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Journal articles on the topic 'Phenyl mercury'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Ullah, Hashmat, and Muhammad Farid Khan. "BLOOD." Professional Medical Journal 22, no. 03 (2015): 365–69. http://dx.doi.org/10.29309/tpmj/2015.22.03.1358.

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All forms of mercury are global pollutants having no environmental limits.Human exposure to mercury occurs basically through food chain due to accumulation oforganic forms of mercury in fish. Objectives: The purpose of the present study was to analyzethe effect of phenyl mercuric acetate on plasma and cytosolic fraction GSH. Study Design:Experimental Study. Setting: Department of Pharmaceutical Chemistry, Faculty of Pharmacy,Gomal University, Dera Ismail Khan. Period: 29 January 2011 to 11 march 2012 .StatisticalAnalysis: One-way ANOVA followed by Dunnet’s HSD test. Results: For the estimation

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2

Black, DS, GB Deacon, GL Edwards, and BM Gatehouse. "Organomercury Compounds. XXXI. Preparations and 199Hg N.M.R. Spectra of Organomercury Derivatives of 2-Phenylpyridine, Benzo[h]quinoline, 1-Phenylpyrazole and 3,4,5-Trimethyl-1-phenylpyrazole, and the X-Ray Crystal Structure of Bis[2-(pyridin-2'-yl)phenyl]mercury." Australian Journal of Chemistry 46, no. 9 (1993): 1323. http://dx.doi.org/10.1071/ch9931323.

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2-(Pyridin-2'-yl) phenylmercuric acetate has been prepared by mercuration of 2-phenylpyridine. Symmetrization of the corresponding chloride by alkaline sodium stannite gave bis [2-(pyridin-2'-yl)phenyl]mercury, which was also prepared from 2-(2'-aminophenyl)pyridine by the diazo method and treatment of the initial product with copper powder and aqueous ammonia. Mercuration of benzo [h] quinoline and 3,4,5-trimethyl-1-phenylpyrazole with mercuric acetate followed by treatment with lithium chloride yielded benzo [h]quinolin-10-ylmercuric chloride and 2-(3',4',5'-trimethylpyrazol-1'-yl) phenylmer

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3

Lai, Chian Sing, and Edward R. T. Tiekink. "Phenyl(pyrrolinedithiocarbamato)mercury(II)." Acta Crystallographica Section E Structure Reports Online 58, no. 11 (2002): m674—m675. http://dx.doi.org/10.1107/s1600536802019372.

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4

Al-Rubaie, Ali Z., Shaker A. S. Al-Jadaan, Anwar T. Abd Al-Wahed, and Ibraheem A. Raadah. "Synthesis, characterization and biological studies of some new organometallic compounds containing mercury, selenium and tellurium based on p-aminobenzoic acid." Journal of Physics: Conference Series 2063, no. 1 (2021): 012003. http://dx.doi.org/10.1088/1742-6596/2063/1/012003.

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Abstract Ten chalcogen and mercury bearing compounds based on 4-aminobenzoic acid (i.e., (2-amino-5-(ethoxycarbonyl)phenyl)mercury(II) chloride (1), (2-amino-5-(ethoxycarbonyl)phenyl) phenyl selenide (2), (2-amino-5-(ethoxycarbonyl)phenyl) phenyl telluride (3), (4-carboxyphenyl)mercury(II) chloride (4), 4-selenocyanatobenzoic acid (5), 4-tellurocyanatobenzoic acid (6), bis(4-carboxyphenyl) diselenide (7) bis(4-carboxyphenyl) ditelluride (8), bis(4-carboxyphenyl) selenide (9) bis(4-carboxyphenyl) telluride (10) were prepared and characterized by various spectroscopic techniques. All compounds w

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5

Jay, K. Desai and Gunjan. "A brief overview on toxicity effect of mercury in animals." Science World a Monthly e Magazine 3, no. 6 (2023): 926–29. https://doi.org/10.5281/zenodo.7998212.

