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Journal articles on the topic 'Phenylmercury'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Bachman, R. E., B. R. Maughon, D. J. McCord, K. H. Whitmire, and W. E. Billups. "(Bromodichloromethyl)phenylmercury." Acta Crystallographica Section C Crystal Structure Communications 51, no. 10 (1995): 2033–35. http://dx.doi.org/10.1107/s0108270195004501.

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2

Kiyono, Masako, and Hidemitsu Pan-Hou. "The merG Gene Product Is Involved in Phenylmercury Resistance in Pseudomonas Strain K-62." Journal of Bacteriology 181, no. 3 (1999): 726–30. http://dx.doi.org/10.1128/jb.181.3.726-730.1999.

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ABSTRACT The physiological function of a new gene, hereby designatedmerG, located between merA and merBon the broad-spectrum mer operon of Pseudomonasstrain K-62 plasmid pMR26 was investigated. The 654-bp merGgene encodes a protein with a canonical leader sequence at its N terminus. The processing of the signal peptide of this protein was dose-dependently inhibited by sodium azide, a potent inhibitor of protein export. These results suggest that the mature MerG protein (ca. 20 kDa) may be located in the periplasm. Deletion of themerG gene from the broad-spectrum mer operon of pMR26 had no effe

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3

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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4

V�zquez-L�pez, E. M., A. Casti�eiras, A. S�nchez, J. S. Casas, and J. Sordo. "Phenylmercury(II) dithiophosphates. Crystal structure of (O,O?-diethyldithiophosphate) phenylmercury(II)." Journal of Crystallographic and Spectroscopic Research 22, no. 4 (1992): 403–9. http://dx.doi.org/10.1007/bf01195400.

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5

Casas, José S., María D. Couce, Manuel García-Vega, Agustín Sánchez, José Sordo, and Ezequiel M. Vázquez López. "Phenylmercury(ii) sulfanylpropenoates: an example of symmetrization with the 3-(2-methoxyphenyl)-2-sulfanylpropenoato ligand." New Journal of Chemistry 40, no. 8 (2016): 6735–44. http://dx.doi.org/10.1039/c6nj00624h.

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Some new phenylmercury(ii) sulfanylpropenoate complexes were prepared and characterized. The identification of diphenylmercury(ii) reveals the existence of a symmetrization process, which was followed in solution by NMR.

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6

S., K. Srivastava, B. Saxena S., and S. Jain (Mrs.). "Reactivity of phenylmercury-O,O' -alkylenedithiophosphate." Journal Of Indian Chemical Society Vol.78, Jul 2001 (2001): 362–63. https://doi.org/10.5281/zenodo.5878348.

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School of Studies in Chemistry, Jiwaji University, Gwalior-474 011, India <em>Manuscript received 26 August 1999, revised 10 September 2000, accepted 10 February 2001</em> The interactions of phenylmercury-<em>Ο</em>,<em>O</em>'-alkylenedithiophosphate [C<sub>6</sub>H<sub>5</sub>HgS(S)\({POCH_2(CH_2)_3CH_2O]\over}\) with various <em>O- </em>and <em>S</em>-donor Lewis  bases have yielded some new molecular adducts.

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7

Sanjay, K. Srivastava, Sihare Surachna, and Pandey Yogesh. "Synthesis, spectral characterization and ligation behaviour of phenylmercury(II) O, O' -dialkyl/ alkylene dithiophosphates." Journal of Indian Chemical Society Vol. 83, Jun 2006 (2006): 542–46. https://doi.org/10.5281/zenodo.5837751.

