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Journal articles on the topic 'Dimethylglyoxime'

Author: Grafiati

Published: 4 June 2021

Last updated: 26 July 2025

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1

RAJIB, LAL DE, and KUMAR BHAR SANJIB. "Mixed-ligand Complexes of Cobalt(III) with Dimethylglyoxime." Journal of Indian Chemical Society Vol. 71, May 1994 (1994): 245–48. https://doi.org/10.5281/zenodo.5894738.

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Department ot Chemistry, lnorganic Chemistry Section, Jadavpur University, Calcutta-700 032 <em>Manuscript received 9 February 1993, revised 17 June 1993, accepted 23 June 1993</em> Mixed-ligand complexes of cobalt(III) of the types [Co(SBx)(DMGH)] and [Co(SBy)(DMGH)], where SBx = dianion of tetradentate Schiff base; SBy = monoanion of bidentate Schiff base; DMGH = monoanion of dimethylglyoxime, were isolated from the reaction of alcoholic suspension of cobalt(III) dimethylglyoximate dihydrate with Schiff bases in 1 : 1 and 1 : 2 molar ratios for SBx and SHy respectively. Further mixed-ligand

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2

Kia, Reza, Shiva Batmanghelich та Paul R. Raithby. "First heterobimetallic AgI–CoIII coordination compound with both bridging and terminal –NO2 coordination modes: synthesis, characterization, structural and computational studies of (PPh3)2AgI–(μ-κ2 O,O′:κN-NO2)–CoIII(DMGH)2(κN-NO2)". Acta Crystallographica Section C Structural Chemistry 74, № 8 (2018): 882–88. http://dx.doi.org/10.1107/s2053229618009257.

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An unusual heterobimetallic bis(triphenylphosphane)(NO2)AgI–CoIII(dimethylglyoximate)(NO2) coordination compound with both bridging and terminal –NO2 (nitro) coordination modes has been isolated and characterized from the reaction of [CoCl(DMGH)2(PPh3)] (DMGH2 is dimethylglyoxime or N,N′-dihydroxybutane-2,3-diimine) with excess AgNO2. In the title compound, namely bis(dimethylglyoximato-1κ2 O,O′)(μ-nitro-1κN:2κ2 O,O′)(nitro-1κN)bis(triphenylphosphane-2κP)cobalt(III)silver(I), [AgCo(C4H7N2O2)2(NO2)2(C18H15P)2], one of the ambidentate –NO2 ligands, in a bridging mode, chelates the AgI atom in an

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3

Dogari, Haniyeh, Fereshte Hassanzadeh-Afruzi, and Ali Maleki. "ZnFe2O4@dimethylglyoxime: Preparation and Catalyst Application in the Synthesis of 2-Amino-tetrahydro-4H-chromene-3-carbonitrile Derivatives." Cells 3, no. 1 (2020): 89. http://dx.doi.org/10.3390/ecsoc-24-08287.

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Hybrid materials constructed from two or more constituents provide new features and distinctive applications which not found in the single-part material. Spinel ferrites with the general formula of AB2O4, where A denotes divalent ions and B represents trivalent ions, appeared as efficient catalysts for the synthesis of organic compounds. These magnetic nanoparticles have both the Lewis acid and the Lewis base sites in their structure. In the present study, ZnFe2O4 was prepared and modified with dimethylglyoxime to obtain a magnetic ZnFe2O4@dimethylglyoxime hybrid catalyst. Dimethylglyoxime is

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4

Hökelek, Tuncer, Hümeyra Batı, Yunus Bekdemir, and Halil Kütük. "2,3-Dimethylquinoxaline–dimethylglyoxime (1/1)." Acta Crystallographica Section E Structure Reports Online 57, no. 8 (2001): o663—o665. http://dx.doi.org/10.1107/s1600536801010765.

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5

Yang, Yan, Ziping Huang, Haitang Lv, and Aixia Han. "4,4′-Bipyridine–dimethylglyoxime (1/1)." Acta Crystallographica Section E Structure Reports Online 68, no. 1 (2011): o242. http://dx.doi.org/10.1107/s1600536811054341.

