Transformations of 5-(2-arylethynyl)-2-methyl-2H-tetrazoles under superelectrophilic activation

Reaction of 5-arylethynyl-2-methyl-2H-tetrazoles (acetylene tetrazoles) with arenes under the action of Brønsted superacid CF₃SO₃H or acidic zeolite HUSY CBV-720 gives rise to E-/Z-5-(2,2-diarylethenyl)-2-methyl-2H-tetrazoles, as products of hydroarylation of acetylene bond, in yields up to 98% with predominant formation of E-isomers. Cationic intermediates of these reactions have been studied theoretically by DFT calculations. Addition of CF₃SO₃H to the triple bond of acetylene tetrazoles leads to the corresponding E-/Z-vinyl triflates in high yields. Hydration of triple bond in these tetrazoles in H₂SO₄ results in the formation of 5-(2-aryl-2-oxoethyl)-2-methyl-2H-tetrazoles. Tandem hydroarylation-ionic hydrogenation of acetylene tetrazoles in the systems acid(CF₃SO₃H or AlCl₃)-arene-cyclohexane affords 5-(2,2-diarylethyl)-2-methyl-2H-tetrazoles.     

Supramolecular Nested Microbeads as Building Blocks for Macroscopic Self‐Healing Scaffolds

The ability to construct self‐healing scaffolds that are injectable and capable of forming a designed morphology offers the possibility to engineer sustainable materials. Herein, we introduce supramolecular nested microbeads that can be used as building blocks to construct macroscopic self‐healing scaffolds. The core–shell microbeads remain in an “inert” state owing to the isolation of a pair of complementary polymers in a form that can be stored as an aqueous suspension. An annealing process after injection effectively induces the re‐construction of the microbead units, leading to supramolecular gelation in a preconfigured shape. The resulting macroscopic scaffold is dynamically stable, displaying self‐recovery in a self‐healing electronic conductor. This strategy of using the supramolecular assembled nested microbeads as building blocks represents an alternative to injectable hydrogel systems, and shows promise in the field of structural biomaterials and flexible electronics.     

Double Circulant Codes over \mathbb{Z}_4 and Even Unimodular Lattices

With the help of some new results about weight enumerators of self-dual codes over we investigate a class of double circulant codes over , one of which leads to an extremal even unimodular 40–dimensional lattice. It is conjectured that there should be Nine more constructions of the Leech lattice     

Oscillation of forced neutral differential equations with positive and negative coefficients

In this paper the forced neutral difterential equation with positive and negative coefficients d/dt [x(t)-R(t)x(t-r)] P(t)x(t-x)-Q(t)x(t-σ)=f(t),t≥t0,is considered,where f∈L^1(t0,∞)交集C([t0,∞],R^ )and r,x,σ∈(0,∞),The sufficient conditions to oscillate for all solutions of this equation are studied.     

A note on the behavior of blow-up solutions for one-phase Stefan problems

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X-ray structure of 2,6-dimethoxy-7-methylpurine

The title compound (C₈H₁₀N₄O₂) is monoclinic, with a = 7.740(2), b = 17.044(7), c = 6.992(3) Å, = 100.60(1)°, and space group P2₁/c. Two O-methyl groups are coplanar with the pyrimidine ring. Whereas, the O(6)-methyl group is directed away from the imidazole ring toward the N(1) atom, the O(2)-methyl is pointed away from the N(1) atom toward the N(3) atom. Two intermolecular hydrogen bonds H(8)···N(1) and H(711)···O(2) of 2.48(2) and 2.58(3) Å make a linear arrangement of the molecules. The conformation of the O-methyl groups explains some results of thermal rearrangement of 2,6-dialkoxy-7-methylpurines and differences in alkylations of 2,4-dialkoxypyrimidines and 2,6-dialkoxy-7-methylpurines.     

