STM analysis of triosmium carbonyl cluster adsorption at HOPG

The study of metallic carbonyl clusters as precursors in tailoring the heterogeneous metal catalysts has been of great importance. The catalytic nature of the adsorbed clusters in thin film form depends on the chemical properties of the substrate used. The metal-support interaction will determine various properties such as the surface morphology, adsorption features and the structural orientations. We report a scanning tunneling microscopy (STM) study of an osmium carbonyl cluster (Os₃(CO)₁₁(NCCH₃)) adsorbed on highly oriented pyrolytic graphite (HOPG). STM measurements showed that the osmium carbonyl cluster interacts with HOPG in such a way that it adsorbs on the basal plane showing regular lattice structure, whereas the axial planes of the HOPG surface shows no ordered structure. The regular cluster lattice structure of the carbonyl cluster on the basal plane of the graphite has lattice parameters of a=1.4 nm and b=1.5 nm. We believe that the regular orientation of the cluster indicates a monolayer adsorption of the cluster on the graphite basal planes. Scanning tunneling spectroscopy (STS) measurements also indicated an insulating behavior for the cluster molecules on HOPG, with a significant energy gap value of ca. 300 mV. The cluster interaction at the active sites, i.e. axial planes of the graphite, was also observed by in situ STM measurements.     

A new class of self-assembly multinuclear Pt(II) coordination cages by a modular approach

The formation of three examples of a new class of self-assembly Pt(II) cage molecules of general formula [Pt_m(ligand)_n](NO₃)_2m is achieved from Pt(II) and ligands. The compounds are observed in solution state and confirmed from the similarity of their proton NMR behavior as compared with that of reported Pd(II) compounds of the formula [Pd_m(ligand)_n](NO₃)_2m.     

Photobleaching of xanthene dyes in a poly(vinyl alcohol) matrix

Photobleaching of three different xanthene dyes namely, Erythrosin B (ERB), Eosin Y (EOY) and Rose Bengal (ROB) in Poly(Vinyl Alcohol) (PVA) matrix has been studied. Quantum yield values of photobleaching using an argon-ion laser (514.5 nm) were determined in presence of an electron donor (TriEthAnolamine, TEA) and/or Cr(VI). Evaluated quantum yield values suggest that erythrosin B undergoes faster photobleaching than eosin Y or rose bengal in presence of TEA. Presence of Cr(VI) in addition to TEA drastically decreases the quantum yield. Possible reaction pathways of photobleaching are discussed.     

Electron transfer. 147. Reductions with gallium(I)

Solutions 0.03-0.05 M in gallium(I) can be generated by treatment of the "mixed" halide Ga(I)Ga(III)Cl(4) with cold water under argon and then removing the precipitated metallic gallium and Ga(OH)(3) by centrifugation. Ga(I) is lost from such preparations with a half-life of about 3 h at 0 degrees C. These solutions, which may be handled by conventional techniques, readily reduce I(3)(-), IrCl(6)(2)(-), Fe(bipy)(3)(3+), Fe(NCS)(2+), aquacob(III)alamin, and a group of ring-substituted derivatives of Ru(NH(3))(5)(py)(3+) but are inert to (NH(3))(5)CoCl(2+) and (NH(3))(5)CoBr(2+). All reactions give Ga(III). Reduction of HCrO(4)(-) in 2-ethyl-2-hydroxybutanoate buffers (pH 3.6) yields a Cr(IV) chelate of the buffering anion but forms Cr(III) when carried out in 0.01 M H(+). Reactions of le(-) oxidants proceed via successive single changes with the conversion Ga(II) --> Ga(III) much more rapid than Ga(I) --> Ga(II). Only for the reactions of I(3)(-) and Fe(NCS)(2+) is there evidence for redox bridging.     

Synthesis of differentially protected/functionalised acetylenic building blocks from p-benzoquinone and their use in the synthesis of new enediynes

Sequential addition of two different lithium acetylides to p-benzoquinone yielded diastereomeric mixtures of 1,4-diethynylcyclohexa-2,5-diene-1,4-diols wherein the two ethynyl groups bear different protective/functional groups. Selective deprotection to the terminal acetylene followed by Pd(0) mediated coupling with Z-1,2-dichloroethene yielded new enediynes bearing cyclohexa-2,5-diene units.     

Computational description of quantum chemical calculations and pharmacological studies of the synthesized chalcone derivative: A promising NLO material