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6

Wu, Kang, Junyang Wang, Qi Li, et al. "In situ synthesis of a nickel concentration gradient structure of Ni-rich LiNi0.8Co0.15Al0.05O2 with promising superior electrochemical properties at high cut-off voltage." Nanoscale 12, no. 20 (2020): 11182–91. http://dx.doi.org/10.1039/d0nr01557a.

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7

Ma, Jinxiu, Wen Meng, Lahong Zhang, Feng Li, and Taohai Li. "Effective oil–water mixture separation and photocatalytic dye decontamination through nickel-dimethylglyoxime microtubes coated superhydrophobic and superoleophilic films." RSC Advances 11, no. 9 (2021): 5035–43. http://dx.doi.org/10.1039/d0ra09240a.

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The nickel-dimethylglyoxime microtubes were synthesized by a facile coprecipitation method. The as-prepared superhydrophobic and superoleophilic films showed excellent oil–water separation efficiency and effective photocatalytic degradation.

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8

Ding, Qing-Rong, Gui-Lan Xu, Jian Zhang, and Lei Zhang. "Synergistic ligand effect for the construction of titanium–oxo clusters with planar chirality and high solution stability." Dalton Transactions 49, no. 13 (2020): 4030–33. http://dx.doi.org/10.1039/d0dt00197j.

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Synergistic effect between dimethylglyoxime and nonlinear dicarboxylate ligands has been developed for the construction of planar chiral titanium-oxo clusters, which showed high solution stability confirmed by recrystallization studies.

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9

Fadeeva, I. V., O. V. Prokopova, E. V. Volchkova, et al. "Heterometallic (Nickel, Titanium)-dimethylglyoximates as precursors for nickel titanate coating." Perspektivnye Materialy 8 (2023): 57–67. http://dx.doi.org/10.30791/1028-978x-2023-8-57-67.

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Heterometallic (nickel, titanium) dimethylglyoximate (II) with a nickel:titanium ratio of 1, was synthesized. based on nickel dimethylglyoximate (I) and titanium tetrachloride TiCl4 in chloroform The obtained complex II was characterized by XRD, IR and EPR spectroscopy, and elemental analysis. It was shown that the synthesized complex II is a solvate. On the basis of the analysis results, an assumption was made about the possible structure of complex II. It was found that the thermal decomposition of complex II starts at 44 °C. A constant mass of the decomposition product is observed in the te

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10

Lance, K. A., W. K. Lin, D. H. Busch, and N. W. Alcock. "A BF2-bridged cobalt dimethylglyoxime complex." Acta Crystallographica Section C Crystal Structure Communications 47, no. 7 (1991): 1401–3. http://dx.doi.org/10.1107/s0108270191000628.

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11

Szabó, Andrea, and Attila Kovács. "Structure and molecular vibrations of dimethylglyoxime." Journal of Molecular Structure 651-653 (June 2003): 615–19. http://dx.doi.org/10.1016/s0022-2860(02)00688-9.

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12

Hall, H. L. "Radiochemical extraction of palladium with dimethylglyoxime." Journal of Radioanalytical and Nuclear Chemistry Articles 158, no. 1 (1992): 211–14. http://dx.doi.org/10.1007/bf02034787.

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13

Georgieva, Marija, and Blagoja Andonovski. "Study of the Reaction of Platinum(IV) with Dimethylglyoxime by UV Spectrophotometry." Collection of Czechoslovak Chemical Communications 68, no. 6 (2003): 1065–75. http://dx.doi.org/10.1135/cccc20031065.

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The complex formation of dimethylglyoxime and platinum(IV) in alkaline medium has been investigated by ultraviolet spectroscopy. This study has shown that more than one complex species exists in solution. The effects of pH variation of ammonia buffer solution from 6.0 to 13.0 were investigated with respect to the absorption spectra. The molar ratios method, the Job's method and the method of relative recovery of complex species were used. It was found that the stoichiometric ratio Pt(IV)/dimethylglyoxime was 1:1, 1:2 and 2:1. The molar absorptivity (log ε = 4.1 at 260 nm) and the formation con

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14

Saidakhon, Ubaydullayeva, Sodikov Usmonali, Yunusova Nozima, and Azimbek Amirov. "SELECTION OF OPTIMAL CONDITIONS FOR COMPLEX COMBINATION OF NICKEL (II) ION WITH DIMETHYLGLYOXIME REAGENT." American Journal Of Applied Science And Technology 02, no. 04 (2022): 29–34. http://dx.doi.org/10.37547/ajast/volume02issue04-04.