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<strong>Poisonous Compounds</strong> Mercuric oxide, mercuric chloride, mercuric iodide, mercuric cyanide, mercuric nitrate, mercurous chloride (calomel) and mercurous nitrate. <strong>Organic Preparations</strong> Merbromin (mercurochrome), thimersol (merthiolate), nitromersol (metaphen), phenyl mercuric acetate, phenyl mercuric nitrate, mercurial diuretics (neptal, tt1iomerin sodium and mercurophylline), phenyl mercuric chloride (PMC), phenyl mercuric acetate (PMA), ethyl mercuric chloride, iodide and phosphate and methyl mercuric hydroxide.

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6

Weiden, Norbert, Alarich Weiss, Gary Wulfsberg та ін. "Activation Energies for Fluxional Behavior in Aryl(pentachlorocyclopentadienyl)mercurials, η1 -C5Cl5 HgR, from 35Cl NQR Relaxation Times". Zeitschrift für Naturforschung A 45, № 3-4 (1990): 503–10. http://dx.doi.org/10.1515/zna-1990-3-450.

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Abstract Solid-state activation energies for fluxional behavior in three aryl-subsituted (pentachlorocyclo-pentadienyl)phenylmercury compounds RHgC5 Cl5 : (pentachlorocyclopentadienyl)(pentamethyl-phenyl)mercury (I, R = C6 (CH3)5 , Eact = 19.3 kJ mol-1); (pentachlorocyclopentadienyl)(2,4,6-tris-(terf-butyl)phenyl)mercury (II, R = 2,4,6-C 6 H 2 (C(CH3)3)3 , Eact = 59.5 kJ mol-1); and (pentachloro-cyclopentadienyl)(phenyl)mercury (III, R = C6H5 , E act = 62.8 kJ mol-1) have beeb obtained from 35Cl NQR spin-lattice relaxation-time measurements. II has also been shown to be fluxional in solution b

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7

Tahya, Candra Y., Hanoch J. Sohilait, and Serly J. Sekewael. "Synthesis Of 1-phenyl-4-(3â€™, 4â€™-dimethoxy phenyl)-1-Buten-3-on From Eugenol." Indonesian Journal of Chemical Research 2, no. 1 (2014): 124–30. http://dx.doi.org/10.30598/ijcr.2014.2-can.

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The synthesis of 1-phenyl-4-(3â€™, 4â€™-dimethoxy phenyl)-1-buten-3-one from eugenol has been done through four reaction steps. The metilation of eugenol with dimethyl sulphate yields 81.81% of methyl eugenol. Oxymercuration-demercuration of methyl eugenol with mercury acetate yields 67.27% of methyl eugenyl alcohol. Oxidation of methyl eugenyl alcohol with pyridinium chloro chromate (PCC) yields 45.31% of methyl eugenyl ketone. Aldol condensation reaction of methyl eugenyl ketone with benzaldehide catalyzed by potasium hydroxyde yields 7.38% of 1-phenyl4-(3â€™,4â€™-dimethoxyphenyl)-1-buten-3-

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8

Gupta, Anand, Harkesh B. Singh та Ray J. Butcher. "Crystal structure of {2,6-bis[(dimethylamino)methyl]phenyl-κ3N,C1,N′}(bromido/chlorido)mercury(II)". Acta Crystallographica Section E Crystallographic Communications 73, № 11 (2017): 1679–82. http://dx.doi.org/10.1107/s2056989017014682.

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In the molecular structure of the title compound, {2,6-bis[(dimethylamino)methyl]phenyl-κ3N,C1,N′}[bromido/chlorido(0.30/0.70)]mercury(II)–{2,6-bis[(dimethylamino)methyl]phenyl-κ3N,C1,N′}[bromido/chlorido(0.24/0.76)]mercury(II) (1/1), [HgBr0.30Cl0.70(C12H19N2)]·[HgBr0.24Cl0.76(C12H19N2)], there are two molecules in the asymmetric unit of formulaLHgX{L= 2,6-bis[(dimethylamino)methyl]phenyl andX= Cl/Br}. In each molecule, the halide site is mixed Cl/Br, with occupancies of 0.699 (7):0.301 (7) and 0.763 (7):0.237 (7), respectively. The two molecules are linked into dimers by a combination of Hg..

