Relevant bibliographies by topics / Organometallic mercury compounds

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters

Academic literature on the topic 'Organometallic mercury compounds'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Organometallic mercury compounds"

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Deacon, GB, and GN Stretton. "Organomercury Compounds. XXVII. The Synthesis and Properties of Some Carboxylato- and Carboxy-pyridinylmercurials." Australian Journal of Chemistry 38, no. 3 (1985): 419. http://dx.doi.org/10.1071/ch9850419.

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Decarboxylation of mercuric pyridine-2,3-dicarboxylate in hot dimethyl sulfoxide or hexamethylphosphoramide gives a mixture of 2-carboxylatopyridin-3-ylmercury(II) (major product) and 3- carboxylatopyridin-2-ylmercury(II) (minor product). The mixture reacts ( i ) with acidified halide ions ( Cl - or I-) to yield a mixture of the corresponding carboxypyridinyl ( halogeno )mercury(II) derivatives, (ii) with tribromide ions to give the bromo ( carboxypyridinyl )mercury(ii) complexes, 3-bromopyridine-2-carboxylic acid, and 2-bromopyridine-3- carboxylic acid, and (iii) with iodide ions in hot aqueo
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2

Moscoso-Pérez, C., V. Fernández-González, J. Moreda-Piñeiro, P. López-Mahía, S. Muniategui-Lorenzo, and D. Prada-Rodríguez. "Multivariate optimization of PTV-GC-MS method for simultaneous determination of organometallic compounds of mercury, lead and tin." Analytical Methods 8, no. 42 (2016): 7702–10. http://dx.doi.org/10.1039/c6ay02212j.

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3

Hoke, W. E., P. J. Lemonias, and R. Korenstein. "An examination of organometallic thermal stability and its relevance to low-temperature MOCVD growth of HgCdTe." Journal of Materials Research 3, no. 2 (1988): 329–34. http://dx.doi.org/10.1557/jmr.1988.0329.

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A well-established stability model for hydrocarbon molecules is reviewed and then applied to organometallic compounds used in the epitaxial growth of HgCdTe films. For hydrocarbon molecules, the strength of carbon-hydrogen bonds is modified by neighboring organic groups. The mechanism for this effect is delocalization of the free radical electronic charge by the neighboring groups. The delocalization effect is present in organometallic compounds and is illustrated for tellurium, mercury, and cadmium compounds. An important application of the delocalization effect is the development of a low-te
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4

Schwerdtfeger, Peter, Peter D. W. Boyd, Stephane Brienne, et al. "The mercury-mercury bond in inorganic and organometallic compounds. A theoretical study." Inorganica Chimica Acta 213, no. 1-2 (1993): 233–46. http://dx.doi.org/10.1016/s0020-1693(00)83833-5.

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5

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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6

Busato, Matteo, Jesús Castro, Domenico Piccolo, and Marco Bortoluzzi. "Mercury Monohalides as Ligands in Transition Metal Complexes." Molecules 30, no. 1 (2025): 145. https://doi.org/10.3390/molecules30010145.

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The main categories of transition metal–mercury heterometallic compounds are briefly summarized. The attention is focused on complexes and clusters where the {Hg-Y} fragment, where Y represents a halide atom, interacts with transition metals. Most of the structurally characterized derivatives are organometallic compounds where the transition metals belong to the Groups 6, 8, 9 and 10. More than one {Hg-Y} group can be present in the same compound, interacting with the same or with different transition metals. The main synthetic strategies are discussed, and structural data of representative co
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Holloway, Clive E., and Milan Melník. "Mercury organometallic compounds. Classification and analysis of crystallographic and structural data." Journal of Organometallic Chemistry 495, no. 1-2 (1995): 1–31. http://dx.doi.org/10.1016/0022-328x(95)05395-6.

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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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HOLLOWAY, C. E., and M. MELNIK. "ChemInform Abstract: Mercury Organometallic Compounds. Classification and Analysis of Crystallographic and Structural Data." ChemInform 26, no. 44 (2010): no. http://dx.doi.org/10.1002/chin.199544282.

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10

Schumann, Herbert, Silke Freitag, Frank Girgsdies, Holger Hemling, and Gabriele Kociok-Köhn. "Homoleptic Organometallic Compounds of Zinc, Cadmium, and Mercury, Intramolecularly Stabilized by Amine Ligands." European Journal of Inorganic Chemistry 1998, no. 2 (1998): 245–52. http://dx.doi.org/10.1002/(sici)1099-0682(199802)1998:2<245::aid-ejic245>3.0.co;2-t.

