Generation and measurement of relativistic electron bunches characterized by a linearly ramped current profile

We report the first successful attempt to generate ultrashort (1-10 ps) relativistic electron bunches characterized by a ramped longitudinal current profile that rises linearly from head to tail and then falls sharply to zero. Bunches with this type of longitudinal shape may be applied to plasma-based accelerator schemes as an optimized drive beam, and to free-electron lasers as a means of reducing asymmetry in microbunching due to slippage. The scheme used to generate the ramped bunches employs an anisochronous dogleg beam line with nonlinear correction elements to compress a beam having an initial positive time-energy chirp. The beam current profile is measured using a deflecting mode cavity, and a pseudoreconstruction of the beam's longitudinal phase space distribution is obtained by using this diagnostic with a residual horizontal dispersion after the dogleg.     

The Diels-Alder reactions of quinone imine ketals: a versatile synthesis of highly substituted 5-methoxyindoles

[reaction: see text]. N-benzoylated quinone imine ketals undergo smooth cycloadditions in a [4 + 2] sense to yield the expected cycloadducts. The crude cycloadducts, when subjected to a short series of simple transformations, produce synthetically useful quantities of 5-methoxyindoles in excellent overall yields.     

The elastic scattering of 33 MeV He particles from Ni,Cu and Zn

Differential cross sections have been measured for the elastic scattering of 33 MeV ³He particles from targets of ^58,60,62,64Ni,^63,65Cu and ^64,66,68Zn over the angular range 5° to 175°. The data have been analysed with the optical model, with particular emphasis on the investigation of the ambiguities in the real potential, the form of the imaginary potential and the use of a spin-orbit term.     

Bayesian stratified random sampling using auxiliary information

Summary Smith (1976,J. R. Statist. Soc., A,139, 183–204) has argued that survey statisticians should attempt to model finite population structures in the same way that statisticians in other disciplines have to provide models of finite or infinite populations. Following this argument, we suggest in this paper that an obvious model for a stratified population when auxiliary information regarding variate values is available, is the one way analysis of covariance model with unequal variances and we consider the problem of estimating the finite population mean. Finally a possible extension of this result is discussed.     

Investigation of 91Zr by high resolution (d,p), (p,p′) and (p,d) reactions

Energy spectra and angular distributions of light particles (Z = 3–8) produced in the reactions ¹³C+^{58, 60, 64}Ni have been measured at 105 MeV. Coincidence events between light outgoing particles Li, Be, B and α, p have been observed for the first time in the ¹³C+⁵⁸Ni and ¹³C+⁶⁴Ni reactions. The results show that at least part of the ‘deep-inelastic’ events are due to many-particle reactions.     

Iron-catalyzed C2-C3 bond cleavage of phenylpyruvate with O2: insight into aliphatic C-C bond-cleaving dioxygenases

Iron(II)-phenylpyruvate complexes of tetradentate tris(6-methyl-2-pyridylmethyl)amine (6-Me3-TPA) and tridentate benzyl bis(2-quinolinylmethyl)amine (Bn-BQA) were prepared to gain insight into C-C bond cleavage catalyzed by dioxygenase enzymes. The complexes we have prepared and characterized are [Fe(6-Me3-tpa)(prv)][BPh4] (1), [Fe2(6-Me3-tpa)2(pp)][(BPh4)2] (2), and [Fe2(6-Me3-tpa)2(2'-NO2-pp)][(BPh4)2] (3), [Fe(6-Me3-tpa)(pp-Me)][BPh4] (4), [Fe(6-Me3-tpa)(CN-pp-Et)][BPh4] (5), and [Fe(Bn-bqa)(pp)] (8), in which PRV is pyruvate, PP is the enolate form of phenylpyruvate, 2'-NO2-PP is the enolate form of 2'-nitrophenylpyruvate, PP-Me is the enolate form of methyl phenylpyruvate, and CN-PP-Et is the enolate form of ethyl-3-cyanophenylpyruvate. The structures of mononuclear complexes 1 and 5 were determined by single-crystal X-ray diffraction. Both the PRV ligand in 1 and the CN-PP-Et ligand in 5 bind to the iron(II) center in a bidentate manner and form 5-membered chelate rings, but the alpha-keto moiety is in the enolate form in 5 with concomitant loss of a C-H(beta) proton. The PP ligands of 2, 3, 4, and 8 react with dioxygen to form benzaldehyde and oxalate products, which indicates that the C2-C3 PP bond is cleaved, in contrast to cleavage of the C1-C2 bond previously observed for complexes that do not contain alpha-ketocarboxylate ligands in the enolate form. These reactions serve as models for metal-containing dioxygenase enzymes that catalyze the cleavage of aliphatic C-C bonds.     

Siderophore-Mediated Iron Uptake Promotes Yeast–Bacterial Symbiosis

In the present study, siderophore produced by the marine yeast Aureobasidium pullulans was characterized as hydroxamate by chemical and bioassays. The hydroxamate assignment was supported by the appearance of peaks at 1,647.21?C1,625.99?cm^?1 and at 1,435.04?cm^?1 in the infrared spectrum. The purified siderophore exhibited specific growth-promoting activity under iron-limited conditions for siderophore auxotrophic probiotic bacteria. Cross-utilization of siderophore indicates a symbiotic relationship between the yeast A. pullulans and the selected probiotic bacterial strains. Statistical optimization of medium components for improved siderophore production in A. pullulans was depicted by response surface methodology. The shift in UV?CVis spectroscopy indicates the photoreactive property and subsequent oxidative cleavage of purified siderophore on exposure to sunlight.     

The effect of titanium dioxide exposure on the thermal properties of Zebrafish (<Emphasis Type="Italic">Danio rerio</Emphasis>) bones

This article presents the changes in the thermal properties of the control and titanium dioxide (TiO₂), both nano and bulk exposed Zebrafish bones by using thermo analytical techniques. The result shows that the mass loss due to the thermal decomposition occurs in three distinct steps due to loss of water, organic and inorganic materials. The titanium dioxide exposed bones present a different thermal behaviour compared to the control bones. The residue masses are found to be increased due to titanium dioxide exposure. In particular, nano titanium dioxide exposure increases the residue mass level significantly (three fold) when compared to titanium dioxide bulk exposure. These thermal characteristics can be used as a qualitative method to check the metal oxide intoxication in biological samples.