Electrochemical studies on surfactant-modified cellulose acetate membrane

The possibility of electrochemical modification of cellulose acetate membrane upon immobilization of the anionic surfactant (SDS) has been explored on the basis of membrane potential studies. Surface tension measurements with and without cellulose acetate membrane were carried out to ascertain the extent of immobilization of the surfactant. Cellulose acetate membrane practically does not exhibit any ion selectivity. However, modified membrane exhibits cation selectivity which varies with concentration of the surfactant till its critical micelle concentration is reached. An attempt has also been made to demonstrate correspondence between the immobilized surfactant and the permselectivity of the membrane.     

Plasma treatment of polyester fabric to impart the water repellency property

Polyester fabric is treated with DCDMS solution by two methods: dipping the fabric directly in DCDMS solution for different intervals and dipping the fabric in DCDMS solution after its exposure into RF plasma chamber for different durations at optimized exposure power conditions. The physical properties of polyester fabric treated with DCDMS in the presence or absence of air plasma have been compared with control fabric. Different characterization techniques like scanning electron microscope, attenuated total reflectance-IR and Dataflash 100 colour measurement spectrophotometer are used to assess the surface morphology, composition and change in colour parameters. Water repellency property of both untreated and modified polyester fabric is studied using AATCC test method 39 (1971). The effectiveness of the water repellency property of modified polyester fabric is checked by repeated washing up to ten cycles. This article was presented at the Second International Conference on the Frontiers of Plasma Physics and Technology, 21–25 February 2005, Goa, India.     

UV excitable Y2? x ? y Gd y SiO5:Ce x phosphors for cool white light emission

Cool white light was realized in Y_2−x−y Gd _x SiO₅: Ce _y phosphor under near UV excitation, due to the occupation Ce³⁺ in Y³⁺ 1st and 2nd site, synthesized using solid state carbothermal reduction route. SEM with elemental analysis show the existence of Gd in Y₂SiO₅:Ce enhances the particles size in comparison to Y₂SiO₅:Ce phosphors alone. Gd³⁺ (0.00≤x≤0.75) and Ce³⁺ (0.02≤y≤0.10) concentration was optimized to 0.50 and 0.08 in Y₂SiO₅, respectively. The CIE chromaticity color coordinates (0.24, 0.20) are close to cool white light value which could be useful for the fabrication of cool white LED.     

Synthesis and characterization of cadmium selenide nanostructures on porous aluminum oxide templates by high frequency alternating current electrolysis

We have successfully deposited nanostructured cadmium selenide (CdSe) inside anodic aluminum oxide (AAO) templates from aqueous electrolyte containing cadmium sulfate, selenium oxide and mercuric chloride by using high frequency alternating current (19 V_rms, 200 Hz). Addition of mercury ions aids in the deposition of CdSe inside anodic oxide pores. Scanning and transmission electron microscopy studies of the deposit etched in phosphoric acid showed the presence of end standing nanostrips. Energy dispersive X-ray analysis of the deposit confirmed the presence of cadmium and selenium in the deposit. X-ray diffraction (XRD) studies of the deposit showed small but broad diffraction peaks consistent with the presence of hexagonal CdSe. Optical studies revealed blue shift in band gap energy due to quantum confinement.     

A Novel Synthesis of Berbines- Condensation of 2-(3,4-Dimethoxyphenyl) Ethyl Bromide with 1,4-Dihydro-6,7-Dimethoxy-3 (2H) Isoquinolone-Synthesis of (+)-Xylopinine

Recently we reported an efficient synthesis of the berbine alkaloids^3,4 by the use of the bromo esters⁵ prepared from 3-isochromanones. Now a new general synthetic route to the berbine alkaloids beginning with the condensation of the phenethylbromide 3 and 3-(2H) isoquinolone 2 is being described. The method gains added advantage of placing desired substitution on both rings A and D of the berbine, emerging from the easy availability of the starting compounds. In conclusion, the present results have not only added one more efficient example to more than a dozen successful procedures of the berbine synthesis⁶ but also offer a potential route to the structurally parallel indoloquinolizidine alkaloids.     

Asymmetric routes to pentadec-1-en-4-ol: application to the syntheses of aculeatins F and epi-F, (R)- and (S)-5-hexadecanolide and a formal synthesis of solenopsin

A short and simple route to the synthesis of pentadec-1-en-4-ol, an important synthetic building block for the aculeatins F and epi-F, insect pheromone 5-hexadecanolide, solenopsin and various other natural products has been developed via proline-catalyzed α-aminoxylation of an aldehyde and hydrolytic kinetic resolution of a terminal epoxide. While the synthesis of aculeatins F and epi-F has been accomplished using a PIFA promoted oxidative spirocyclization/dithiane deprotection reaction sequence and linchpin coupling as key steps, the synthesis of hexadecanolide and a formal synthesis of solenopsin was performed using ring-closing metathesis (RCM) as key step.     

Validated HPTLC method for the simultaneous quantification of diterpenoids in Vitex trifolia L.

Vitex trifolia L. is an important Indian medicinal plant with diverse pharmacological properties. In a recent study, we reported the isolation and antitubercular activity evaluation of three new diterpenoids from its leaves; here we have developed a validated rapid, simple, precise, and accurate high‐performance TLC method for the simultaneous quantification of isolated diterpenoids in V. trifolia. Diterpenoids, 6α,7α‐diacetoxy‐13‐hydroxy‐8(9),14‐labdadien ( A ), 13‐hydroxy‐5(10),14‐halimadien‐6‐one ( B ), and 9‐hydroxy‐13(14)‐labden‐16,15‐olide ( C ) were separated on silica gel 60F₂₅₄ high‐performance TLC plates using chloroform/acetone (98:2, v/v) as mobile phase. The quantitation of diterpenoids was carried out using densitometric reflection/absorption mode at 610 nm after postchromatographic derivatization using a vanillin/sulfuric acid reagent. A precise and accurate quantification can be performed for compounds A and B in the linear working concentration range of 333–1000 ng/band and for C in the range of 670–2000 ng/band with good correlations (r = 0.9984, 0.9991, and 0.9994, respectively). The method was validated for peak purity, precision, accuracy, robustness, LOD, and LOQ, as per the ICH guidelines. The method reported here is simple, reproducible and may be applied for the quantitative analysis of the above diterpenoids in the leaves of V. trifolia.     

A Novel Synthesis of the Yohimbane Skeleton-Course of the Synthesis of 15,16,17,18,19,20-Hexadehydroyohimbane by Use of Palladium Catalyzed Insertion of Carbon Monoxide

In the course of our continuing synthetic experiments on benzoquinolizidine² and indoloquinolizidine alkaloids³, we have recently utilized palladium catalyzed amidation⁴ for the synthesis of the berbine alkaloids⁵. In this present paper we wish to report, what we believe is the first successful utilization of the palladium catalyzed amidation for the synthesis of the hexadehydroyohimbane skeleton.     

Catalyst-free synthesis of 3-substituted-3-hydroxy-2-oxindoles by reaction of isatin and cyclic enaminone in water

An easy protocol for the synthesis of enaminone attached 3-substituted-3-hydroxy-2-oxindoles has been demonstrated by reaction of isatin and cyclic enaminone in water. The developed catalyst-free reaction has the advantage of being atom-economical, eco-friendly, and benign reaction conditions. The broader substrate scope, experimentally simple procedures, and easy purification of products with high yield further make this method attractive and useful.