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Dissertations / Theses on the topic "Organometallic mercury compounds"

1

Haque, Rosenani S. M. Anwarul. "Silver, mercury and ruthenium complexes of N-heterocyclic carbene linked cyclophanes." University of Western Australia. Chemistry Discipline Group, 2008. http://theses.library.uwa.edu.au/adt-WU2008.0236.

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This thesis describes the synthesis and isolation of silver, mercury, ruthenium and palladium complexes of bidentate N-heterocyclic carbenes (NHCs), derived from imidazolium-linked cyclophanes and related bis-imidazolium salts. The cyclophane structures contain two imidazolyl links between ortho- and meta- substituted aromatic rings and the related structures are ortho-, meta- and para-xylyl linked bis-imidazolium salts. The complexes have been characterised by NMR spectroscopy and X-ray crystallography. The synthesis of five new silver complexes has been achieved via a simple complexation rea
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2

Nsengimana, Hermogene. "Speciation of organometallic of tin, lead and mercury in environmental samples." Thesis, 2008. http://hdl.handle.net/10539/4538.

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Abstract Organic derivatives of tin, lead, mercury are the most widely distributed organometallic ecotoxicants in the environment. While some of these organometallic compounds exist in the environment as a result of direct discharge, anthropogenic emissions alone cannot explain the ubiquity, for example, of the organomercury and organolead compounds in marine and fresh waters, sediments and biota. It is known that some organometallic compounds are formed via a bioconversion from the inorganic contaminants. Depending on the source, they can enter the environment in varied forms inorgani
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Books on the topic "Organometallic mercury compounds"

1

1939-, Wardell J. L., ed. Organometallic compounds of zinc, cadmium, and mercury. Chapman and Hall, 1985.

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2

Wardell, J. L., ed. Organometallic Compounds of Zinc, Cadmium and Mercury. Springer US, 1985. http://dx.doi.org/10.1007/978-1-4899-7162-3.

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(Editor), Dietrich K. Breitinger, and Wolfgang A. Herrmann (Editor), eds. Copper, Silver, Gold, Zinc, Cadmium, and Mercury (Synthetic Methods of Organometallic and Inorganic Chemistry, Vol 5). Georg Thieme Verlag, 1999.

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Book chapters on the topic "Organometallic mercury compounds"

1

Macintyre, J. E. "Hg Mercury." In Dictionary of Organometallic Compounds. Springer US, 1986. http://dx.doi.org/10.1007/978-1-4615-6847-6_22.

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2

MacIntyre, Jane E. "Hg Mercury." In Dictionary of Organometallic Compounds. Springer US, 1996. http://dx.doi.org/10.1007/978-1-4899-6848-7_24.

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3

Macintyre, J. E., F. M. Daniel, D. J. Cardin, et al. "Hg Mercury." In Dictionary of Organometallic Compounds. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4757-4966-3_24.

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4

Wardell, J. L. "Hg Mercury." In Organometallic Compounds of Zinc, Cadmium and Mercury. Springer US, 1985. http://dx.doi.org/10.1007/978-1-4899-7162-3_2.

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5

Wardell, J. L. "Cd Cadmium." In Organometallic Compounds of Zinc, Cadmium and Mercury. Springer US, 1985. http://dx.doi.org/10.1007/978-1-4899-7162-3_1.

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6

Wardell, J. L. "Zn Zinc." In Organometallic Compounds of Zinc, Cadmium and Mercury. Springer US, 1985. http://dx.doi.org/10.1007/978-1-4899-7162-3_3.

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7

Mullin, J. B., and S. J. C. Irvine. "Mechanisms in the Photochemical Growth of Cadmium Mercury Telluride." In Mechanisms of Reactions of Organometallic Compounds with Surfaces. Springer US, 1989. http://dx.doi.org/10.1007/978-1-4899-2522-0_27.

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8

"1.3 Organometallic Compounds of Copper." In Copper, Silver, Gold, Zinc, Cadmium and Mercury, edited by Wolfgang A. Herrmann and Dietrich K. Breitinger. Georg Thieme Verlag, 1999. http://dx.doi.org/10.1055/b-0035-128054.

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9

"2.3 Organometallic Compounds of Silver." In Copper, Silver, Gold, Zinc, Cadmium and Mercury, edited by Wolfgang A. Herrmann and Dietrich K. Breitinger. Georg Thieme Verlag, 1999. http://dx.doi.org/10.1055/b-0035-128058.

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10

"3.3 Organometallic Compounds of Gold." In Copper, Silver, Gold, Zinc, Cadmium and Mercury, edited by Wolfgang A. Herrmann and Dietrich K. Breitinger. Georg Thieme Verlag, 1999. http://dx.doi.org/10.1055/b-0035-128062.

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