2-[(R-phenyl)amine]-1,4-naphthalendiones as photosystem I electron acceptors: structure-activity relationship of m- and p-PAN compounds with QSAR analysis

Nineteen 2-[(R-phenyl)amine]-1,4-naphthalendione derivatives (PAN) were tested on spinach thylakoids for their activity as electron acceptors. These molecules act as photosystem I electron acceptors in the micromolar range. AC(50) values varied from 5 nM to 24 microM. QSAR analysis revealed a linear correlation of the m-PAN derivative log [1/AC(50)] with the energy difference of the LUMO and HOMO orbitals. The biological activity of p-PAN derivatives correlates linearly with structural parameters. Electron affinity is being the most important. The half wave I potential values (E(1/2)) of PAN compounds (from -213 to -569 mV vs. NHE) match with the mid-point potentials of the A(0) to F(X) niche of PSI electron transport carriers. The logP values of PAN derivatives were 3.35 and 3.88, indicating that they are hydrophobic compounds. Therefore PAN compounds accept electrons at the hydrophobic A(0) to F(X) niche of PSI.     

Chemoenzymatic and yeast-catalysed synthesis of diastereomeric ethyl γ-phenyl and γ-(n-pyridyl)paraconates

The synthesis of γ-phenyl and γ-(n-pyridyl)paraconates was accomplished by chemical reduction of their respective ketodiester precursors followed by cyclisation of the resulting hydroxy diester intermediates. The cis- and trans-lactones thus obtained were separated and separately subjected to enzymatic hydrolysis with HLAP. The cis-lactonic esters had enantiomeric excesses ranging from 94% to 99%, while for the trans-isomers the ee’s ranged from 80% to 93%. The same ketodiester precursors were subjected to reduction with a series of yeasts. The absolute configuration of trans-(−)-2-pyridyl paraconic acid was assigned by means of X-ray analysis of its hydrobromide salt, while the absolute configurations of the other lactones were determined via analysis of their respective CD curves.     

Unique intermolecular reaction of simple porphyrins at a metal surface gives covalent nanostructures

Deposition of a porphyrin onto metallic copper followed by heating leads to an unprecedented type of linking of the molecules giving a mixture of covalent multiporphyrin nanostructures at the surface.     

Quality control of Amazonian cocoa (<Emphasis Type="Italic">Theobroma cacao</Emphasis> L.) by-products and microencapsulated extract by thermal analysis

The mineralogical characterization and pyrolysis kinetics of raw oil shale from Moroccan Rif region and the corresponding bitumen-free material were investigated using various analytical techniques. The structural analysis results showed the siliceous character of mineral matrix and the presence of complex organic components in both oil shales studied. Non-isothermal pyrolysis kinetic measurements indicated that bitumen-free oil shale exhibits a single behavior pyrolysis in the oil-producing stage as compared to raw oil shale. The activation energies estimated by using isoconversional methods reveal that the pyrolysis reaction occurred by one-step kinetic process. The kinetic parameters, determined from a nonlinear fitting method using various kinetic models g(α) and iterative Kissinger–Akahira–Sunose energy calculations, reveal that the pyrolysis mechanism is well described by the nth order kinetics (Fn), with n = 1.071, for bitumen-free oil shale, and n = 1.550, for kerogen of raw oil shale. The mechanism of the whole pyrolysis process of raw oil shale seems not to be affected by the elimination of bitumen, but only some kinetic changes have been recorded in the reaction order mechanism. The process pyrolysis is represented by independent reactions and consequently considered as parallel processes. Besides, the thermodynamic functions of activated complexes (?S ^≠ , ?H ^≠ and ?G ^≠) were also calculated and the pyrolysis is found as non-spontaneous process in agreement with the thermal analysis data.     

