Search results for "COBALT"
showing 10 items of 1098 documents
Influence of Sodium on the Structure and HDS Activity of Co–Mo Catalysts Supported ON Silica and Aluminosilicate
2000
Abstract Structural changes and catalytic performances of hydrodesulfurization (HDS) Co–Mo catalysts, supported on amorphous aluminosilicate (ASA) and amorphous SiO 2 were investigated as a function of the amount of sodium ions added to the supports. The catalysts were prepared according to the incipient wet impregnation method using (NH 4 ) 6 Mo 7 O 24 as molybdenum precursor and CoCl 2 or Co(NO 3 ) 2 as cobalt precursor. Structural and morphological characterisations of the materials were performed with X-ray diffraction (XRD) and surface area measurements (BET). In the case of the ASA-supported catalysts, increasing the amount of sodium resulted in a gradual decrease of the catalyst surf…
Cover Feature: The Missing Link in the Magnetism of Hybrid Cobalt Layered Hydroxides: The Odd–Even Effect of the Organic Spacer (Chem. Eur. J. 3/2021)
2020
Preparation of dithiacycloalkynes by cyclization reactions applying the cesium effect
1993
Abstract The strained dithiacycloalkynes 3a,b and the larger heterocyclic alkynes 3c and 4 are obtained by cesium assisted cyclization reactions of the dithiols 1a–c and 1,4-dibromo-2-butyne (2). The reactivity of 3a–c was studied in cycloaddition and complexation reactions generating the adducts 5a,b and 6 and the silver and cobalt complexes 7 and 8.
Field-induced slow relaxation of magnetization in a mononuclear Co(II) complex of 2,6-bis(pyrazol-1-yl)pyridine functionalized with a carboxylic acid
2018
Abstract Combining Co(II) with the 2,6-bis-(pyrazol1-yl)pyridine ligand functionalized with a carboxylic acid group (bppCOOH) results in the compound [CoII(bppCOOH)2](ClO4)2·2Me2CO, which shows a field-induced slow relaxation of magnetization as a result of the magnetic anisotropy of the distorted octahedral coordination of high-spin Co(II). Co(II)/Fe(II) solid solutions of bppCOOH have been prepared to study the influence of Co(II) on the spin crossover properties of Fe(II). Magnetic characterization of [Fe0.92Co0.08(bppCOOH)2](ClO4)2 indicates that the Cobalt dopant leads to a reduction of T1/2 and a loss of cooperativity of the spin transition.
Magnetic phase transition and magnetic bistability in oxamato-based CoIICuII bimetallic MOF thin films
2019
Abstract Thin films of an anionic oxamato-bridged cobalt(II)–copper(II) 3D MOF have been growth at 120 °C in DMSO through a one-pot reaction from Co(NO3)2·6H2O and (Me4N)2[Cu(2,6-Et2pa)2]·6H2O (2,6-Et2pa = N-2,6-diethylphenyloxamate) over Si(111) surfaces functionalized with carboxylic acid terminating groups. These heterobimetallic CoII2CuII3 MOF thin films (2) of about ten nanometers thickness show a ferrimagnetically ordered phase below ca. 10 K with a relatively large magnetic hysteresis similar to that of the bulk material of formula (Me4N)2[Co2Cu3(2,6-Et2pa)6]·5H2O (1).
2017
Eight coordination compounds of formulae [FeII(L˙)2][ReIVCl6] (1a), [FeII(L˙)2][ReIVBr6] (1b), [CoII(L˙)2][ReIVCl6]·CH3CN (2a), [CoII(L˙)2][ReIVBr6] (2b), [NiII(L˙)(CH3CN)3][ReIVCl6]·CH3CN (3a), [NiII(L˙)(CH3CN)3][ReIVBr6]·3CH3CN (3b), [CuII(L˙)2][ReIVCl6] (4a) and [CuII(L˙)2][ReIVBr6] (4b), where L˙ is the aminoxyl radical chelating ligand, 4,4′-dimethyl-2,2′-di(2-pyridyl)oxazolidine-N-oxide, have been synthesised. Structural and magnetic studies reveal metal–radical intramolecular antiferromagnetic interactions in the [MII(L˙)2]2+ cations in the iron, cobalt and copper based compounds (1a, 1b, 2a, 2b, 4a and 4b) with the central metal ion low-spin in the case of iron (1a and 1b) and a gra…
Strongly Coupled Cyclometalated Ruthenium Triarylamine Chromophores as Sensitizers for DSSCs
2016
A series of anchor-functionalized cyclometalated bis(tridentate) ruthenium(II) triarylamine hybrids [Ru(dbp-X)(tctpy)](2-) [2 a](2-) -[2 c](2-) (H3 tctpy=2,2';6',2''-terpyridine-4,4',4''-tricarboxylic acid; dpbH=1,3-dipyridylbenzene; X=N(4-C6 H4 OMe)2 ([2 a](2-) ), NPh2 ([2 b](2-) ), N-carbazolyl [2 c](2-) ) was synthesized and characterized. All complexes show broad absorption bands in the range 300-700 nm with a maximum at about 545 nm. Methyl esters [Ru(Me3 tctpy)(dpb-X)](+) [1 a](+) -[1 c](+) are oxidized to the strongly coupled mixed-valent species [1 a](2+) -[1 c](2+) and the Ru(III) (aminium) complexes [1 a](3+) -[1 c](3+) at comparably low oxidation potentials. Theoretical calculati…
Studies on coordination compounds—VIII. Syntheses, structural, magnetic, spectral and thermal properties of some cobalt(II), nickel(II) and copper(II…
1995
Abstract The complexes bis[triaqua(2-aminopyrimidine)-μ-sulphato-O,O′-cobalt(II)] dihydrate (1), catena-[diaqua(2(2-aminopyrimidine))-μ-sulphato-O,O′nickel(II)]2-amino-pyrimidine (2), [pentaaqua(2-aminopyrimidine)nickel(II)]sulphate 2-aminopyrimidine (3) and catena-[aqua(2(2-aminopyrimidine))-μ-sulphato-O,O′-copper(II)] dihydrate (4) were prepared, structure determined by X-ray methods and physical properties studied by magnetic, IR, NMR, EPR and reflectance methods. The thermal behaviour was studied by TG and mass spectrometric methods. The results are discussed on a structural basis.
Cobalt Corroles with Bis‐Ammonia or Mono‐DMSO Axial Ligands. Electrochemical, Spectroscopic Characterizations and Ligand Binding Properties
2018
International audience; Four bis-ammonia ligated cobalt corroles and four mono-DMSO ligated cobalt corroles with different mesoaryl substituents on the macrocycle (A 2 Band A 3-corroles) were synthesized and investigated as to their electrochemical and spec-troscopic properties under different solution conditions. The complexation energies of the investigated cobalt corroles were theoretically calculated to illustrate the propensity of the cobalt center for pentacoordination or hexa-coordination with various axial ligands (DMSO, CO, py and NH 3). The structure of one hexacoordinate bis-NH 3 cobalt corrole complex was also determined by X-ray diffraction.