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School of Studies in Chemistry, Jiwaji University, Gwalior-474 011, Madhya Pradesh, India <em>E-mail</em> : sksrivas5@yahoo.com Chemistry Department, Bipin Behari (P.G.) College, Jhansi, Uttar Pradesh, India <em>Manuscript received 18 January 2006, accepted 6 March 2006</em> The phenylmercury(Il) complexes having composition [C<sub>6</sub>H<sub>5</sub>H<sub>g</sub>S(S)P(OCH<sub>2</sub>CH<sub>2</sub>CH<sub>2 </sub>[C<sub>2</sub>H<sub>5</sub>HgS(S)POCH<sub>2</sub>OC(CH<sub>2</sub>)<sub>2</sub>CH<sub>2</sub>O}] and [C<sub>2</sub>H<sub>5</sub>HgS(S)POCH<sub>2</sub>C(CH<sub>3</sub>)<sub>2</sub

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8

Bilodeau, Denis, and André L. Beauchamp. "Methyl- and phenylmercury complexes of azaindolyl–azaindole." Inorganica Chimica Acta 261, no. 1 (1997): 7–13. http://dx.doi.org/10.1016/s0020-1693(96)05571-5.

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9

Farhangi, Y. "Reaction of phenylmercury acetate with Lewis bases." Inorganica Chimica Acta 129, no. 1 (1987): 11–13. http://dx.doi.org/10.1016/s0020-1693(00)85894-6.

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10

Chen, Beibei, Yunli Wu, Xueqin Guo, Man He, and Bin Hu. "Speciation of mercury in various samples from the micro-ecosystem of East Lake by hollow fiber-liquid–liquid–liquid microextraction-HPLC-ICP-MS." Journal of Analytical Atomic Spectrometry 30, no. 4 (2015): 875–81. http://dx.doi.org/10.1039/c4ja00312h.

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A novel method by combining hollow fiber-liquid–liquid–liquid microextraction (HF-LLLME) with HPLC-ICP-MS was developed for the speciation of inorganic mercury (Hg<sup>2+</sup>) and organomercury including methylmercury (MeHg<sup>+</sup>), ethylmercury (EtHg<sup>+</sup>) and phenylmercury (PhHg<sup>+</sup>), in the micro-ecosystem of East Lake (Wuhan, China).

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11

Tiekink, E. R. T. "(O-Ethyl dithiocarbonato-κS)phenylmercury, [Hg(C3H5OS2)(C6H5)]". Acta Crystallographica Section C Crystal Structure Communications 50, № 6 (1994): 861–62. http://dx.doi.org/10.1107/s0108270194000259.

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12

Chang, Shenghe, Zhengjing Wu, Wei Sun, and Haiyan Shu. "The Construction of an Engineered Bacterial Strain and Its Application in Accumulating Mercury from Wastewater." Applied Sciences 8, no. 9 (2018): 1572. http://dx.doi.org/10.3390/app8091572.

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To remove organic and inorganic mercury from wastewater, an engineered bacterial strain, BL21-7, was constructed that contained the artificial operon P16S-g10-merT-merP-merB1-merB2-ppk-rpsT. For BL21-7, the minimum inhibitory concentrations of mercuric chloride, methylmercury chloride and phenylmercury chloride in Luria-Bertani (LB) medium were 100 µmol/L, 60 µmol/L and 80 µmol/L, respectively. After being cultured in three media (liquid LB containing 80 µmol/L mercuric chloride, 40 µmol/L methylmercury chloride or 60 µmol/L phenylmercury chloride) for 72 h, the engineered bacteria accumulated

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13

S., K. Srivastava, S. Sihare (Mrs.), Rastogi R., and A. Gaur (Mrs.). "Synthesis, structural aspects and ligation behaviour of phenylmercury(II) dithio complexes having Hg-S bonds." Journal of Indian Chemical Society Vol. 84, Sep 2007 (2007): 867–71. https://doi.org/10.5281/zenodo.5827036.

