Thermal and Microwave‐Assisted Conjugate Additions of Indole on Electron‐Deficient Nitro‐olefins

Conjugate addition of indole on nitro‐olefins was carried out by three different methods: (i) thermal heating in a sealed tube, (ii) reaction with indolyl magnesium iodide, and (iii) microwave irradiation. Comparison of the results indicated that the microwave technique is most efficient.     

Investigation on the effect of Zr doping in ZnO thin films by spray pyrolysis

Zirconium doped zinc oxide thin films with enhanced optical transparency were prepared on Corning 1737 glass substrates at the substrate temperature of 400 °C by spray pyrolysis method for various doping concentrations of zirconium (IV) chloride in the spray solution. The X-ray diffraction studies reveal that the films exhibit hexagonal crystal structure with polycrystalline grains oriented along (0 0 2) direction. The crystalline quality of the films is found to be deteriorating with the increase of doping concentration and acquires amorphous state for higher concentration of 8 at.% in precursor solution. The average transmittance for 5 at.% (solution) zirconium doped ZnO film is significantly increased to ∼92% in the visible region of 500-800 nm. The room temperature photoluminescence (PL) spectra of films show a band edge between 3.41 and 3.2 eV and strong blue emission at 2.8 eV irrespective of doping concentration and however intensity increases consistently with doping levels. The vacuum annealing at 400 °C reduced the resistivity of the films significantly due to the coalescence of grains and the lowest resistivity of 2 × 10⁻³ Ω cm is observed for 3 at.% (solution) Zr doped ZnO films which envisages that it is a good candidate for stable TCO material.     

Ene-sulfides as Reaction Partners of Organometallic Compounds

A comparison of the reactivity of ene-sulfides and en-ethers towards organometallic reagents reveals some remarkable differences. With the thio compounds metallation at the olefinic site next to the hetero atom dominates clearly over the alternative deprotonation of an allylic position. Only with propenyl phenyl sulfide both exchange modes were observed simultaneously, whereas with all higher homologues of it as well as vinyl phenyl sulfide the metal was exclusively attached to the olefinic α-carbon atom.     

Determination of boron at sub-ppm levels in uranium oxide and aluminum by hyphenated system of complex formation reaction and high-performance liquid chromatography (HPLC)

Boron, at sub-ppm levels, in U3O8 powder and aluminum metal, was determined using complex formation and dynamically modified reversed-phase high-performance liquid chromatography (RP-HPLC). Curcumin was used for complexing boron extracted with 2-ethyl-1,3-hexane diol (EHD). Separation of complex from excess reagent and thereafter its determination using the online diode array detector (DAD) was carried out by HPLC. Calibration curve was found to be linear for boron amounts in the sample ranging from 0.02 microg to 0.5 microg. Precision of about 10% was achieved for B determination in samples containing less than 1 ppmw of boron. The values obtained by HPLC were in good agreement with the data available from other analytical techniques. The precision in the data obtained by HPLC was much better compared to that reported by other techniques. The present hyphenated methodology of HPLC and complex formation reaction is interesting because of cost performance, simplicity, versatility and availability when compared to other spectroscopic techniques like ICP-MS and ICP-AES.     

Use of the Pictet-Spengler reaction for the synthesis of 1,4-disubstituted-1,2,3,4-tetrahydro-β-carbolines and 1,4-disubstituted-β-carbolines: formation of γ-carbolines

Microwave-assisted conjugate addition of indole on nitro-olefins furnished nitro compounds, which were reduced to tryptamines. Further, by using Pictet-Spengler condensation, new 1,4-disubstituted-1,2,3,4-tetrahydro-β-carbolines were synthesized in diastereoselective manner. Dehydrogenation of the tetrahydro-β-carbolines produced new 1,4-disubstituted-β-carbolines. As a new observation, in some of the cases, Pictet-Spengler condensation and dehydrogenation gave two products, namely 1,4-disubstituted-β-carbolines and 1,4-disubstituted-γ-carbolines. A mechanism is proposed for this observation.     

Hydrogen switches and sensors fabricated by combining electropolymerization and Pd electrodeposition at microgap electrodes

Here we describe a simple electrochemical approach to fabricate devices which behave as hydrogen sensors and switches. Devices fabricated by the electrodeposition of Pd directly across a 5 microm gap interdigitated array (IDA) of gold electrodes behaved as "hydrogen sensors". These devices had initial currents on the 10(-3) A level at -0.3 V and exhibited fast and reversible decreases in current in the presence of H(2) concentrations in a N(2) carrier gas with an average detection limit of 400 ppm. The current decrease is due to the formation of the more resistive PdH(x) in the presence of H(2). Devices fabricated by polyphenol electropolymerization on one set of electrodes and Pd electrodeposition on the other set behaved as "hydrogen switches". These devices displayed very low baseline currents of 10-100 pA at -0.3 V due to the presence of polphenol in the Electrode1/Pd/Polyphenol/Electrode 2 junction, and the current increased a remarkable 7-8 orders of magnitude in the presence of > or = 1.0% H(2) due to volume expansion upon PdH(x) formation, which leads to a direct connection between Pd (as PdH(x)) and Electrode 2 through the porous 4-10 nm thick polyphenol insulating film. The response and recovery time for the "hydrogen sensor" ranged from 20 to 60 s while that for the "hydrogen switch" ranged from 10 to >100 s. The response and recovery time generally decreased for the "hydrogen switch" as the number of polyphenol electrochemical cycles decreased.     

