The solution photochemistry of αβ-unsaturated sulphones

1-Phenyl-2-(benzenesulphonyl)-ethylene and 1-phenyl-2-(benzenesulphonyl)-prop-1-ene have been shown to undergo $\text{Z}$,$\text{E}$-photoisomerisation, whereas 2-benzenesulphonylindene readily forms [_π2 + _π2] photoadducts with 2,3-dimethylbut-2-ene, cyclopentene, and cyclohexene.     

Thermal and mass spectrometric fragmentation of esters of deuterated long chain carboxylic acids

A method combining thermal fragmentation and mass spectrometry for the determination of the position of double bonds in an unsaturated ester is presented. The thermal fragmentation of methyl esters of deuterated long chain carboxylic acids yields a homologous series of olefins plus a homologous series of unsaturated esters. The positions of the deuterium atoms in the original ester are revealed by the deuterium content of its fragments as determined by mass spectrometry. Therefore, the positions of double bonds of a polyunsaturated acid can be determined by pyrolysis after saturation by deuterium. The structures of the unsaturated fragments are ascertained by mass spectrometric method, and the formation of the ion [M – 32] in the mass spectrometric fragmentation of unsaturated methyl esters is studied by means of deuterium labeling.     

Spectrophotometric determination of aromatic primary amines and nitrite by flow injection analysis

Aromatic primary amines are determined by injection into dilute hydrochloric acid carrier which merges sequentially with 4-N-methylaminophenol and dichromate. The purple-red color formed by oxidative coupling of amines with 4-N-methylaminophenol is measured at 530 nm. In contrast to the manual procedure, the flow-injection procedure avoided errors arising from the instability of the coupling intermediate, oxidation of the amine, and too great an excess of the oxidant. The method improves the selectivity for certain amines in the presence of those which are sterically hindered or have an electron-deficient aromatic nucleus. Nitrite is determined by diazotization of sulfanilamide and quantifying the residual sulfanilamide by oxidative coupling. The sample thourghout for the assay of amines (0.05–20 μg ml^?1 NH₂-N) and nitrite (1–10 μg ml^?1 NO₂^--N) was 120 h^?1. A system for the consecutive determination of aromatic primary amines and nitrite is decribed.     

A hybrid level set method for modelling detonation and combustion problems in complex geometries

We present an accurate and fast wave tracking method that uses parametric representations of tracked fronts, combined with modifications of level set methods that use narrow bands. Our strategy generates accurate computations of the front curvature and other geometric properties of the front. We introduce data structures that can store discrete representations of the location of the moving fronts and boundaries, as well as the corresponding level set fields, that are designed to reduce computational overhead and memory storage. We present an algorithm we call stack sweeping to efficiently sort and store data that is used to represent orientable fronts. Our implementation features two reciprocal procedures, a forward ‘front parameterization’ that constructs a parameterization of a front given a level set field and a backward ‘field construction’ that constructs an approximation of the signed normal distance to the front, given a parameterized representation of the front. These reciprocal procedures are used to achieve and maintain high spatial accuracy. Close to the front, precise computation of the normal distance is carried out by requiring that displacement vectors from grid points to the front be along a normal direction. For front curves in two dimensions, a cubic interpolation scheme is used, and G ¹ surface parameterization based on triangular patches is used for the three-dimensional implementation to compute the distances from grid points near the front. To demonstrate this new, high accuracy method we present validations and show examples of combustion-like applications that include detonation shock dynamics, material interface motions in a compressible multi-material simulation and the Stephan problem associated with dendrite solidification.     

Finite-difference solution of the united atom,one-centre expansion for H2 +

An analytical expression of dipolar absorption, obtained by truncating the memory function hierarchy to the first order is compared to experimental results on Furan and Chloroform at different temperatures. The proposed method permits the prediction of the form of the correlation functions if the high frequencies absorption spectrum only, is known.     

Differentiation of Escherichia coli serotypes using DC gradient insulator dielectrophoresis

Bacteria play a significant role in both human health and disease. An estimated 9.4 million cases of foodborne illness occur in the United States each year. As a result, rapid identification and characterization of microorganisms remains an important research objective. Despite limitations, selective culturing retains a central role among a cadre of identification strategies. For the past decade, separations-based approaches to rapid bacterial identification have been under investigation. Gradient insulator dielectrophoresis (g-iDEP) promises benefits in the form of rapid and specific separation of very similar bacteria, including serotypes of a single species. Furthermore, this approach allows simultaneous concentration of analyte, facilitating detection and downstream analysis. Differentiation of three serotypes or strains of Escherichia coli bacteria is demonstrated within a single g-iDEP microchannel, based on their characteristic electrokinetic properties. Whole cells were captured and concentrated using a range of applied potentials, which generated average electric fields between 160 and 470 V/cm. Bacteria remained viable after exposure to these fields, as determined by cellular motility. These results indicate the potential g-iDEP holds in terms of both separatory power and the possibility for diagnostic applications.     

Adenosine Nucleoside Analog Synthesis via Electrophilic Activation of Electron Rich Alkenes

Aminomercuration and aminoselenation of electron rich alkenes provides a useful route to adenosine nucleoside analogs.