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School of Studies in Chemistry, Jiwaji University, Gwalior-474 011, Madhya Pradesh, India <em>E-mail </em>: sksrivas7@yahoo.com <em>Manuscript received 28 June 2007, accepted 2 July 2007</em> Reactions of C<sub>6</sub>H<sub>5</sub>HgOH with CS<sub>2</sub> and 2-alkyl amino ethanol at -20 <sup>o</sup>c yield neutral two coordinate unsymmetrically substituted phenylmercury(II) <em>N</em>-alkyl, <em>N</em>·hydroxyethyl dithiocarbamate complexes,[C<sub>6</sub>H<sub>5</sub>HgS(S)CN(R)CH<sub>2</sub>CH<sub>2</sub>OH] [R =CH<sub>3</sub> (1), C<sub>2</sub>H<sub>5</sub> (2), <em>n</em>-C<sub>4</s

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14

Eschwege, Karel von, Fabian Muller та Alfred Muller. "[1,5-Bis(2-methoxyphenyl)thiocarbazonato-κ2N1,S]phenylmercury(II)". Acta Crystallographica Section E Structure Reports Online 67, № 12 (2011): m1804. http://dx.doi.org/10.1107/s1600536811049099.

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15

Singh, Vikram, Ratna Chauhan, Abhinav Kumar, Lal Bahadur, and Nanhai Singh. "Efficient phenylmercury(ii) methylferrocenyldithiocarbamate functionalized dye-sensitized solar cells." Dalton Transactions 39, no. 41 (2010): 9779. http://dx.doi.org/10.1039/c0dt00575d.

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16

de la Fournière, Emmanuel M., Ana G. Leyva, Eduardo A. Gautier, and Marta I. Litter. "Treatment of phenylmercury salts by heterogeneous photocatalysis over TiO2." Chemosphere 69, no. 5 (2007): 682–88. http://dx.doi.org/10.1016/j.chemosphere.2007.05.042.

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17

Miranda, Cristian, Jorge Yáñez, David Contreras, Claudio Zaror, and Héctor D. Mansilla. "Phenylmercury degradation by heterogeneous photocatalysis assisted by UV-A light." Journal of Environmental Science and Health, Part A 48, no. 13 (2013): 1642–48. http://dx.doi.org/10.1080/10934529.2013.815453.

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18

Casas, José S., Alfonso Castiñeiras, María D. Couce, et al. "3-(Aryl)-2-sulfanylpropenoates of mercury(II) and phenylmercury(II)." Polyhedron 27, no. 11 (2008): 2436–46. http://dx.doi.org/10.1016/j.poly.2008.04.034.

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19

Chauhan, A. K. S., Rita Sharma, and R. C. Srivastava. "Phenylmercury(II) Haloacetates and their Complexes with Group VB Donors." Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry 25, no. 1 (1995): 151–62. http://dx.doi.org/10.1080/15533179508218210.

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20

Chen, Kwan-Tin, Fuh-An Yang, Jyh-Horung Chen, Shin-Shin Wang та Jo-Yu Tung. "A novel bismercury(II) complex of bidentate N21,N22-bridged porphyrin: [((benzamido-κN)phenylmercury-κHg–N21,N22)-meso-tetraphenylporphyrinato-N23,N24]phenylmercury(II) toluene solvate". Polyhedron 27, № 9-10 (2008): 2216–20. http://dx.doi.org/10.1016/j.poly.2008.03.029.

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21

Nagata, Takeshi, Masako Kiyono, and Hidemitsu Pan-Hou. "Involvement of Aromatic Amino Acids in Phenylmercury Transport by MerT Protein." JOURNAL OF HEALTH SCIENCE 52, no. 4 (2006): 475–77. http://dx.doi.org/10.1248/jhs.52.475.

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22

Eschwege, Karel G. von, Fabian Muller та Alfred Muller. "[1,5-Bis(4-fluorophenyl)thiocarbazonato-κ2N5,S]phenylmercury(II) dichloromethane hemisolvate". Acta Crystallographica Section E Structure Reports Online 67, № 12 (2011): m1858—m1859. http://dx.doi.org/10.1107/s1600536811050331.

