Fluoroalkyl-s-triazines

A series of symmetrically and asymmetrically substituted s-triazines was synthesized by condensation of fluorocarbon nitriles (Scheme II, compounds 1a-c ) and by cyclodehydration of a fluorocarbon imidoylamidine utilizing a fluorocarbon anhydride (Scheme III, compounds 2a-e ). Among the new nitriles prepared for incorporation in these reaction paths were 11-H-4,9-dioxahexadecylfluoroundecanenitrile ( 3 ) and 6-chloro-6-H-4-oxaheptafluorohexanenitrile ( 4 ), prepared by Scheme 1.     

A comparison of CeS and CeAl2

The compression curve (to 200 kbars) and the ambient resistivity versus temperature (1.5K <T < 300K) of CeS have been measured. The results are compared to the analogous experiments on the compound CeAl₂. A high pressure valence instability and ambient pressure crystalline electric field, spin fluctuation and magnetic order effects are found to be common to both compounds.     

A simple-minded direct approach to estimating the calibration parameter for proportionate data

In non-destructive assay there exist techniques founded on physics principles and experimental design for which the quantity of interest y_True to be estimated is expected to vary in direct proportion to the true value x_True of the experimentally observed predictor quantity x. In other words, the calibration is a straight line passing through the origin, so that the assay method is fully described by a single parameter, the slope. In principle a single reference item is sufficient to estimate the slope. However, there are good reasons for including more than a single item in the calibration procedure. When multiple items are used questions arise regarding how to make best use of all the available calibration data in estimating the slope. This paper shows that the usual weighted least squares curve fitting approach can be circumvented by using only the familiar notion of a weighted arithmetic mean. In particular we draw attention to the ease with which uncertainties in both x and y can be incorporated using this simple and direct approach. Moreover the uncertainty in the calibration parameter is estimated using familiar techniques and with an appropriate magnitude for subsequent use, for instance, in setting reasonable uncertainties on assay results performed using the calibration. For completeness, weighted least squares accounting for nonzero covariances among the measurements y of y_True together with an errors in predictors approach accounting for errors in x is also presented.     

Fusion around the barrier for 7Li+12C

Fusion cross-sections for the ⁷Li + ¹²C reaction have been measured at energies above the Coulomb barrier by the direct detection of evaporation residues. The heavy evaporation residues with energies below 3 MeV could not be separated out from the α-particles in the spectrum and hence their contribution was estimated using statistical model calculations. The present work indicates that suppression of fusion cross-sections due to the breakup of ⁷Li may not be significant for ⁷Li + ¹²C reaction at energies around the barrier.     

Validation of gamma-ray true coincidence summing effects modeled by the Monte Carlo code MCNP-CP

When radionuclides decay by cascading photons, the accuracy of the measured nuclide activity may be affected by true coincidence summing effects. The effects can be quantified by Monte Carlo simulations that can handle correlated γ-and X-ray emissions from a radionuclide. Analysis techniques are also available commercially to correct for the effects due to cascading γ-rays. The MCNP-CP code was used to compute the effects in high purity germanium detectors for several commonly used nuclides and geometries and the results were compared to measurements and an analysis technique. Excellent agreement in true coincidence summing corrections predicted by MCNP-CP and the analysis technique was obtained. In addition, the X-ray true coincidence summing effects were evaluated.     

Generation and stereoselective transformations of 3-phenylcyclopropene

A convenient and inexpensive approach to the generation of 3-phenylcyclopropenes is described. Reaction of these compounds with a range of dienophiles and dipolarophiles led to the stereoselective formation of [4+2]- and [3+2]-cycloadducts, which were exclusively exo-3-phenyl-cis-1,2-disubstituted cyclopropanes. Efficient trapping of 1-lithio-3-phenylcyclopropene with different electrophiles is also discussed. Ab initio calculations suggest that the lowest energy conformation of 3-phenylcyclopropene has the plane of the benzene ring perpendicular to the cyclopropene π-bond but with a low rotation barrier.     

The potential use of continuous-flow isotope-ratio mass spectrometry as a tool in forensic soil analysis: a preliminary report

The use of continuous-flow isotope-ratio mass spectrometry (CF-IRMS) as a tool in soil analysis has been assessed as part of a larger study using a number of geological techniques applied in a forensic context. Carbon and nitrogen isotopic ratios, delta13C and delta15N, have been analysed to investigate situations which have arisen from crime casework. Three questions have been addressed: the role of spatial variation found over the short-scale (less than 20 m), temporal variation over a period of almost 2 years, and the variation found between source soils and soil transferred to footwear soles during a simple one-stage transfer process. Results are presented for the three experiments. The use of carbon and nitrogen isotopes has been shown to be useful in discriminating between soil types and sample locations, even when sampling occurs at a different time (as might be the case with a crime scene). In cases of primary transfer (from a source soil by a one-stage transfer to another surface, in this case, shoes and boots), the combination of carbon and nitrogen isotope ratios is a valuable tool in discriminating between sites and in showing the relationship of the transferred samples to the relevant source soils. Used in combination with other analytical techniques, isotopic analysis may prove to be a useful tool in a forensic context.