Search results for "Qualitative inorganic analysis"
showing 10 items of 16 documents
Selective chromo-fluorogenic detection of trivalent cations in aqueous environments using a dehydration reaction
2016
[EN] Trivalent cations (Al3+, Fe3+, Cr3+, As3+, In3+ and Ga3+) induced a dehydration reaction of a chemodosimeter in water that is coupled with colour and emission changes.
Interactions of Dioxouranium(VI) with Amines in Aqueous Solution
2010
The interaction of the dioxouranium(VI) ion with five low molecular weight polyamines (ethylenediamine, putrescine, cadaverine, spermidine, and spermine) and with poly(allyl)amine (15 kDa) was studied potentiometrically (ISE-H + glass electrode) at T ) 298.15 K. Investigations were carried out in NaNO3 ionic medium, at I ) 0.1 mol · L -1 (and 0.5 mol · L -1 for poly(allyl)amine only), in the pH range 3.5 to 5.5, before the formation of uranyl insoluble species. The results gave evidence for the formation of two species, namely, UO2L 2+ and UO2L(OH) + for the diamine systems (ethylenediamine, putrescine, cadaverine), UO2L 2+ and UO2LH 3+ for spermidine, and UO2LH 3+ and UO2LH2 4+ for spermin…
The interaction of native DNA with Zn(II) and Cu(II) complexes of 5-triethyl ammonium methyl salicylidene orto-phenylendiimine
2007
The interaction of native calf thymus DNA with the Zn(II) and Cu(II) complexes of 5-triethyl ammonium methyl salicylidene orto-phenylendiimine (ZnL(2+) and CuL(2+)), in 1 mM Tris-HCl aqueous solutions at neutral pH, has been monitored as a function of the metal complex-DNA molar ratio by UV absorption spectrophotometry, circular dichroism (CD) and fluorescence spectroscopy. The results support for an intercalative interaction of both ZnL(2+) and CuL(2+) with DNA, showing CuL(2+) an affinity of approximately 10 times higher than ZnL(2+). In particular, the values of the binding constant, determined by UV spectrophotometric titration, equal to 7.3x10(4) and 1.3x10(6)M(-1), for ZnL(2+) and CuL…
Preliminary studies on the synthesis of alkaline-free large crystals of ZSM-5
1988
Single crystals of ZSM-5 were synthesized in three systems containing Na + -TPA, Li + -TPA, and NH 4 + -TPA, respectively. Applying a reaction mixture of the molar composition 8 TPA + 123(NH 4 ) 2 O + Al 2 O 3 + 59 SiO 2 + 2280 H 2 O, alkaline-free, homogeneous, and pure single crystals of ZSM-5 were prepared up to a length of 350 μm. The crystal size and yield were found to be dependent on the water content of the starting reaction mixture and on the type of aluminium source; for example, boehmite and aluminiumtriisopropylate.
Interaction of metal ions with N-glycosylamines: isolation and characterization of the products of 4,6-O-benzylidene-N-(o-carboxyphenyl)-β-D-glucopyr…
2001
Metal-ion complexes of Li+, Na+, K+, Mg2+, Ca2+, Ba2+, Pb2+, Cd2+, Hg2+ with 4,6–O–benzylidene–N–(o–carboxyphenyl)–β–D–glucopyranosylamine were synthesized and isolated as solid products and characterized by analytical means as well as by spectral techniques, such as, 1H and 13C NMR, FTIR, absorption, FAB mass spectrometry, optical rotation and CD. While the alkali metal ions formed ML type of complexes, the other metal ions formed ML2 type complexes. Molecular weights of the complexes of Li+, Na+ and K+ were established based on the molecular-ion peaks in the FAB mass spectra. The saccharide portion remians in the β-anomeric form even after the complexation. The spectral data, as well as t…
Lawrencium chemistry: no evidence for oxidation states lower than 3+ in aqueous solution
1988
Lawrencium (3-min 260Lr) together with other actinides, was produced in the bombardment of a 249Bk target with 18O ions. There was no sign of a reduction of Lr3+ in dilute hydrochloric acid by V2+ or Cr2+, although in the same experiments, Md3+ was reduced to Md2+ (E°=−0.2 V). The resulting limit for the reduction potential of the Lr3+/Lr1(2)+ couple is E° < −0.44 V.
Co2+ Translocation in a Terpyridine−Cyclam Ditopic Receptor
2001
The coordination behaviour of the ditopic receptor of 1-[p-(2,2′:6′,2′′-terpyrid-4′-yl)tolyl]-1,4,8,11-tetraazacyclotetradecane (L1) towards Co2+ in acetonitrile/water (70:30, v/v) has been investigated. At acidic pH values, the L1−H+−Co2+ system shows an oxidation wave at 150 mV vs. SCE, characteristic of Co2+ in a bis(terpyridine) environment. Upon addition of OH−, a reduction in the intensity of the wave at 150 mV is observed and a new oxidation wave appears at 1.30 V. This new wave is close to that found for [Co(cyclam)]2+ under similar working conditions. The electrochemical data thus suggest that there is a pH-controlled translocation of the Co2+ ion from the bis(terpyridine) to the c…
Synthesis and coordination properties of an azamacrocyclic Zn(II) chemosensor containing pendent methylnaphthyl groups
2008
The synthesis of a polyazamacrocycle constituted by two diethylenetriamine bridges functionalized at their central nitrogen with naphth-2-ylmethyl units and interconnected through 2,6-dimethylpyridine spacers (L1) is reported. The protonation behaviour of the new macrocycle in water and in water-ethanol 70/30 v/v mixed solvent has been examined by means of pH-metric, UV-Vis and steady-state fluorescence techniques. The fluorescence emission is slightly quenched following the deprotonation of the central tertiary amines and more deeply quenched upon deprotonation of the secondary amino groups. pH-Metric titrations show that in water-ethanol 70/30 v/v L1 forms stable mononuclear complexes wit…
Aza–oxa macrocyclic ligands functionalised with naphthylmethyl fluorescent groups
2000
Abstract Compounds L 1 and L 2 were obtained by reaction of 2-(bromomethyl)naphthalene with 1,4,10-trioxa-7,13-diazacyclopentadecane and 1,4,7-trioxa-10-azacyclododecane, respectively. These receptors contain aza–oxa crowns attached covalently to fluorescent groups. The protonation and coordination behaviour of L 1 and L 2 against metal ions has been studied in dioxane:water (70:30 v/v, 25°C, 0.1 M potassium nitrate) using potentiometric methods. All metal ions studied form complexes with L 1 and L 2 with the logarithm of the formation constants L+M 2+ =[M(L)] 2+ in the sequence Cd 2+ ≅Pb 2+ , Zn 2+ 2+ for L 1 and Zn 2+ 2+ 2+ 2+ 2+ for L 2 . The fluorescent behaviour of L 1 and L 2 was stud…
Solubility of some calcium-carboxylic ligand complexes in aqueous solution
1994
Insoluble species were identified in the systems Ca(2+)-hemimellitate, Ca(2+)-1,2,3,4-butanetetracarboxylate and Ca(2+)-citrate, and their solubilities were determined in aqueous solution at T = 25 degrees C. Values of pK(s0) were obtained for the species CaLH (L = benzene-1,2,3-tricarboxylate or hemimellitate), Ca(2)L (L = 1,2,3,4-butanetetracarboxylate), CaLH and Ca(3)L(2) (L = citrate), together with their dependence on ionic strength. Solid compounds were also characterized by thermogravimetry. The complex formation in solution for the system Na(+) - and Ca(2+)-hemimellitate was studied too.