Technology of production of red figure pottery from Attic and southern Italian workshops

Samples from Greek figure vases were investigated by scanning electron microscopy coupled with energy dispersive X-ray analysis, X-ray diffraction, thermomechanical analysis and reflectance spectroscopy to achieve a technological characterisation. The vases, dating from the end of the sixth to the fourth century BC, had been excavated at Locri Epizephiri (Calabria, Italy) and attributed to Attic or local workshops, respectively. Information on the morphology of black slip areas and firing temperatures was compared with that previously obtained for Attic and local black gloss pottery from the same site; results show that the peculiar technique required for the production of black slips was mastered by both Attic and local potters and employed for monochrome and figured products. The black coating is usually well vitrified and 15- to 20-m thick; the evaluated maximum firing temperature is around 900°C, while a temperature lower than 800°C is generally estimated for ceramic body re-oxidation.     

Automated headspace solid-phase dynamic extraction to analyse the volatile fraction of food matrices

High concentration capacity headspace techniques (headspace solid-phase microextraction (HS-SPME) and headspace sorptive extraction (HSSE)) are a bridge between static and dynamic headspace, since they give high concentration factors as does dynamic headspace (D-HS), and are as easy to apply and as reproducible as static headspace (S-HS). In 2000, Chromtech (Idstein, Germany) introduced an inside-needle technique for vapour and liquid sampling, solid-phase dynamic extraction (SPDE), also known as "the magic needle". In SPDE, analytes are concentrated on a 50 microm film of polydimethylsiloxane (PDMS) and activated carbon (10%) coated onto the inside wall of the stainless steel needle (5 cm) of a 2.5 ml gas tight syringe. When SPDE is used for headspace sampling (HS-SPDE), a fixed volume of the headspace of the sample under investigation is sucked up an appropriate number of times with the gas tight syringe and an analyte amount suitable for a reliable GC or GC-MS analysis accumulates in the polymer coating the needle wall. This article describes the preliminary results of both a study on the optimisation of sampling parameters conditioning HS-SPDE recovery, through the analysis of a standard mixture of highly volatile compounds (beta-pinene, isoamyl acetate and linalool) and of the HS-SPDE-GC-MS analyses of aromatic plants and food matrices. This study shows that HS-SPDE is a successful technique for HS-sampling with high concentration capability, good repeatability and intermediate precision, also when it is compared to HS-SPME.     

Reliability of fibres in solid-phase microextraction for routine analysis of the headspace of aromatic and medicinal plants

This article evaluates the HS-SPME recovery repeatability, intermediate precision and their performance over time when applied to HS-SPME sampling for quality control of medicinal and aromatic plants. Experiments were carried out on two sets of fibres coated with two different coatings and belonging to different lots (i.e 100 microm polydimethylsyloxane (PDMS) and Carboxen/divinylbenzene/PDMS 50/30 microm, l: 1 cm (CAR/DVB/PDMS)) and on chamomile (Matricaria chamomilla L.), sage (Salvia lavandulifolia Vahl.) and a standard solution containing 3-hexanol, isoamyl acetate, 1,8-cineole and menthol in diisobutyl phthalate. The performance of each set of fibres was evaluated by determining a group of complementary statistical parameters including: (i) repeatability of the absolute areas of each marker from each matrix with each fibre; (ii) intra-fibre repeatability of the total absolute areas of the markers of each matrix obtained with each fibre of each set; (iii) inter-fibre intermediate precision of the total absolute areas of the markers of each matrix obtained with all fibres of each set; and (iv) analysis of variance by one-way ANOVA with Fisher and Tukey tests. The influence of the number of analyses on fibre effectiveness (fibre life-time) was studied by linear regression analysis (LRA). The results proved that HS-SPME can successfully be used for routine control analysis of aromatic ad medicinal plants since both types of fibres showed good repeatability and intermediate precision of analytes recovery and consistency over time. Unlike data previously reported by other authors, CAR/DVB/PDMS coated fibres gave better results than those coated with PDMS. The fibre-life seemed mainly to be influenced by the number and conditions of samplings and nature of the matrix investigated.     

