Fractionation and redox speciation of antimony in agricultural soils by hydride generation--atomic fluorescence spectrometry and stability of Sb(III) and Sb(V) during extraction with different extractant solutions

This stability of Sb(III) and Sb(V) species was studied during single extraction from soils by water. EDTA, diluted H2SO4 and H3PO4, and oxalic acid/oxalate solutions, with and without ascorbic acid, were used as stabilizing reagent of both Sb species. Antimony redox speciation in soil extracts was performed by selective hydride generation-atomic fluorescence spectrometry. Simulated extraction procedures (without soil) showed that, except in oxalate medium, Sb(III) was oxidized to Sb(V), and this reaction was avoided with ascorbic acid. Recovery studies from a spiked agricultural soil showed that no oxidation but sorption of Sb(III) occurred during the extraction process in water and H2SO4 medium, and quantitative oxidation in EDTA and oxalate medium. With ascorbic acid, this oxidation was totally avoided in EDTA and partially avoided in oxalate solution. A new sequential extraction procedure was proposed and applied to the fractionation and redox speciation of antimony in agricultural soils, using EDTA + ascorbic acid, pH 7 (available under complexing and moderately reducible conditions); oxalic acid/oxalate + ascorbic acid (extractable in reducible conditions) and HNO3 + HCl + HF (residual fraction). The proposed extraction scheme can provide information about the availability and mobility of antimony redox species in agricultural soils.     

2,3,6,7‐Tetra­hydroxy‐9,10‐di­methyl‐9,10‐di­hydro‐9,10‐ethano­anthracene bis(1,4‐dioxane) solvate

2,3,6,7‐Tetra­hydroxy‐9,10‐di­methyl‐9,10‐di­hydro‐9,10‐ethano­anthracene crystallizes with 1,4‐dioxane to give a bis‐solvate, C₁₈H₁₈O₄·2C₄H₈O₂. The bis­(catechol) mol­ecule is located on a twofold axis and the two aromatic rings form a dihedral angle of 130.61 (4)°. Hydro­gen bonds are formed between the hydroxyl groups and either a neighbouring bis­(catechol) mol­ecule or the ether‐O atom of a dioxane mol­ecule.     

Physiological aspects of resistant starch and in vivo measurements

Resistant starch (RS) is the sum of starch and products of starch degradation not absorbed in the small intestine of healthy individuals. There are a number of RS with different characteristics which may have a different fate in the colon. As a consequence, all RS should not be considered equivalent as far as physiological properties are concerned; indeed, they may have a different impact on colonic health. This statement may explain part of the apparent contradictions in the literature on RS and cancer or inflammatory disease prevention. RS is fermented in the large intestine into short-chain fatty acids and, among those, butyrate, which is recognized as the main nutrient of the colonocyte. This fermentation pattern seems to be responsible for most of the effects of RS on colonic health. Another important property is linked to its ability to lower colonic pH, which is usually considered as beneficial for mineral biovailability in the colon or cancer prevention. Due to their fate in the digestive tract, RS materials do not seem to have any significant impact on glucose absorption or metabolism. On the contrary, they may have a hypocholesterolemic effect, but available information is contradictory.     

Efficient acyclic stereocontrol using the tethered aminohydroxylation reaction

[reaction: see text] The tethered aminohydroxylation (TA) of acyclic allylic carbamates has been achieved in a stereospecific and stereoselective manner. Unusually high levels of stereocontrol were observed in the oxidation of 1,1-disubstituted substrates.     

Temperature dependence of X- and Q-band EPR spectra of the dinuclear manganese(II) complex [(NO2Bpmp)Mn2(mu-OAc)2]+: determination of the exchange constant and of the spin parameters for the S=1, 2, and 3 spin states

A new dinuclear manganese(II) complex was synthesised with the biscompartimental ligand 2,6-bis[bis(2-pyridylmethyl)aminomethyl]-4-nitrophenol (NO(2)BpmpH) and characterised by X-ray crystallography. Magnetic susceptibility measurements revealed that the two high-spin Mn(II) ions are antiferromagnetically coupled with a singlet-to-triplet separation of 7.2 cm(-1). The powder EPR spectra were recorded for both X- and Q-bands between 1.8 K and 35 K. A detailed analysis of these spectra led to the determination of three out of five individual spin-state zero-field splitting parameters. From the proposed simulations, the exchange coupling constant J and the intermetallic distance have been computed.     

