Cyclometallated 1,2,3-triazol-5-ylidene iridium(III) complexes: synthesis,structure, and photoluminescence properties

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Synthesis,X-ray and DFT Studies of 6-halo-3-(hydroxymethyl)cinnolin-4(1H)-ones

Chemistry of Heterocyclic Compounds - The Richter cyclization was used for the synthesis of 6-halo-3-(hydroxymethyl)cinnolin-4(1H)-ones. X-ray analysis revealed that these compounds exist as dimers...     

Solving q-Virasoro constraints

Letters in Mathematical Physics - We show how q-Virasoro constraints can be derived for a large class of (q, t)-deformed eigenvalue matrix models by an elementary trick of inserting...     

Crystal Structure of Cl-Deficient Analogue of Taseqite from Odikhincha Massif

An eudialyte group mineral, found in pegmatites of the Odikhincha massif (the northern part of the Siberian platform), has been investigated using X-ray diffraction, IR spectroscopy, and Raman spectroscopy. The mineral is characterized by a high strontium content and a low chlorine content. It has a trigonal unit cell with the following parameters: a = 14.2700(6) Å and c = 30.057(1) Å; V = 5300.6(1) ų; sp. gr. R3m. The structure has been refined to R = 0.047 in the anisotropic approximation of atomic displacements using 1697F > 4σ(F). The idealized formula (Z = 3) was found to be Na₁₂Sr₂Ca₆Fe ₃ ²⁺ Zr₃NbSi₂₅O₇₂(OH,O)₄Cl(Н₂О)_0.2. The chemical composition and structure of this mineral are close to those of taseqite; however, it differs from the holotype sample by a low chlorine content and peculiarities of cation distribution over basic structure sites. A comparative analysis of strontium-rich eudialytes has revealed their important crystallochemical feature: selective concentration of strontium in the N4 site. Thus, taseqite, along with heterophyllosilicates, may play a role of strontium concentrator in agpaitic pegmatites.     

Resonance Assisted Chalcogen Bonding as a New Synthon in the Design of Dyes

Intramolecular chalcogen bonding in arylhydrazones of sulfamethizole is strengthened by conjugation in the π-system of a noncovalent five-membered ring. The S⋅⋅⋅O distance in the sulfamethizole moiety of these compounds ranges from 2.698(3) to 2.806(15) Å, which indicates its strong dependence on the attached arylhydrazone fragments. Information on the nature of the intramolecular chalcogen bond was afforded by DFT calculations.     

Spectral Photoluminescent Parameters of Barley Seeds (Hordéum vulgáre) Infected with Fusarium ssp

We needed effective and sustainable technologies for better microbiological control of crops, including Fusarium. However, photoluminescent UV–Vis methods are potential for diagnosing plant diseases with Fusarium. It has not been sufficiently studied despite the application of these methods for other biological researches. The excitation spectrum of the seeds during infection shifts to the shorter wavelength and a new maximum appears in the region λ ≈ 232 nm. The photoluminescence of infected seeds increases with excitation by radiation of wavelengths λ_e,1 = 232 nm, λ_e,2 = 362 nm and λ_e,3 = 424 nm by 1.33–3.14 times, and λ_e,3 = 424 nm—decreases by 1.1 times. Statistical moments μ₃ and μ₄, asymmetry and kurtosis change only with short-wave excitation. When analyzing the decomposition of the frequency spectrum into Gaussian curves, the most informative ratio is the ratio of right-handed and left-handed Gaussians under excitation λ_e,2 = 362 nm and λ_e,3 = 424 nm. The ratios of their maxima change during infection by 1.36–3.2 times, and for excitation by radiation λ_e,2, the frequency boundaries of Gaussians change. The results of measurements and calculations provide a basis for the development of a method and device for photoluminescence diagnostics of fusarium seeds in UV–Vis ranges.