Syntheses,Physico‐Chemical Studies and Antioxidant Activities of Transition Metal Complexes with a Perimidine Ligand

A series of mononuclear complexes of the type, [MLCl₂] [M = Co^II, Ni^II, Cu^II, and Zn^II] with a pyrimidene‐type ligand, which was synthesized by the reaction of 2‐furaldehyde and 1, 8‐diaminonaphthalene, was obtained. The ligand and its complexes were characterized by elemental analysis, IR, NMR, EPR, and UV/Vis spectroscopy, ESI‐mass spectrometry, magnetic susceptibility, molar conductivity, and thermogravimetric analyses. On the basis of UV/Vis spectroscopic and magnetic susceptibility data, an octahedral arrangement was assigned around all metal ions. The low molar conductivity data for all the complexes show their non‐electrolytic nature. The thermal behavior of the complexes was studied by TGA analyses. The electrochemical study carried out on the Cu^II complex exhibits a quasi reversible redox process. The ligand and its complexes showed potential antioxidant and antimicrobial activities.     

Synthesis,structural chemistry and antimicrobial activity of −(−) borneol derivative

Borneol is a monoterpene that is a part of traditional Chinese and Japanese medicine. (−) borneol reacted with methanesulfonyl chloride in THF/pyridine to afford the new 1,7,7-trimethylbicyclo[2.2.1]hept-2-yl methane sulfonate derivative in excellent yield. The product is characterized by H1NMR, C¹³NMR, mass spectroscopy as well as elemental analysis and its structure was identified by X-ray single crystal diffraction. The packing of 1,7,7-trimethylbicyclo[2.2.1]hept-2-yl methanesulfonate exhibits the non-classical C-H···O hydrogen bonding in C(4) and R² ₂(8) chain and ring motifs as structural determinants. This was also confirmed by the analysis of Hirshfeld surfaces. The 1,7,7-trimethylbicyclo[2.2.1]hept-2-yl methane sulfonate antimicrobial activity was tested and compared with its parent (−) borneol against three different pathogens. Particularly, 1,7,7-trimethylbicyclo[2.2.1]hept-2-yl methane sulfonate showed high sensitivity, compared to Chloramphenicol reference material, against Escherichia coli.      

Copper(I)-catalyzed hydrophosphination of styrenes

Hydrophosphination of styrenes has been accomplished with metal salts for the first time. (CuOTf)₂·toluene complex is the catalyst of choice, but CuCl can also be used. “In-situ” EPR and NMR studies suggest Cu(I) as the catalytically active metal species, giving exclusively the anti-Markovnikov product. Phosphine oxides or β-ketophosphine oxides can be prepared in one-pot by oxidation with molecular oxygen.     

Advanced Photoelectrochemical Hydrogen Generation by CdO-g-C3N4 in Aqueous Medium under Visible Light

Herein, hydrothermal fabrication of CdO-g-C₃N₄ photocatalyst for a substantially better photocatalytic recital in water splitting is presented. The XRD analysis confirms the cubic phase of CdO-g-C₃N₄, whereas FTIR and UV-VIS studies revealed the presence of respective groups and a median band gap energy (2.55 eV) of the photocatalyst, respectively, which further enhanced its photo-electrochemical (PEC) properties. The SEM displays the oblong structures of g-C₃N₄ sheets and nano rod-like morphology of CdO and CdO-g-C₃N₄, respectively. The HR-TEM exhibits morphology & orientation of the grains and substantiates the polycrystal-line nature of CdO-g-C₃N₄ nanocomposite. The photocatalytic water-splitting concert is evaluated by PEC experiments under 1 SUN visible light irradiation. Linear sweep voltammetry (LSV), chronoamperometry (CA), and electrochemical impedance spectroscopy (EIS) comprehend the CdO-g-C₃N₄ as a hydrogen evolution photocatalyst. A photocurrent density beyond ≥5 mA/cm² is recorded from CdO-g-C₃N₄, which is 5–6 folds greater than pure CdO and g-C₃N₄. The efficient separation and transfer of charges allocated to CdO-g-C₃N₄ and fabricating heterojunctions between g-C₃N₄ and CdO suppresses the unfavorable electron-hole pairs recombination process. Thus, it recesses charge transfer resistance, augmenting enhanced photocatalytic performance under 1 SUN irradiation.     

