Capillary electrophoretic-ultraviolet method for the separation and estimation of zineb, maneb, and ferbam in food samples

A simple and sensitive capillary electrophoretic method with ultraviolet detection has been developed for the separation and determination of ferbam [iron(III)-dimethyldithiocarbamate], maneb [manganese(II)-ethylenebisdithiocarbamate] and zineb [zinc(II)-ethylenebisdithiocarbamate], in borate buffer, after their acidic decomposition and complexation with CDTA (trans-1,2-diaminocyclohexane-N,N,N',N'-tetraacetic acid monohydrate), as CDTA-metal complexes of Fe+3, Mn +2, and Zn+2. The determination is dependent on the pH and the nature of the buffer solutions. In this method, the detection limit (signal-to-noise ratio = 3) is 0.0013, 0.0022, and 0.0023 mM for ferbam, maneb, and zineb, respectively. The relative standard deviation for the analysis of 1 mM of each was found to be 1.5 +/- 0.2%. The method was successfully applied for the analysis of red beans and grain samples spiked with ferbam, maneb, and zineb. The applicability of capillary electrophoresis as a useful tool for the simultaneous determination and analysis of ferbam, maneb, and zineb is demonstrated.     

Ring-closing metathesis of sulfoximine-substituted N-tethered trienes: modular asymmetric synthesis of medium-ring nitrogen heterocycles

A synthesis of sulfoximine-substituted medium-ring nitrogen heterocycles (MRNHs) having a high degree of substitution has been developed. Its key steps are the modular asymmetric synthesis of sulfoximine-substituted N-tethered trienes and their Ru-catalyzed ring-closing metathesis (RCM) reaction. The highly substituted N-tethered trienes were obtained enantio- and diastereopure through 1) the diastereoselective aminoalkylation of sulfoximine-substituted allyltitanium complexes with N-tert-butylsulfonyliminoester, 2) N-allylation of homoallylic N-sulfonyl amines, 3) allylation, hydroxylalkylation, and formylation of α-lithioalkenylsulfoximines, and 4) allylation of α-formylalkenylsulfoximines. The Ru-catalyzed RCM reaction of the sulfoximine-substituted 1,7,10- and 1,7,12-trienes stereoselectively afforded the corresponding nine-, ten-, and eleven-membered MRNHs in good yields. An interesting difference in reactivity was noted in the case of a sulfoximine-substituted 1,7,10-triene and its corresponding 1,10-diene. While the triene readily underwent a RCM reaction, the diene reacted only in the presence of Ti(OiPr)(4) under formation of the corresponding MRNH. The feasibility of a removal of the sulfoximine auxiliary and the N-sulfonyl protecting group from the MRNHs were demonstrated through reduction and cleavage, respectively, of a nine-membered heterocycle, both of which proceeded readily and gave the corresponding cyclic alkene and amine, respectively.     

Steady state self-focusing, self-modulation of laser beam in an inhomogeneous plasma

Laboratory as well as PIC simulation experiments reveal strong flow of energetic electrons co-moving with laser beam in laser plasma interaction. Equation governing the evolution of complex envelope in slowly varying envelope approximation is nonlinear parabolic equation. Variational approach is used to solve this problem and a Lagrangian for the problem is set up. Assuming a trial Gaussian profile, authors solve the reduced Lagrangian problem for beam width and curvature. Two scale lengths for inhomogenity along the direction of propagation, one for nonlinearity and other for diffraction management are introduced. Self-focusing, self-modulation as well as self-trapping of the laser-electron-beam plasma system is studied under variety of parameters.     