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23

Rodríguez, Antonio, Antonio Sousa-Pedrares, José A. García-Vázquez, Jaime Romero, and Antonio Sousa. "Phenylmercury(II) complexes with pyrimidine-2-thionato ligands: Synthesis and characterization." Journal of Organometallic Chemistry 695, no. 9 (2010): 1271–75. http://dx.doi.org/10.1016/j.jorganchem.2010.02.022.

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24

Lin, Yang-Wei, and Huan-Tsung Chang. "Detection of mercury and phenylmercury ions using DNA-based fluorescent probe." Analyst 136, no. 16 (2011): 3323. http://dx.doi.org/10.1039/c1an15117g.

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25

Semin, G. K., S. I. Gushchin, S. B. Karpov, E. V. Bryukhova, L. S. Golovchenko, and D. N. Kramov. "127I and79Br NQR spectra of halo-substituted phenols and phenylmercury phenoxides." Russian Chemical Bulletin 45, no. 3 (1996): 573–76. http://dx.doi.org/10.1007/bf01435784.

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26

Srivastava, S. K., Sharmila Jain, and S. B. Saxena. "Synthesis, Characterisation and Reactivity of Phenylmercury(II) Compounds Containing Hg-S Bonds." Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry 28, no. 9 (1998): 1431–44. http://dx.doi.org/10.1080/00945719809351687.

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27

Graham, Garry G., Diarmaid Gordon, and Peter J. Sadler. "Reactions of the Antiarthritic Drug Aurothiomalate With Phenylmercury(II) Compounds: NMR Studies." Metal-Based Drugs 3, no. 6 (1996): 269–76. http://dx.doi.org/10.1155/mbd.1996.269.

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Clinical formulations of the antiarthritic drug aurothiomalate sometimes contain phenylmercury(ll) compounds as antimicrobial preservative agents and, in the presence of para-chloromercuri-benzoate, aurothiomalate is a potent inhibitor of collagenase. By H1 NMR spectroscopy, para-hydroxymercuribenzoate and para-hydroxymercuriphenylsulphonate were shown to react with aurothiomalate by complexing only with the terminal thiomalate of aurothiomalate oligomers, thereby converting them to ring complexes. The reaction was also detected by UV spectroscopy. The arylmercury complexes produced no change

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28

Pombrik, S. I., A. A. Bezrukova, L. S. Golovchenko, A. S. Peregudov, A. Z. Rubezhov, and D. N. Kravtsov. "Redox-demercuration of phenylmercury 4-fluorothiophen-oxide by tetrakis(triphenylphosphine)platinum(0)." Journal of Organometallic Chemistry 293, no. 1 (1985): C1—C4. http://dx.doi.org/10.1016/0022-328x(85)80253-9.

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29

Cerrillos, C., M. A. Pradera Adrian, and J. A. Navio. "UV photolytic degradation of phenylmercury compounds in water-acetonitrile (1:1) media." Journal of Photochemistry and Photobiology A: Chemistry 84, no. 3 (1994): 299–303. http://dx.doi.org/10.1016/1010-6030(94)03866-x.

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30

Klapötke, Thomas M., Burkhard Krumm, and Richard Moll. "Synthetic and Structural Studies on Methyl-, tert-Butyl- and Phenylmercury(II) Azide." Zeitschrift für anorganische und allgemeine Chemie 637, no. 5 (2011): 507–14. http://dx.doi.org/10.1002/zaac.201000036.

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31

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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32

Dushenko, G., I. Mikhaylov, O. Mikhaylova, R. Minyayev, and V. Minkin. "Structure and fluxional behavior of phenylmercury derivatives of N,N’-diarylform(benz)amidines." Доклады академии наук 482, no. 3 (2018): 292–96. http://dx.doi.org/10.31857/s086956520003114-8.

