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Journal articles on the topic 'Transition metal sulphur compounds'

Author: Grafiati

Published: 4 June 2021

Last updated: 15 February 2022

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1

Brz⊙zka, Zbigniew. "Transition metal ion-selective membrane electrodes based on complexing compounds with heteroatoms. Part II. Complexing compounds containing sulphur atoms." Analyst 113, no. 12 (1988): 1803–5. http://dx.doi.org/10.1039/an9881301803.

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2

Tarique, Mohammad. "Cr(III),Mn(II),Fe(III),Co(II),Ni(II),Cu(II) and Zn(II) Complexes with Diisobutyldithiocarbamato Ligand." E-Journal of Chemistry 8, no. 4 (2011): 2020–23. http://dx.doi.org/10.1155/2011/348475.

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The synthesis of sulphur and nitrogen containing dithiocarbamato ligand derived from diisobutylamine as well as its coordination compounds with 3d series transition metals is presented. These synthesized compounds were characterized on the basis of elemental analysis, conductometric measurements and IR spectral studies. The analytical data showed the stoichiometry 1:2 and 1:3 for the compounds of the types ML2{M=Mn(II), Co(II), Ni(II), Cu(II) and Zn(II)} and M'L3{M'=Cr(III) and Fe(III)} respectively. The conductometric measurements proved the non-electrolytic behaviour of all the compounds. Th

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3

Dannenbauer, Nicole, Ana Kuzmanoski, Claus Feldmann, and Klaus Müller-Buschbaum. "1,3-Thiazole as Suitable Antenna Ligand for Lanthanide Photoluminescence in [LnCl3(thz)4]·0.5thz, Ln = Sm, Eu, Gd, Tb, Dy." Zeitschrift für Naturforschung B 69, no. 2 (2014): 255–62. http://dx.doi.org/10.5560/znb.2014-3292.

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The series of luminescent monomeric lanthanide thiazole complexes [LnCl3(thz)4]⋅0.5thz (Ln = Sm, Eu, Gd, Tb, Dy; thz=1,3-thiazole) has been synthesised and characterised by powder and singlecrystal X-ray diffraction, IR and photoluminescence spectroscopy, DTA/TG as well as elemental analysis. The colourless compounds exhibit photoluminescence in the visible region with varying quantum efficiencies up to QY = 48% for [TbCl3(thz)4]⋅0.5thz. Both, the lanthanide ions as well as the thiazole ligand contribute to the luminescence. Excitation can be achieved via intra-4 f transitions and by exciting

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4

Alrefai, Riyadh, Henri Eggenweiler, Hartmut Schubert, and Andreas Berkefeld. "Understanding Factors that Control the Structural (Dis)Assembly of Sulphur-Bridged Bimetallic Sites." Inorganics 7, no. 4 (2019): 42. http://dx.doi.org/10.3390/inorganics7040042.

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Bimetallic structures of the general type [M2(µ-S)2] are omnipresent in nature, for biological function [M2(µ-S)2] sites interconvert between electronically distinct, but isostructural, forms. Different from structure-function relationships, the current understanding of the mechanism of formation and persistence of [M2(µ-S)2] sites is poorly developed. This work reports on bimetallic model compounds of nickel that interconvert between functional structures [Ni2(µ-S)2]+/2+ and isomeric congeners [2{κ-S–Ni}]2+/+, S = Aryl-S−, in which the nickel ions are geometrically independent. Interconversio

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5

Ionov, A. M., M. R. Kobrin, R. N. Mozhchil, A. S. Sigov, Yu V. Syrov, and V. V. Fomichev. "SYNTHESIS AND STUDY OF RHENIUM(IV) DISULPHIDE." Fine Chemical Technologies 12, no. 6 (2017): 83–90. http://dx.doi.org/10.32362/2410-6593-2017-12-6-83-90.