Cloud Point Studies of Tween and Glycol in the Presence of Salts

This article deals with the cloud point studies of ethoxylated sorbitan ester, Tween in the presence of glycols, and salts. Cloud point temperature of Tween 20 (5 mol dm^?3) and Tween 80 (1 mol dm^?3) has been determined in the presence of various salts in addition to glycols. The glycols chosen for these studies were triethylene glycol (TEG), and ethylene glycol mono butylether (EGMBE). At concentration below 0.02 M these salts have no significant effect on cloud point temperature in all cases. The cloud point temperature of Tween+TEG and Tween+EGMBE found to decrease in the presence of sodium chloride (NaCl) and potassium chloride (KCl). The cloud point temperature of Tween 20 + TEG and Tween 20 + EGMBE found to increase in the presence of urea and nicotinamide. The change in cloud point was found to be more in case of nicotinamide as compare to urea. The influence of an additive on the cloud point depends on how it affects the intermicellar interactions. An effort has been made to understand the interaction between solvent and additives leading to a change in solubility of Tween.     

Effect of various additives on the performance of a newly developed PVC based potentiometric sensor for anionic surfactants

A new poly(vinyl chloride) PVC membrane electrode to determine monomer concentrations of dodecylbenzenesulphonate ions (DBS⁻) based on a neutral ion-pair carrier complex of dodecyltrimethylammonium–dodecylbenzenesulphonate (DTA⁺–DBS⁻), is reported here. The electrode exhibits a slope of 51.25 mV per decade for DBS⁻ ions. The DBS⁻ ion selective electrode (ISE) can determine monomer units down to concentrations as low as 3.32 × 10⁻⁴ M. The effect of three kinds of additives, i.e. alcohols, glycols and triblock polymers on the performance of the surfactant selective electrode is studied systematically. The effect of foreign anions along with primary ions on the performance of ion-selective electrode is investigated in terms of potentiometric selectivity coefficients, which were determined using the fixed interference method (FIM) at 1.0 × 10⁻² M concentration of foreign anions. The sensor responds well to the surfactant ions in the presence of additives at lower concentration. The Gibbs free energy of micelle formation (ΔG_m) of sodium dodecylbenzenesulphonate (SDBS) in the presence of various additives is calculated and found to vary differently with respect to the increase in the amount of additives. The sensor worked in the acidic pH range with a short response time of 30 s. The lifetime of the sensor is more than three months. The sensor was further used to determine the amount of DBS⁻ in local detergents. This method of determining anionic surfactants was found to be quite accurate when compared with classical methods.     

Investigation of Silver(I) Ion Sensing Property of Ruthenium(II) Thiosemicarbazone Complex Using Coated Graphite and Polymeric Membrane Electrodes

A ruthenium(II) complex [Ru(PPh₃)₂(pytsc)₂] {Hpytsc = pyridine‐2‐carbaldehydethiosemicarbazone, (C₅H₅N)C²(H)=N³‐N²(H)‐C¹(=S)N¹H} has been used as an ion carrier for the selective determination of silver(I) ions in solution. Silver(I) ion‐selective coated graphite based (CGE) and PVC polymeric membrane based (PME) electrodes exhibit Nernstian slope for silver(I) ions over a wide concentration range from 1.0 × 10⁻¹ M to 5.0 × 10⁻⁶ M (with CGE) and 1.0 × 10⁻¹ M to 2.0 × 10⁻⁵ M (with PME). The working pH range of these electrodes has been found to be from 1.2 to 7.2 for CGE and 2.2 to 6.5 for PME. The proposed CGE sensor exhibits better analytical features like sensitivity and selectivity towards different secondary ions in comparison to the corresponding PME with no interference from mercury(II) ions . These electrodes also act as indicator electrodes in potentiometric titration and have been successfully used for the determination of silver content in solution of real samples (1 gm dissolved in 100 mL of dilute nitric acid) such as silver ornaments and thin silver foils. Silver content determined by the use of ion selective electrode was found to vary in the concentration range from 1.20 x 10⁻² M to 7.45 x 10⁻² M and results were found to be comparable with those obtained from the traditional volumetric method of analysis. It is the first report of a metal‐ligand complex used as an ion carrier in ion selective electrode, which is selective for a metal ion other than the one used in the complex.     

