium(IV) in perchloric acid medium." Journal of Indian Chemical Society Vol. 82, Apr 2005 (2005): 290–94. https://doi.org/10.5281/zenodo.5827184.

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P. G. Department of Chermistry Government J D B Girls College Kota-324 001 Indra <em>E-mail</em>: iconota@datarntosys.net <em>Manuscript received 21 January 2003 revised 5 April 2004 accepted 22 July 2004</em> The kinetics of the silver(I) catalyzed oxidation of alanine with cerium(IV) has been studied in perchloric acid medium An usual decrease in rate with increasing concentration of cerium-(IV) is observed and the detailed quantitative analysis of this behaviour is presented on the basis of dimeruation of cerium(IV) The reaction exhibits tractional dependence on alanine and that has been ac

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13

IMAMURA, S. "Oxidation of carbon monoxide catalyzed by manganese-silver composite oxides." Journal of Catalysis 109, no. 1 (1988): 198–205. http://dx.doi.org/10.1016/0021-9517(88)90198-4.

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14

Gallyas, F., and I. Merchenthaler. "Copper-H2O2 oxidation strikingly improves silver intensification of the nickel-diaminobenzidine (Ni-DAB) end-product of the peroxidase reaction." Journal of Histochemistry & Cytochemistry 36, no. 7 (1988): 807–10. http://dx.doi.org/10.1177/36.7.2898497.

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We propose an improved silver procedure for intensification of peroxidase staining. It utilizes the high argyrophilia of polymerized Ni-DAB as a chromogen of peroxidase histochemistry, and the capacity of Cu++-catalyzed H2O2 oxidation to suppress tissue argyrophilia without influencing the argyrophilia of the polymerized Ni-DAB. This procedure is much more effective than any previously proposed intensification technique. When used in somatostatin histochemistry, it reveals perikarya, fibers, and nerve terminals in locations at which they have never been detected in preparations where only the

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15

Tiwari, Anjali, D. V. Prabhu, and Harichandra A. Parbat. "BIOGENICALLY SYNTHESIZED SILVER NANOPARTICLES CATALYZED OXIDATION OF ALIPHATIC AND CYCLIC ALCOHOLS BY KIO4: KINETIC AND THERMODYNAMIC STUDY." RASAYAN Journal of Chemistry 17, no. 03 (2024): 1299–308. http://dx.doi.org/10.31788/rjc.2024.1738867.

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The ability to generate valuable products through oxidation makes it one of the most pivotal industrial processes. While organic oxidants have traditionally been the focus in converting alcohols into carbonyl compounds, inorganic oxidants have been relatively underutilized. In this study, we delve into the influence of Potassium periodate (KIO4) in an acidic environment on the oxidation of selected alcohols, comparing its performance with that of catalyst silver nanoparticles prepared from two distinct plant sources: Madhuca longifolia flowers and Ziziphus jujuba leaves. The reactions were int

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16

Tang, Dianyong, Zhongzhu Chen, Jianping Hu, Guofeng Sun, Shenzhuang Lu, and Changwei Hu. "CO oxidation catalyzed by silver nanoclusters: mechanism and effects of charge." Physical Chemistry Chemical Physics 14, no. 37 (2012): 12829. http://dx.doi.org/10.1039/c2cp41845b.

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17

Chakraborty, Debashis, Ravikumar R. Gowda, and Payal Malik. "Silver nitrate-catalyzed oxidation of aldehydes to carboxylic acids by H2O2." Tetrahedron Letters 50, no. 47 (2009): 6553–56. http://dx.doi.org/10.1016/j.tetlet.2009.09.044.

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18

Iyer, Meera R., and Girish K. Trivedi. "Silver(I) Oxide Catalyzed Oxidation ofo-Allyl- ando-(1-Propenyl)phenols." Bulletin of the Chemical Society of Japan 65, no. 6 (1992): 1662–64. http://dx.doi.org/10.1246/bcsj.65.1662.

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19

Hsu, Ming-Tsung, Yi-Hung Liu, and Shiuh-Tzung Liu. "Synthesis of 2-Benzylidene-3-Pyrrolines and Their Synthetic Transformation." Reactions 1, no. 2 (2020): 47–53. http://dx.doi.org/10.3390/reactions1020005.

