Search results for "Perchlorate"
showing 10 items of 643 documents
Complex Formation of the Uranyl (UO22+) Ion with the Diethylene Triaminopentaacetate (DTPA) Ligand at 25 °C in 3 M Sodium Perchlorate
2011
The complex formation between the uranyl (UO22+) ion and the diethylene triaminopentaacetate ligand (DTPA) has been investigated at 25 °C, in a 3 M sodium perchlorate medium. The overall protonation constants βjH of the free ligand have been previously determined in this ionic medium: six protonated species (HjA), with j ranging from 1 to 6, together with the free anion A5− have been identified in the concentration range from (3·10−3 to 13·10−3) mol·kg−1. Four complex species, H2UO2A−, HUO2A2−, UO2A3−, and UO2AOH4−, have been identified in the total uranyl concentration range from (1.1·10−3 to 5.7·10−3) mol·kg−1, and their overall stability constants determined, keeping the metal to ligand …
A new N6 hexadentate ligand and a novel heptacoordinated N6O-type Fe(III) compounds: Synthesis, characterization and structure of [Fe(dimpyen)(OH)](A…
2011
Abstract In this contribution, we report the syntheses of a novel N6 donor set ligand, dimpyen = N1,N2-di[(1-methyl-1H-2-imidazolyl) methyl]-N1,N2-di(2-pyridilmethyl)-1,2-ethanediamine. This type of ligand was designed to modulate the properties of the metal ions bound to it. The reaction with Fe(II) gives off a new heptacoordinated iron(III) complex. We study the spectroscopic (UV–Vis), magnetic and electrochemical behavior and also made the structural determination with X-ray diffraction at 134 K and a heptacoordinated N6O-type derivative of Fe(III) is reported as well. This complex crystallize as perchlorate or hexafluorophosphate and the formula of these derivatives are [Fe(dimpyen)(OH)…
A non-heme dinuclear iron(II) complex containing a single, unsupported hydroxo bridge.
2006
Complexation of the tetrapodal pentadentate NN4 ligand 2,6-C5H3N[CMe(CH2NH2)2]2 (I) with iron(II) perchlorate hydrate in methanol, in the presence of N-methylimidazole, produces a diferrous complex with a single, unsupported mu-OH ligand between two {(I)FeII} coordination modules.
Ligand mediated structural diversity of copper(II)-azido moiety: Synthesis, structure and magnetic study
2022
Abstract Two copper azido complexes [Cu4(L1)4(µ1,1-N3)3(N3)] (1) and [{Cu2(L2)(N-benzylen)(µ1,1-N3)3(µ1,1,3-N3(N3)]n (2) have been synthesized by the reaction of aqueous solution of sodium azide to a methanolic solution of copper perchlorate hexahydrate and corresponding Schiff-base ligands. Schiff bases HL1 and HL2 act as blocking coligands are derived from the 1:1 condensation of N-benzyl ethylenediamine with Salicyldehyde and 2-hydroxy-5-chloroacetophenone respectively (N-benzylen is the N-benzyl ethylenediamine). These two complexes are characterized by the elemental analysis, FT-IR, single crystal X-ray diffraction, powder XRD and also TGA. Single crystal X-ray structural study reveals…
Automated determination of clomipramine and its major metabolites in human and rat serum by high-performance liquid chromatography with on-line colum…
1998
A fully automated method including column-switching and isocratic high-performance liquid chromatography (HPLC) was developed for simultaneous determination of the tricyclic antidepressant clomipramine and its metabolites demethylclomipramine, 2-, 8-, and 10-hydroxyclomipramine, 2-, and 8-hydroxydemethylclomipramine and didemethylclomipramine in serum. After serum injection into the HPLC system and on-line sample clean-up on a clean-up column (Hypersil CN; 10 x 4.6 mm) by an eluent consisting of 35% acetonitrile and 65% deionized water, the chromatographic separation was performed on an analytical column (LiChrospher CN; 250 x 4.6 mm I.D.) by an eluent consisting of 38% acetonitrile and 62%…
Macroscopic and local electrochemical studies of austempered ductile iron in perchlorate solutions.