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33

Antipin, M. Y., F. M. Dolgushin, A. A. Yakovenko, J. H. Gallegos, and T. V. Timofeeva. "Mixed crystal of bidentate and tridentate perfluoro-phenylmercury Lewis acids with organic molecules." Acta Crystallographica Section A Foundations of Crystallography 64, a1 (2008): C488—C489. http://dx.doi.org/10.1107/s0108767308084304.

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34

UNO, Yoshio, Masako KIYONO, Toshiyuki TEZUKA, and Hidemitsu PAN-HOU. "Phenylmercury Transport Mediated by merT-merP Genes of Pseudomonas K-62 Plasmid pMR26." Biological & Pharmaceutical Bulletin 20, no. 1 (1997): 107–9. http://dx.doi.org/10.1248/bpb.20.107.

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35

Dushenko, G. A., I. E. Mikhailov, O. I. Mikhailova, R. M. Minyaev, and V. I. Minkin. "Structure and Fluxional Behavior of Phenylmercury Derivatives of N,N'-Diarylform(benz)amidines." Doklady Chemistry 482, no. 1 (2018): 189–94. http://dx.doi.org/10.1134/s0012500818090069.

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36

Mascarenhas, Y. P., K. Tomita, C. O. P. Santos, and J. S. Casas. "Crystalline and molecular structure of (2-mercaptobenzoxalate) methylmercury(II) and (2-mercaptobenzoxolate) phenylmercury(II)." Acta Crystallographica Section A Foundations of Crystallography 43, a1 (1987): C180. http://dx.doi.org/10.1107/s0108767387080632.

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37

Parkin, J. E. "Interference by Disodium Edetate with the Reaction of Phenylmercury Ions with Dithiocarbamate Derivatising Agents." Journal of Liquid Chromatography 15, no. 3 (1992): 441–49. http://dx.doi.org/10.1080/10826079208017183.

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38

López-Torres, Elena, and M. Antonia Mendiola. "Synthesis and molecular structures of methyl and phenylmercury(II) complexes with benzaldehyde-4,4-dimethylthiosemicarbazone." Journal of Organometallic Chemistry 725 (February 2013): 28–33. http://dx.doi.org/10.1016/j.jorganchem.2012.11.032.

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39

Lee, Ching-Hui, Ruey-Hseng Lin, Shing Hwa Liu, and Shoei-Yn Lin-Shiau. "Distinct genotoxicity of phenylmercury acetate in human lymphocytes as compared with other mercury compounds." Mutation Research/Genetic Toxicology and Environmental Mutagenesis 392, no. 3 (1997): 269–76. http://dx.doi.org/10.1016/s1383-5718(97)00081-8.

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40

Parkin, J. E. "High-performance liquid chromatography of mercury and phenylmercury as the N-disubstituted dithiocarbamate complexes." Journal of Chromatography A 472 (January 1989): 401–5. http://dx.doi.org/10.1016/s0021-9673(00)94140-2.

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41

Alegret, S., E. Martínez-Fàbregas, and J. M. Paulís. "Determination of phenylmercury(II) by photometric titration with dithizone in a mixed organic medium." Journal of Pharmaceutical and Biomedical Analysis 9, no. 9 (1991): 769–71. http://dx.doi.org/10.1016/0731-7085(91)80219-y.

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42

Singh, Nanhai, Abhinav Kumar, Kieran C. Molloy, and Mary F. Mahon. "Syntheses, crystal and molecular structures, and properties of some new phenylmercury(ii) dithiolate complexes." Dalton Transactions, no. 37 (2008): 4999. http://dx.doi.org/10.1039/b804635b.

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43

Chauhan, Ratna, Gabriele Kociok-Köhn, Manoj Trivedi, Suryabhan Singh, Abhinav Kumar, and Dinesh P. Amalanerkar. "Phenylmercury(II) methylferrocenyldithiocarbamate-functionalized dye-sensitized solar cells with hydroxy as an anchoring group." Journal of Solid State Electrochemistry 19, no. 3 (2014): 739–47. http://dx.doi.org/10.1007/s10008-014-2660-3.