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Synthesis and study of complex chalcogenides in the low oxidation state opens unexpected new opportunities of studying some fundamental problems of condensed matter physics. Dichalcogenides of transition metals, i.e., compounds with the general formula MX2, where M is molybdenum, tungsten, rhenium etc., and X is sulphur, selenium or tellurium, are especially interesting. These dichalcogenides find applications in optoelectronic devices, radiophotonics, in laser physics, communication technology, etc. This study contains a survey of literature concerning the synthesis of sulphides of transition

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6

Moroz, O. M., S. O. Hnatush, C. I. Bohoslavets, G. V. Yavorska та N. V. Truchym. "Usage of ferrum (ІІІ) and manganese (IV) ions as electron acceptors by Desulfuromonas sp. bacteria". Biosystems Diversity 24, № 1 (2016): 87–95. http://dx.doi.org/10.15421/011610.

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The toxicity of metal ions to microorganisms, in particular at high concentrations, is one of the main impediments to their usage in remediation technologies. The purpose of this work is to analyze the possibility of usage by bacteria of the Desulfuromonas genus, isolated by us from Yavorivske Lake, of ferrum (ІІІ) and manganese (IV) ions at concentrations in the medium of 1,74–10,41 mM as electron acceptors of anaerobic respiration to assesss resistance of sulphur reducing bacteria strains to heavy metal compounds. Cells of Desulfuromonas acetoxidans ІМV V-7384, Desulfuromonas sp. Yavor-5 and

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7

Nasir, H. M., T. A. Saki, and M. Y. Al-Luaibi. "Synthesis, identification and thermal study of some new inorganic polymers based on bis-dithiocarbamate ligands with silicone, tellurium and some transition metals." Innovaciencia Facultad de Ciencias Exactas Físicas y Naturales 7, no. 1 (2019): 1–13. http://dx.doi.org/10.15649/2346075x.507.

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Introduction: In recent years, there has been considerable interest in dithiocarbamate complexes because of its diverse biological roles, very few reports have been made on polymeric bis- dithiocarbamate compounds with carbon chain of n-propyl or hexamethelene with transition metals in addition of the absence of any report of organosilicone or tellurium halides with such compounds Our interest in this report based on the preparation of new series of polymers with an expected activity as a fungi side compounds followed by the using of prepared amino compound as a hardners for epoxy paints Mater

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8

Ghoneim, M., E. Mabrouk, A. Hassanein, M. El-Attar, and E. Hesham. "Voltammetric and potentiometric studies of some sulpha drug-Schiff base compounds and their metal complexes." Open Chemistry 5, no. 3 (2007): 898–911. http://dx.doi.org/10.2478/s11532-007-0035-7.

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AbstractThe electrochemical behavior of some sulpha drug-Schiff bases at a mercury electrode was examined in the Britton-Robinson universal buffer of various pH values (2.5–11.7) containing 20% v/v) of ethanol using DC-polarography, cyclic voltammetry and controlled-potential electrolysis. The DC-polarograms and cyclic voltammograms of the examined compounds exhibited a single, 2-electron, irreversible, diffusion-controlled cathodic step within the entire pH range which is attributed to the reduction of the azomethine group-CH=N- to -CH2-NH-. The symmetry transfer coefficient (α) of the electr

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9

Karimov, Kirill, Denis Rogozhnikov, Evgeniy Kuzas, Oleg Dizer, Dmitry Golovkin, and Maksim Tretiak. "Deposition of Arsenic from Nitric Acid Leaching Solutions of Gold–Arsenic Sulphide Concentrates." Metals 11, no. 6 (2021): 889. http://dx.doi.org/10.3390/met11060889.

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At present, the processing of refractory gold–arsenic sulphide concentrates is becoming more relevant due to the depletion of rich crude ore reserves. In the process of the nitric acid leaching of arsenic sulphide minerals, solutions are formed containing 20–30 g/L of arsenic (III). Since market demand for arsenic compounds is limited, such solutions are traditionally converted into poorly soluble compounds. This paper describes the investigation of precipitating arsenic sulphide from nitric acid leaching solutions of refractory sulphide raw materials of nonferrous metals containing iron (III)

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10

Chivers, Tristam, and Frank Edelmann. "Transition-metal complexes of inorganic sulphur-nitrogen ligands." Polyhedron 5, no. 11 (1986): 1661–99. http://dx.doi.org/10.1016/s0277-5387(00)84846-9.