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The study of the effect of nickel on dimethylglyoxime from the composition of adsorbents used in this article showed that the optimal conditions for this are graphically determined using a spectrophotometer. The analysis was detected in a photocolorimeter.

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15

Westenbrink, W. W., J. A. Page, and G. W. VanLoon. "The voltammetric determination of cobalt(II) in seawater – adsorptive preconcentration of the dimethylglyoxime complex." Canadian Journal of Chemistry 68, no. 2 (1990): 209–13. http://dx.doi.org/10.1139/v90-027.

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Conditions for the determination of trace Co in seawater are described. The method involves formation of the dimethylglyoxime complex and adsorptive accumulation onto a hanging mercury drop electrode at an applied potential of −0.70 or −0.96 V vs. SCE. The adsorbed complex is then reduced by scanning the electrode potential to −1.20 V; the reduction peak potential (Ep) is −1.12 V. Nickel behaves in a similar manner with Ep of −0.99 V but the Co complex appears to be preferentially adsorbed, making analysis for Co possible even in the presence of a large excess of Ni. Adsorption of organic matt

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16

DIEFALLAH, El-H., S. AL-THABAITI, A. EL-BELLIHI, et al. "Kinetics of Thermal Decomposition of Nickel Dimethylglyoxime." Journal of King Abdulaziz University-Science 10, no. 1 (1998): 103–13. http://dx.doi.org/10.4197/sci.10-1.8.

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17

Kim, Jandee, Sechul Kim, and Choong Kyun Rhee. "Adsorptive Behavior of Dimethylglyoxime on Au(111)." Langmuir 27, no. 23 (2011): 14638–46. http://dx.doi.org/10.1021/la202594s.

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18

Lin, H., and W. S. Wu. "Crystal structure of dimethylglyoxime 2-picoloylhydrazone, C10H12N4O2." Zeitschrift für Kristallographie - New Crystal Structures 218, no. 4 (2003): 525–26. http://dx.doi.org/10.1524/ncrs.2003.218.4.525.

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19

Lin, H., and W. S. Wu. "Crystal structure of dimethylglyoxime 2-picoloylhydrazone C10H12N4O2." Zeitschrift für Kristallographie - New Crystal Structures 218, JG (2003): 557–58. http://dx.doi.org/10.1524/ncrs.2003.218.jg.557.

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20

Taqui Khan, M. M., K. Venkatasubramanian, S. H. R. Abdi, M. M. Bhadbhade, and B. Tyagi. "Structure of tris(dimethylglyoxime)ruthenium(II) dichloride." Acta Crystallographica Section C Crystal Structure Communications 48, no. 8 (1992): 1402–5. http://dx.doi.org/10.1107/s010827019101510x.

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21

Dong, Zhi-Yong, Xuan-Wen Liu, Xiao-Qing Wang, Ru-Ji Wang, and Guang-Qiu Shen. "Aqua(azido)(dimethylglyoximato)(dimethylglyoxime)cobalt(III) monohydrate." Acta Crystallographica Section E Structure Reports Online 59, no. 5 (2003): m260—m262. http://dx.doi.org/10.1107/s1600536803003520.

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22

Zhao, Zaofan, and Zhiquang Gao. "Single sweep polarography of palladium-dimethylglyoxime complex." Journal of Electroanalytical Chemistry and Interfacial Electrochemistry 256, no. 1 (1988): 65–75. http://dx.doi.org/10.1016/0022-0728(88)85007-1.

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23

Ramírez, Silvana A., and Gabriel J. Gordillo. "Adsorption and reduction of palladium–dimethylglyoxime complex." Journal of Electroanalytical Chemistry 629, no. 1-2 (2009): 147–51. http://dx.doi.org/10.1016/j.jelechem.2009.02.006.

