FeIII in a high-spin state in bis(5-bromosalicylaldehyde 4-ethylthiosemicarbazonato-κ3 O,N 1,S)ferrate(III) nitrate monohydrate, the first example of such a cationic FeIII complex unit

The synthesis and crystal structure (100 K) of the title compound, [Fe(C10H11BrN3OS)2]NO3·H2O, is reported. The asymmetric unit consists of an octahedral [FeIII(HL)2]+ cation, where HL − is H-5-Br-thsa-Et or 5-bromosalicylaldehyde 4-ethylthiosemicarbazonate(1−) {systematic name: 4-bromo-2-[(4-ethylthiosemicarbazidoidene)methyl]phenolate}, a nitrate anion and a noncoordinated water molecule. Each HL − ligand binds via the thione S, the imine N and the phenolate O atom, resulting in an FeIIIS2N2O2 chromophore. The ligands are orientated in two perpendicular planes, with the O and S atoms in cis and the N atoms in trans positions. This [Fe(HL)2](anion)·H2O compound contains the first known cationic FeIII entity containing two salicylaldehyde thiosemicarbazone derivatives. The FeIII ion is in the high-spin state at 100 K. In addition, a comparative IR spectroscopic study of the free ligand and the ferric complex is presented, demonstrating that such an analysis provides a quick identification of the degree of deprotonation and the coordination mode of the ligand in this class of metal compounds. The variable-temperature magnetic susceptibility measurements (5–320 K) are consistent with the presence of a high-spin FeIII ion with a zero-field splitting D = 0.439 (1) cm−1.

Sample stacking – Capillary electrophoretic determination of nitrate and nitrite contents as nitric oxide metabolites in honey varieties originated from Anatolia

Nitrate and nitrite ions taken from food are the sources of bioavailable nitric oxide (NO) in the nitrogen cycle. Some beneficial effects of honey on health are attributed to the ability of honey to increase NO production. The variation of nitrate and nitrite levels of honey samples collected from different Anatolia regions were clarified using capillary electrophoresis technique. The sensitivities of both anions were improved with the application of the sample stacking method. Separation buffer consisted of 30 mmol L−1 formic acid and 30 mmol L−1 sodium sulfate at a pH of 4.0. The CE technique revealed that 18 honey samples contained nitrate anion ranged between 2.53 and 31.8 mg kg−1. Nitrite amounts were found in lower amounts in the honey samples as between non-detected and 0.533 mg kg−1. The observed differences in nitrate levels between honey varieties may be a way to determine honey's origin.

Di-μ-nitrato-bis(μ-octaethyl pyrophosphoramide)bis[aquadinitratocalcium(II)]

The title compound, di-μ-nitrato-κ3 O,O′:O;O:O,O′-bis(μ-octaethyl pyrophosphoramide-κ2 O:O′)bis[aquabis(nitrato-κ2 O,O′)calcium(II)], [Ca2(NO3)4(C16H40N4O3P2)2(H2O)2] was obtained as a side product during the work up of the synthesis of octaethyl pyrophosphoramide and represents the first structurally characterized complex of this ligand. The compound crystallizes in the monoclinic space group P21/n and the asymmetric unit contains one pyrophosphoramide molecule and one Ca2+ ion coordinated to two nitrate ions and one water molecule. The complex exists as a dimer with a centre of inversion located between two eight-coordinate calcium(II) centres, which are bridged by two nitrate ions and two octaethyl pyrophosphoramide ligands. Each Ca2+ cation is also coordinated to a further nitrate anion, acting as a bidentate ligand, and a water molecule. The complexes stack parallel to the a axis and are held in place by a network of intermolecular O—H...O hydrogen bonds also running parallel to a.

(Nitrato-κO)(2,2′:6′,2′′-terpyridine-κ3 N,N′,N′′)palladium(II) nitrate

The title complex, [Pd(NO3)(C15H11N3)]NO3, comprises a cationic PdII complex and a nitrate anion. In the complex, the PdII cation is four-coordinated in a distorted square-planar coordination geometry defined by the three N atoms of the tridentate 2,2′:6′,2′′-terpyridine ligand and one O atom from the NO3 − anion. In the crystal, the complex molecules are stacked in columns along the a axis being connected by π–π stacking [closest inter-centroid separation between pyridyl rings = 3.878 (3) Å]. The connections between columns and anions to sustain a three-dimensional architecture are C—H...O hydrogen bonds.