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9

Flower, Kevin R., and Robin G. Pritchard. "Bis[2-(2-methylphenylimino)phenyl]mercury(II)." Acta Crystallographica Section E Structure Reports Online 62, no. 7 (2006): m1467—m1468. http://dx.doi.org/10.1107/s1600536806020149.

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10

Akbarzadeh, Abolfath, Reza Soleymani, Milad Taheri, Halimeh Rajabzadeh, and Mehdi Daryani. "Synthesis and Studies of Potential Antifungal and Antibacterial Agents New Aryl Thiazolyl Mercury (II) Derivatives Compounds." Journal of Chemistry 2013 (2013): 1–6. http://dx.doi.org/10.1155/2013/186531.

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Combination of mercaptothiazoles and mercury phenyl chloride synthesized some new compounds of thiazoles. Firstly some mercaptothiazoles with different sorts have been synthesized, and then synthesized compounds were reacted with different mercury phenyl chloride structures. At last, each of these synthesized compounds was purified. Consequently, these structures were recrystallized using oil ether. Forming product through chromatogram (TLC) and combination ofRfwith other compound'sRfof were identified, and their purity percent was recognized. The1H-NMR and other methods like FT-IR and mass sp

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11

Anufriev, S. А., S. V. Timofeev, D. I. Nasyrova, I. B. Sivaev, and V. I. Bregadze. "Synthesis of C-mercuro derivatives of ortho-carborane. Crystal structure of bis(2-phenyl-ortho-carboran-1-yl)mercury." Žurnal neorganičeskoj himii 69, no. 5 (2024): 659–64. http://dx.doi.org/10.31857/s0044457x24050014.

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Many carborane derivatives, first synthesized during the rapid development of this field of chemistry in the 60s of the last century, remained completely uncharacterized by modern spectral and structural methods. In this work, a series of C-mercuro derivatives of ortho-carborane 1-PhHg-2-Ph-1,2-C2B10H10 and (2-R-1,2-C2B10H10)2Hg (R = H, Me, Ph) were newly synthesized and characterized by NMR spectroscopy. The molecular crystal structure of bis(2-phenyl-ortho-carboran-1-yl)mercury was determined by single crystal X-ray diffraction.

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12

K., M. RAO, and JAYARAMA REDDY S. "Voltammetric Reductions of some Substituted-phenacyl Bromides." Journal of Indian Chemical Society Vol. 65, Jun 1988 (1988): 411–14. https://doi.org/10.5281/zenodo.6298910.

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Department of Chemistry, S. V. University, Tirupati-517 502 <em>Manuscript  received 11 February 1988, accepted 6 April 1988</em> Substituted-phenacyl bromides, such as <em>m</em>-nitro, <em>p</em>-phenyl, <em>p</em>-methyl, <em>p</em>-methoxy and <em>m</em>-methoxyphenacyl bromides have been reduced electrochemically at dropping mercury electrode and hanging mercury drop electrode using d c. polarography and cyclic voltammetry in 50% (v/v) ethanol- water and DMF- water mixtures. Comparative account of their reduction behaviour in different buffer systems is discussed.  The effect of

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13

Flower, Kevin R., and Robin G. Pritchard. "Bis[2-(2-isopropylphenylimino)phenyl]mercury(II)." Acta Crystallographica Section E Structure Reports Online 62, no. 7 (2006): m1469—m1470. http://dx.doi.org/10.1107/s1600536806020150.

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The structure of the centrosymmetric cyclomercurated 2-phenyliminophenyl title compound, [Hg(C16H16N)2], has been determined at 120 (2) K. The coordination geometry at the Hg atom is essentially square planar.

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14

K., MASTAN RAO, and J. REDDY S. "Electrochemical Reduction and Evaluation of Kinetic Parameters of some Substituted Phenacyl Bromides in Non-aqueous Media." Journal of Indian Chemical Society Vol.70, Jun 1993 (1993): 523–25. https://doi.org/10.5281/zenodo.5913815.