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44

Abbas, M. N., N. B. El-assy, and Sh Abdel-Moniem. "Determination of Traces of Mercury (II) and Phenylmercury by Direct Polyurethane foam Thin-Layer Spectrophotometry." Analytical Letters 22, no. 11-12 (1989): 2575–85. http://dx.doi.org/10.1080/00032718908052376.

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45

Bravo, Jorge, Jose S. Casas, Maria V. Castano, et al. "Methyl- and phenylmercury(II) derivatives of 2-mercaptobenzothiazole. Crystal structure of (2-benzothiazolylthio)methylmercury(II)." Inorganic Chemistry 24, no. 21 (1985): 3435–38. http://dx.doi.org/10.1021/ic00215a027.

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46

Wilhelm, Michaela, Wolfgang Saak, and Henry Strasdeit. "Phenylmercury Chloride: Its Single-Crystal X-Ray Structure and Some Aspects of its Biological Chemistry." Zeitschrift für Naturforschung B 55, no. 1 (2000): 35–38. http://dx.doi.org/10.1515/znb-2000-0107.

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A single crystal of phenylmercury chloride (PhHgCl) was obtained by serendipity from a solution of diphenylmercury (HgPh2) and dihydrolipoic acid in tetrahydrofuran / carbon tetrachloride. The crystal structure of PhHgCl is pseudotetragonal. It is best described in the orthorhombic space group Cmma with a = 6.856(1), b = 6.882(1), c = 14.309(2) Å (at 193 K), and Z = 4. The Cl-Hg-C moiety of the PhHgCl molecule is exactly linear. The bond lengths at the Hg atom are Hg-Cl 2.345(2) and Hg-C 2.044(9) Å. In the crystal, the molecules are arranged in double layers parallel to the a,b plane. In a mod

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47

Singh, Nanhai, Abhinav Kumar, Rajendra Prasad, Kieran C. Molloy, and Mary F. Mahon. "Syntheses, crystal, photoluminescence and electrochemical investigation of some new phenylmercury(ii) dithiocarbamate complexes involving ferrocene." Dalton Transactions 39, no. 10 (2010): 2667. http://dx.doi.org/10.1039/b917871f.

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48

Zukerman-Schpector, J., E. M. Vázquez-López, A. Sánchez, J. S. Casas, and J. Sordo. "Synthesis and structural characterization of diphenldithiophosphinates of methyl- and phenylmercury(II). Crystal structure of MeHgS2PPh2." Journal of Organometallic Chemistry 405, no. 1 (1991): 67–74. http://dx.doi.org/10.1016/0022-328x(91)83157-y.

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49

P., P. SINGH, and SRIVASTAVA BEENA. "Bimetallic Complexes involving Schiff Base." Journal of Indian Chemical Society Vol. 63, Sep 1986 (1986): 797–800. https://doi.org/10.5281/zenodo.6298761.

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Chemistry Department, M L. K. (P. G.) College, Balrampur-271 201 <em>Manuscript received 6 May 1985, revised 19 May 1986, accepted 18 June 1986</em> Phenylmercury derivative (phHgSA) of Schiff base SAH derived from salicylaldehyde and aniline have been prepared. Reaction of this derivative with M(NCS)<sub>2</sub>, where M - Co<em><sup>II</sup></em>, Ni<em><sup>II</sup></em>, Cu<em><sup>ll</sup></em> and Zn<em><sup>II</sup></em>, gave complexes of general formulae (phHgSA)<sub>2</sub>M(NCS)<sub>2.</sub> These complexes on further reaction with pyridine or bipyridine (L) furnished addu

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Feo, J. C., and A. J. Aller. "Speciation of mercury, methylmercury, ethylmercury and phenylmercury by Fourier transform infrared spectroscopy of whole bacterial cells." Journal of Analytical Atomic Spectrometry 16, no. 2 (2001): 146–51. http://dx.doi.org/10.1039/b005767n.

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