Development of versatile CdMoO4/g-C3N4 nanocomposite for enhanced photoelectrochemical oxygen evolution reaction and photocatalytic dye degradation applications

Fabrication of an efficient, stable, and versatile photocatalysts for the energy and environment remediation applications is an urgent task for the current researchers. In this work, we have successfully synthesized a versatile hybrid photocatalysts, i.e.; CdMoO₄/g-C₃N₄ (CMO/CN) by a facile and simple one-pot in-situ hydrothermal method. Here CdMoO₄ (CMO) microspheres were deposited on the g-C₃N₄ (CN) sheets. Fabricated CN, CMO, and CMO/CN composite photocatalysts were analyzed with various characterization techniques like UV–visible diffuse reflectance spectra (UV–Vis DRS), photoluminescence spectroscopy (PL), time-resolved fluorescence lifetime (TRFL), electrochemical impedance spectroscopy (EIS), powder X-ray diffraction (PXRD), Fourier transform infrared spectroscopy (FT-IR), Scanning electron microscopy–energy-dispersive X-ray analysis (SEM-EDX), transmission electron microscope (TEM), thermogravimetric analysis (TGA), X-ray photoelectron spectroscopy (XPS), and Brunauer–Emmett–Teller (BET). The results reveal that the formation of a strong heterojunction between two semiconductors leads to the formation of active photocatalyst. Furthermore, as-synthesized materials were tested for the photoelectrocatalytic (PEC) oxygen evolution reactions (OERs) in acidic medium, and photocatalytic (PC) degradation of methylene blue (MB) under light irradiation. Among all tested samples, CMO/CN-10 has shown the highest current density 52.74 mA cm^?2 at 1.95 V with lowest over potential of 0.70 mV on glassy carbon electrode for OER in acidic medium under the light irradiation. The PC degradation rate constant of CMO/CN-10 composite in MB solution is k = 2.0 × 10^?2 min^?1, whereas for the pure CMO and CN degradation rate constant is k = 5.7 × 10^?3 min^?1 and k = 1.2 × 10^?2 min^?1, respectively. This enhancement in PEC and PC properties is due to the fast migration of photo-induced electrons in the case of CMO/CN-10 nanocomposite. Trapping experiment results reveal the major reactive species for PC degradation of MB is ?OH (hydroxyl radicals) and h⁺ (holes), respectively, and suitable PC reaction mechanism also proposed for CMO/CN-10 composites. Based on the above remarkable results, it would be a potential nanocomposite for the PEC oxygen evolution and PC degradation of MB under light illumination.     

Reactive sensing of gold (III) by coumarin tethered fluorescent probe through alkyne activation

A novel strategy, involving anchoring and un-anchoring of coumarin based fluorophore, has been established for the selective detection of Au³⁺ species. Selective sensing of Gold (Au³⁺) was triggered due to alkynophilicity of gold ions to create lateral fluorescence of a latent fluorophore. The 4-methyl-2-oxo-2H-chromen-7-yl 2-(2-phenylethynyl) benzoate (CEB) probe was synthesized by reacting 7-hydroxy-4-methylcoumarin with iodo-benzoic acid. CEB probe has an absorption at 300 nm and 335 nm which decreases gradually and new absorption appeared at 406 nm due to Au³⁺ promoted ester hydrolysis selectively over other metal ions with great sensitivity, which accompanies a turn on fluorescence change produced by 7-hydroxy coumarin. The principle behind this sensing strategy is activation of triple bond induced uniquely by Au⁺³ ions leading to cascade and delivers active fluorophore. The sensing mechanism was proposed and supported by ¹H NMR, MS and TD-DFT experiments. The density functional theory (DFT) and time dependent density functional theory (TD-DFT) theoretical results of the CEB-probe and Au³⁺ reaction is in good agreement with the experimental results. Additionally, probe could be well incorporated onto the test strips for effective detection of Au^3+.     