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24

Dakhel, A. A. "DC conduction processes in nickel-dimethylglyoxime films." Crystal Research and Technology 41, no. 1 (2006): 68–71. http://dx.doi.org/10.1002/crat.200410532.

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25

Fedotov, Aleksandr, Tat'yana Vahnina, and Sergey Kotikov. "THE INFLUENCE OF PRODUCTION PROCESS FACTORS ON THE INDICATORS OF PLYWOOD ON MODIFIED PHENOL-FORMALDEHYDE BINDER." Forestry Engineering Journal 11, no. 1 (2021): 88–100. http://dx.doi.org/10.34220/issn.2222-7962/2021.1/8.

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To reduce production costs, FSF plywood is produced by pressing at a reduced temperature. However, at the same time, the resite stage is not provided for the phenol-formaldehyde binder, which results in a decrease in the physical and mechanical properties of plywood. In the world and Russian practice of scientific work, this problem is solved in various ways: by modifying the binder at the stage of its synthesis, by preliminary surface treatment of veneer, by modifying phenol-formaldehyde binder at the stage of synthesis or “on site”. To develop a rational combination of the values of the prod

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26

YOSHIOKA, Takahiro, Kazuki MATSUSHIMA, Goro HIHARA, and Hiroshi MIYAMAE. "Crystal Structure of cis-Dichlorobis(dimethylglyoxime)nickel(II)." Analytical Sciences: X-ray Structure Analysis Online 22 (2006): x205—x206. http://dx.doi.org/10.2116/analscix.22.x205.

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27

SHIBUTANI, Yasuhiko, Yutaka KAWAMINAMI, Chuya MATSUMOTO, and Koichiro SHINRA. "Thermal analysis of cobalt(III) complexes of dimethylglyoxime." NIPPON KAGAKU KAISHI, no. 7 (1985): 1379–84. http://dx.doi.org/10.1246/nikkashi.1985.1379.

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28

Gerbeleu, N. V., Yu A. Simonov, O. A. Bologa, P. N. Bourosh, and E. B. Koropchanu. "Transamination reaction of dimethylglyoxime on cobalt(III) matrix." Russian Journal of Inorganic Chemistry 51, no. 5 (2006): 717–19. http://dx.doi.org/10.1134/s0036023606050056.

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29

Ramirez, Silvana, Gabriel J. Gordillo, and Dionisio Posadas. "The adsorption of nickel dimethylglyoxime complex on mercury." Journal of Electroanalytical Chemistry 407, no. 1-2 (1996): 219–25. http://dx.doi.org/10.1016/0022-0728(95)04481-7.

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30

Rath, Meenakshi, Laxmi Priya Behera, Barsha Dash, Abdul Rauf Sheik, and Kali Sanjay. "Recovery of dimethylglyoxime (DMG) from Ni-DMG complexes." Hydrometallurgy 176 (March 2018): 229–34. http://dx.doi.org/10.1016/j.hydromet.2018.01.014.

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31

Hu, Yang, and Qiang Huang. "Effect of Dimethylglyoxime on Cobalt Bottom-up Filling." ECS Meeting Abstracts MA2020-02, no. 25 (2020): 1776. http://dx.doi.org/10.1149/ma2020-02251776mtgabs.

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32

Rosal, Miguel, Xavier Cetó, Núria Serrano, Cristina Ariño, Miquel Esteban, and José Manuel Díaz-Cruz. "Dimethylglyoxime modified screen-printed electrodes for nickel determination." Journal of Electroanalytical Chemistry 839 (April 2019): 83–89. http://dx.doi.org/10.1016/j.jelechem.2019.03.025.

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33

Ding, Hui Ling, and Lan Ping Zeng. "Highly Efficient Oxidation of Toluene to Benzoic Acid Catalyzed by N-Hydroxyphthalimide and Oxime in PEG -1000-Based Dicationic Ionic Liquid." Advanced Materials Research 709 (June 2013): 74–79. http://dx.doi.org/10.4028/www.scientific.net/amr.709.74.