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A series of benzylidene-3-pyrrolines were prepared from chalcone derivatives, arylacetylene and sulfonamide via a three-step sequence without the isolation of intermediates. Typically, the reaction of 1,3-di-p-tolylprop-2-en-1-one with lithium phenylacetylide was followed by substitution with tosylamide and then silver-catalyzed 5-exo-dig cyclization to give N-tosyl-2-benzylidene-3,5-di-p-tolyl-2,5-dihydro-1H-pyrrole with a 86% yield. Furthermore, transformation to the corresponding substituted 3-pyrrolin-2-one and pyrrole by m-chloroperbenzoic acid (mcpba)-oxidation and acid-catalyzed aromati

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20

Koketsu, Mamoru, Amol Sonawane, Yunnus Shaikh, and Dinesh Garud. "Synthesis of Isoquinoline-Fused Quinazolinones through Ag(I)-Catalyzed Cascade Annulation of 2-Aminobenzamides and 2-Alkynylbenzaldehydes." Synthesis 51, no. 02 (2018): 500–507. http://dx.doi.org/10.1055/s-0037-1610910.

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A new route for the expedient synthesis of a specific regioisomer of isoquinoline-fused quinazolinones is reported. Silver(I)-catalyzed cascade cyclization of 2-aminobenzamides and 2-alkynylbenzaldehydes followed by in situ oxidation gives 12-butyl- or 12-aryl-6H-isoquinolino[2,1-a]quinazolin-6-ones in 69–91% yields. The structure of the isoquinoline-fused quinazolinone was confirmed by X-ray crystallography analysis.

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21

Beebe, T. R., V. L. Hensley, F. W. Ng, R. A. Noe, and D. J. Scott. "Light-catalyzed and silver acetate catalyzed oxidation of alcohols with N-iodosuccinimide: two different pathways." Journal of Organic Chemistry 50, no. 16 (1985): 3015–16. http://dx.doi.org/10.1021/jo00216a048.

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22

Choudhary, Meenakshi, Samarjeet Siwal, and Kaushik Mallick. "Single step synthesis of a ‘silver–polymer hybrid material’ and its catalytic application." RSC Advances 5, no. 72 (2015): 58625–32. http://dx.doi.org/10.1039/c5ra09115b.

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23

Du, Jialei, Zuofeng Chen, Chuncheng Chen, and Thomas J. Meyer. "A Half-Reaction Alternative to Water Oxidation: Chloride Oxidation to Chlorine Catalyzed by Silver Ion." Journal of the American Chemical Society 137, no. 9 (2015): 3193–96. http://dx.doi.org/10.1021/jacs.5b00037.

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24

M., B. Yadav, Devra Vijay, and Rani Ashu. "Kinetics and mechanism of uncatalyzed and silver(I) catalyzed oxidation of lysine by cerium(IV) in acid perchlorate medium." Journal of Indian Chemical Society Vol. 86, Jun 2009 (2009): 600–604. https://doi.org/10.5281/zenodo.5811769.

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P. G. Department of Chemistry, Govt. College Kota, Kota-324 001, Rajasthan, India P. G. Department of Chemistry, Govt. J. D. B. Girls College, Kota-324 001. Rajasthan, India Department of Pure and Applied Chemistry, Kota University, Kota-324 005, Rajasthan, India <em>E-mail:</em> ashu.uok@gmail.com <em>Manuscript received 25 February 2009, accepted 12 March 2009</em> The kinetics of the uncatalyzed and silver(I) catalyzed oxidation of lysine with cerium(IV) has been studied in perchloric acid medium. The reaction is second order, that is first order with respect to each reactant. The mode of e

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25

Veeranna, Kirana Devarahosahalli, Kanak Kanti Das, and Sundarababu Baskaran. "Silver oxide mediated novel SET oxidative cyclization: stereoselective synthesis of 3-azabicyclo[n.1.0]alkanes." Chemical Communications 55, no. 53 (2019): 7647–50. http://dx.doi.org/10.1039/c9cc03647d.

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26

Jori, K., M. Mizrahi, L. J. Giovanetti, et al. "Room temperature aerobic oxidation of thiophenes catalyzed by silver 5-atoms clusters." Catalysis Today 449 (April 2025): 115184. https://doi.org/10.1016/j.cattod.2025.115184.

