Structure determination of salisomide and salisoflavan,two new secondary metabolites from Salsola imbricata,by 1D and 2D NMR spectroscopy

Chromatographic analysis of the alcoholic extract from Salsola imbricata yielded two new secondary metabolites, salisomide (1) and salisoflavan (2). Their structures were established with the help of spectroscopic techniques including COSY, HMQC and HMBC NMR experiments. Copyright © 2008 John Wiley & Sons, Ltd.     

Structure–reactivity relationships and the rate–determining step in the reactions of methyl salicylate with primary amines

The aqueous cleavage of methyl salicylate has been studied in the buffer solutions of various primary mono- and di-amines as well as secondary amines at 30°C. Both ionized (MS^?) and nonionized (MSH) methyl salicylate are reactive toward primary mono- and di-amines. The second-order rate constants for the reactions of MS^? with primary mono- and di-amines of pK_a > 9.4 exhibit Bronsted plot of slope (β_nuc) of 0.82. This high value of β_nuc is attributed to an intramolecular proton transfer in a thermodynamically unfavorable direction in the rate-determining step in a stepwise process for the formation of monoanionic tetrahedral intermediate. However, a concerted process for the formation of a monoanionic tetrahedral intermediate in the reactions of MS^? with amine nucleophiles wherein expulsion of leaving group is a rate-determining step is not completely ruled out. The α-effect nitrogen nucleophiles hydroxylamine and hydrazine reveal, respectively, ca. 10⁴- and 10³-fold higher reactivity compared to other amine nucleophiles of comparable basicity. The value of β_nuc of 1.03 obtained for the reactions of primary monoamines with MSH is ascribed to the expulsion of leaving group as the rate-determining step. The significantly lower value of β_nuc of 0.60 obtained in the reactions of MSH with both monoprotonated and unprotonated diamines is explained in terms of possible occurrence of intramolecular general acid-base catalysis. Intramolecular general base catalysis is responsible for the enhanced nucleophilic reactivity of primary amines toward MS^?. Dimethylamine, piperidine, morpholine, and piperazine have no detectable nucleophilic reactivity toward MS^?.     

Analysis of laser micro drilled holes through aluminium for micro-manufacturing applications

Conventional laser machining of aluminium with long wavelength lasers has its inherent problems due to the high reflectivity of aluminium to laser radiation (Handbook of Optics, vol 1, 2nd ed. New York: McGraw-Hill; 1995). Laser processing at shorter wavelengths reduces the reflectivity of the workpiece to the incident laser radiation and can also reduce the dimensions of the obtainable machining geometries. This paper reviews the limiting factors in the micro machining of aluminium using a diode pumped solid state (DPSS) Nd:YAG laser operated at 1064, 532, and 355 nm. The geometries of the laser-machined samples were investigated using interferometric, and optical methods to assess how the processing fluence and wavelength will affect the obtainable precision for successful integration of the laser in a micromachining CAD/CAM system.     

Application of H-point standard addition method and partial least squares to the simultaneous kinetic-potentiometric determination of hydrazine and phenylhydrazine

Simultaneous determination of hydrazine (HZ) and phenylhydrazine (PHZ) by H-point standard addition method (HPSAM) and partial least squares (PLS) regression was carried out based on kinetic data from novel potentiometry methods. The rate of chloride ion production in the reaction of HZ and PHZ with N-chlorosuccinimide (NCS) was monitored by a chloride ion-selective electrode. The experimental data show the good ability of ion-selective electrodes (ISEs) as detectors not only for the direct determination of chloride ion but also for simultaneous kinetic-potentiometric analysis using HPSAM and PLS methods. The methods are based on the differences observed in the production rate of chloride ions. The results show that simultaneous determination of HZ and PHZ can be performed in concentration ranges of 0.5 - 20.0 and 0.8 - 25.0 microg mL(-1), respectively. The total relative standard error for applying the PLS method to 8 synthetic samples in the concentration ranges of 1.0 - 16.0 microg mL(-1) for HZ and 2.0 - 16.0 microg mL(-1) for PHZ was 3.96. In order for the selectivity of the method to be assessed, we evaluated the effects of certain foreign ions upon the reaction rate and assessed the selectivity of the method. Both methods (PLS and HPSAM) were evaluated using a set of synthetic sample mixtures and then applied for simultaneous determination of HZ and PHZ in water samples.     

Microwave-assisted Oxidation of Alcohols and Polyarenes with Cetyltrimethylammonium Bromochromate

An efficient and mild methodology for oxidation of alcohols and polyarenes was described using cetyltrimethylammonium bromochromate (CTMABC) under microwave irradiation. Primary and secondary alcohols and polyarenes could be selectively oxidized under microwave irradiation into the corresponding aldehydes and ketones in high yields and short reaction time, using commercially available and magnetically retrievable oxidative material (CTMABC).     