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Dimethylglyoxime (DMG) and N-hydroxyphthalimide (NHPI) were used to catalyze oxidation of toluene to benzoic acid with molecular oxygen under normal pressure in PEG 1000 -based functional dicationic acidic ionic liquid (PEG1000 -DAIL). PEG1000 –DAIL enhanced the efficient catalytic ability of NHPI: 89.82% conversion of toluene with 94.63% selectivity for benzoic acid could be obtained at 80°C in 10 h.

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34

Foersterling, H. U. "Investigations of the adsorption of palladium on carbonaceous adsorbents modified with dimethylglyoxime—I. The adsorption of dimethylglyoxime on selected carbonaceous adsorbents." Carbon 28, no. 1 (1990): 27–34. http://dx.doi.org/10.1016/0008-6223(90)90089-h.

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35

Qiao, Pengyi, Chengwen Tan, Xiaodong Yu, Zishan Xiong, Jianwei Dang, and Hao Chang. "Process research on the preparation of high-purity cobalt chloride by chemical precipitation." Journal of Physics: Conference Series 2539, no. 1 (2023): 012090. http://dx.doi.org/10.1088/1742-6596/2539/1/012090.

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Abstract As the precursor of high-purity cobalt, the purity of cobalt chloride has an important influence on the properties of the cobalt target prepared subsequently. In recent years, in addition to ion exchange and extraction, chemical precipitation is a promising method for the purification of cobalt chloride. High-purity cobalt chloride was prepared by chemical precipitation with ammonium hydroxide and dimethylglyoxime as precipitants. The purification mechanism of high-purity cobalt chloride and the depletion mechanism of the main element Co were studied. Inductively coupled plasma-mass s

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36

Shaikh, AA, Shabed Reza, MS Rahman, and Pradip K. Bakshi. "Preparation and Characterization of Vitamin B₁₂ Model Complexes." Dhaka University Journal of Science 60, no. 1 (2012): 97–101. http://dx.doi.org/10.3329/dujs.v60i1.10345.

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Cobaloxime complexes of the type [CoCl(DMGH)2(L)], where DMGH = dimethylglyoxime monoanion, L = tri-ethanolamine and 1,10- phenanthroline, were synthesized. The compounds were formulated on the basis of cobalt and chloride contents, IR and UV-visible spectral analyses and magnetic moment measurement. Cyclic voltammetric technique was also employed to investigate the interaction between Co(II) and the ligands under studied.DOI: http://dx.doi.org/10.3329/dujs.v60i1.10345Dhaka Univ. J. Sci. 60(1): 97-101 2012 (January)

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37

Anca, Ganescu, Simionescu Andreea, and Dumitru Mihaela-Gabriela. "Dioximates of transitional metals. Syntheses, characterizations, applications." Annals of the University of Craiova Series Chemistry 29, no. 2 (2023): 56–59. http://dx.doi.org/10.52846/aucchem.2023.2.14.

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Several derivates of α benzyldioxime with nickel, platinum and palladium are known to have been synthesized by Ciugaev, and later by F.P.Dwyer and D.P.Mallor. Recently, this reagent has found a wide use for the gravimetric determination of palladium and nickel, especially in semi-microanalysis, because the solubility of the respective chelate formed with α benzyldioxime is lower, and the gravimetric factor has a more appropriate value than in the case of analog derivates of dimethylglyoxime.

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38

K. Nayak, SudhirU, Deepika Amala, and ShrutakirthiD Shenoi. "Nickel release from laptop detected by dimethylglyoxime (DMG) test." Indian Journal of Dermatology 66, no. 6 (2021): 696. http://dx.doi.org/10.4103/ijd.ijd_111_21.

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39

Chen, Xiao-Yan, Peng Cheng, Xuan-Wen Liu, et al. "Binuclear and Tetranuclear Copper(II) Complexes Bridged by Dimethylglyoxime." Chemistry Letters 32, no. 2 (2003): 118–19. http://dx.doi.org/10.1246/cl.2003.118.

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40

Thyssen, Jacob P., Lizbet Skare, Lennart Lundgren, et al. "Sensitivity and specificity of the nickel spot (dimethylglyoxime) test." Contact Dermatitis 62, no. 5 (2010): 279–88. http://dx.doi.org/10.1111/j.1600-0536.2010.01709.x.