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11

Weger, M. "Dehybridization transition in intermetallic transition-metal compounds." Philosophical Magazine B 52, no. 3 (1985): 701–16. http://dx.doi.org/10.1080/13642818508240630.

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12

Dieckmann, Volker, Sebastian Eicke, Kristin Springfeld, and Mirco Imlau. "Transition Metal Compounds Towards Holography." Materials 5, no. 6 (2012): 1155–75. http://dx.doi.org/10.3390/ma5061155.

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13

Kato, M., Y. Tani, T. Imamura, K. Hirota, and K. Yoshimura. "Metal–insulator transition in compounds." Physica B: Condensed Matter 403, no. 5-9 (2008): 1315–17. http://dx.doi.org/10.1016/j.physb.2007.10.135.

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14

Gribanova, T. N., R. M. Minyaev, and V. I. Minkin. "Multidecker transition metal sandwich compounds." Doklady Chemistry 429, no. 1 (2009): 258–63. http://dx.doi.org/10.1134/s0012500809110020.

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15

Bernal, Ivan, Wolfgang Ries, Henri Brunner, and Devendra K. Rastogi. "Optically active transition metal compounds." Journal of Organometallic Chemistry 290, no. 3 (1985): 353–64. http://dx.doi.org/10.1016/0022-328x(85)87298-3.

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16

Bernal, Ivan, George M. Reisner, Henri Brunner, and Georg Riepl. "Optically active transition-metal compounds." Journal of Organometallic Chemistry 284, no. 1 (1985): 115–28. http://dx.doi.org/10.1016/0022-328x(85)80017-6.

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17

Brazhkin, V. V., R. N. Voloshin, S. V. Popova, and A. G. Umnov. "Nonmetal-metal transition in sulphur melt under high pressure." Physics Letters A 154, no. 7-8 (1991): 413–15. http://dx.doi.org/10.1016/0375-9601(91)90043-8.

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18

Chivers, Tristram, Cees Lensink, and John F. Richardson. "Phosphorus(III)-Nitrogen-Sulphur Compounds: Synthesis and Metal Complexes." Phosphorous and Sulfur and the Related Elements 30, no. 1-2 (1987): 189–92. http://dx.doi.org/10.1080/03086648708080554.

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19

Reiher, Markus. "A Theoretical Challenge: Transition-Metal Compounds." CHIMIA International Journal for Chemistry 63, no. 3 (2009): 140–45. http://dx.doi.org/10.2533/chimia.2009.140.

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20

Gill, Martin R., and Katherine A. Vallis. "Transition metal compounds as cancer radiosensitizers." Chemical Society Reviews 48, no. 2 (2019): 540–57. http://dx.doi.org/10.1039/c8cs00641e.

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21

Brookhart, M., M. L. H. Green, and G. Parkin. "Agostic interactions in transition metal compounds." Proceedings of the National Academy of Sciences 104, no. 17 (2007): 6908–14. http://dx.doi.org/10.1073/pnas.0610747104.

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22

Brunner, Henri, Peter Faustmann, and Bernhard Nuber. "Optically active transition metal compounds 113." Journal of Organometallic Chemistry 556, no. 1-2 (1998): 129–40. http://dx.doi.org/10.1016/s0022-328x(97)00745-6.

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23

Brunner, Henri, Andreas Winter, and Bernhard Nuber. "Optically active transition metal compounds 114." Journal of Organometallic Chemistry 558, no. 1-2 (1998): 213–18. http://dx.doi.org/10.1016/s0022-328x(98)00412-4.

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24

Poddar, P., and A. K. Rastogi. "Metal-Insulator Transition in AxVS2 Compounds." physica status solidi (b) 218, no. 1 (2000): 229–32. http://dx.doi.org/10.1002/(sici)1521-3951(200003)218:1<229::aid-pssb229>3.0.co;2-o.

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25

Saito, Yoshihiko. "Structural Studies of Transition Metal Compounds." Journal of the Chinese Chemical Society 38, no. 5 (1991): 405–24. http://dx.doi.org/10.1002/jccs.199100070.