Molecular structure of N-(2-phenylethyl)amide of α-(1,1-ethylenedioxy)-ethyl γ-hydroxybutyric acid (I) and1H NMR spectra of (I) and N-(p-methoxybenzyl)derivative (III)

The spectroscopic and X-ray investigation of the N-(2-phenylethyl) amide of -(1,1-ethylenedioxy)-ethyl--hydroxybutyric acid are reported. The¹H NMR spectra for the title structure and for the N-(p-methoxybenzyl) amide of -(1,1-ethylenedioxy)-ethyl--hydroxybutyric acid are given. The N-(2-phenylethyl)amide of -(1,1-ethylenedioxy)-ethyl--hydroxybutyric acid, C₁₆H₂₃O₄N, crustallizes in the monoclinic space groupP2 ₁/c witha=21.547(5),b=6.333(2),c=11.822(3) Å and =101.01(2)°. The dioxolane ring has a half-chair conformation with C₂(O3)=2.4° and ||_av=18.2°. The inconsiderable deviations from planarity of the six atoms of the amide group are caused mainly by twist around the C4–N1 bond and out-of-plane bending at the N1 atom ((C4–N1)=4°, X_N =7°, X_c =0.4° ). The amide group plane is nearly coplanar with the phenyl ring. The molecules are connected by two intermolecular hydrogen bonds.     

Determination of boron in water samples at nanograms per cubic decimeter levels by reversed-phase partition high-performance liquid chromatography with precolumn complexation reaction using salicylaldehyde and 1-amino-8-naphthol-3,6-disulfonate

A new method for the highly sensitive and selective determination of boron at nanograms per cubic decimeter levels has been developed based on the derivatization reaction of boron using salicylaldehyde and 1-amino-8-naphtol-3,6-disulfonate with reversed-phase partition high-performance liquid chromatography. A detection limit as low as 2.0 nmol/dm³ (22 ng/dm³) was achieved without any preconcentration. No significant interference was observed in the determination of 16 μmol/dm³ of boron with the addition of nine metal ions (Al^III, Cu^II, Co^II, Fe^II, Fe^III, Ni^II, Mn^II, V^V, Zn^II) at concentrations 100 times greater than that of boron without any masking procedure. The proposed method was successfully applied to the determination of boron in river water, tap water, doubly distilled water, and highly purified water. Figure Scheme of formation of boron-azomethine-H complex with salicylaldehyde and 1-amino-8-naphthol-3, 6-disulfonate     

Combination of cloud point extraction and flame atomic absorption spectrometry for preconcentration and determination of trace iron in environmental and biological samples

In the presented work, the conditions for cloud point extraction of iron from aqueous solutions using 7-iodo-8-hydroxyquinolin-5-sulphonic acid (Ferron) was investigated and optimized. The procedure is based on the separation of its ferron complex into the micellar media by adding the surfactant Triton X-114. After phase separation, the surfactant-rich phase was dissolved with 1.0 M HNO3 in methanol. Iron was determined by flame atomic absorption spectrometry. Optimization of the pH, ligand and surfactant quantities, incubation time, temperature, viscosity, sample volume, and interfering ions were investigated. The effects of the matrix ions were also examined. The detection limits for three times the standard deviations of the blank for iron was 0.4 ng m L-1, enrichment factor of 19.6 and preconcentration factor of 30 could be achieved. The validity of cloud point extraction was checked by employing real samples including soil, blood, spinach, milk, meat, liver and orange juice samples using the standard addition method, which gave satisfactory results.In the presented work, the conditions for cloud point extraction of iron from aqueous solutions using 7-iodo-8-hydroxyquinolin-5-sulphonic acid (Ferron) was investigated and optimized. The procedure is based on the separation of its ferron complex into the micellar media by adding the surfactant Triton X-114. After phase separation, the surfactant-rich phase was dissolved with 1.0 M HNO₃ in methanol. Iron was determined by flame atomic absorption spectrometry. Optimization of the pH, ligand and surfactant quantities, incubation time, temperature, viscosity, sample volume, and interfering ions were investigated. The effects of the matrix ions were also examined. The detection limits for three times the standard deviations of the blank for iron was 0.4 ng m L⁻¹, enrichment factor of 19.6 and preconcentration factor of 30 could be achieved. The validity of cloud point extraction was checked by employing real samples including soil, blood, spinach, milk, meat, liver and orange juice samples using the standard addition method, which gave satisfactory results.      

The poset structures admitting the extended binary Golay code to be a perfect code

Brualdi et al. [Codes with a poset metric, Discrete Math. 147 (1995) 57-72] introduced the concept of poset codes, and gave an example of poset structure which admits the extended binary Golay code to be a 4-error-correcting perfect P-code. In this paper we classify all of the poset structures which admit the extended binary Golay code to be a 4-error-correcting perfect P-code, and show that there are no posets which admit the extended binary Golay code to be a 5-error-correcting perfect P-code.