The intended chalcone, (E)-1-(4-aminophenyl)-3-(4-ethoxyphenyl)-prop-2-en-1-one (4A3EP), was synthesized in an alkaline medium by the Claisen–Schmidt condensation reaction of 4-aminoacetophenone with 4-ethoxybenzaldehyde. Spectroscopic analytical techniques such as UV–visible, FT-IR, FT-RAMAN, ¹H NMR, and ¹³C NMR investigations were used to analyze the molecular structure of the title molecule. The optimized molecular structure of the chalcone in gas phase vibrational frequencies and associated vibrational assignments were theoretically studied and compared with experimental results using the B3LYP/6–311++G techniques. All the experimental results were found to be in line with the theoretical values. The non linear optical activity of the title compound was proved from the hyperpolarizability calculations. In addition, E_HOMO (?5.9038 eV), E_LUMO (?2.2833 eV), energy gap (3.6205 eV) and electrophilicity index (4.628) were calculated to explore the reactivity, stability and bio activity of the title compound. The molecular electrostatic potential map was generated in order to spot the electrophilic and nucleophilic sites in the title compound. Natural bond orbital analysis was investigated in order to forecast the stability and charge transfer tendency of a title molecule. FUKUI FUNCTIONS were also calculated using DFT. Its anti-inflammatory, anti-diabetic, and anti-oxidant activities were also investigated. A molecular docking model was used to study the ligand-protein binding interactions of a synthetic chalcone derivative with the main protease of SARS-CoV-2 (the PDB code is 6yb7).     

Induction of drought stress tolerance by ketoconazole in Catharanthus roseus is mediated by enhanced antioxidant potentials and secondary metabolite accumulation

A pot culture experiment was conducted to estimate the drought stress mitigating effect of ketoconazole (KCZ), a fungicide cum plant growth regulator, in Catharanthus roseus plants. The plants under pot culture were subjected to drought stress and drought stress with KCZ from 30 days after sowing (DAS) and regular irrigation was kept as control. Antioxidant contents and activities of antioxidant enzymes were estimated from root, stem and leaf of both control and treated plants. The alkaloid ajmalicine was extracted and estimated from the roots of control, drought stressed and KCZ treated plants. Individual and combined drought stress and KCZ treatments increased ascorbic acid, -tocopherol contents, superoxide dismutase, ascorbate peroxidase, catalase and polyphenol oxidase activities when compared to control. There was a significant enhancement in ajmalicine production under KCZ treated plants under drought stress when compared to well watered control as well as drought stressed plants. The KCZ treatment resulted in partial mitigation of drought stress by increasing the antioxidant potentials in C. roseus plants.     

Formation of five-membered carbocycles by intramolecular palladium-catalyzed ring opening of tert-cyclobutanols

We report herein stereoselective formation of a functionalized five-membered carbocycle bearing a quaternary center by intramolecular palladium-catalyzed ring-opening of o-bromophenyl-tethered tert-cyclobutanols.     

Synthesis,structure, thermal studies on Zn(II), Cd(II) complexes of N-(2-pyridylmethyl)pyridine-2-carbaldimine and N-(2-pyridylmethyl)pyridine-2-methylketimine

The bivalent zinc and cadmium complexes of two Schiff bases N-(2-pyridylmethyl)pyridine-2-carbaldimine (L1), N-(2-pyridylmethyl)pyridine-2-methylketimine (L2), tridentate ligands with an N₃ chromophore and coordinating with two five-membered chelate rings, were synthesized. Complexes [Zn(L1)(NO₃)₂] (1), [Zn(L2)(NO₃)₂] (2), [Cd(L1)(NO₃)₂(H₂O)] (3) and [Cd(L2)(NO₃)₂(CH₃OH)] (4) were characterized by X-ray crystallography. In 1 and 2, Zn(II) has a distorted square-pyramidal geometry where as in 3 and 4, Cd(II) possesses a pseudo-pentagonal-bipyramidal geometry. The following trends in the bond lengths are observed: M–N_im < M–N_py; Zn–N > Zn–O; Cd–N < Cd–O. The final residues from the thermogravimetric analysis are ZnO and CdO, the SEM studies revealed, respectively, their porous and spherical natures. The average activation energy (E) for the loss of pyridine rings obtained from the Friedman fitting of the DSC data, for 1, 2, 3, and 4 are 193.8(2), 114.5(3), 127.1(4), and 63.7(3) kJ mol⁻¹ and their logarithmic pre-exponential factor (A) are 11.22, 5.31, 6.88, and 2.09, respectively.     

Comparative effects of different triazole compounds on antioxidant metabolism of Solenostemon rotundifolius

The effect of different triazole compounds, viz., triadimefon (TDM) and hexaconazole (HEX) treatments on the antioxidant metabolism of Solenostemon rotundifolius Poir., Morton plants was investigated in the present study under pot culture. Plants were treated with TDM at 15 mg l⁻¹ and HEX at 10 mg l⁻¹ separately by soil drenching on 80, 110 and 140 days after planting (DAP). The plants were harvested randomly on 90, 120 and 150 DAP for determining the effect of both the triazoles on non-enzymatic antioxidant contents like ascorbic acid (AA), reduced glutathione (GSH) and -tocopherol (-toc), activities of antioxidant enzymes like superoxide dismutase (SOD) and ascorbate peroxidase (APX). All the analyses were made in leaf, stem and tubers of both control and treated plants. It was found that both these triazole compounds have profound effects on the antioxidant metabolism and caused an enhancement in both non-enzymatic and enzymatic antioxidant potentials under treatments. These results suggest that, the application of triazoles may be a useful tool to increase the antioxidant production in S. rotundifolius and thereby make it an economical food crop.