Magnetic properties of rare earth clusters

We report results of Stern-Gerlach deflection experiments on terbium clusters, which resemble earlier results for gadolinium clusters. As in gadolinium, we observe two distinct behaviors: clusters that are superparamagnetic and clusters that are described by a locked-moment model. The magnetic behavior is highly size dependent. Certain clusters make a transition from locked-moment to superparamagnetic behavior with increasing temperature and, in this process, exhibit an intermediate behavior. Both superparamagnetic and locked-moment clusters have magnetic moments per atom well below the bulk value. We show that oxygen atoms attached to the clusters have little effect on the clusters' magnetic properties and are not responsible for the two distinct behaviors observed in rare earth clusters. We also present preliminary results from studies on dysprosium clusters.     

Internal energy content of n-butylbenzene, bromobenzene, iodobenzene and aniline molecular ions generated by two-photon ionization at 266 nm. A photodissociation study

A technique to investigate photodissociation kinetics on a nanosecond time scale has been devised for molecular ions generated by multiphoton ionization (MPI) using mass-analyzed ion kinetic energy spectrometry. The branching ratio or rate constant has been determined for the photodissociation of the n-butylbenzene, bromobenzene, iodobenzene, and aniline molecular ions generated by MPI at 266 nm. The ion internal energies have been estimated by comparing the measured kinetic data with the previous energy dependence data. The analysis has shown that only those molecular ions generated by two-photon ionization contribute to the photodissociation signals. Around half of the available energy has been found to remain as molecular ion internal energy in the two-photon ionization process. Copyright 1999 John Wiley & Sons, Ltd.     

Photodesorption of alkali anions from alkali-halide cluster anions

Using photoelectron spectroscopy, we have observed alkali anion photodesorption from alkali-halide cluster anions that contain two weakly bound electrons. In the alkali iodides, we have found this type of desorption in almost every (MI)(n)M- cluster we have studied (M=Na, K, Cs; n<9), although it depends on the probe laser frequency and cluster temperature. Using pump-probe techniques, we have shown that the process occurs on a picosecond time scale by way of an electronic excitation of the cluster's spin-paired electrons.     

A rapid and precise assay for peroxide as 'active oxygen' in products, by flow injection analysis in a high pressure system with spectrophotometric detection

A simple, rapid and automated assay for ‘active oxygen’ originating from hydrogen peroxide, or other organic peroxides, in products is presented employing flow injection (FI) analysis. The product is dispersed and peroxide dissolved in a solvent of 5% (v/v) acetic acid, which constitutes the carrier stream. Ammonium molybdate can be added to this carrier stream to increase sensitivity as required. The sample solution is injected into the acid carrier stream, which is then merged with iodide ion in situ in a two-stream manifold. The ‘active oxygen’ in the product oxidises acidified iodide to iodine, which is detected spectrophotometrically at 350 nm. The closed conditions prevent interference from atmospheric oxygen and the short reaction time minimises the potential for interference from side reactions. Standard HPLC equipment is used throughout, employing a back-pressure to improve precision (high pressure flow injection). Conditions have been investigated using screening multivariate experimental design (two-level quarter fractional factorial design incorporating centre points) to identify and optimise the critical variables. The method has been fully validated (with sample solution R.S.D.s typically < 0.5%, LOQs of 0.04 or 0.006 μg ml⁻¹ as ‘active oxygen’ for acid or acid/molybdate carriers respectively) and is quicker and simpler than the currently employed manual titration approach. It should be applicable to a range of ‘active oxygen’ products.     

Development of a contact call in black-capped chickadees (Poecile atricapillus) hand-reared in different acoustic environments

The tseet contact call, common to black-capped (Poecile atricapillus) and mountain chickadees (P. gambeli), is the most frequently produced vocalization of each species. Previous work has characterized the tseet call of black-capped and mountain chickadees from different geographic locations in terms of nine acoustic features. In the current study, using similar methods, the tseet call of black-capped chickadees that were hand reared with either conspecifics, heterospecifics (mountain chickadees), or in isolation from adult chickadees are described. Analysis of call features examined which acoustic features were most affected by rearing environment, and revealed that starting frequency and the slope of the descending portion of the tseet call differed between black-capped chickadees reared with either conspecific or heterospecific adults. Birds reared in isolation from adults differed from the other hand-reared groups on almost every acoustic feature. Chickadee tseet calls are more individualized when they are reared with adult conspecifics or heterospecifics compared to chickadees that are reared in isolation from adults. The current results suggest a role of learning in this commonly used contact call.     

Evidence for the direct ejection of clusters from alkali-halides during laser vaporization

We have studied the formation of clusters of alkali halides during laser vaporization. Measurements of the abundances of cluster ions produced by several different source configurations indicate that clusters are ejected directly from the source sample and do not necessarily grow from an atomic or molecular vapor. Using samples consisting of mixed alkali halide powders, we have found that unalloyed clusters are easily produced in a source that prevents growth from occurring after the clusters leave the sample surface. Melting the sample or encouraging growth after vaporization lead to the production of alloyed cluster species. We also obtain information about the relative binding energies for substituted halogen ions bound to alkali halide clusters.     

Room temperature, palladium-mediated p-arylation of secondary phosphine oxides

We show that a broad range of aryl iodides are efficiently coupled with secondary phosphine oxides using 1 mol % of a catalyst formed in situ from tris(dibenzylideneacetone)dipalladium and Xantphos (1). Scalemic (S)-methylphenylphosphine oxide [(S)-2e] is shown to undergo arylation without detectable stereoerosion. The application of this method to the synthesis of novel P-chiral phosphines and PCP ligands is demonstrated.     

Photofragmentation of mass resolved carbon cluster ions

The results of a detailed study of the photodissociation of carbon cluster ions, C ₃ ⁺ to C ₂₀ ⁺ , are presented and discussed. The experiments were performed using internally cold cluster ions derived from pulsed laser evaporation of a graphite target rod in a helium buffer gas followed by supersonic expansion. The mass selected clusters were photodissociated using 248 nm and 351 nm light from an excimer laser. Photofragment branching ratios, photodissociation cross sections and data on the laser fluence dependence of photodissociation are reported. For almost all initial clusters, C _n ⁺ , the dominant photodissociation pathway was observed to be loss of a C₃ unit to give a C _n?3 ⁺ ion. This observation is interpreted as indicating that dissociation occurs by a statistical unimolecular process rather than by direct photodissociation. The photodissociation was found to be linear with laser fluence forn>5 with 248 nm and 351 nm light; quadratic forn=5 for 248 nm and 351 nm; and linear forn=4 at 248 nm. Dissociation energies for the carbon cluster ions implied by these results are discussed. The photodissociation cross sections were found to change dramatically with cluster size and with the wavelength of the photodissociating light.