Search results for "COBALT"
showing 10 items of 1098 documents
Strong Exchange Coupling in a Trimetallic Radical-Bridged Cobalt(II)-Hexaazatrinaphthylene Complex.
2016
Reducing hexaazatrinaphthylene (HAN) with potassium in the presence of 18-c-6 produces [{K(18-c-6)}HAN], which contains the S=1/2 radical [HAN](.-) . The [HAN](.-) radical can be transferred to the cobalt(II) amide [Co{N(SiMe3 )2 }2 ], forming [K(18-c-6)][(HAN){Co(N'')2 }3 ]; magnetic measurements on this compound reveal an S=4 spin system with strong cobalt-ligand antiferromagnetic exchange and J≈-290 cm(-1) (-2 J formalism). In contrast, the Co(II) centres in the unreduced analogue [(HAN){Co(N'')2 }3 ] are weakly coupled (J≈-4.4 cm(-1) ). The finding that [HAN](.-) can be synthesized as a stable salt and transferred to cobalt introduces potential new routes to magnetic materials based on …
CCDC 732637: Experimental Crystal Structure Determination
2010
Related Article: E.Colacio, H.Aouryaghal, A.J.Mota, J.Cano, R.Sillanpaa, A.Rodriguez-Dieguez|2009|CrystEngComm|11|2054|doi:10.1039/b906382j
CCDC 1569643: Experimental Crystal Structure Determination
2017
Related Article: Bin Fei, Jian Zhou, Zheng Yan, Sergii I. Shylin, Vadim Ksenofontov, Il'ya A. Gural'skiy, Xin Bao|2017|CrystEngComm|19|7079|doi:10.1039/C7CE01826F
CCDC 1569644: Experimental Crystal Structure Determination
2017
Related Article: Bin Fei, Jian Zhou, Zheng Yan, Sergii I. Shylin, Vadim Ksenofontov, Il'ya A. Gural'skiy, Xin Bao|2017|CrystEngComm|19|7079|doi:10.1039/C7CE01826F
CCDC 1435056: Experimental Crystal Structure Determination
2016
Related Article: Kwang Soo Lim, José J. Baldoví, Woo Ram Lee, Jeong Hwa Song, Sung Won Yoon, Byoung Jin Suh, Eugenio Coronado, Alejandro Gaita-Ariño, and Chang Seop Hong|2016|Inorg.Chem.|55|5398|doi:10.1021/acs.inorgchem.6b00410
Metallic nanoparticles exhibit paradoxical effects on oxidative stress and pro-inflammatory response in endothelial cells in vitro
2007
Particulate matter is associated with different human diseases affecting organs such as the respiratory and cardiovascular systems. Very small particles (nanoparticles) have been shown to be rapidly internalized into the body. Since the sites of internalization and the location of the detected particles are often far apart, a distribution via the blood stream must have occurred. Thus, endothelial cells, which line the inner surface of blood vessels, must have had direct contact with the particles. In this study we tested the effects of metallic nanoparticles (Co and Ni) on oxidative stress and proinflammatory response in human endothelial cells in vitro. Exposure to both nanoparticle types…
CoS2/TiO2 Nanocomposites for Hydrogen Production under UV Irradiation
2019
Transition metal chalcogenides have intensively focused on photocatalytic hydrogen production for a decade due to their stronger edge and the quantum confinement effect. This work mainly focuses on synthesis and hydrogen production efficiencies of cobalt disulfide (CoS2)-embedded TiO2 nanocomposites. Materials are synthesized by using a hydrothermal approach and the hydrogen production efficiencies of pristine CoS2, TiO2 nanoparticles and CoS2/TiO2 nanocomposites are compared under UV irradiation. A higher amount of hydrogen production (2.55 mmol g&minus
Equilibrium and structural studies of complexes with a hexadentate ligand containing amide, amine and pyridyl nitrogen donors. Crystal structures of …
2002
A novel potentially hexadentate ligand, 1,8-bis(2-pyridylcarbamoyl)-3,6-diazaoctane (pyctrien) has been synthesised as its tetrahydrochloride salt; its protonation constants and the stability constants of the copper(II) and nickel(II) chelates have been determined by potentiometry. Amide group deprotonation permits the formation of [MLH−1]+ and [MLH−2] species in all cases, whereas the detection of the neutral or the protonated species depends on the nature of the metal ions. The solid complexes of copper, nickel and cobalt with the neutral and the deprotonated ligand have been synthesised and characterised by IR and UV–VIS spectroscopy. The amidic groups are coordinated through the oxygen …
Self-Assembled Molecular Rafts at Liquid|Liquid Interfaces for Four-Electron Oxygen Reduction
2011
The self-assembly of the oppositely charged water-soluble porphyrins, cobalt tetramethylpyridinium porphyrin (CoTMPyP(4+)) and cobalt tetrasulphonatophenyl porphyrin (CoTPPS(4-)), at the interface with an organic solvent to form molecular "rafts", provides an excellent catalyst to perform the interfacial four-electron reduction of oxygen by lipophilic electron donors such as tetrathiafulvalene (TTF). The catalytic activity and selectivity of the self-assembled catalyst toward the four-electron pathway was found to be as good as that of the Pacman type cofacial cobalt porphyrins. The assembly has been characterized by UV-visible spectroscopy, Surface Second Harmonic Generation, and Scanning …
Characterization of Cobalt Catalysts on Biomass-Derived Carbon Supports
2017
Cobalt catalysts are known to have a high activity and selectivity in the Fischer–Tropsch reaction converting synthesis gas to higher hydrocarbons (C5+). These catalysts have been supported by different porous materials. Porous carbon materials like activated carbon (AC) have physical and chemical surface properties that affect the preparation of supported metal catalysts and can easily be tailored. In this study, AC was produced by carbonization and steam activation of lignin, a waste fraction from the Kraft pulping process. A series of Co/AC-catalysts was produced and characterized by several techniques. According to the results, tailored properties (high surface area, mesoporosity) were …