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26

KAUZLARICH, S. M. "ChemInform Abstract: Transition Metal Zintl Compounds." ChemInform 28, no. 49 (2010): no. http://dx.doi.org/10.1002/chin.199749281.

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27

Bartol, Jessica, Peter Comba, Michael Melter, and Marc Zimmer. "Conformational searching of transition metal compounds." Journal of Computational Chemistry 20, no. 14 (1999): 1549–58. http://dx.doi.org/10.1002/(sici)1096-987x(19991115)20:14<1549::aid-jcc8>3.0.co;2-f.

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28

HÜFNER, S. "ELECTRONIC STRUCTURE OF TRANSITION METAL COMPOUNDS." International Journal of Modern Physics B 07, no. 01n03 (1993): 324–32. http://dx.doi.org/10.1142/s0217979293000688.

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The basic features of the electronic structure of transition metal oxides is discussed. It is found that the bands of the anions are well understood whereas the exact nature of the d-bands is still uncertain. There is a competition between local excitonic like excitations and excitations which reflect with some renormalization the band structure. The nature of gap states in NiO is discussed.

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29

TSUJI, Jiro, and Kiyotaka OHNO. "Decarbonylation Reactions Using Transition Metal Compounds." Synthesis 1969, no. 04 (2002): 157–69. http://dx.doi.org/10.1055/s-1969-34197.

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30

Saito, Yoshihiko. "Structural studies on transition metal compounds." International Reviews in Physical Chemistry 8, no. 2-3 (1989): 235–73. http://dx.doi.org/10.1080/01442358909353230.

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31

H�fner, S. "Mott insulation in transition metal compounds." Zeitschrift f�r Physik B Condensed Matter 61, no. 2 (1985): 135–38. http://dx.doi.org/10.1007/bf01307767.

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32

Vos, Johannes G., and Mary T. Pryce. "Photoinduced rearrangements in transition metal compounds." Coordination Chemistry Reviews 254, no. 21-22 (2010): 2519–32. http://dx.doi.org/10.1016/j.ccr.2010.04.010.

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33

Neumann, K. U., J. Crangle, S. Lipinski, J. G. Smith, N. K. Zayer, and K. R. A. Ziebeck. "Superweak ferromagnetism in transition metal compounds." Journal of Magnetism and Magnetic Materials 140-144 (February 1995): 195–96. http://dx.doi.org/10.1016/0304-8853(94)00698-9.

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34

Yemelyanova, V. S., T. V. Shakieva, Zh K. Kairbekov, E. M. Shakiev, and B. B. Baizhomartov. "Low-Temperature Catalytic Clearing of Gases of Thermal Power Station from Harmful Impurity in the Presence of the Cobalt Complexes Fixed on a Polymeric Matrix." Advanced Materials Research 807-809 (September 2013): 1586–92. http://dx.doi.org/10.4028/www.scientific.net/amr.807-809.1586.

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The results of optimization of catalysts for gases clearing from sulfur dioxide using processes of oxidation are presented in this work. The researches carried out with the help of modern methods: kinetic, IR-, UV-spectrophotometric, viscometry, LG-chromatography, redox-potentiometric. It is shown, that developed complexes of transitive metals immobilized on a polymeric matrix are highly effective and stable catalysts for the sulphur dioxide oxidation processes. By the example of cobalt compounds the reactions kinetic investigated in details, the kinetic equation is received, allowing to optim

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35

YAMADA, Teruaki, and Yoshio KAMIYA. "Mechanism of antioxidant action of sulphur containing transition metal complexes." Journal of Synthetic Organic Chemistry, Japan 43, no. 1 (1985): 67–75. http://dx.doi.org/10.5059/yukigoseikyokaishi.43.67.

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36

BRUNNER, H. "ChemInform Abstract: Optically Active Transition Metal Compounds Containing Chiral Transition Metal Atoms." ChemInform 28, no. 9 (2010): no. http://dx.doi.org/10.1002/chin.199709215.

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37

Parker, L. J., M. Hasegawa, T. Atou, and J. V. Badding. "High Pressure Synthesis of Alkali Metal-Transition Metal Compounds." REVIEW OF HIGH PRESSURE SCIENCE AND TECHNOLOGY 7 (1998): 1049–53. http://dx.doi.org/10.4131/jshpreview.7.1049.