Optimisation of ICPMS collision/reaction cell conditions for the simultaneous removal of argon based interferences of arsenic and selenium in water samples

The optimisation of ICPMS collision/reaction cell conditions for the simultaneous analysis of arsenic and selenium is described. A mixture of 3.8 mL min⁻¹ of H₂ and 0.5 mL min⁻¹ of He was found to be suitable for the removal of both ArAr⁺ and ArCl⁺ interferences. Detection limits down to 30 ng (element) L⁻¹ in total analysis, and between 81 and 230 ng (element) L⁻¹ in speciation analysis were achieved in chloride matrix (1 g L⁻¹ NaCl). After validation, the method was applied to commercially available mineral waters.     

Oxygen and nitrogen Lewis base adducts of [UO2(OTf)2]. Crystal structures of polypyridine complexes with out-of-plane uranyl equatorial coordination

Dissolution of [UO2(OTf)2](1) in anhydrous thf, dme or py led to the formation of the complexes [UO2(OTf)2(thf)3](2), [UO2(OTf)2(dme)](3) and [UO2(OTf)2(py)3](4), respectively. Compounds 2 and 4 are neutral monomers in the solid state as well as the chloride [UO2Cl2(py)3](5) which was prepared in a similar way as for from the dimer [[UO2Cl2(thf)2]2]. Addition of 4 equivalents of triphenylphosphine oxide (tppo) to 1 afforded, in pyridine, the dicationic species [UO2(tppo)4][OTf]2 (6). The bi- or terdentate nitrogen molecules 2,2'-bipy, phen or terpy reacted with 1 in acetonitrile or pyridine to give [UO2(OTf)2(bipy)2](7), [UO2(phen)3][OTf]2(8), [UO2(OTf)2(terpy)](9) and [UO2(terpy)2][OTf]2(10), respectively. The hydroxide compound [[UO2(OH)(terpy)]2][OTf]2(11) was obtained by hydrolysis in air of 1 in a mixture of acetonitrile and ethanol in the presence of terpyridine. The X-ray crystal structures of , and reveal a novel coordination geometry for the uranyl ion, the uranium atom being in a rhombohedral environment; the six coordinating ligands atoms of the [UO2]2+ ion are separated into two parallel and staggered equilateral triangles and the UO2 axis is perpendicular to these triangles, passing through their centre. The structures of the mono(terpy) complexes 9 and 11 show the uranium atoms in a distorted pentagonal bipyramidal configuration with the nitrogen atom of the central pyridine ring of the terpy ligand significantly displaced from the equatorial plane.     

A Complex between C-Methylcalix[4]resorcinarene and Triethylammonium Nitrate

Abstract

The synthesis and crystal structure of the complex formed by the all-cis epimer of C-methylcalix[4]resorcinarene (1) and triethylammonium nitrate are reported. “1.(HNEt⁺ ₃)₄. (NO^? ₃)₄(2)”, crystallizes in the monoclinic space group P2₁/n, a=25.796(2), b=16.6048(11), c=29.5659(10) Å, β=94.636(4)°, V=12623(2) ų, Z=8. Refinement led to a final conventional R₁ value of 0.128 for 12428 reflections and 1473 parameters. The resorcinarene displays the usual bowl-type shape, with four hydroxyl protons involved in intramolecular hydrogen bonds, whereas the remaining four make hydrogen bonds with four bridging nitrate ions, which results in the formation of infinite chains. Those chains are arranged so as to form layers, between which the triethylammonium ions and the remaining nitrate ions are hydrogen-bonded one to another.     

Synthesis of Coleon U

The recent publication by Matsumoto¹ of a synthesis of Coleon U²(1) prompts us to present our own preparation of this poly-hydroxy diterpene as the tri-O-methyl (12a) and tetra-O-methyl ethers (12b). In a previous communication³ we outlined our approach which is aimed at several similar natural products such as Coleon C⁴ (1b), Lycoxanthol⁵ (2), etc. and differs considerably from that of the Japanese group. Formally at least, the two syntheses start with the same material, (+) ferruginol methyl ether 5a. In our case the latter was prepared by recorded methods from methyl O-methyl podocarpate after introducing the iso-propyl sidechain⁶ (→4), transforming the C.4 methoxycarbonyl residue to a methyl⁷ (→5a, ferruginol methyl ether) which was oxidised at the benzylic position of the B ring to give sugiol methyl ether 5b.     

Novel C1-symmetric dibenzophosphole ligands: application in hydroformylation reactions

A new family of non-symmetrical disubstituted dibenzophospholes possessing different steric and electronic effects have been synthesized and characterized. Their preliminary evaluation in rhodium-catalyzed hydroformylation reactions is presented.