A Determination of Standard Potentials and Related Primary pH Standards in the 50 Mass Percent (N-Methyl-2-Pyrrolidinone + Water) Mixture at Various Temperatures

Following the IUPAC-endorsed procedure, the primary pH standards offered by the equimolal phosphate buffer (Na₂HPO₄ (0.01 mol⋅kg⁻¹) + KH₂PO₄ (0.01 mol⋅kg⁻¹)) in the (N-methyl-2-pyrrolidinone + water) solvent mixture of 50 mass percent composition at various temperatures have been determined from potential difference measurements with the reversible Harned cell. Since the essential prerequisite of the above procedure is the knowledge of the (hitherto unknown) standard potential difference of Harned’s cell, a parallel supplementary series of potential difference measurements has been carried out with the reversible cell, Pt|H₂|HCl(m)|AgCl|Ag|Pt according to the classical thermodynamic procedure. The problem of comparability of the pH scale in the (N-methyl-2-pyrrolidinone + water) solvent with that in the pure water solvent is duly discussed in terms of primary medium effects.     

Conventional and narrow bore short capillary columns with cyclodextrin derivatives as chiral selectors to speed-up enantioselective gas chromatography and enantioselective gas chromatography-mass spectrometry analyses

The analysis of complex real-world samples of vegetable origin requires rapid and accurate routine methods, enabling laboratories to increase sample throughput and productivity while reducing analysis costs. This study examines shortening enantioselective-GC (ES-GC) analysis time following the approaches used in fast GC. ES-GC separations are due to a weak enantiomer-CD host-guest interaction and the separation is thermodynamically driven and strongly influenced by temperature. As a consequence, fast temperature rates can interfere with enantiomeric discrimination; thus the use of short and/or narrow bore columns is a possible approach to speeding-up ES-GC analyses. The performance of ES-GC with a conventional inner diameter (I.D.) column (25 m length x 0.25 mm I.D., 0.15 microm and 0.25 microm d(f)) coated with 30% of 2,3-di-O-ethyl-6-O-tert-butyldimethylsilyl-beta-cyclodextrin in PS-086 is compared to those of conventional I.D. short column (5m length x 0.25 mm I.D., 0.15 microm d(f)) and of different length narrow bore columns (1, 2, 5 and 10 m long x 0.10 mm I.D., 0.10 microm d(f)) in analysing racemate standards of pesticides and in the flavour and fragrance field and real-world-samples. Short conventional I.D. columns gave shorter analysis time and comparable or lower resolutions with the racemate standards, depending mainly on analyte volatility. Narrow-bore columns were tested under different analysis conditions; they provided shorter analysis time and resolutions comparable to those of conventional I.D. ES columns. The narrow-bore columns offering the most effective compromise between separation efficiency and analysis time are the 5 and 2m columns; in combination with mass spectrometry as detector, applied to lavender and bergamot essential oil analyses, these reduced analysis time by a factor of at least three while separation of chiral markers remained unaltered.     

Steric and Electronic Effects on the Configurational Stability of Residual Chiral Phosphorus‐Centered Three‐Bladed Propellers: Tris‐aryl Phosphanes

A series of tris‐aryl phosphanes, structurally designed to exist as residual enantiomers or diastereoisomers, bearing substituents differing in size and electronic properties on the aryl rings, were synthesized and characterized. Their electronic properties were evaluated on the basis of their electrochemical oxidation potential determined by voltammetry. The configurational stability of residual phosphanes, evaluated by dynamic HPLC on a chiral stationary phase or/and by dynamic ¹H and ³¹P NMR spectroscopy, was found to be rather modest (barriers of about 18–20 kcal mol^?1), much lower than that shown by the corresponding phosphane oxides (barriers of about 25–29 kcal mol^?1). For the first time, the residual antipodes of a tris‐aryl phosphane were isolated in enantiopure state and the absolute configuration assigned to them by single‐crystal anomalous X‐ray diffraction analysis. In this case, the racemization barrier could be calculated also by CD signal decay kinetics. A detailed computational investigation was carried out to clarify the helix reversal mechanism. Calculations indicated that the low configurational stability of tris‐aryl phosphanes can be attributed to an unexpectedly easy phosphorus pyramidal inversion which, depending upon the substituents present on the blades, can occur even on the most stable of the four conformers constituting a single residual stereoisomer.