Growth and characterization of glycine picrate single crystal

Glycine picrate (GP), an organic material, was synthesized and successfully grown by solution growth method. Cell parameters of the grown crystals were obtained from the single crystal X-ray diffraction analysis and the presence of functional groups was identified by FTIR study. Its optical properties were examined by UV-vis-NIR analysis, which shows that the crystal is transparent between the wavelengths 400 nm and 1000 nm. Thermal analysis carried out for the glycine picrate reveals that the crystal exhibits a single sharp weight loss at 214 degrees C. The fluorescence spectrum of glycine picrate was recorded. The Vicker's microhardness values were measured for the grown crystal.     

Design and synthesis of bioactive 1,2-annulated adamantane derivatives

Adamantanopyrrolidines 8, 9 and 10, adamantanopyrrolidines 16 and 18, adamantanoxazolone 20, adamantanopyrazolone 23, adamantanopyrazolothione 24 and adamantanocyclopentanamine 32 were synthesized and tested for anti-influenza A virus and trypanocidal activity. The stereoelectronic requirements for optimal antiviral and trypanocidal potency were investigated. Pyrrolidine 16 proved to be the most active of the compounds tested against influenza A virus, being 4-fold more active than amantadine, equipotent to rimantadine and 19-fold more potent than ribavirin. Oxazolone 20 showed significant trypanocidal activity against bloodstream forms of the African trypanosome, Trypanosoma brucei, being approximately 3 times more potent than rimantadine and almost 50-fold more active than amantadine.     

Glutathione S-transferase inhibiting chemical constituents of Caesalpinia bonduc

Glutathione S-transferase inhibition assay-guided fractionations on the ethanolic extract of the bark of Caesalpinia bonduc resulted in the isolation of a new sterol, 17-hydroxy-campesta-4,6-dien-3-one (1) along with four known compounds, 13,14-seco-stigmasta-5,14-dien-3alpha-ol (2), 13,14-seco-stigmasta-9(11),14-dien-3alpha-ol (3), caesaldekarin J (4) and pipataline (5) as active constituents. Structures of compounds 1-5 were established on the basis of extensive NMR spectroscopic studies. The compounds (1-5) were isolated on the basis of their inhibitory activity against glutathione S-transferase, an enzyme that has been implicated in resistances during treatment of cancer and parasitic infections. Efforts to study structure-activity relationships of compounds 2 and 3 were also made by modifying their structures. The IC50 values of these compounds and their derivatives ranged from 57-380 microM and were compared to the inhibitory effects due to sodium taurocholate, an isoprene-derived GST inhibitor (IC50=398 microM). A plausible biosynthesis of 13,14-seco-steroids has also been proposed.     

Single- and two-photon properties of a dye-derivatized Roussin's red salt ester (Fe2(mu-RS)2(NO)4) with a large TPA cross section

The synthesis, characterization, photochemistry, and two-photon photophysical properties of a new dye-derivatized iron sulfur nitrosyl cluster Fe2(mu-RS)2(NO)4 (AFX-RSE, RS = 2-thioethyl ester of N-phenyl-N-(3-(2-ethoxy)phenyl)-7-(benzothiazol-2-yl)-9,9-diethyl-fluoren-2-yl-amine) were investigated. Under continuous photolysis, AFX-RSE decomposes with modest quantum yields (Phi(diss) = (4.9 +/- 0.9) x 10(-3) at lambda(irr) = 436 nm) as measured from the loss of the nitrosyl bands in the IR absorbance spectrum. Nitric oxide (NO) was qualitatively demonstrated to be photochemically produced via single-photon excitation through the use of an NO-specific electrode. Steady-state luminescence measurements have shown that AFX-RSE fluorescence is about 88% quenched relative to the model compound AF-tosyl. This is attributed to a relatively efficient energy transfer from the excited states of the antenna chromophores to the dinuclear metal center, with the subsequent production of NO. In addition, the two-photon absorption (TPA) cross sections (delta) were measured for the AF-chromophores via the two-photon excitation (TPE) photoluminescence technique using a femtosecond excitation source. The TPA cross section of AFX-RSE was found with this technique to be delta = 246 +/- 8 GM (1 GM = 10(-50) cm4 s photon(-1) molecule(-1)).