Investigation of self-association of the selected glycols on cellulose sorbents

A comparison was performed of the selected glycols, i.e., 1,2-ethanediol, 1,3-propanediol, 1,4-butanediol, and 1,5-pentanediol, in respect of their ability to form intramolecular hydrogen bonds. The following analytical techniques were employed: ir absorption spectroscopy and a new method taking advantage of chromatographic paper.     

RuO4-catalyzed oxidative polycyclization of squalene. Determination of the configuration of the penta-tetrahydrofuranyl diol product

The configuration of the penta-tetrahydrofuranyl diol (penta-THF) product obtained by a single-step, RuO₄-catalyzed oxidative polycyclization of squalene, has been determined as cis-threo-cis-threo-trans-threo-trans-threo-trans. The cis-cis-trans-trans-trans sequence for the five contiguous THF rings has been established through extensive 2D-NMR spectroscopic studies carried out both on the intact molecule and on some of its derivatives, including the oxidative cleavage products obtained by degradation of the penta-THF with PCC/AcOH. Four different chemical approaches were devised to determine each of the four threo relationships within each carbon pair connecting adjacent THF rings in the molecule. To this aim, studies have been carried out either on some intermediates of the process leading to penta-THF, obtained by stopping the oxidation of squalene prior to completion, or on a degradation product of the penta-THF, obtained from the latter through a bidirectional double oxidative degradation with PCC.     

Optically active polymer carbon nanotube composite

A completely soluble optically active polyaniline-multiwalled carbon nanotube composite was investigated by spectroscopic and microscopic techniques. It was found that the polymer's optical activity was retained in the presence of carbon nanotubes. Solutions were found to be easily processable into thin films, which exhibited dendritic structures only in the presence of nanotubes.     

Residue analysis of organophosphorus pesticides in animal matrices by dual column capillary gas chromatography with nitrogen-phosphorus detection

Organophosphorus pesticides (OPPs) were determined in matrices of animal origin by dual column capillary gas chromatography using nitrogen-phosphorus detection (NPD). This method was tested on cow milk and on liver and muscle of wild boar. The isolation of these pesticides was performed by liquid partition followed by cleanup with solid phase cartridge (SPE C18), after extraction from the matrix. The analytes identification was obtained by comparing the retention times in two columns with different polarity. The quantification of each OPP was obtained using parathion-ethyl as internal standard. The method was developed in a UNI EN ISO 9001:2000 certified laboratory. The recovery, investigated by analyzing samples spiked at 5, 10 and 50 ppb, ranged from 59 to 117% in milk, from 60 to 81% in liver and from 68 to 76% in muscle. The limit of quantification (LOQ) and limit of detection (LOD) were, respectively, 5 and 1 ppb for each compound and allowed quantifying the residues below the legal limits.     

Synthesis of novel tricyclic isoindole derivatives

Novel 3-methylene-2,5-dioxo-3H,9bH-oxazolo[2,3-a]isoindoles were prepared from the thermolysis of (3R,9bS)-5-oxo-2,3,5,9b-tetrahydrothiazolo[2,3-a]isoindole-3-carboxylic acids in acetic anhydride. The structure of 3-methylene-2,5-dioxo-3H,9bH-oxazolo[2,3-a]isoindole 6a was determined by X-ray crystallography.     

Capillary electrophoresis-mass spectrometry for the analysis of quaternary ammonium herbicides

Conditions for the simultaneous determination of the three herbicides paraquat, diquat and difenzoquat and the two plant growth regulators chlormequat and mepiquat by pressure-assisted capillary electrophoresis coupled to mass spectrometry (ion-trap) using electrospray as ionisation source have been established. A 200 mM formic acid-ammonium formate buffer solution at pH 3.0 with 50% of methanol was used as carrier electrolyte. Some capillary electrophoresis-mass spectrometry parameters such as sheath liquid and sheath gas flow-rates, sheath liquid composition, electrospray voltage andthe CE capillary position were optimised. The MS and MS-MS spectra of positive ions were studied in order to obtain structural information for the confirmation of the identity. The use of labelled standards allowed to confirm fragment ions assignation. The detection limits, based on a signal-to-noise ratio of 3:1, were between 0.5 and 2.5 mg l(-1) with hydrodynamic injection (10 s) and between 1 and 10 microg l(-1) with elecrokinetic injection (20 s, 10 kV) using standards in ultrapure water. Quality parameters such as linearity and run-to-run precision (n=6) were established. Quantitation was carried out using labelled standards. The method has been applied to the analysis of contaminated irrigation water and spiked mineral water samples.     

Role of surface oxygen groups in incorporation of nitrogen to activated carbons via ethylmethylamine adsorption

Coal origin and wood origin activated carbons were used in this study. To broaden the spectrum of surface features, the surface of the initial samples was modified using oxidation with nitric acid or impregnation with urea followed by heat treatment. Boehm and potentiometric titrations, thermal analysis, and sorption of nitrogen were used to characterize the pore structure and surface chemistry. Then adsorption of ethylmethylamine from aqueous solutions was carried out without controlling the pH of the carbon suspension. The isotherms were measured at 299 K and fitted to the Freundlich equation. The results showed that the amount of ethylmethylamine adsorbed on all carbons at a high concentration is dependent on the total number of surface groups whereas at low concentration it depends on the type of surface groups. The latter was observed exclusively for initial and oxidized carbons where acidic groups are present. The ethylmethylamine adsorption is mainly governed by dipole-dipole, hydrogen bonding, or specific acid-base interactions. Those interactions play a crucial role in incorporation of nitrogen to the carbon matrix at elevated temperatures.     

Expedient one-pot synthesis of novel chiral 2-substituted 5-phenyl-1,4-benzodiazepine scaffolds from amino acid-derived amino nitriles

An efficient and stereocontrolled synthesis of phenylalanine- and tryptophan-derived 5-phenyl-1,4-benzodiazepines is described. This new methodology involves, as a key step, the synthesis of 5-phenyl-2,3-dihydro-1H-1,4-benzodiazepines by a one-pot cyano reduction and reductive cyclization of the appropriate amino nitrile, which were obtained via a modified Strecker reaction of N-protected alpha-amino aldehydes with 2-aminobenzophenone and trimethylsilyl cyanide. The subsequent reduction of these 2,3-dihydro-1H-1,4-benzodiazepines, followed by regioselective alkylation or acylation at position 4, led to 2,4-disubstituted-5-phenyl-2,3,4,5-tetrahydro-1H-1,4-benzodiazepine.