Relevant bibliographies by topics / Organocopper compounds. Complex compounds. Ligands

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Academic literature on the topic 'Organocopper compounds. Complex compounds. Ligands'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Organocopper compounds. Complex compounds. Ligands"

1

Ion, Emilia, Mirela Calinescu, Ana Emandi, Victoria Badea, and Dumitru Negoiu. "Copper(II) Complex Compounds with Mixed Hydrazone Ligands." Revista de Chimie 59, no. 1 (2008): 12–16. http://dx.doi.org/10.37358/rc.08.1.1697.

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Three Cu(II) complex compounds with mixed hydrazone ligands have been prepared and characterized in view of their potential biological activity. The complex compounds have the formulas: [Cu(HLa)(Lc)Br], [CuLaLc] and [CuLbLc] . Na, where HLa = 4-dimethylamino benzaldehyde-2-benzothiazolyl hydrazone, H2Lb = 2-hydroxybenzaldehyde-2-benzothiazolyl hydrazone and HLc = 2-hydroxy-1-naphthyliden-N,N-dimethyl hydrazone. The complexes have been characterized by elemental and thermogravimetrical analysis, infrared, electronic and EPR spectra. EPR spectral studies of the complexes gave axial symmetry, wit
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2

JITARU, IOANA, MARIANA BICHER, OANA JINGA, and DAN JINGA. "COMPLEX COMPOUNDS WITH PHOSPHORUS AND NITROGEN CONTAINING LIGANDS." Phosphorus Research Bulletin 10 (1999): 708–13. http://dx.doi.org/10.3363/prb1992.10.0_708.

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3

Molteni, Roberto, Rüdiger Bertermann, Katharina Edkins, and Andreas Steffen. "An unexpected transmetalation intermediate: isolation and structural characterization of a solely CH3 bridged di-copper(i) complex." Chemical Communications 52, no. 28 (2016): 5019–22. http://dx.doi.org/10.1039/c6cc01510g.

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A dicopper(i) complex, [Cu(PPh<sub>3</sub>)<sub>2</sub>(μ-Me)CuMe] (2), in which two metal centres are solely bridged by a methyl group and experience stabilizing metallophilic interactions, has been isolated and structurally characterized, showing a new bonding mode of CH<sub>3</sub> and giving further inside into transmetalation reactions of organocopper compounds.
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4

LANG, H., and M. WEINMANN. "ChemInform Abstract: Bis(alkynyl) Titanocenes as Organometallic Chelating Ligands for the Stabilization of Monomeric Organocopper(I) Compounds." ChemInform 27, no. 19 (2010): no. http://dx.doi.org/10.1002/chin.199619287.

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5

Golichenko, Alexander, and Alexander Shtemenko. "HYDROLYSIS OF RHENIUM(III) CLUSTER COMPOUNDS." Ukrainian Chemistry Journal 85, no. 3 (2019): 27–34. http://dx.doi.org/10.33609/0041-6045.85.3.2019.27-34.

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Study of hydrolysis of cis-tetrachlorodi-m-carboxylates of dirhenium (III) was carried out due to the electronic adsorption and IR spectroscopy and pHmeter. As a result, itwas shown that the hydrolysis is a multistage process which can be attributed to the reactions of the pseudo-first order. It is also shown that the electronic absorption spectroscopy (EAS) is a reliable method of investigation to study the hydrolysis of rhenium (III) complex compounds. This conclusion is based on the fact that in the systems with halide and carboxylic ligands, each of the five structural types can be clearly
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6

Golichenko, Alexander, and Alexander Shtemenko. "HYDROLYSIS OF RHENIUM(III) CLUSTER COMPOUNDS." Ukrainian Chemistry Journal 85, no. 3 (2019): 27–34. http://dx.doi.org/10.33609/6045.85.3.2019.27-34.

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Abstract:
Study of hydrolysis of cis-tetrachlorodi-m-carboxylates of dirhenium (III) was carried out due to the electronic adsorption and IR spectroscopy and pHmeter. As a result, itwas shown that the hydrolysis is a multistage process which can be attributed to the reactions of the pseudo-first order. It is also shown that the electronic absorption spectroscopy (EAS) is a reliable method of investigation to study the hydrolysis of rhenium (III) complex compounds. This conclusion is based on the fact that in the systems with halide and carboxylic ligands, each of the five structural types can be clearly
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7

Scrase, Tom G., Simon M. Page, Paul D. Barker, and Sally R. Boss. "Folates are potential ligands for ruthenium compounds in vivo." Dalton Trans. 43, no. 22 (2014): 8158–61. http://dx.doi.org/10.1039/c4dt00081a.

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A labile ruthenium(ii) complex has been observed to chelate to folates under physiologically relevant conditions. The diastereomeric complexes formed would interfere with the one-carbon carrying role of folate in vivo. This highlights the importance of considering small molecules alongside macromolecules when determining the chemical origins of cytotoxicity of metallodrug candidates.
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8

Ranskiy, Anatoliy, and Natalia Didenko. "Direct Synthesis of Cuprum(II) Complex Compounds Based on Thioamide Ligands." Chemistry & Chemical Technology 8, no. 4 (2014): 371–78. http://dx.doi.org/10.23939/chcht08.04.371.

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9

Chomi¹, J., K. Györyová, E. Szunyogová, and J. Kováéová. "Thermal study of zinc(II) salicylate complex compounds with bioactive ligands." Journal of Thermal Analysis and Calorimetry 76, no. 1 (2004): 33–41. http://dx.doi.org/10.1023/b:jtan.0000027800.14514.c2.

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10

Domonov, Denis P., and S. I. Pechenyuk. "Thermal decomposition of double complex compounds of 3D metals." Herald of Kola Science Centre of the RAS 12, no. 3-2020 (2020): 5–15. http://dx.doi.org/10.37614/2307-5228.2020.12.3.001.

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The paper is devoted to the study of thermolysis of double complex compounds (DCС) of metalsin the I transition series. 30 DCСwith various combinations of metal-central atoms (Co-Fe, Cu-Fe, Ni-Fe Cr-Fe, Cr-Co,) and ligands (ammonia, urea (ur), ethylenediamine (en), 1,3-diaminopropane (tn), cyanide, oxalate and nitrite anions) were synthesized and characterized. A complete study of the thermal proper-ties of these DCCs in three atmospheres was carried out: oxidizing (air), inert (Ar, N2, partly He) and re-ducing (H2), in the temperature range of 20–1000°Cand at constant heating rate of 10°C/min
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