Search results for "PALLADIUM"
showing 10 items of 956 documents
Sorption of Pd(II) ion by calcium alginate gel beads at different chloride concentrations and pH. A kinetic and equilibrium study
2016
Abstract A kinetic and thermodynamic study on the sorption ability of calcium alginate gel beads towards Pd(II) ion was made in aqueous solution at different pH and chloride concentrations. The experimental conditions adopted in the sorption experiments were established on the basis of a speciation study on the Pd 2+ -AA system in which all the side reactions, such as the hydrolysis of Pd(II), the protonation of alginate and the interactions of the ligand and the metal ion with ions of ionic medium were taken into account. In the pH range 2–5 and at chloride concentration in the range 0 ⩽ C Cl - /mmol L −1 ⩽ 10 the gel beads showed good sorption ability towards Pd(II) ion as confirmed by k…
Protonation and methylation reactions of 2-pyridyl-palladium(II) and -platinum(II) complexes
1983
Abstract The reactions of strong acids HX and HClO4 with the 2-pyridyl complexes [PdX(μ-C5H4N-C2,N)(PPh3)]2 (X = Cl, Br), trans-[PdCl(C5H4N-C2)(PEt3)2] and [PdCl(C5H4N-C2)(dppe)] yield the N-protonated derivatives cis-[PdX2-(C5H5N-C2)(PPh3)], trans-[PdCl(C5H5N-C2)(PEt3)2]ClO4 and [PdCl-(C5H5N-C2)(dppe)]ClO4, respectively. The terminal 2-pyridyl group of trans-[PdCl(C5H4N-C2)(PEt3)2] and [PdCl(C5H4N-C2)(dppe)] also reacts with Me2SO4/NaClO4 to give trans-[PdClC5H4(l-Me)N-C2(PEt3)2]ClO4 and [PdClC5H4(l-Me)N-C2(dppe)]ClO4. Analogous N-protonation or N-methylation reactions occur with trans-[PtBr(C5H4N-C2)(L)2] (L = PEt3, PPh3). The complexes trans-[MX(C5H5N-C2)(PMe2Ph)2]ClO4 (M = Pd, X = Cl an…
Selective palladium-catalysed dimerisation of methyl acrylate in ionic liquids: towards a continuous processThis work was presented at the Green Solv…
2003
The activity and stability of cationic palladium complexes [Pd(PBu3)2S2]2+ used for the selective tail-to-tail dimerisation of methyl acrylate are significantly improved with the utilisation of ionic liquids like [BMIM][BF4] or the protonated N-butyl-imidazole, [HBIM][BF4]. Problems related to product inhibition and catalyst recycling are overcome by running the reaction in a two-phase mode, toluene being used as extractant. Catalyst stabilisation is further improved by trapping the ancillary ligand into the ionic liquid with an ionic tail: with the use of 1-dibutylphosphino-2-dimethylaminoethane, the catalyst is stable for more than 100 h, therefore demonstrating the feasibility of a conti…
Photo-assisted formation of a chelating diphos ligand from PPh3 and a cyclometallated [P(C6H4)(C6H5)2]− ligand. Crystal structure of Pd{η2-o-[P(C6H5)…
2000
Abstract The cyclometallated palladium compound, Pd[η2-(C6H4)P(C6H5)2]Br[P(C6H5)3] (1), in the solid state by action of light, evolves to give Pd{η2-o-[P(C6H5)2]2(C6H4)}Br2 (2). This compound contains the diphosphine, o-[P(C6H5)2]2(C6H4), as chelated ligand that is formed by a couple reaction of the metallated ligand η2-[(C6H4)P(C6H5)2]− and the coordinated arylphosphine. A study by NMR spectroscopy confirms that the o-phenylene bridge in the diphosphine ligand in 2 comes from the metallated phosphine ligand in 1.
