Search results for "organometalli"
showing 10 items of 395 documents
Coordinating behaviour of a new pyridylhydrazone; tris-complexes of manganese(II), cobalt(II), nickel(II), copper(II) and zinc(II) with 2-pyridylcarb…
1991
The preparation and characterization oftris-complexes of MnII, CoII, NiII, CuII and ZnII with a new pyridylhydrazone, 2-pyridylcarbaldehyde-N,N-dimethylhydrazone (pch), are described. In all the complexes pch behaves as a bidentate ligand binding through the pyridine and azomethyne nitrogen atoms. The complexes appear to be monomeric, high spin six-coordinate, and a distorted octahedral stereochemistry around the metal is suggested. The e.p.r. results for both CuII compounds indicate a mainly dx2−y2 ground state with a static Jahn-Teller distortion, whilst for the MnII complex the e.p.r. data indicates a very low symmetry for the MnN6 polyhedron.
Tungsten(VI) complexes formed in an excess of gluconic acid: A polarimetric and spectrophotometric study
1985
The tungsten(VI)-gluconic acid system in an excess of this organic reagent has been spectroscopically and polarimetrically studied and four species, two mononuclear with stoichiometry 1∶2 (metal∶ligand) and two dinuclear with composition 2∶2, have been identified. The non-formation of a binuclear species with stoichiometry 2∶1 (metal∶ligand) demonstrates some preference towards coordination of carboxylate group.
Cimetidine complexes derived from cobalt(II), nickel(II) and copper(II) salts of polyatomic anions
1986
Cobalt(II), nickel(II) and copper(II) complexes [M(CM)2]X2 (X = BF4 or NO3) have been prepared with cimetidine (CM). Powder data, molar conductivities, magnetic moments, i.r. and electronic spectra support apseudo-octahedral stereochemistry with MN2N 2 ⋆ S2 chromophore and tentative structures are proposed for the complexes. Their properties are compared with these of previously prepared complexes.
High oxidation state aqueous organometallics: synthesis and structure of a dinuclear oxo(pentamethylcyclopentadienyl)acetato complex of molybdenum(IV…
2003
International audience; The zinc reduction of Cp*2Mo2O5 in a MeOH–H2O mixture in the presence of acetic acid affords the diamagnetic dinuclear compound [Cp*MoO(O2CCH3)]2. An X-ray structural investigation reveals a novel dioxo- and diacetato-bridged structure, with a relatively strong metal–metal bond [2.5524(3) Å]. The compound exhibits a reversible one-electron oxidation process in the cyclic voltammogram. A comparison with other related structures reveals the effect of the electric charge on the mononuclear or dinuclear structural choice.Zinc reduction of Cp*2Mo2O5 in water–methanol in the presence of acetic acid affords compound Cp*2Mo2O2(O2CCH3)2, whose dinuclar tetrabridged structure …
Fluorescence emission and enhanced photochemical stability of Zn(II)-5-triethyl ammonium methyl salicylidene ortho-phenylendiiminate interacting with…
2010
Abstract The photophysical and photochemical properties of the cationic Zn II complex of 5-triethyl ammonium methyl salicylidene ortho-phenylendiimine (ZnL 2+ ) interacting with native DNA were investigated by steady state and time-resolved fluorescence spectroscopies. Experimental results indicate that, in the presence of DNA, ZnL 2+ is efficiently protected from a photochemical process, which occurs when it is in the free state dispersed in aqueous solution. The analysis of the absorption and emission spectra of ZnL 2+ , both stored in the dark and after exposure to tungsten lamp light for 24 h, corroborated by quantum chemical calculations, allowed us to point out that ZnL 2+ undergoes a…
Fluorescent organometallic rhodium(I) and ruthenium(II) metallodrugs with 4-ethylthio-1,8-naphthalimide ligands: Antiproliferative effects, cellular …
2018
Fluorescent 4-ethylthio-1,8-naphthalimides containing rhodium(I) N-heterocyclic carbene (NHC) and ruthenium (II) NHC fragments were synthesised and evaluated for their antiproliferative effects, cellular uptake and DNA-binding activity. Both types of organometallics triggered ligand dependent efficient cytotoxic effects against tumor cells with the rhodium(I) NHC derivatives causing stronger effects than the ruthenium (II) NHC analogues. Antiproliferative effects could also be observed against several pathogenic Gram-positive bacterial strains, whereas the growth of Gram-negative bacteria was not substantially affected. Cellular uptake was confirmed by atomic absorption spectroscopy as well…
Luminescent Ionic Transition-Metal Complexes for Light-Emitting Electrochemical Cells
2012
Higher efficiency in the end-use of energy requires substantial progress in lighting concepts. All the technologies under development are based on solid-state electroluminescent materials and belong to the general area of solid-state lighting (SSL). The two main technologies being developed in SSL are light-emitting diodes (LEDs) and organic light-emitting diodes (OLEDs), but in recent years, light-emitting electrochemical cells (LECs) have emerged as an alternative option. The luminescent materials in LECs are either luminescent polymers together with ionic salts or ionic species, such as ionic transition-metal complexes (iTMCs). Cyclometalated complexes of Ir(III) are by far the most util…
Reversible Colorimetric Probes for Mercury Sensing
2005
The selectivity and sensitivity of two colorimetric sensors based on the ruthenium complexes N719 [bis(2,2'-bipyridyl-4,4'-dicarboxylate)ruthenium(II) bis(tetrabutylammonium) bis(thiocyanate)] and N749 [(2,2':6',2' '-terpyridine-4,4',4' '-tricarboxylate)ruthenium(II) tris(tetrabutylammonium) tris(isothiocyanate)] are described. It was found that mercury ions coordinate reversibly to the sulfur atom of the dyes' NCS groups. This interaction induces a color change in the dyes at submicromolar concentrations of mercury. Furthermore, the color change of these dyes is selective for mercury(II) when compared with other ions such as lead(II), cadmium(II), zinc(II), or iron(II). The detection limit…
Enantioselective Henry addition of methyl 4-nitrobutyrate to aldehydes. Chiral building blocks for 2-pyrrolidinones and other derivatives.
2010
A catalytic highly enantioselective Henry addition of methyl 4-nitrobutyrate to aldehydes using a Cu(II)-amino pyridine complex as catalyst is described. The products resulting from this reaction constitute a new, highly versatile family of chiral building blocks as a result of the presence of three different functional groups on the molecule. These products have been transformed into nonracemic chiral gamma-lactams, 5-hydroxy-5-substituted levulinic acid derivatives, and delta-lactones.
The construction of open GdIII metal–organic frameworks based on methanetriacetic acid: New objects with an old ligand
2010
11 páginas, 11 figuras, 2 esquemas.-- et al.