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Department of Chemistry, Regional Engineering College, Warangal-506 004 Department of Chemistry, S. V. University, Tirupati-517 502 <em>Manuscript received 4 June 1992, revised 8 February 1993, accepted 19 February 1993</em> Substituted phenacyl bromides, like <em>m</em>-nitro, <em>m</em>-methoxy, <em>p</em>-phenyl, <em>p</em>-methoxy, <em>p</em>-methylphenacyl bromides have been reduced electrochemically under dropping mercury electrode and hanging mercury drop electrode employing d.c. polarography and cyclic voltammetry in 50% (v/v) DMF-water mixture. The cleavage of C-Br bond involves two-e

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15

Habibi, Mohammad Hossein, Abdollah Fallah-Shojaiea, Kazem Barati, and William Clegg. "Synthesis and crystal structure of bis[N-(phenyl)-3,5-dinitrothiobenzamidato]mercury(II) and bis[N-(phenyl)-4-nitrothiobenzamidato]mercury(II)." Journal of Coordination Chemistry 62, no. 22 (2009): 3712–18. http://dx.doi.org/10.1080/00958970802695805.

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16

Habibi, Mohammad Hossein, Shahram Tangestaninejad, Abdollah Fallah-Shojaei, Kazem Barati, Neil R. Brooks, and William Clegg. "Synthesis and crystal structures of bis(N-phenyl-3,5-dinitrothiobenzamidato)mercury(II) and bis(N-phenyl-4-nitrothiobenzamidato)mercury(II)." Journal of Coordination Chemistry 63, no. 4 (2010): 579–85. http://dx.doi.org/10.1080/00958970903556096.

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17

Adams, Richard D., Zhongwen Luo, and Yuen Onn Wong. "Bridging phenyl ligands. Unsaturated mercury-triosmium carbonyl cluster complexes containing bridging phenyl ligands." Journal of Organometallic Chemistry 784 (May 2015): 46–51. http://dx.doi.org/10.1016/j.jorganchem.2014.08.009.

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18

Elena, Marettová, Maretta M., Legat J., and Nad P. "The effect of selenium on phenyl mercury toxicity and mercury retention in chicken." Acta veterinaria 53, no. 4 (2003): 211–18. http://dx.doi.org/10.2298/avb0304211m.

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19

Deacon, Glen B., Craig M. Forsyth, Dominique Freckmann, et al. "Adventitiously Obtained Rare-Earth Peroxide Complexes and Their Structural Characterisation." Australian Journal of Chemistry 67, no. 12 (2014): 1860. http://dx.doi.org/10.1071/ch14410.

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The structures of three adventitiously obtained peroxolanthanoid complexes have been determined, namely, [Yb2(Cp)4(μ-O)2/3(μ-O2)1/3(thf)2] (1) (Cp = cyclopentadienyl; thf = tetrahydrofuran), which has disorder between the bridging oxide and peroxide, [Nd2(o-PhPhForm)4(thf)4(μ-O2)] (2) (o-PhPhForm = N,N′-bis(2-phenylphenyl)formamidinate), and [Eu4(FForm)6(μ-OH)2(μ3-O2)2(μ-diglyme)2]·2diglyme (3) (FForm = N,N′-bis(2-fluorophenyl)formamidinate, diglyme = bis(2-methoxyethyl) ether). In the first two complexes, the peroxide bridges side-on between metals, whereas in the last complex, each peroxide

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20

Rajeev, Jain, K. Halve A., Guru Aribam Nirupama, and Jadon Nimisha. "Synthesis, antibacterial and electrochemical studies of 4-[(E)-{[(4-substituted]- sulfonyl]substitutedimino}methyl](substituted)phenyl acetate." Journal of Indian Chemical Society Vol. 92, Jul 2015 (2015): 1173–80. https://doi.org/10.5281/zenodo.5607303.

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School of Studies in Chemistry, Jiwaji University, Gwalior-474 011, Madhya Pradesh, India <em>E-mail</em> : rajeevjain54@yahoo.co.in School of Studies in Environmental Chemistry, Jiwaji University, Gwalior-474 011, Madhya Pradesh, India <em>Manuscript received online 30 October 2014, accepted 27 November 2014</em> A new series of 4-[(<em>E</em>)-{[(4-substituted]sulfonyl]substitutedimino}methyl](substituted)phenyl acetate were synthesized by coupling of 3-methoxy-4-acetyloxy benzaldehyde with different sulphanalamide derivatives. Electrochemical behaviour of 4-[(<em>E</em>)-{[(4-substituted]su

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21

Hoang, Hien Thai, and Dong Van Nguyen. "Determination of methyl mercury and total mercury in sediment samples collected from canals in HoChiMinh city." Science and Technology Development Journal 19, no. 4 (2016): 123–36. http://dx.doi.org/10.32508/stdj.v19i4.680.