Organometallic Palladium Complexes with a Water-Soluble Iminophosphorane Ligand As Potential Anticancer Agents
2012
The synthesis and characterization of a new water-soluble iminophosphorane ligand TPA=N-C(O)-2BrC(6)H(4) (C,N-IM; TPA = 1,3,5-triaza-7-phosphaadamantane) 1 is reported. Oxidative addition of 1 to Pd(2)(dba)(3) affords the orthopalladated dimer [Pd(μ-Br){C(6)H(4)(C(O)N=TPA-kC,N)-2}](2) (2) as a mixture of cis and trans isomers (1:1 molar ratio) where the iminophosphorane moeity behaves as a C,N-pincer ligand. By addition of different neutral or monoanionic ligands to 2, the bridging bromide can be cleaved and a variety of hydrophilic or water-soluble mononuclear organometallic palladium(II) complexes of the type [Pd{C(6)H(4)(C(O)N=TPA-kC,N)-2}(L-L)] (L-L = acac (3); S(2)CNMe(2) (4); 4,7-Diph…
Etherification of Functionalized Phenols with Chloroheteroarenes at Low Palladium Loading: Theoretical Assessment of the Role of Triphosphane Ligands…
2011
The present study highlights the potential of robust tridentate ferrocenylphosphanes with controlled conformation as catalytic auxiliaries in CO bond formation reactions. Air-stable palladium triphosphane systems are efficient for selective heteroaryl ether synthesis by using as little as 0.2 mol% of catalyst. These findings represent an economically attractive and clean etherification of functionalized phenols, electron-rich, electron-poor and para-, meta- or ortho-substituted substrates, with heteroaryl chlorides, including pyridines, hydroxylated pyridine, pyrimidines and thiazole. The etherification tolerates very important functions in various positions, such as cyano, methoxy, amino, …
Triplet-triplet energy transfer controlled by the donor-acceptor distance in rigidly held palladium-containing cofacial bisporphyrins.
2005
Eleven new complexes, including mono-, heterobi-, and homobimetallic cofacial bisporphyrins, (Pd)H 2 DPS, (M)H 2 DPX, (M)H 2 DPB, (PdZn)DPS, (PdZn)DPX, (Pt) 2 DPX, (M) 2 DPB (M=Pd, Pt), and (Pt)P (DPS 4 - = 4,6-bis[5-(2,8,13,17-tetraethyl-3,7,12,18-tetramethylporphyrinyl)]dibenzothiophene tetraanion, DPX 4 - = 4,5-bis[5-(2,8,13,17-tetraethyl-3,7,12,18-tetramethylporphyrinyl)]-9,9-dimethylxanthene tetraanion, DPB 4 - =1,8-bis[5-(2,8,13,17-tetraethyl-3,7,12,18-tetramethylporphyrinyl)]biphenylene tetraanion, P 2 - = 5-phenyl-2,8,13,17-tetraethyl-3,7,12,18-tetramethylporphyrin dianion) have been synthesized and characterized. The photophysical properties of the donor (M)P (M=Pd or Pt, P= porphy…
Intermolecular hydrogen bonding H···Cl− in the solid palladium(II)-diaminocarbene complexes
2017
Abstract Weak intermolecular non-covalent H···Cl− interactions in the solid chelated palladium(II)-diaminocarbene complex cis-[PdCl(CNXyl){C(NHXyl)=NHC6H2Me2 NH2}]Cl (3; Xyl=2,6-Me2C6H3) were studied by XRD followed by appropriate DFT calculations. The N–H···Cl contacts for both NH groups in the carbene moiety are different (N1–H···Cl2 3.5258(19), N2–H···Cl2 3.0797(17) Å). The DFT calculations and topological analysis of the electron density distribution within the formalism of Bader’s theory (QTAIM method) were performed for a model cluster of the carbene complex 3. The theoretical data confirmed that the strength of intermolecular HB H···Cl− is different for two NH-protons of the carbene …
Nanostructured electrodes for hydrogen production in alkaline electrolyzer
2018
Abstract Ever-widespread employment of renewable energy sources, such as wind and sun, request the simultaneous use of effective energy storage systems owing to the intermittent and unpredictable energy generation by these sources. The most reliable storage systems currently under investigation are batteries and electrochemical cells for hydrogen production from water splitting. Both systems store chemical energy which can be converted on demand. The low power density is the weakness of the batteries while the high production cost limits currently the wide use of hydrogen from electrochemical water splitting. In this work, attention was focused on the use of nanostructured Ni as a cathode f…
A nanostructured sensor of hydrogen peroxide
2017
Abstract A nanostructured electrochemical sensor of hydrogen peroxide was fabricated growing self-standing Pd nanowires (Pd NWs) into polycarbonate (PC) membranes through a simple metal galvanic deposition. Conditions of deposition were adjusted in order to attain 2–5 μm long Pd wires. Characterization of Pd-NWs was performed by scanning electrode microscopy, energy-dispersive X-ray spectroscopy and X-ray diffraction. Properties of the nanostructured sensor were studied by cyclic voltammetry and chronoamperometry in phosphate buffer—ethanol solution. Addition of pure ethanol to the test solution was essential in order to increase wettability of the nanostructures. Sensing features were comp…