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41

Zhang, Baofeng, Sheng Chu, Xiaoqing Wang, Guangqiu Shen, and Ru-Ji Wang. "A new tetranuclear copper(II) complex bridged by dimethylglyoxime." Acta Crystallographica Section E Structure Reports Online 59, no. 7 (2003): m504—m506. http://dx.doi.org/10.1107/s1600536803013382.

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42

Hemmingsen, Jens, David Larkin, and Thomas Martin. "Homogeneous precipitation of nickel as the dimethylglyoxime complex: revisited." Analytical Chemistry 58, no. 9 (1986): 2087–88. http://dx.doi.org/10.1021/ac00122a034.

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43

Rami´rez, Silvana, Gabriel J. Gordillo, and Dionisio Posadas. "The reduction of nickel dimethylglyoxime complex preadsorbed on mercury." Journal of Electroanalytical Chemistry 431, no. 2 (1997): 171–81. http://dx.doi.org/10.1016/s0022-0728(97)00183-6.

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44

Dakhel, A. A., and Y. Ali-Mohamed Ahmed. "Electrical properties of thermally evaporated nickel-dimethylglyoxime thin films." Journal of Physics and Chemistry of Solids 66, no. 6 (2005): 1080–84. http://dx.doi.org/10.1016/j.jpcs.2005.02.006.

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45

Qureshi, Anjum, N. L. Singh, A. K. Rakshit, F. Singh, D. K. Avasthi, and V. Ganesan. "Ion beam modification of nickel dimethylglyoxime dispersed polymer films." Surface and Coatings Technology 201, no. 19-20 (2007): 8225–29. http://dx.doi.org/10.1016/j.surfcoat.2006.02.083.

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46

Huang, Q., T. W. Lyons, and W. D. Sides. "Electrodeposition of Cobalt for Interconnect Application: Effect of Dimethylglyoxime." Journal of The Electrochemical Society 163, no. 13 (2016): D715—D721. http://dx.doi.org/10.1149/2.1111613jes.

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47

Ramesh, P., A. SubbiahPandi, P. Jothi, C. Revathi та A. Dayalan. "Dichlorido(dimethylglyoximato-κ2N,N′)(dimethylglyoxime-κ2N,N′)cobalt(III)". Acta Crystallographica Section E Structure Reports Online 64, № 2 (2008): m300—m301. http://dx.doi.org/10.1107/s1600536807068407.

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48

Lawson, E. E., H. G. M. Edwards, and A. F. Johnson. "Vibrational spectroscopic characterization of cobalt dimethylglyoxime boron difluoride ag." Spectrochimica Acta Part A: Molecular Spectroscopy 50, no. 11 (1994): 1899–907. http://dx.doi.org/10.1016/0584-8539(94)80202-5.

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49

Adonaylo, Viviana N., Adriana Stahl, Carlos O. Cañellas, Alicia B. Pomilio, and Arturo A. Vitale. "Technetium-99m-dimethylglyoxime (99mTc-DMG) as renal imaging agent." Journal of Labelled Compounds and Radiopharmaceuticals 33, no. 6 (1993): 443–53. http://dx.doi.org/10.1002/jlcr.2580330602.

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50

SOMA, GANGOPADHYAY, DAS ASIM, and BANERJEA D. "Studies on the Kinetics and Mechanisms of Reactions of Dimethylglyoxime with Iron(II), Cobalt(II) and Copper(II) Ions in Ethanol-Water Media." Journal Of India Chemical Society Vol.66, Aug-Oct 1989 (1989): 517–20. https://doi.org/10.5281/zenodo.5959130.

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Laboratory of Chose Professor of Chemistry, Inorganic Chemisty Division, University College of Science, 92 A. P. 0. Road, CalCutta-700 009 Reactions of dimethyiglyoxime with iron(II), cobalt(II) and copper(II) ions in (20%, v/v) ethanol—water media have been studied by stopped-flow spectrophotometry. The results indicate that in all the cases the initial reaction is a rather fast formation of the bis(dimethylglyoximato) complex of M(II) followed by further reaction in a slower step which involves oxidation of the cobalt(II) complex to a cobalt(III) species by the free ligand in solution,

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