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In this study, the analysis of methyl mercury (MeHg) and total mercury (T-Hg) was studied using gas chromatographic separation/atomic fluorescence spectrometric detection and cold vapour atomic absorption spectrometry respectively. MeHg was extracted from sediment matrix using HNO3/KCl/CuSO4 into dichloromethane followed ethylation with NaB(C2H5)4 in hexane. Total mercury was digested using three different procedures: EPA 245.1, AOAC 971.21 and our proposed one. The reliability of the analytical method for MeHg was evaluated by the use of the certified reference material ERM CC-580. In additio

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22

Barek, Jiří, and Dagmar Civišová. "The polarographic and voltammetric determination of 1-phenyl-5-hydroxy-3-carbamoylpyrazol-4-azo-(4'-ethoxycarbonylbenzene)." Collection of Czechoslovak Chemical Communications 52, no. 1 (1987): 81–87. http://dx.doi.org/10.1135/cccc19870081.

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The polarographic reduction of the title azodye has been studied, a mechanism has been proposed for this process and conditions have been found for the determination of this substance by TAST polarography, with a detection limit of 7 . 10-7 mol l-1, differential pulse polarography at a dropping mercury electrode with a detection limit of 3.5 . 10-7 mol l-1, fast scan differential pulse voltammetry at a static mercury drop electrode with a detection limit of 6.9 . 10-9 mol l-1 and voltammetry with linearly increasing voltage at a hanging mercury drop with a detection limit of 1.6 . 10-9 mol l-1

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23

Dürüst, Yaşar, Cevher Altuğ, Çetin Bozkurt, and Frank R. Fronczek. "Bis(3-phenyl-1,2,4-thiadiazole-5-thiolato)mercury(II)." Acta Crystallographica Section C Crystal Structure Communications 61, no. 9 (2005): m442—m444. http://dx.doi.org/10.1107/s0108270105025734.

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24

Stoermer, Martin, and John Pinhey. "[(Z)-5-Phenyl-2-penten-2-yl]mercury Bromide." Molecules 3, no. 8 (1998): M68. http://dx.doi.org/10.3390/m68.

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25

Stoermer, Martin, and John Pinhey. "[(Z)-5-Phenyl-2-penten-2-yl]mercury Acetate." Molecules 3, no. 8 (1998): M69. http://dx.doi.org/10.3390/m69.

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26

Stoermer, Martin, and John Pinhey. "bis-[(Z)-5-Phenyl-2-penten-2-yl]mercury." Molecules 3, no. 8 (1998): M70. http://dx.doi.org/10.3390/m70.

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27

Casado, Juan, and Iluminada Gallardo. "On the electroreduction mechanism of halobenzenes: Detection of intermediates in reduction of monohalobenzenes." Collection of Czechoslovak Chemical Communications 54, no. 4 (1989): 900–910. http://dx.doi.org/10.1135/cccc19890900.

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Experimental results from electrochemical behaviour of halobenzenes in DMF at a mercury cathode are used to discuss alternative mechanisms of reduction. Intermediates of these mechanisms, such as phenyl anion, phenylmercury radical and phenylmercury cation have been detected at the electrode by using cyclic voltammetry and a rotating ring-disk electrode.

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28

Taylor, C. G., and W. Tickle. "Radiometric studies of mercury loss from fungicidal paints. 1. Loss of phenyl mercuric acetate." Journal of Applied Chemistry 19, no. 1 (2007): 1–7. http://dx.doi.org/10.1002/jctb.5010190101.

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29

Garrard, WNC, and FG Thomas. "On the Electrochemical-Behavior of Pyrylium Ions at the Mercury-Electrode. II. Aromatically Substituted Ions in Acetonitrile." Australian Journal of Chemistry 39, no. 6 (1986): 865. http://dx.doi.org/10.1071/ch9860865.

