66 research outputs found
trans-N,N,N′,N′-Tetrakis(carboxymethyl)cyclohexane-1,2-diammonium tetrachloridocadmium(II) tetrahydrate
In the title compound, (C14H24N2O8)[CdCl4]·4H2O, the Cd atom in the tetrahedral [CdCl4]2− anion lies on a twofold rotation axis, and the diprotonated organic molecule, trans-N,N,N′,N′-tetrakis(carboxymethyl)cyclohexane-1,2-diammonium, has 2 symmetry with the twofold rotation axis running through the mid-point of two C—C bonds in the cyclohexane unit. In the crystal structure, classical intramolecular O—H⋯O and N—H⋯O and intermolecular O—H⋯O, N—H⋯O, O—H⋯Cl and C—H⋯Cl hydrogen bonds are observed
Tuning the Reversible Binding of NO to Iron(II) Aminocarboxylate and Related Complexes in Aqueous Solution
Fenton reagent reduces the level of arsenic in paddy rice grain
Hydroponic and pot experiments were conducted to examine the effects of Fenton reagent on paddy rice plant growing in arsenic-contaminated soils. Fenton reagent significantly reduced arsenic phytotoxicity, uptake by the plants and accumulation in rice grain. This is attributed to oxidation of As3+ to As5+ by hydroxyl radicals and immobilization of arsenate by reacting with precipitating Fe3+ to form practically insoluble compounds. Although this process enhanced the formation of Fe-enriched coatings on root surface, it appears that root plaque had limited effects on inhibiting As uptake since most of the young roots were not covered by iron plaque. It is more likely that As immobilization in the bulk soils play a major role in reducing As flux towards rhizosphere. The findings have implications for understanding As behavior in paddy field receiving rainwater-borne hydrogen peroxide and developing cost-effective techniques for reducing As level in rice grain produced from As-contaminated soil
Unexpected Differences in the Dynamics and in the Nuclear and Electronic Relaxation Properties of the Isoelectronic [EuII(DTPA)(H2O)]3- and [GdIII(DTPA)(H2O)]2- Complexes (DTPA = Diethylenetriaminepentaacetate)
Unexpected Differences in the Dynamics and in the Nuclear and Electronic Relaxation Properties of the Isoelectronic [Eu II (DTPA)(H 2 O)] 3 - and [Gd III (DTPA)(H 2 O)] 2 - Complexes (DTPA = Diethylenetriamine Pentaacetate) 1
International audienc
Unexpected Differences in the Dynamics and in the Nuclear and Electronic Relaxation Properties of the Isoelectronic [Eu II
Solution and solid-state characterization of Eu(II) chelates: a possible route towards redox responsive MRI contrast agents.
We report the first solid state X-ray crystal structure for a Eu(II) chelate, [C(NH2)3]3[Eu(II)(DTPA)(H2O)].8H2O, in comparison with those for the corresponding Sr analogue, [C(NH2)3]3[Sr(DTPA)(H2O).8H2O and for [Sr(ODDA)].8H2O (DTPA5 = diethylenetriamine-N,N,N',N",N"-pentaacetate, ODDA2- =1,4,10,13-tetraoxa-7,16-diazacyclooctadecane-7,16-diacetate ). The two DTPA complexes are isostructural due to the similar ionic size and charge of Sr(2+) and Eu(2+). The redox stability of [Eu(II)(ODDA)(H2O)] and [Eu(II)(ODDM)]2- complexes has been investigated by cyclovoltammetry and UV/Vis spectrophotometry (ODDM4- =1,4,10,13-tetraoxa-7,16-diaza-cyclooctadecane-7,16-++ +dimalonate). The macrocyclic complexes are much more stable against oxidation than [Eu(II)(DTPA)(H2O)]3- (the redox potentials are E1/2 =-0.82 V, -0.92 V, and -1.35 V versus Ag/AgCl electrode for [Eu(III/II)(ODDA)(H2O)],[Eu(III/II)(ODDM)], and [Eu(III/II)(DTPA)(H2O)], respectively, compared with -0.63 V for Eu(III/II) aqua). The thermodynamic stability constants of [Eu(II)(ODDA)(H2O)], [Eu(II)(ODDM)]2-, [Sr(ODDA)(H2O)], and [Sr(ODDM)]2- were also determined by pH potentiometry. They are slightly higher for the EuII complexes than those for the corresponding Sr analogues (logK(ML)=9.85, 13.07, 8.66, and 11.34 for [Eu(II)(ODDA)(H2O)], [Eu(II)(ODDM)]2-, [Sr(ODDA)(H2O)], and [Sr(ODDM)]2-, respectively, 0.1M (CH3)4NCl). The increased thermodynamic and redox stability of the Eu(II) complex formed with ODDA as compared with the traditional ligand DTPA can be of importance when biomedical application is concerned. A variable-temperature 17O-NMR and 1H-nuclear magnetic relaxation dispersion (NMRD) study has been performed on [Eu(II)(ODDA)(H2O)] and [Eu(II)(ODDM)]2- in aqueous solution. [Eu(II)(ODDM)]2- has no inner-sphere water molecule which allowed us to use it as an outer-sphere model for [Eu(II)(ODDA)(H2O)]. The water exchange rate (k298(ex)= 0.43 x 10(9)s(-1)) is one third of that obtained for [Eu(II)(DTPA)(H2O)]3-. The variable pressure 17O-NMR study yielded a negative activation volume, deltaV (not=) = -3.9cm3mol(-1); this indicates associatively activated water exchange. This water exchange rate is in the optimal range to attain maximum proton relaxivities, which are, however, strongly limited by the fast rotation of the small molecular weight complex
Solution and Solid-State Characterization of EuII Chelates: A Possible Route Towards Redox Responsive MRI Contrast Agents
International audienceWe report the first solid state X-ray crystal structure for a Eu(II) chelate, [C(NH2)3]3[Eu(II)(DTPA)(H2O)].8H2O, in comparison with those for the corresponding Sr analogue, [C(NH2)3]3[Sr(DTPA)(H2O).8H2O and for [Sr(ODDA)].8H2O (DTPA5 = diethylenetriamine-N,N,N',N",N"-pentaacetate, ODDA2- =1,4,10,13-tetraoxa-7,16-diazacyclooctadecane-7,16-diacetate ). The two DTPA complexes are isostructural due to the similar ionic size and charge of Sr(2+) and Eu(2+). The redox stability of [Eu(II)(ODDA)(H2O)] and [Eu(II)(ODDM)]2- complexes has been investigated by cyclovoltammetry and UV/Vis spectrophotometry (ODDM4- =1,4,10,13-tetraoxa-7,16-diaza-cyclooctadecane-7,16-++ +dimalonate). The macrocyclic complexes are much more stable against oxidation than [Eu(II)(DTPA)(H2O)]3- (the redox potentials are E1/2 =-0.82 V, -0.92 V, and -1.35 V versus Ag/AgCl electrode for [Eu(III/II)(ODDA)(H2O)],[Eu(III/II)(ODDM)], and [Eu(III/II)(DTPA)(H2O)], respectively, compared with -0.63 V for Eu(III/II) aqua). The thermodynamic stability constants of [Eu(II)(ODDA)(H2O)], [Eu(II)(ODDM)]2-, [Sr(ODDA)(H2O)], and [Sr(ODDM)]2- were also determined by pH potentiometry. They are slightly higher for the EuII complexes than those for the corresponding Sr analogues (logK(ML)=9.85, 13.07, 8.66, and 11.34 for [Eu(II)(ODDA)(H2O)], [Eu(II)(ODDM)]2-, [Sr(ODDA)(H2O)], and [Sr(ODDM)]2-, respectively, 0.1M (CH3)4NCl). The increased thermodynamic and redox stability of the Eu(II) complex formed with ODDA as compared with the traditional ligand DTPA can be of importance when biomedical application is concerned. A variable-temperature 17O-NMR and 1H-nuclear magnetic relaxation dispersion (NMRD) study has been performed on [Eu(II)(ODDA)(H2O)] and [Eu(II)(ODDM)]2- in aqueous solution. [Eu(II)(ODDM)]2- has no inner-sphere water molecule which allowed us to use it as an outer-sphere model for [Eu(II)(ODDA)(H2O)]. The water exchange rate (k298(ex)= 0.43 x 10(9)s(-1)) is one third of that obtained for [Eu(II)(DTPA)(H2O)]3-. The variable pressure 17O-NMR study yielded a negative activation volume, deltaV (not=) = -3.9cm3mol(-1); this indicates associatively activated water exchange. This water exchange rate is in the optimal range to attain maximum proton relaxivities, which are, however, strongly limited by the fast rotation of the small molecular weight complex
Melt Extruded Open-Cell Microcellular Foams for Membrane Separation: Processing and Cell Morphology Relationship
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