Novel Pd(ii)-salen complexes showing high in vitro anti-proliferative effects against human hepatoma cancer by modulating specific regulatory genes

We have reported the synthesis of a novel salen ligand and its mononuclear Pd-salen complexes derived from 2-{[2-hydroxy-3-{[(E)-(2-hydroxyphenyl)methylidene]amino}propyl)imino]methyl}phenol. The newly synthesized and isolated Pd(ii) complexes have been identified and fully characterized by various physico-chemical studies viz., elemental analyses, IR, UV-Vis, (1)H, (13)C NMR spectroscopy, electron spray ionization mass spectrometry (ESI-MS) and TGA/DTA studies. The molecular structure of the salen ligand has been ascertained by single-crystal XRD and it is coordinated to Pd(ii) ion through two nitrogen and two oxygen atoms. The UV-Vis data clearly suggest a square-planar environment around both the Pd(ii) ions. The DNA binding studies of the synthesized compounds has been investigated by electron spectroscopy and fluorescence measurements. The results suggest that Pd(ii) complexes bind to DNA strongly as compared to the free ligand. The free salen ligand and its Pd(ii) complexes have also been tested against human hepatoma cancer cell line (Huh7) and results manifested exceptional anti-proliferative effects of the Pd(ii) complexes. The anti-proliferative activity of Pd(ii) complexes has been modulated by specific regulatory genes.     

Structural and optical properties of laser irradiated nano structured cadmium oxide thin film synthesized by sol-gel spin coating method

Cadmium oxide CdO nanostructured thin films are synthesized using sol-gel spin coating method. The prepared samples of CdO thin films are irradiated with 10 mJ laser from pulsed Q-Switched Nd:YAG laser at 1064 and 532 nm wavelength. The samples were exposed to 45 pulses of 7 ns pulse duration. Morphology and structural analysis were carried out with scanning electron microscope (SEM) micrographs and X-ray diffraction (XRD) patterns. Optical investigations were obtained with spectrometer and fluorospectrometer from Shimadzu. SEM micrographs confirm the nanostructure of the CdO film and indicate agglomeration of nanoparticles with laser irradiation. XRD patterns show decrease in the intensity of orientation peaks after laser irradiation. Variation in band gap energy, absorption peaks, and photoluminescence spectra with laser irradiation are observed.     

Grindstone Chemistry: Design,One-Pot Synthesis,and Promising Anticancer Activity of Spiro[acridine-9,2′-indoline]-1,3,8-trione Derivatives against the MCF-7 Cancer Cell Line

In this study, the synthesis of one-pot 10-phenyl-3,4,6,7-tetrahydro-1H-spiro [acridine-9,2′-indoline]-1,3,8-trione derivatives was achieved via a four-component cyclocondensation reaction, which was carried out in solvent-free conditions, and using p-toluenesulfonic acid (p-TSA) as a catalyst. The product was confirmed by FT-IR, ¹H-NMR, ¹³C-NMR, mass spectra, and elemental analysis. Furthermore, the anticancer activity was screened for all compounds. Among these compounds, compound 1c was more effective (GI₅₀ 0.01 µm) against MCF-7 cancer cell lines than standard and other compounds. Therefore, the objective of this study was achieved with a few promising molecules having been demonstrated to be potential anticancer agents.     

Effect of Sn additions on the microstructure,mechanical properties,corrosion and bioactivity behaviour of biomedical Ti–Ta shape memory alloys

Ti–Ta and Ti–Ta–xSn shape memory alloys (SMAs) were produced successfully by microwave sintering. Tin element was added to Ti–Ta SMA with three different atomic percentages (0.37, 0.745 and 2.26 at.%). The influences of Sn addition on microstructure, transformation temperatures, mechanical properties, shape memory behaviours, corrosion resistance and bioactivity were investigated. It was found that the morphologies of the modified and unmodified Ti–Ta alloys contain a plate-like and needle-like structure, where the former structure is related to the β phase and the latter related to the α phase. The transformation temperatures of M _s to M _f with and without Sn additions were observed to be in the range of 389.65 to 355 K, while the transformation temperatures of A _s to A _f were found to be in the range of 250.42 to 365.8 K. By increasing the proportion of Sn, the compressive fracture strength and shape memory behaviour were enhanced; however, the corrosion resistance tended to be decreased. Based on the bioactivity results, antibacterial activity was improved with the addition of Sn. In conclusion, the existent results indicate that Ti–30 at.% Ta SMAs may be a convenient alternative to Ni–Ti for certain biomedical applications.