2006
The corrosion behavior of austempered ductile iron (ADI) in alkaline environment has been investigated at the microscale by means of the electrochemical microcell technique, surface analysis methods, and at the macroscale using classical electrochemical techniques. Local electrochemical investigations have revealed that the matrix (ausferrite), far from spheres, undergoes passivation in 1 M NaClO 4 , pH 10 solution within a wide potential range, from the corrosion potential (of about -280 mV/SCE) until 800 mV/SCE. Surface observations combined with local electrochemical analysis have shown that corrosion of ADI first occurs in the close vicinity of some graphite spheres and then around oxid…
[Di-aqua-sesqui(nitrato-κO)hemi(perchlorato-κO)copper(II)]-μ-{bis-[5-methyl-3-(pyridin-2-yl)-1H-pyrazol-4-yl] selenide}-[tri-aqua-(perchlorato-κO)cop…
2013
In the binuclear title complex, [Cu2(ClO4)1.5(NO3)1.5(C18H16N6Se)(H2O)5]NO3·H2O, both Cu(II) ions are hexa-coordinated by O and N atoms, thus forming axially elongated CuO4N2 octa-hedra. The equatorial plane of each octa-hedron is formed by one chelating pyrazole-pyridine fragment of the organic ligand and two water mol-ecules. The axial positions in one octa-hedron are occupied by a water mol-ecule and a monodentately coordinated perchlorate anion, while those in the other are occupied by a nitrate anion and a disordered perchlorate/nitrate anion with equal site occupancy. The pyrazole-pyridine units of the organic selenide are trans-oriented to each other with a C-Se-C angle of 96.01 (14)…
(μ-Acetato-κ2 O:O′)[μ-2,6-bis({bis[(pyridin-2-yl-κN)methyl]amino-κN}methyl)-4-methylphenolato-κ2 O:O](methanol-κO)dizinc bis(perchlorate)
2014
The binuclear title complex, [Zn2(C33H33N6O)(CH3COO2)(CH3OH)](ClO4)2, was synthesized by the reaction between 2,6-bis({[bis(pyridin-2-yl)methyl]amino}methyl)-4-methylphenol (H-BPMP), Zn(OAc)2and NaClO4. The two ZnIIions are bridged by the phenolate O atom of the octadentate ligand and the acetate group. An additional methanol ligand is terminally coordinated to one of the ZnIIions, rendering the whole structure unsymmetric. Other symmetric dizinc complexes of BPMP have been reported. However, to the best of our knowledge, the present structure, in which the two ZnIIions are distinguishable by the number of coordinating ligands and the coordination geometries (octahedral and square-pyramidal…
Dehydrogenation versus Oxygenation in Two-Electron and Four-Electron Reduction of Dioxygen by 9-Alkyl-10-methyl-9,10-dihydroacridines Catalyzed by Mo…
2004
Dehydrogenation of 10-methyl-9,10-dihydroacridine (AcrH(2)) by dioxygen (O(2)) proceeds efficiently, accompanied by the two-electron and four-electron reduction of O(2) to produce H(2)O(2) and H(2)O, which are effectively catalyzed by monomeric cobalt porphyrins and cofacial dicobalt porphyrins in the presence of perchloric acid (HClO(4)) in acetonitrile (MeCN) and benzonitrile (PhCN), respectively. The cobalt porphyrin catalyzed two-electron reduction of O(2) also occurs efficiently by 9-alkyl-10-methyl-9,10-dihydroacridines (AcrHR; R = Me, Et, and CH(2)COOEt) to yield 9-alkyl-10-methylacridinium ion (AcrR+) and H(2)O(2). In the case of R = Bu(t) and CMe(2)COOMe, however, the catalytic two…
Ferromagnetic Cu(II)4, Co(II)4, and Ni(II)6 azido complexes derived from metal-assisted methanolysis of di-2,6-(2-pyridylcarbonyl)pyridine.
2009
Reaction of copper(II) perchlorate with di-2,6-(2-pyridylcarbonyl)pyridine (pyCOpyCOpy, dpcp) in the presence of sodium azide yields complex [Cu(4)(N(3))(2){pyC(OMe)(O)pyC(OMe)(O)py}(2)(MeOH)(2)](ClO(4)) x 2 MeOH (1 x 2 MeOH), which crystallizes in the monoclinic P2(1)/c space group. Similar reaction of cobalt(II) nitrate yields complex [Co(4)(N(3))(2)(NO(3))(2){pyC(OMe)(O)pyC(OMe)(O)py}(2)] x 0.5 MeOH (2 x 0.5 MeOH) which crystallizes in the monoclinic I2/m space group. Reaction of nickel(II) perchlorate yields complex [Ni(6)(CO(3))(N(3))(6){pyCOpyC(O)(OMe)py}(3)(MeOH)(2)(H(2)O)][Ni(6)(CO(3))(N(3))(6){pyCOpyC(O)(OMe)py}(3) (MeOH)(3)](ClO(4))(2) x 1.8 MeOH (3 x 1.8 MeOH), which crystallizes…