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The electrochemical behaviour of the 2,4,6-triphenylpyrylium ( tpp +) and 7-phenyl-5,6,8,9-tetrahydrodibenzo[ c,h ] xanthylium (thx+) ions in acetonitrile in the presence of 0.1 M tetrabutylammonium perchlorate is reported. The reduction of both ions proceeds by two, one-electron steps. The initial product of the first reduction is the corresponding radical, which may dimerize to give isomeric bipyrans in the case of tpp + or a phenyl-phenyl or phenyl- pyranyl dimer in the case of thx+. The corresponding anions are the initial products of the second reduction step. The tpp - anion reacts with

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30

Kushwaha, Shilpi, and Padmaja P. Sudhakar. "Adsorption of mercury(II), methyl mercury(II) and phenyl mercury(II) on chitosan cross-linked with a barbital derivative." Carbohydrate Polymers 86, no. 2 (2011): 1055–62. http://dx.doi.org/10.1016/j.carbpol.2011.06.028.

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31

Taylor, C. G., W. Tickle, and A. Dwyer. "Radiometric studies of mercury loss from fungicidal paints. II. Comparison of three phenyl mercury compounds." Journal of Applied Chemistry 19, no. 1 (2007): 8–11. http://dx.doi.org/10.1002/jctb.5010190102.

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32

Habibi, Mohammad Hossein, Shahram Tangestaninejad, A. Fallah-Shojaie, I. Mohammadpoor-Baltork, and S. F. Tayyari. "Preparation and Spectral Investigation of Bis[N(2-methyl-phenyl) 4-Nitro-thiobenzamidato] mercury(II), Bis[N(2-methoxy-phenyl) 4-Nitro-thiobenzamidato]mercury(II), and Bis[N(2-chloro-phenyl) 4-Nitro-thiobenzamidato]mercury(II) Complexes." Phosphorus, Sulfur, and Silicon and the Related Elements 180, no. 8 (2005): 1863–71. http://dx.doi.org/10.1080/104265090889521.

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33

Abouelfida, Abdesselam, Jean Paul Pradère, Michel Jubault, and André Tallec. "Réduction électrochimique de 4H-1,3-thiazines: obtention de 6H-1,3-thiazines et (ou) de pyrroles substitués." Canadian Journal of Chemistry 70, no. 1 (1992): 14–20. http://dx.doi.org/10.1139/v92-003.

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Controlled potential electroreduction (protic medium, mercury cathode) of substituted 2-ethoxy and 2-phenyl-4H-1,3-thiazines leads to 6H-1,3-thiazines and (or) pyrroles. The nature of the isolated products appears strongly dependent on pH of the medium and type of substitution: pyrrole formation takes place in acidic medium (0.5 mol L−1 H2SO4) and is favoured by phenyl and alkoxycarbonyl groups at positions 2 and 4, respectively; formation of 6H-1,3-thiazines and their reduction products (substituted thiobenzamides, carbamates and 2-thiazoline) occurs in weakly acidic (acetate buffer) or basic

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34

Colorado-Solís, David, Rodrigo Castro-Ramírez, Francisco Sánchez-Bartéz, Isabel Gracia-Mora, and Norah Barba-Behrens. "Novel Sulfone 2-Aminobenzimidazole Derivatives and Their Coordination Compounds: Contribution of the Ethyl and Phenyl Substituents on Non-Covalent Molecular Interactions; Biological Antiproliferative Activity." Inorganics 11, no. 10 (2023): 392. http://dx.doi.org/10.3390/inorganics11100392.

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New sulfone 2-aminobenzimidazole derivatives were designed and synthesized. Their nickel(II), copper(II), zinc(II), cadmium(II) and mercury(II) compounds were obtained and fully characterized by spectroscopic and analytical techniques. Single crystal X-ray structural analysis was performed in order to study the relevant intra and inter non-covalent interactions, mainly H···π, lone pair···π, and π···π, highlighting the difference between the terminal ethyl and phenyl groups in such interactions. Dimeric and trimeric supramolecular syntons were found for some of these compounds. Additionally, th

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35

Wang, Hongxing, Wenxiang Gu, Gaoju Zhang, Zhenwei Huan, and Jin-Pei Cheng. "Revisiting the Reactions of Phenyl(trihalomethyl)mercury with Tetraphenylcyclone (TPCP)." Journal of Chemical Research 23, no. 6 (1999): 348–49. http://dx.doi.org/10.1177/174751989902300602.