Antimicrobial,Antioxidant, Anti-Acetylcholinesterase,Antidiabetic, and Pharmacokinetic Properties of Carum carvi L. and Coriandrum sativum L. Essential Oils Alone and in Combination

Herbs and spices have been used since antiquity for their nutritional and health properties, as well as in traditional remedies for the prevention and treatment of many diseases. Therefore, this study aims to perform a chemical analysis of both essential oils (EOs) from the seeds of Carum carvi (C. carvi) and Coriandrum sativum (C. sativum) and evaluate their antioxidant, antimicrobial, anti-acetylcholinesterase, and antidiabetic activities alone and in combination. Results showed that the EOs mainly constitute monoterpenes with γ-terpinene (31.03%), β-pinene (18.77%), p-cymene (17.16%), and carvone (12.20%) being the major components present in C. carvi EO and linalool (76.41%), γ-terpinene (5.35%), and α-pinene (4.44%) in C. sativum EO. In comparison to standards, statistical analysis revealed that C. carvi EO showed high and significantly different (p < 0.05) antioxidant activity than C. sativum EO, but lower than the mixture. Moreover, the mixture exhibited two-times greater ferric ion reducing antioxidant power (FRAP) (IC₅₀ = 11.33 ± 1.53 mg/mL) and equipotent chelating power (IC₅₀ = 31.33 ± 0.47 mg/mL) than the corresponding references, and also potent activity against 2,2-diphenyl-1-picrylhydrazyl (DPPH) (IC₅₀ = 19.00 ± 1.00 mg/mL), β-carotene (IC₅₀ = 11.16 ± 0.84 mg/mL), and superoxide anion (IC₅₀ = 10.33 ± 0.58 mg/mL) assays. Antimicrobial data revealed that single and mixture EOs were active against a panel of pathogenic microorganisms, and the mixture had the ability to kill more bacterial strains than each EO alone. Additionally, the anti-acetylcholinesterase and α-glucosidase inhibitory effect have been studied for the first time, highlighting the high inhibition effect of AChE by C. carvi (IC₅₀ = 0.82 ± 0.05 mg/mL), and especially by C. sativum (IC₅₀ = 0.68 ± 0.03 mg/mL), as well as the mixture (IC₅₀ = 0.63 ± 0.02 mg/mL) compared to the reference drug, which are insignificantly different (p > 0.05). A high and equipotent antidiabetic activity was observed for the mixture (IC₅₀ = 0.75 ± 0.15 mg/mL) when compared to the standard drug, acarbose, which is about nine times higher than each EO alone. Furthermore, pharmacokinetic analysis provides some useful insights into designing new drugs with favorable drug likeness and safety profiles based on a C. carvi and C. sativum EO mixture. In summary, the results of this study revealed that the combination of these EOs may be recommended for further food, therapeutic, and pharmaceutical applications, and can be utilized as medicine to inhibit several diseases.     

A study of optical absorption in some sodium titanium silicate glasses

A series of glass specimens was prepared from mixtures of SiO₂, TiO₂ and Na₂O, and their optical absorption coefficients measured as functions of photon energy in the range 2.1–3.3 eV. From the results, values of the optical energy gap are calculated and found to be dependent on the glass compositions. The results are analysed in terms of a mechanism of optical absorption arising from forbidden indirect transitions.     

Unroofing history of the Sillai Patti granite gneiss, Pakistan: constraints from zircon fission-track dating

A group of alkaline igneous rocks is exposed in the north of the Peshawar Plain, extending from Tarbela in the east up to Loe–Shilman near the Pakistan–Afghanistan border in the west. The alkaline rocks consist mainly of granites, syenites, gabbros, ijolites and carbonatites. Granitic gneisses of Paleozoic age are exposed at the Malakand and further westward at Sillai Patti. However, the fission-track dating studies on zircon, based on the present work, indicate that the age of the Sillai Patti granite gneiss is less than the absolute age of granite gneisses. Therefore, the zircon fission-track age of 24.28±2.97 Ma of the Sillai Patti granite gneiss, represents a time of post-metamorphic denudation history of the area, when these rocks passed through the 210°C isotherm, corresponding to a depth of about 6.7 km inside the earth's crust from their present position if a paleogeothermal gradient of 30°C/km is assumed to have prevailed. Our average fission-track zircon age of 24.28±2.97 Ma is very similar to the average fission-track zircon age of 25.4±0.7 Ma of Mansehra granites. Average cooling rates of the Mansehra and Sillai Patti granite gneisses have been computed to be (8.00±0.22)°C/Ma and (8.00±0.98)°C/Ma, while the average denudation rates of the Mansehra and Sillai Patti granite gneisses have been computed to be (0.262±0.007) and (0.274±0.034) mm/yr, respectively, on the basis of zircon fission-track ages for the period between 25 Ma and the present time. This indicates that the two complexes have experienced similar average cooling/uplift-induced denudation histories during the last 25 Ma or so.