Search results for "PERCHLORATE"
showing 10 items of 643 documents
Synthesis, characterization, cellular uptake and interaction with native DNA of a bis(pyridyl)-1,2,4-oxadiazole copper(II) complex
2010
The copper(II) complex of 3,5-bis(2'-pyridyl)-1,2,4-oxadiazole was synthesized and characterized. X-Ray crystallography revealed that the complex consists of a discrete [Cu(3,5-bis(2'-pyridyl)-1,2,4-oxadiazole)(2)(H(2)O)(2)](2+) cation and two ClO(4)(-) anions. The Cu(II) coordination sphere has a distorted octahedral geometry and each ligand chelates the copper ion through the N(4) nitrogen of the oxadiazole ring and the nitrogen of one pyridine moiety. The coordinated water molecules are in cis position and each of them is H-bonded to the 5-pyridyl nitrogen of the oxadiazole ligand and to an oxygen of the perchlorate anion. Biological assays showed that, despite the free ligand not being …
Mössbauer effect study of the electronic ground state of iron(II)in tris(2-chlorophenanthroline)iron(II) perchlorate
1976
Abstract Mossbauer spectra of [Fe(2-Cl-phen) 3 ](ClO 4 ) 2 ·H 2 O have been measured in the temperature range 293 − 5 K. The spectra indicate that the iron atom in this compound possesses a spin quintet ground state throughout the temperature range under study, in contradiction to the suggested high spin-low spin transition, which has been concluded from a magnetic susceptibility study by other authors. From a theoretical analysis of the temperature dependence of the quadrupole splitting, with trigonal distortion, spin-orbit coupling, and effects of covalency taken into account, the ground term of iron(II) in this compound has been elucidated as being 5 A 1 ( 5 T 2g ), separated from the 5 …
Nucleophilic attack by 2-pyridylpalladium(II) and platinum(II) complexes on the organic chlorides ClCH2R (R COMe, CN, Ph, Cl)
1992
Abstract The 2-pyridyl complexes trans-[MCl(C5H4NC2)(PPh3)2] (M = Pd, 1a; M = Pt, 1b), [MCl(C5H4NC2)(dppe)] (M = Pd, 2a; M = Pt, 2b) and [M(dmtc)(C5H4NC2) (PPh3)] (M = Pd, 3a; M = Pt,3b) react with the chlorides ClCH2R(R COMe, CN, Ph) to give cationic products containing the 2-pyridylium ligands (1-CH2R)C5H4NC2. The rate of nucleophilic displacement of the chloride ion from ClCH2R depends on the central metal (Pt > Pd), on the coordination geometry (1 ~ 3) and on the substituent R (COMe > CN > Ph for the reactions with 3b). Like 1b and 2b, complex 3b also reacts with dichloromethane to give [Pt(dmtc){(1-CH2Cl)C5H4NC2}(PPh3)]+. The reaction of the binuclear compound [{PdCl(μ-C5H4NC2,…
Effect of Lithium Perchlorate on the Kinetics of the Anionic Polymerization of Methyl Methacrylate in Tetrahydrofuran
1999
The kinetics of the anionic polymerization of methyl methacrylate in the presence of lithium perchlorate (LiClO 4 ) are investigated in THF using 1,1-diphenylhexyllithium as initiator in a flow-tube reactor between -30 and 0 °C. The rate constants of propagation determined in the presence of LiClO 4 are lower than those obtained in the absence of the salt, similar to the effect observed for LiCl. For propagation, the reaction order with respect to active center concentration is found to be 0.5 in both cases, which indicates that LiClO 4 does not effectively perturb the aggregation of the enolate ion pair. The formation of various mixed aggregates is proposed. The polydispersity index of the…
Complex formation of Tb3+ with glycolate, D-gluconate and α-isosaccharinate in neutral aqueous perchlorate solutions
2003
Summary An electromigration technique was used for measurements of metal-ligand formation constants of non-carrier-free 160Tb3+ with glycolate, D-gluconate and α-isosaccharinate ligands. The overall ion mobilities of Tb at different concentrations of the ligands were measured in chemically inert perchlorate solutions (pH 7 and T= 298.1K) with an overall ionic strength μ = 0.1. The stepwise stoichiometric stability constants are: Tb3+/glycolate: log K 1=2.72(18), log K 2=1.73(19), log K 3= 1.12(17), Tb3+/D-gluconate: log K 1=2.96(11), log K 2=2.60(11), log K 3=1.13(9), Tb3+/α-ISA: log K 1=3.07(8), log K 2 = 2.69(11), log K 3 = 1.80(12).