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36

Casas, José S., Eduardo E. Castellano, M. S. García Tasende, et al. "(Dicyclohexyldithiophosphinato-S,S′)[2-(2-pyridyl-N)phenyl]mercury(II)." Acta Crystallographica Section C Crystal Structure Communications 56, no. 2 (2000): 182–83. http://dx.doi.org/10.1107/s0108270199015048.

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37

Cornu, David, Peter B. Hitchcock, Michael F. Lappert, and Patrick G. H. Uiterweerd. "Some 2,6-bis(dimethylamino)phenyl–mercury(II) and –boron complexes." Polyhedron 21, no. 5-6 (2002): 635–40. http://dx.doi.org/10.1016/s0277-5387(01)01037-3.

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38

Wang, Hongxing, Wenxiang Gu, Gaoju Zhang, Zhenwei Huan, and Jin-Pei Cheng. "Revisiting the Reactions of Phenyl(trihalomethyl)mercury with Tetraphenylcyclone (TPCP)." Journal of Chemical Research, no. 6 (1999): 348–49. http://dx.doi.org/10.1039/a900516a.

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39

Bai, Su-Zhen, Xin-Hua Lou, Hong-Mei Li, and Hui Shi. "Chlorido[(E)-2-hydroxy-6-(isonicotinoylhydrazonomethyl)phenyl]mercury(II) monohydrate." Acta Crystallographica Section E Structure Reports Online 65, no. 7 (2009): m842—m843. http://dx.doi.org/10.1107/s1600536809023824.

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40

Lai, Chian Sing, and Edward R. T. Tiekink. "Crystallographic report: Phenyl(N,N-di-n-propyldithiocarbamato)mercury(II)." Applied Organometallic Chemistry 17, no. 3 (2003): 194. http://dx.doi.org/10.1002/aoc.395.

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Hernández, Guadalupe, Sylvain Bernès, Oscar Portillo, Alejandro Ruíz, Gloria E. Moreno, and René Gutiérrez. "Crystal structures of three mercury(II) complexes [HgCl2L] whereLis a bidentate chiral imine ligand." Acta Crystallographica Section E Crystallographic Communications 71, no. 12 (2015): 1462–66. http://dx.doi.org/10.1107/s2056989015020368.

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The crystal structures of three complexes [HgCl2L] were determined, namely, (S)-(+)-dichlorido[1-phenyl-N-(pyridin-2-ylmethylidene)ethylamine-κ2N,N′]mercury(II), [HgCl2(C14H14N2)], (S)-(+)-dichlorido[1-(4-methylphenyl)-N-(pyridin-2-ylmethylidene)ethylamine-κ2N,N′]mercury(II), [HgCl2(C15H16N2)], and (1S,2S,3S,5R)-(+)-dichlorido[N-(pyridin-2-ylmethylidene)isopinocampheylamine-κ2N,N′]mercury(II), [HgCl2(C16H22N2)]. The complexes consist of a bidentate chiral imine ligand coordinating to HgCl2and crystallize with four independent molecules in the first complex and two independent molecules in the

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Parish, R. V., Jonathan P. Wright, and Robin G. Pritchard. "Mercury(II) and gold(III) derivatives of 2-phenyl pyridines and 2-phenyl-4-(methylcarboxylato)quinoline." Journal of Organometallic Chemistry 596, no. 1-2 (2000): 165–76. http://dx.doi.org/10.1016/s0022-328x(99)00645-2.

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Ghaedi, Mehrorang, Abdolah Falah Shojaie, Morteza Montazerozohori, Bahador Karami, and Shiva Gharaghani. "Iodide-Selective Electrodes Based on Bis[N(2-methyl-phenyl) 4-Nitro-thiobenzamidato]mercury(II) and Bis[N-phenyl 3,5-Dinitro-thiobenzamidato]mercury(II) Carriers." Electroanalysis 17, no. 19 (2005): 1746–54. http://dx.doi.org/10.1002/elan.200503278.