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27

Kestenbaum, Harry, Armin Lange de Oliveira, Wolfgang Schmidt, et al. "Silver-Catalyzed Oxidation of Ethylene to Ethylene Oxide in a Microreaction System." Industrial & Engineering Chemistry Research 41, no. 4 (2002): 710–19. http://dx.doi.org/10.1021/ie010306u.

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28

Mitsudome, Takato, Shusuke Arita, Haruhiko Mori, Tomoo Mizugaki, Koichiro Jitsukawa, and Kiyotomi Kaneda. "Supported Silver-Nanoparticle-Catalyzed Highly Efficient Aqueous Oxidation of Phenylsilanes to Silanols." Angewandte Chemie International Edition 47, no. 41 (2008): 7938–40. http://dx.doi.org/10.1002/anie.200802761.

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29

Mitsudome, Takato, Shusuke Arita, Haruhiko Mori, Tomoo Mizugaki, Koichiro Jitsukawa, and Kiyotomi Kaneda. "Supported Silver-Nanoparticle-Catalyzed Highly Efficient Aqueous Oxidation of Phenylsilanes to Silanols." Angewandte Chemie 120, no. 41 (2008): 8056–58. http://dx.doi.org/10.1002/ange.200802761.

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30

Wan, Wen, Jialiang Li, Guobin Ma, et al. "Ag(i)-Catalyzed oxidative decarboxylation of difluoroacetates with activated alkenes to form difluorooxindoles." Organic & Biomolecular Chemistry 15, no. 25 (2017): 5308–17. http://dx.doi.org/10.1039/c7ob00955k.

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31

Li, Wanli, Cai-Fu Li, Fengpei Lang, et al. "Self-catalyzed copper–silver complex inks for low-cost fabrication of highly oxidation-resistant and conductive copper–silver hybrid tracks at a low temperature below 100 °C." Nanoscale 10, no. 11 (2018): 5254–63. http://dx.doi.org/10.1039/c7nr09225c.

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32

Reza Hormozi Jangi, Saeed. "Biochemical characterization of enzyme-like silver nanoparticles toward nanozyme-catalysed oxidation reactions." Micromaterials and Interfaces 1, no. 1 (2023): 60. http://dx.doi.org/10.59429/mi.v1i1.60.

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In this contribution, the biochemical characterization of enzyme-like nanosilvers was performed toward nanozyme-catalyzed oxidation reactions. In this regard, silver nanoparticles were synthesized via a simple chemical reduction method and then characterized by the TEM imaging method. Afterward, their enzyme-like activity was investigated toward catalysis of the oxidation reaction of 3,3’,5,5’-tetramethyl-benzidine (TMB) as one of the most popular peroxidase substrates. The results exhibited a specific nanozymatic activity as high as 5400 nM min−1 for the as-synthesized nanosilvers toward TMB

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33

Cui, Huanhuan, Wei Wei, Daoshan Yang, et al. "Silver-catalyzed direct spirocyclization of alkynes with thiophenols: a simple and facile approach to 3-thioazaspiro[4,5]trienones." RSC Advances 5, no. 103 (2015): 84657–61. http://dx.doi.org/10.1039/c5ra16548b.

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34

Wang, Junjiao, and Shangdong Yang. "A silver triflate-catalyzed cascade of in situ-oxidation and allylation of arylbenzylamines." Tetrahedron Letters 57, no. 31 (2016): 3444–48. http://dx.doi.org/10.1016/j.tetlet.2016.06.076.

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35

Dash, Anadi C., Guru C. Pradhan, and Rabindra K. Nanda. "Kinetics and mechanism of silver(I) catalyzed oxidation of coordinated formate by peroxydisulphate." Transition Metal Chemistry 15, no. 2 (1990): 160–63. http://dx.doi.org/10.1007/bf01023908.

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36

PRAKASH, MOHANTY, DAS NIGAMANANDA, and KUMAR DEI JASHODA. "Silver catalysed Oxidation of cis-(Diglycinato )bis( ethylenediamine )cobalt(III) Ion by Potassium Peroxydisulphate in Aqueous Perchlorate Medium." Journal of Indian Chemical Society Vol. 71, March 1994 (1994): 143–45. https://doi.org/10.5281/zenodo.5894038.