The Durrmeyer type modification of the q-Baskakov type operators with two parameter α and β

In this paper, we are dealing with q analogue of Durrmeyer type modified the Baskakov operators with two parameter α and β, which introduces a new sequence of positive linear q-integral operators. We show that this sequence is an approximation process in the polynomial weighted space of continuous function defined on the interval [0, ∞). We study moments, weighted approximation properties, the rate of convergence using a weighted modulus of smoothness, asymptotic formula and better error estimation for these operators.     

A Facile Synthesis of 3,7-Diphenyl-4,8-distyryl-2,6-dioxo-2H,6H-benzo[1,2-b:3,4-b′] Dipyrans and Their Antifeedant Activity.

The synthesis, characterisation and antifeedant activity of some new angular dicoumarins prepared from 2,4-diacetyl resorcinol has been reported.     

Copper(II) complexes with N-(2-hydroxyethyl)-2-iminodiacetic acid and imidazoles: crystal structure,spectroscopic studies and superoxide dismutase activity

Abstract  

Two new copper(II) complexes, [Cu(Hhida)(BenzImH)]·H₂O (1) and [Cu(Hhida)(EtImH)]·2H₂O (2) have been synthesized by the interaction of basic copper carbonate with N-(2-hydroxyethyl)-2-aminodiacetic acid (Hhida²⁻) and benzimidazole (BenzImH) or (2-ethylimidazole (EtImH)). The structures of both complexes were studied by single crystal X-ray diffraction. The geometry around the copper(II) atom can be best described as distorted square pyramidal as indicated by the value of the trigonal index τ = 0.32 for (1) and 0.21 for (2). Spectroscopic and electrochemical studies were performed in order to correlate structural features of the complexes with their superoxide scavenger activity. The ability of the complexes to scavenge superoxide anions was also evaluated.     

Unusual sulfanylation through ring transformation of arene-tethered 2H-pyran-2-ones by in situ built Michael adduct

A novel synthesis of highly functionalized alkylsulfanylmethyl arenes 8a-m through the ring transformation of 6-aryl-4-methyl/ethylsulfanyl-2H-pyran-2-one-3-carbonitriles 1a-j, by reaction with methyl vinyl ketone 2, is delineated and illustrated. To ascertain the course of reaction, 3-arylsulfanylmethyl-2-methyl-6-methylsulfanyl-4-phenylbenzonitriles 8k-m were also prepared from the reaction of 1 with 4-arylsulfanyl-butan-2-ones 7c,d.     

Bromodimethylsulfonium bromide (BDMS) in ionic liquid: a mild and efficient catalyst for Beckmann rearrangement

Bromodimethylsulfonium bromide (BDMS)-catalyzed Beckmann rearrangement of a variety of ketoximes has been carried out in the imidazolium-based ionic liquid [bmim]PF₆ under mild conditions without using any additional cocatalyst or solvent to afford excellent conversion and selectivity. The ionic liquid is recovered and reused for up to three runs without any loss of efficiency.     

A convenient synthesis of partially reduced benzo[c]phenanthrenes, its ketals and ketones

A concise and convenient synthesis of various partially reduced 6-sec-amino-1,2,3,4,7,8-hexahydro-, 6-sec-amino-1,2,7,8-tetrahydrobenzo[c]phenanthrene-5-carbonitriles, 6-sec-amino-3,4,7,8-tetrahydro-1H-benzo[c]phenanthrene-2-one-5-carbonitrile cycloalkene ketals, pendant with electron donor and acceptor substituents has been described through base catalyzed ring transformation of 2-oxo-4-sec-amino-5,6-dihydro-2H-benzo[h]chromene-3-carbonitriles by cyclohexanone, 2-cyclohexen-1-one, 1,4-cyclohexanedione monocycloalkene ketals. The acid catalyzed deketalation of 6-sec-amino-3,4,7,8-tetrahydro-1H-benzo[c]phenanthrene-2-one-carbonitrile ketals led to yield 6-sec-amino-3,4,7,8-tetrahydro-1H-benzo[c]phenanthrene-3-carbonitrile-2-ones in excellent yield. We also performed the X-ray studies of the molecules 3d and 6a to know the degree of non-planarity.