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An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.
The facile hydrothermal method was used to prepare low-dimensional doped Ag<sub>2</sub>O/Sb<sub>2</sub>O<sub>3</sub> nanoparticles (NPs) at low temperature in alkaline medium. The calcined NPs were characterized in detail by FTIR, UV/vis, FESEM, XPS, EDS, and XRD. A thin layer of Ag<sub>2</sub>O/Sb<sub>2</sub>O<sub>3</sub> NPs was deposited onto a glassy carbon electrode (GCE) using Nafion (5% Nafion suspension in ethanol) conducting binder, which formed the working electrode of the selective 3-methoxyphenol electrochemical sensor probe. The proposed chemical sensor exhibits high sensitivity, long-term stability, and enhanced electrochemical responses towards 3-methoxyphenol. Response to 3-methoxyphenol is linear over the concentration range (LDR) of 0.09 nM to 0.09 mM. The analytical parameters of the sensor such as sensitivity, stability, response time, linearity, LDR, robustness, selectivity <i>etc.</i> were evaluated by an electrochemical approach. The sensor probe fabricated with Ag<sub>2</sub>O/Sb<sub>2</sub>O<sub>3</sub> NPs seems to be a promising candidate for effective and reliable electrochemical detection of hazardous and carcinogenic chemicals in the environment and health care fields in large scales.
1,3-Diethyl-5-(2-methoxybenzylidene)-2-thioxodihydropyrimidine-4,6(1H,5H)-dione 3 was prepared by Knoevenagel condensation of 2-methoxybenzaldehyde 1 and N,N-diethylthiobarbituric acid 2 in ethanol using piperidine as a base [1,2].[...]
In the title hydrate, C13H10N4O2S·H2O, the dihedral angles between the central pyrazole ring and its pendant phenyl and thia-diazole rings are 9.93 (8) and 4.56 (7)°, respectively. In the crystal, the components are linked by N-H⋯O, O-H⋯N and O-H⋯O hydrogen bonds, generating [100] chains incorporating R 4 (4)(10) loops. A weak C-H⋯O inter-action helps to consolidate the packing.
Carbon-based solar photocatalysts for overall water splitting could provide H<sub>2</sub> as an energy vector in a clean and sustainable way. Band engineering to align energy levels can be achieved, among other ways, by doping. Herein, it is shown that phosphorous doping of microporous graphitic carbons derived from pyrolysis of α-, β-, and γ-cyclodextrin increases the valence band edge energy of the material, and the energy value of the conduction band decreases with the P content. In this way, P doping increases the activity of these metal-free materials in photocatalytic overall water splitting under simulated sunlight and visible-light illumination. The optimal P-doped photocatalyst in the absence of any metal as a cocatalyst affords, after 4 h of irradiation with simulated sunlight, a H<sub>2</sub> production of 2.5 mmol of H<sub>2</sub> × g<sub>catalyst</sub><sup>-1</sup> in the presence of methanol as the sacrificial agent or 225 μmol of H<sub>2</sub> × g<sub>catalyst</sub><sup>-1</sup> from pure H<sub>2</sub>O.
A pyridine-pyrazoline (2-(3-(pyridin-2-yl)-5-(3,4,5-trimethoxyphenyl)-4,5-dihydro-1H-pyrazol-1-yl)benzo[d]thiazole) (PTPB) has been designed and synthesized by the reaction of chalcone with 2-hydrazinylbenzo[d]thiazole. PTPB was further conformed by the FT-IR, 1H-NMR and 13 F. Ran, Y. Liu, D. Zhang, M. Liu, and G. Zhao, “Discovery of Novel Pyrazole Derivatives as Potential Anticancer Agents in MCL,” Bioorganic and Medicinal Chemistry Letters 29, no. 9 (2019): 1060–4.[Crossref], [PubMed], [Web of Science ®] , [Google Scholar]N-NMR spectroscopic techniques. The solvatochromic behavior of PTPB with electron donating and accepting group was investigated in nonpolar, polar aprotic and protic solvents experimentally. The photophysical behavior of the PTPB in different solvent was attributed to the intramolecular charge transfer (ICT) of the compound along with specific and nonspecific interaction with different solvents. On view of the effect of different type of interaction on the photophysical parameters such as stokes shift, dipole moment oscillator strength and fluorescence quantum yields have been calculated with respect to polarity of the solvent. In addition, pyridine-pyrazoline (PTPB) can use as fluorescent chemosensor to determine the Fe3+ metal ion with high selectivity among the series of cations in aqueous dimethylformamide (DMF). The recognition mechanism of PTPB toward Fe3+ has been investigated in detail by Benesi–Hildebrand, Stern–Volmer and job’s plot measurements and PTBP forms 1:1 complex with Fe3+ metal ion and displays fluorescent quenching behavior.
In the title compound, C(22)H(14)BrN(3), the fused-ring system is buckled owing to the ethyl-ene linkage in the central ring; the two flanking aromatic rings are twisted by 25.9 (1) ° with respect to each other. The phenyl ring is twisted by 77.0 (1)° relative to the amino- and cyano-bearing aromatic ring. In the crystal, adjacent mol-ecules are linked by two N-H⋯N hydrogen bonds, generating a zigzag chain along [101].