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Giri, Amit Kumar, Deep Saurabh Singh, and Suresh Kumar. "Studies of Complexes of Para Bromo Phenyl mercury Thiocyanates with M| (BIS Salicylidene 1:2 propane diamine)." ESSENCE International Journal for Environmental Rehabilitation and Conservation 9, no. 1 (2018): 142–51. http://dx.doi.org/10.31786/09756272.18.9.1.117.

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Bond, A. M., R. T. Gettar, N. M. McLachlan, and G. B. Deacon. "Oxidation of mercury electrodes in the presence of phenyl-mercury, -lead and -bismuth organometallic compounds in dichloromethane." Inorganica Chimica Acta 166, no. 2 (1989): 279–89. http://dx.doi.org/10.1016/s0020-1693(00)80821-x.

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Vigo, Ludmila, Pekka Salin, Raija Oilunkaniemi та Risto S. Laitinen. "catena-Poly[[chlorido(methyl phenyl sulfide-κS)mercury(II)]-μ-chlorido]". Acta Crystallographica Section E Structure Reports Online 64, № 6 (2008): m809. http://dx.doi.org/10.1107/s1600536808013718.

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Zhang, Wen-Shen, Zhi-Juan Liu, Feng Xu та Qi-Ning Xun. "Dibromidobis{1-[4-(pyridin-4-yl)phenyl]ethanone-κN}mercury(II)". Acta Crystallographica Section E Structure Reports Online 67, № 12 (2011): m1849. http://dx.doi.org/10.1107/s1600536811049993.

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Fernández -G, Juan M., María J. Rosales, and R. A. Toscano. "The reactivity of [Os3(CO)10(C2Ph2)] towards phenyl mercury halides." Polyhedron 7, no. 21 (1988): 2159–63. http://dx.doi.org/10.1016/s0277-5387(00)81796-9.

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Arkawazi, Hayder Dawood Jasim. "Synthesis and characterization of the new Tetradentate Schiff base ligand type N4 derived From 4-animoantipyrine,4-dimethylaminobenzaldehyde, ethylenediamine and furfural, towards Fe(III), Co(II), Cu(II), Zn(II) and Hg(II) Ions." Journal of Wasit for Science and Medicine 8, no. 2 (2015): 138–56. http://dx.doi.org/10.31185/jwsm.345.

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Iron(III), Cobalt(II), Cupper(II), Zinc(II) and Mercury(II) complexes have been synthesized by reaction of their chloride salt with a new tetradentate Schiff base ligand type N4: (N1Z,N2Z)-N1-(4-((Z)-4-(dimethylamino)benzylideneamino)-2,3-dimethyl-1-phenyl 1,2dihydropyrazol-5-ylidene)-N2(4((Z)-furan-2-ylmethyleneamino)-2,3-dimethyl-1-phenyl-1,2dihydropyrazol-5-ylidene)ethane1,2–diamine. All the prepared complexes were characterized by the spectroscopic methods (FT.IR, UV-Vis) Atomic Absorption, Magnetic Susceptibility, Melting Point, Elemental Analysis and Molar Conductivity, as well as the H1

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Möhrle, Hans, and Michael Gehlen. "Reaktionsbeteiligung Von Oximfunktionen Bei Der Dehydrierung Von 2-Phenylpiperidin-Derivaten." Zeitschrift für Naturforschung B 62, no. 6 (2007): 841–53. http://dx.doi.org/10.1515/znb-2007-0614.

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Mercury(II)-induced dehydrogenation of α-(2-phenylpiperidin-1-yl)-acetophenone oximes 7 gives rise to two different iminium compounds which subsequently react with the neighbouring oxime group. With the mercury(II)-EDTA reagent, (E)-7 forms the cyclic nitrones 9 and 11a, b, whereas (Z)-7 is transformed into oxadiazines 12 and 13a, b. The pairs of diastereomers 11a, b and 13a, b result from the equilibrium involving an iminium oximate species. The introduction of electron donor or acceptor groups into the phenyl substituent in (E)-15 and (E)-16 does not influence significantly the direction of

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