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Department of Chemistry, Utkal Umverstty, Bhubancswar-751 004 Regional Research Laboratory, Bhubaneswar-751 013 <em>Manuscript received 8 February 1993. revised 7 May 1993, accepted 14 May 1993</em> Silver catalysed Oxidation of cis-(Diglycinato )bis( ethylenediamine )cobalt(III) Ion by Potassium Peroxydisulphate in Aqueous Perchlorate Medium.

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37

Trupti, Purohit, Banerji Jayshree, Kotai Laszlo, Sajo I., K. Banerji K., and K. Sharma Pradeep. "Kinetics and mechanism of the oxidation of substituted benzaldehydes with bis(pyridine)silver permanganate." Journal of Indian Chemical Society Vol. 89, Aug 2012 (2012): 1045–52. https://doi.org/10.5281/zenodo.5767214.

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Department of Chemistry, J. N. V. University, Jodhpur-342 011, Rajasthan, India <em>E-mail</em> : drpkvs27@yahoo.com Department of Chemistry, RGP Mahavidyalaya, Kolar Road, Bhopal-462 042, Madhya Pradesh, India chemical Research Center, Hungarian Academy of Sciences, H-1025, Pusztaszeri u. 59-67, Budapest, Hungary Faculty of Science, National Law University, Mandore, Jodhpur-342 304, Rajasthan, India <em>Manuscript received 17 April 2012, accepted 20 April 2012</em> The oxidation of thirty-six <em>ortho</em>-, <em>meta</em>- and para-substituted benzaldehydes by bis(pyridine)silver permanganat

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38

Yao, Qian, Xin Zhou, Xiuli Zhang, Cong Wang, Peng Wang, and Ming Li. "Convenient synthesis of 6-alkyl phenanthridines and 1-alkyl isoquinolines via silver-catalyzed oxidative radical decarboxylation." Organic & Biomolecular Chemistry 15, no. 4 (2017): 957–71. http://dx.doi.org/10.1039/c6ob02331b.

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39

B., L. HIRAN, and N. JOSHI S. "Kinetics of Silver(I)-catalysed Oxidation of n-Butyl Mandelate by Peroxydisulphate." Journal of Indian Chemical Society Vol. 72, Apr 1995 (1995): 271–73. https://doi.org/10.5281/zenodo.5902292.

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Department of Chemistry, College of Science, Sukhadia University, Udaipur-313 001 <em>Manuscript received 7 September 1993, accepted 2 December 1993</em> Kinetics of Silver(I)-catalysed Oxidation of n-Butyl Mandelate by Peroxydisulphate

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40

Gallyas, F., and J. R. Wolff. "Metal-catalyzed oxidation renders silver intensification selective. Applications for the histochemistry of diaminobenzidine and neurofibrillary changes." Journal of Histochemistry & Cytochemistry 34, no. 12 (1986): 1667–72. http://dx.doi.org/10.1177/34.12.3537114.

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Physical developers can increase the visibility of end products of certain histochemical reactions, such as oxidative polymerization of diaminobenzidine and selective binding of complex silver iodide ions to Alzheimer's neurofibrillary changes. Unfortunately, this intensification by silver coating is generally superimposed on a nonspecific staining originating from the argyrophil III reaction, which also takes place when tissue sections are treated with physical developers. The present study reveals that the argyrophil III reaction can be suppressed when tissue sections are treated with certai

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41

Shiraishi, Yukihide, and Naoki Toshima. "Oxidation of ethylene catalyzed by colloidal dispersions of poly(sodium acrylate)-protected silver nanoclusters." Colloids and Surfaces A: Physicochemical and Engineering Aspects 169, no. 1-3 (2000): 59–66. http://dx.doi.org/10.1016/s0927-7757(00)00417-9.

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42

Beier, Matthias J., Bjoern Schimmoeller, Thomas W. Hansen, Jens E. T. Andersen, Sotiris E. Pratsinis, and Jan-Dierk Grunwaldt. "Selective side-chain oxidation of alkyl aromatic compounds catalyzed by cerium modified silver catalysts." Journal of Molecular Catalysis A: Chemical 331, no. 1-2 (2010): 40–49. http://dx.doi.org/10.1016/j.molcata.2010.08.001.