Structure and properties of 2-cyanopyridinium perchlorate [2-CNPyH][ClO4]
2006
The crystal structure of 2-cyanopyridinium perchlorate, [2-CNPyH][ClO4], has been determined at 100 (phase II) and 293 K (phase I). It is monoclinic P 21 at 100 K and orthorhombic P 212121 at 293 K. The dynamic properties of the crystal were studied by differential scanning calorimetry, dilatometry, pyroelectric, dielectric, proton (1H NMR), chlorine (35Cl NMR) magnetic resonance spectroscopies and the infrared method. The crystal undergoes a structural phase transition () at 170 K characterized by a complex mechanism involving both 'order–disorder' and 'displacive' contributions. It reveals pyroelectric properties below 170 K. The dielectric relaxation existing over phase I is due to the m…
Static and MAS 35CI NMR and Molecular Motions of ClO −4 Ions in the Various Phases of Multimethylammonium Perchlorates
1986
Static and MAS*) 35CI NMR data of CIO−4 ions in the low-, intermediate- and high-temperature phases of trimethylammonium, dimethylammonium and monomethylammonium perchlorates are reported. The observed solid-solid phase transitions are interrelated with the motional state of the perchlorate ions. In the low-temperature phase III of trimethylammonium perchlorate there is an anisotropic motion of the ClO−4 ions with a constant quadrupole frequency of 185 kHz and an increasing value of the asymmetry parameter when approaching phase transition III-II. The activation energy for this motion is found to be 44.3 kj/mol. At the transition III-II the ClO−4 ions gain orientational degrees of freedom m…
Calix[4]arenes as Selective Extracting Agents. An NMR Dynamic and Conformational Investigation of the Lanthanide(III) and Thorium(IV) Complexes
2000
The lanthanide and Th4+ complexes with calix[4]arene ligands substituted either on the narrow or at the wide rim by four coordinating groups behave totally differently as shown by an NMR investigation of the dia- and paramagnetic complexes. Solutions of complexes were prepared by reacting anhydrous metal perchlorate salts with the ligands in dry acetonitrile (CAUTION). Relaxation time T1 titrations of acetonitrile solutions of Gd3+ by calixarenes indicate that ligands subsituted on the narrow rim form stable 1:1 complexes whether they feature four amide groups (1) or four phosphine oxide functions. In contrast, a ligand substituted by four (carbamoylmethyl)-diphenylphosphine oxide moieties …
Electrochemical and Spectroelectrochemical Studies of Diphosphorylated Metalloporphyrins. Generation of a Phlorin Anion Product
2015
Two series of diphosphoryl-substituted porphyrins were synthesized and characterized by electrochemistry and spectroelectrochemistry in nonaqueous media containing 0.1 M tetra-n-butylammonium perchlorate (TBAP). The investigated compounds are 5,15-bis(diethoxyphosphoryl)-10,20-diphenylporphyrins (Ph)2(P(O)(OEt)2)2PorM and 5,15-bis(diethoxyphosphoryl)-10,20-di(para-carbomethoxyphenyl)porphyrins (PhCOOMe)2(P(O)(OEt)2)2PorM where M = 2H, Co(II), Ni(II), Cu(II), Zn(II), Cd(II), or Pd(II). The free-base and five metalated porphyrins with nonredox active centers undergo two ring-centered oxidations and two ring-centered reductions, the latter of which is followed by a chemical reaction of the por…
Electrochemical Growth and Physico-Chemical Characterization in Organic Medium of Nb2O5 Thin Films
2008
Investigations about the energetics and the electrical properties of niobium thin film, electrochemically grown, were performed in an organic solution of acetonitrile and lithium perchlorate. The study of the energetics of the Nb2O5/organic solution interface was performed by means of a non-destructive optical technique, photocurrent spectroscopy. By means of this technique, it was possible estimating the value of the flat band potential and locating conduction and valence band. A more cathodic value of flat band potential in respect with acidic solution was found in organic medium. From impedance spectra, the electrical circuit that gives best fitting values is constituted by two resistanc…