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38

SARLIS, JOHN, and DIMITRIOS BERK. "REDUCTION OF SULPHUR DIOXIDE BY METHANE OVER TRANSITION METAL OXIDE CATALYSTS." Chemical Engineering Communications 140, no. 1 (1995): 73–85. http://dx.doi.org/10.1080/00986449608936455.

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39

OGAWA, Akiya, and Noboru SONODA. "Transition Metal-Catalyzed Reactions of Chalcogen Compounds." Journal of Synthetic Organic Chemistry, Japan 51, no. 9 (1993): 815–25. http://dx.doi.org/10.5059/yukigoseikyokaishi.51.815.

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40

Nagasima, T., K. Saikawa, and H. Yamada. "Itinerant-electron ferrimagnetism of transition-metal compounds." Journal of Magnetism and Magnetic Materials 164, no. 1-2 (1996): 115–18. http://dx.doi.org/10.1016/s0304-8853(96)00392-7.

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41

Motome, Yukitoshi, Hiroki Nakano, and Masatoshi Imada. "Metal-insulator transition in Mn perovskite compounds." Materials Science and Engineering: B 63, no. 1-2 (1999): 58–64. http://dx.doi.org/10.1016/s0921-5107(99)00052-5.

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42

Clerjaud, B. "Transition-metal impurities in III-V compounds." Journal of Physics C: Solid State Physics 18, no. 19 (1985): 3615–61. http://dx.doi.org/10.1088/0022-3719/18/19/005.

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43

Krishnamoorthy, Bellie Sundaram, Samia Kahlal, Boris Le Guennic, Jean-Yves Saillard, Sundargopal Ghosh, and Jean-François Halet. "Molecular transition-metal boron compounds. Any interest?" Solid State Sciences 14, no. 11-12 (2012): 1617–23. http://dx.doi.org/10.1016/j.solidstatesciences.2012.03.026.

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44

Krasovskiy, Arkady, Alexander Tishkov, Vicente del Amo, Herbert Mayr, and Paul Knochel. "Transition-Metal-Free Homocoupling of Organomagnesium Compounds." Angewandte Chemie International Edition 45, no. 30 (2006): 5010–14. http://dx.doi.org/10.1002/anie.200600772.

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45

Comba, Peter, Marion Kerscher, Michael Merz, et al. "Structural Variation in Transition-Metal Bispidine Compounds." Chemistry - A European Journal 8, no. 24 (2002): 5750–60. http://dx.doi.org/10.1002/1521-3765(20021216)8:24<5750::aid-chem5750>3.0.co;2-p.

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46

Bogdanović, Borislav, and Manfred Schwickardi. "Transition Metal Catalyzed Preparation of Grignard Compounds." Angewandte Chemie International Edition 39, no. 24 (2000): 4610–12. http://dx.doi.org/10.1002/1521-3773(20001215)39:24<4610::aid-anie4610>3.0.co;2-o.

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47

Bruce, Michael I. "ChemInform Abstract: Organo-Transition Metal Cluster Compounds." ChemInform 30, no. 39 (2010): no. http://dx.doi.org/10.1002/chin.199939247.

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48

Comba, Peter, Wolfgang Goll, Bernhard Nuber, and Katalin Várnagy. "Transition Metal Coordination Compounds of Bisamidobispyridyl Ligands." European Journal of Inorganic Chemistry 1998, no. 12 (1998): 2041–49. http://dx.doi.org/10.1002/(sici)1099-0682(199812)1998:12<2041::aid-ejic2041>3.0.co;2-s.

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49

Natarajan, Srinivasan, and Sukhendu Mandal. "Open-Framework Structures of Transition-Metal Compounds." Angewandte Chemie International Edition 47, no. 26 (2008): 4798–828. http://dx.doi.org/10.1002/anie.200701404.

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50

BRUCE, M. I. "ChemInform Abstract: Organo-Transition Metal Cluster Compounds." ChemInform 29, no. 47 (2010): no. http://dx.doi.org/10.1002/chin.199847301.

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