Properties and Use of Water Activated by Plasma of Piezoelectric Direct Discharge

The distilled water was exposed to a cold atmospheric plasma (CAP) generated by the piezotransformer. The treatment was carried out on a six-well plate. Exposure time was from 30 s to 10 min. The emission spectra were obtained. Physical and chemical changes of activated water were observed for 8 days. The reactive oxygen and nitrogen species (RONS) were investigated. RONS production dependence on the exposure time and RONS lifetime in the treated liquid was determined using absorbance spectra. Quantitative assessment was made of the nitrite and nitrate concentration change over time after treatment. The medium conductivity and redox potential varied linearly depending on exposure time. The pH value change correlates with nitrate anion concentration. The concentration of peroxide hydrogen increased depending on CAP water treatment duration. The RONS concentration after liquid media processing with piezoelectric direct discharge CAP is a novel result. Biogeosystem Technique provides CAP activated water agriculture synergetic effect.

Efficient Exfoliation of Layered Double Hydroxides; Effect of Cationic Ratio, Hydration State, Anions and Their Orientations

The exfoliation ability of nitrate based Mg1−xAlx(OH)2(NO3)x·mH2O layered double hydroxides (Mg-Al LDH) in formamide into single or multilayer nanosheets depends strongly on nitrate anion orientation and layer charge. Our systematic studies used materials that were likely to disclose differences with respect to anion type and their concentrations in the interlayer gallery. We assured to avoid any carbonate incorporation into the galleries for nitrate, chloride, iodide, and sulfate based Mg-Al LDHs. Furthermore, the comparative exfoliation experiments were conducted for fully hydrated samples with as similar particle morphology as possible. The exfoliation of nitrate Mg-Al LDH is far superior to similar clays with carbonate, sulfate, chloride, or iodide as charge balancing anions. Quantitative analysis of exfoliation yield for pre-treated, fully hydrated samples, shows an optimum composition for exfoliation into single nanosheets of around x ≈ 0.25, while double or triple layered sheets are encountered for other x-values. We observe a clear correlation between the expansion of the interlayer gallery due to progressing tilts of nitrate anions and water molecules out of the horizontal interlayer plane, suspension turbidity, and degree of exfoliation. The established correlations extends to nitrate Ni-Al LDH materials. We finally claim that morphology is a dominating parameter, with house-of-card morphology particles exfoliation far less than platelet-like particles. Hence, hydrothermal treatment may be favorable to enhance exfoliation yields.

Single-Ion Magnet and Photoluminescence Properties of Lanthanide(III) Coordination Polymers Based on Pyrimidine-4,6-Dicarboxylate

Herein, we report the magnetic and photoluminescence characterization of coordination polymers (CP) built from the combination of lanthanide(III) ions, pyrimidine-4,6-dicarboxylate (pmdc) ligand and a co-ligand with formula {[Dy(μ-pmdc)(μ-ox)0.5(H2O)3]·2H2O}n (1-Dy), {[Dy(μ3-pmdc)(μ-ox)0.5(H2O)2] ~2.33H2O}n (2-Dy), {[Dy2(μ3-pmdc)(μ4-pmdc)(μ-ox)(H2O)3]·5H2O}n (3-Dy), {[Ln(μ3-pmdc)(μ-ox)0.5(H2O)2]·H2O}n (where Ln(III) = Nd (4-Nd), Sm (4-Sm), Eu (4-Eu) and Dy (4-Dy)) and {[Dy(μ4-pmdc)(NO3)(H2O)]·H2O}n (5-Dy). It must be noted the presence of oxalate anion acting as ditopic co-ligand in compounds 1-Dy, 2-Dy, 3-Dy and 4-Ln, whereas in 5-Dy the nitrate anion plays the role of terminal co-ligand. Direct current measurements carried out for the dysprosium-based CPs reveal almost negligible interactions between Dy3+ ions within the crystal structure, which is confirmed by computed values of the exchange parameters J. In addition, alternating current measurements show field-induced single-molecule magnet (SMM) behavior in compounds 1-Dy, 2-Dy, 4-Dy and 5-Dy, whereas slight-frequency dependence is also observed in 3-Dy. Solid state emission spectra performed at room temperature for those compounds emitting in visible region confirm the occurrence of significant ligand-to-lanthanide charge transfer in view of the strong characteristic emissions for all lanthanide ions. Emission decay curves were also recorded to estimate the emission lifetimes for the reported compounds, in addition to the absolute quantum yields. Among them, the high quantum yield of 25.0% measured for 4-Eu is to be highlighted as a representative example of the good emissive properties of the materials.