Search results for "Ammonium"

Anion-Exchange Properties of Trifluoroacetate and Triflate Salts of N-Alkylammonium Resorcinarenes

2016

The synthesis of N-benzyl- and N-cyclohexylammonium resorcinarene trifluoroacetate (TFA) and triflate (OTf) salt receptors was investigated. Solid-state analysis by single-crystal X-ray diffraction revealed that the N-alkylammonium resorcinarene salts (NARSs) with different upper substituents had different cavity sizes and different affinities for anions. Anion-exchange experiments by mixing equimolar amounts of N-benzylammonium resorcinarene trifluoroacetate and N-cyclohexylammonium resorcinarene triflate, as well as N-benzylammonium resorcinarene triflate and N-cyclohexylammonium resorcinarene trifluoroacetate showed that the NARS with flexible benzyl groups preferred the larger OTf anion…

Synthesis and structure of tetrakis(tetramethylammonium) octacosachlorooctaantimonate(III) [(CH3)4N]4Sb8Cl28

2000

Abstract The reaction between antimony trichloride and tetramethylammonium chloride in nitromethane gives transparent, irregular crystals of tetrakis(tetramethylammonium) octacosachlorooctaantimonate(III) [(CH 3 ) 4 N] 4 Sb 8 Cl 28 . Crystals are triclinic, space group P-1, a =11.846(2), b =12.217(2), c=14.120(3) A , α =95.71(3), β =101.39(3), γ =118.59(3)°, V=1713.7(5) A 3 , Z =1, d c =2.193, d m =2.17(2) Mg m −3 . The structure contains a structurally novel Sb 8 Cl 28 4- anion. It is composed of eight deformed octahedra, connected with each other by faces. In cavities formed by inorganic sublattice are located two crystallographically nonequivalent tetramethylammonium cations. One of them…

General biological properties of antioxidant permeatoxins and their influence on natural and model membranes

1994

Protonation thermodynamics of 2,2'-bipyridyl in aqueous solution. Salt effects and weak complex formation

1993

Abstract Protonation constants of 2,2'-bipyridyl (bipy) have been determined potentiometrically, using (H + )-glass electrode, in different aqueous media (alkali and alkaline earth chlorides, tetramethylammonium chloride and tetramethylammonium iodide) at different temperatures and ionic strengths. The differences in log K H values are explained using a complex formation model. Formation thermodynamic parameters are given.

Preparation, characterization and catalytic properties of vanadium oxides supported on calcined Mg/Al-hydrotalcite

1995

Abstract Vanadium oxide supported on calcined hydrotalcite has been investigated for the oxidehydrogenation of n-butane in the 500–550°C temperature interval. Hydrotalcite (Mg/Al atomic ratio of 2.77), consisting of a single phase only, has been employed as a support precursor. The vanadium catalysts (0–50, referred as wt.-% V 2 O 5 ) were prepared by impregnation of calcined hydrotalcite (450°C) with ammonium metavanadate (in an aqueous solution) or vanadyl acetylacetonate (in a methanolic solution), and then calcined at 600°C for 4 h. During the impregnation step, the support is transformed into hydrotalcite if aqueous solutions are used. However, it is not modified if methanolic solution…

Thermodynamics of transfer of some nitroalkanes from aqueous to dodecyltrimethylammonium bromide micellar phases

1988

Abstract The enthalpies of mixing of some aqueous n-nitroalkane solutions with dodecyltrimethylammonium bromide micellar solutions were determined. The experimental data were treated by using a previously reported approach giving the enthalpies of transfer of solute from the aqueous to the micellar phases and the distribution constant of solute between the two phases at the same time. From these, the standard thermodynamic quantities of transfer (ΔtrfG°, ΔtrfH° and ΔtrfS°) are derived. In order to study the effect of the nature of both the solvent and the head group of solute, these properties are compared with those from water to octane and with those of alcohols and nitriles from aqueous …

Novel water-swellable beads based on an acryloylated polyaspartamide

2001

Spherical polymeric microparticles have been prepared by a reverse-phase suspension polymerization technique. The starting polymer was α,β-poly (N-2-hydroxyethyl)-dl-aspartamide (PHEA) partially functionalised with glycidylmethacrylate (GMA) in order to introduce reactive vinyl groups in the side chain. The PHEA–GMA copolymer obtained (PHG) was cross-linked in a mixture of water/hexane–carbon tetrachloride in the presence of sorbitan trioleate (Span 85) as surfactant and ammonium persulfate/N,N,N′,N′-tetramethylethylenediamine as initiator system. The reaction was also carried out in the presence of N,N′-dimethylacrylamide as comonomer or N,N′-ethylenebisacrylamide as a cross-linking agent.…

Catalytic reduction of nitrates and nitrites in water solution on pumice-supported Pd–Cu catalysts

2000

Abstract Two series of pumice-supported palladium and palladium–copper catalysts, prepared by impregnation with different palladium and copper precursors, were tested for the hydrogenation of aqueous nitrate and nitrite solutions. Measurements were performed in a stirred tank reactor, operating in batch conditions, in buffered water solution at atmospheric pressure and at 293 K. The activities of the catalysts were calculated in terms of nitrate and/or nitrite removal. With the monometallic Pd/pumice, the reduction of nitrite is highly selective; only 0.2% of the initial nitrite content is converted to ammonium ions. The activity in terms of turn over frequency (TOF) is higher as compared t…

Protonation of Carbonate in Aqueous Tetraalkylammonium Salts at 25°C.

2006

Protonation constants of carbonate were determined in tetramethylammonium chloride (Me4NClaq 0.1≤I/mol kg−1 ≤4) and tetraethylammonium iodide (Et4NIaq 0.1≤I/mol kg−1 ≤1) by potentiometric ([H+]-glass electrode) measurements. Dependence of protonation constants on ionic strength was taken into account by modified specific ion interaction theory (SIT) and by Pitzer models. Literature data on the protonation of carbonate in NaClaq (0.1≤I/mol kg−1 ≤6) were also critically analysed. Both protonation constants of carbonate follow the trend Et4NI>Me4NCl > NaCl. An ion pair formation model designed to take into account the different protonation behaviours of carbonate in different supporting electr…

Influence of chloride anions on the electrodeposition and electroactivity of the polymer matrix in polypyrrole, poly( N -methylpyrrole) and polypyrro…

2004

We report electrochemical studies on the influence of a small concentration of chloride ions on the electroactivity of the polymer matrix of polypyrrole (PPy), poly(N-methylpyrrole) [p(N-MePy)] and a poly(titanocene-propyl-pyrrole) derivative, p(Tc3Py) [Tc(CH2)3NC4H4; Tc=CpCp′TiCl2; Cp=C5H5; Cp′=C5H4] in acetonitrile (AN), tetrahydrofuran (THF) and N,N-dimethylformamide (DMF). The polymer films were obtained on Pt disc electrodes from AN solutions of the monomers containing 0.1 M tetrabutylammonium hexafluorophosphate (TBAPF6) as the supporting electrolyte and then transferred to the corresponding monomer-free solution. Studies in Cl−-containing solutions have shown that the p(Tc3Py) matrix…