Simultaneous quantification of withanolides in Withania somnifera by a validated high-performance thin-layer chromatographic method

This paper describes a sensitive, selective, specific, robust, and validated densitometric high-performance thin-layer chromatographic (HPTLC) method for the simultaneous determination of 3 key withanolides, namely, withaferin-A, 12-deoxywithastramonolide, and withanolide-A, in Ashwagandha (Withania somnifera) plant samples. The separation was performed on aluminum-backed silica gel 60F254 HPTLC plates using dichloromethane-methanol-acetone-diethyl ether (15 + 1 + 1 + 1, v/v/v/v) as the mobile phase. The withanolides were quantified by densitometry in the reflection/absorption mode at 230 nm. Precise and accurate quantification could be performed in the linear working concentration range of 66-330 ng/band with good correlation (r2 = 0.997, 0.999, and 0.996, respectively). The method was validated for recovery, precision, accuracy, robustness, limit of detection, limit of quantitation, and specificity according to International Conference on Harmonization guidelines. Specificity of quantification was confirmed using retention factor (Rf) values, UV-Vis spectral correlation, and electrospray ionization mass spectra of marker compounds in sample tracks.     

HPTLC Densitometric Quantification of Hydrolyzable Tannins from Triphala churna

JPC – Journal of Planar Chromatography – Modern TLC - A simple high-performance thin-layer chromatographic (HPTLC) method has been established for simultaneous quantification of...     

Increased Availability of Tryptophan in 5-Methyltryptophan-Tolerant Shoots of Catharanthus roseus and Their Postharvest in vivo Elicitation Induces Enhanced Vindoline Production

Ten 5-methyltryprophan (5-MT)-resistant multiple shoot culture lines in three genotypes of Catharanthus roseus were selected in vitro. The variant shoot lines displayed a differential threshold tolerance limit against the analogue stress, ranged from 20 to 70?mg/l 5-MT in the medium. The lines tolerant to 40?mg/l 5-MT stress were most stable and fast proliferating. All the selected lines in the presence of 5-MT stress recorded increased level of tryptophan in their free amino acid pool. Highest tryptophan accumulation occurred in lines P40, P30, D40, and N40 (i.e., 296.5, 241.0, 200.6, and 202.0???g/g dry wt., respectively). A concomitant increase in the total alkaloid content (2.3?C3.8?% dry wt.) under the analogue stress was also noticed in these lines when compared to 1.0?C1.58?% dry wt. in the respective wild-type shoot maintained on a stress-free medium. The HPLC analysis of the alkaloid extracts of the 5-MT-tolerant lines grown under analogue stress also revealed vindoline as a major constituent with maximum accumulation in lines N40, N30, D30, D40, and P40 (0.046, 0.032, 0.034, and 0.022?% dry wt., respectively). The rooted shoots of 5-MT-tolerant lines were successfully acclimatized under glasshouse environment wherein they grew normally and set seeds. Flowering twigs or leaves excised from 1-year-old glasshouse-grown plants of 5-MT variant lines upon postharvest in vivo elicitation with 30?mg/l 5-MT or 5.0?mg/l tryptophan registered an eight-to-tenfold increment in their vindoline content within 24?C48?h.     

An Efficient and Simple One-Pot Synthesis of Novel 2-Amino-5-aza-6-(dinitrilomethylene)-4,7,7-trimethylbicyclo[2.2.2]octane-1,3-dicarbo-nitrile and its Crystal Structure

Abstract  

The title compound was prepared by the reaction of 4-methyl-pent-3-en-2-one and malononitrile, at room temperature, in the presence of indium-triflate and triethylamine. The structure of the molecule was established by spectral analysis and X-ray diffraction studies. The compound crystallizes in the monoclinic space group C2/c with unit cell parameters: a = 14.269 (2), b = 10.141 (2), c = 19.743 (3) ?, β = 95.523(4)°, Z = 8. The crystal structure was solved by direct methods and refined to R = 0.0526 for 2,690 observed reflections. The isoquinuclidine rings adopt boat conformation. The molecules in the unit cell are arranged in layers. The crystal structure is stabilized by N–H⋯N interactions.