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43

SHARMA, Priyamvada, Riya SAILANI, Deepmala PAREEK, and Chandra Lata KHANDELWAL. "Kinetics of silver(I)-catalyzed oxidation of allyl alcohol by peroxodiphosphate in acetate buffers." TURKISH JOURNAL OF CHEMISTRY 42 (2018): 158–69. http://dx.doi.org/10.3906/kim-1701-32.

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44

Matheswaran, Manickam, Subramanian Balaji, Sang Joon Chung, and Il Shik Moon. "Silver ion catalyzed cerium(IV) mediated electrochemical oxidation of phenol in nitric acid medium." Electrochimica Acta 53, no. 4 (2007): 1897–901. http://dx.doi.org/10.1016/j.electacta.2007.08.042.

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45

Hamal, Khagendra B., Paban Sitaula, and Wesley A. Chalifoux. "Synthesis of Dihydroisobenzofuran Carboxaldehyde Derivatives by a Silver-Catalyzed Sequential Protodesilylation/Cyclization/Oxidation Reaction." European Journal of Organic Chemistry 2019, no. 6 (2019): 1225–28. http://dx.doi.org/10.1002/ejoc.201801606.

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46

Lin, Feng, Yu Chen, Baoshuang Wang, Wenbing Qin, and Liangxian Liu. "Silver-catalyzed TEMPO oxidative homocoupling of indoles for the synthesis of 3,3′-biindolin-2-ones." RSC Advances 5, no. 46 (2015): 37018–22. http://dx.doi.org/10.1039/c5ra04106f.

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A silver-catalyzed TEMPO oxidative homo dimerization of indoles was first successful demonstrated. This new methodology is both atom and step efficient, allowing the synthesis of substituted C3–C3′ bisindolin-2-ones in moderate to excellent yields.

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47

Kudale, Vishal Suresh, Mohana Reddy Mutra, Ching-Piao Chu, and Jeh-Jeng Wang. "Unusual C3-acetylation of quinoxalin-2(1H)-one via oxidative C–C and C–O bond cleavages of PEG-400." Organic & Biomolecular Chemistry 19, no. 25 (2021): 5567–71. http://dx.doi.org/10.1039/d1ob00769f.

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Aerobic oxidative tandem conversion of PEG-400 to acetyl radical via C–C and C–O bond cleavages followed by silver-catalyzed menisci-type addition to the C<sub>3</sub> position of quinoxalin-2(1H)-one is described.

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48

O. Suliman, Fakhr Eldin, and Kauther Al-Hadhrami. "Luminol Chemiluminescence Catalyzed by Silver Nanoparticles for the Sensitive Determination of Penicillamine." Sultan Qaboos University Journal for Science [SQUJS] 22, no. 2 (2018): 63. http://dx.doi.org/10.24200/squjs.vol22iss2pp63-72.

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A sequential injection method for the determination of penicillamine (PA) was developed based on quenching the chemiluminescence generated by oxidation of luminol by hydrogen peroxide in presence of silver nanoparticles (AgNPs). The chemiluminescence (CL) of the reaction was found to greatly enhance in presence of AgNPs due to the increased catalyst surface area. The method was sensitive and found suitable for analysis of penicillamine in pharmaceutical preparations. Linear calibration curve is obtained in the range 0.2-1.0 mg mL-1 with a relative standard deviation less than 2%. A recovery pe

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Banerjee, Rupendranath, Kaushik Das, Amitava Das, and Subrata Dasgupta. "Kinetics of silver(I)-catalyzed oxidation of formic acid by the (ethylenebis(biguanidine))silver(III) cation in acid perchlorate media." Inorganic Chemistry 28, no. 3 (1989): 585–88. http://dx.doi.org/10.1021/ic00302a038.

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Wei, Wen-Ting, Mu-Jia Luo, Fan Teng, Ren-Jie Song та Jin-Heng Li. "Silver-catalyzed oxidative 1,2-alkyletherification of unactivated alkenes with α-bromoalkyl carbonyls: facile access to highly substituted 2,3-dihydrofurans". Chemical Communications 55, № 74 (2019): 11111–14. http://dx.doi.org/10.1039/c9cc05695e.

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