Observation of high soft x-ray drive in large-scale hohlraums at the National Ignition Facility

The first soft x-ray radiation flux measurements from hohlraums using both a 96 and a 192 beam configuration at the National Ignition Facility have shown high x-ray conversion efficiencies of ～85%-90%. These experiments employed gold vacuum hohlraums, 6.4 mm long and 3.55 mm in diameter, heated with laser energies between 150-635 kJ. The hohlraums reached radiation temperatures of up to 340 eV. These hohlraums for the first time reached coronal plasma conditions sufficient for two-electron processes and coronal heat conduction to be important for determining the radiation drive.     

Synthesis of internal fluorinated alkenes via facile aryloxylation of substituted phenols with aryl trifluorovinyl ethers

Nucleophilic addition-elimination of ortho- or para-substituted phenols to aryl trifluorovinyl ethers (TFVEs) in N,N-dimethylformamide was studied. Using sodium hydride as a base afforded vinyl substitution products R-Ar-O-CF=CF-O-Ar-R', where R or R' = H, Br, OMe, tert-Bu, or Ph. The vinyl substitution products produced mixtures of (Z)/(E)-isomers and this isomer ratio was influenced by substitution with more sterically encumbered phenol nucleophiles. Reactions using caesium carbonate afforded addition products R-Ar-O-CHFCF(2)-O-Ar-R' whereas upon dehydrofluorination using sodium hydride produced vinyl substitution products. The preparation of vinyl substituted and addition products proceeded in overall good isolated yields and were elucidated using (1)H and (19)F NMR, GC-MS, and X-ray analysis. Vinyl substituted products were inert to UV light and chemical reactivity using common polymerization promoters. Thermal activation of the (Z)/(E)-fluoroolefin (-CF=CF-) was observed at an onset of 310 °C in nitrogen using differential scanning calorimetry (DSC) producing insoluble network material. The synthesis, characterization, and mechanism for stereoselectivity are discussed.     

A two step route to indoles from haloarenes--a versatile variation on the Fischer indole synthesis

In a new variation on the Fischer indole synthesis, readily available haloarenes are converted into a wide range of indoles in just two steps by halogen-magnesium exchange, quenching with di-tert-butyl azodicarboxylate, followed by reaction with ketones under acidic conditions.     

Factors affecting the quality of plutonium deposits by electrodeposition

Ultra-high resolution alpha spectrometry by microcalorimetry has demonstrated a dramatic improvement in alpha energy resolution over silicon based detectors. To characterize the optimal resolution obtained by the microcalorimeter alpha spectrometers, high quality deposits that are virtually massless are required; electrodeposition is the preferred method for the preparation of high quality deposits. In order to better understand the factors that contribute to lower alpha energy resolution and deposit yield, we have conducted a study to determine the effect of some of the parameters that are used for preparing electrodeposits. We have compared four different electrodeposition methods and four different substrate materials to determine the effect on the deposit yield and alpha energy resolution of plutonium as measured by full width at half maximum using silicon based detectors. Furthermore, we wanted to understand the effect of contaminants from environmental samples on electrodeposits. Therefore, the effect on deposit yield and alpha energy resolution with several common soil constituents (Al³⁺, Eu³⁺, Fe³⁺, K⁺, Lu³⁺, Mg²⁺, Na⁺, Zn²⁺) have been studied.     

Chiral N-Acetyl Selone-Promoted Aldol Reactions

The chiral oxazolidineselone functionality was found to be an excellent partner in the stereospecific acetate aldol reaction with aldehydes via the titanium enolates. Good stereocontrol was obtained as determined by NMR spectroscopy. The oxazolidineselone also provided a straightforward way to establish the stereopurity of the coupling reaction through ⁷⁷Se NMR spectroscopy.     

Natural products containing a diazo group

Although diazo compounds are probably best known for their involvement as versatile intermediates in modern synthetic organic chemistry, a small number of such compounds also occur naturally. Many of the early examples, such as azaserine, originally isolated in the 1950s, have antitumour properties and consist of modified α-amino acids. More recently, other more complex diazo compounds have been isolated from natural sources, and these include diazobenzoquinones, diazonaphthoquinones, such as the SF2415 and A80915 antibiotics, and the diazofluorene-based kinamycins and lomaiviticins. This report will cover the isolation, biosynthesis, biological activity and synthesis of natural products containing a diazo group.     

Synthesis of balsaminone A, a naturally occurring pentacyclic dinaphthofuran quinone

A short synthesis of the natural product balsaminone A, a dinaphthofuran quinone, is described. The key steps of the synthesis are base-induced coupling of 1,4-dihydroxy-2-naphthaldehyde with 2,3-dichloronaphthoquinone to give a pentacyclic dinaphthofuran directly, followed by conversion of the aldehyde into the desired methoxy group via the corresponding phenol. The synthesis, in which the structure of a key pentacyclic intermediate is corroborated by X-ray crystallography, confirms the original structural assignment of the natural product.     

Dworkin’s argument revisited: Point processes,dynamics, diffraction,and correlations

The setting is an ergodic dynamical system (X,μ)$(X,\mu )$ whose points are themselves uniformly discrete point sets Λ$\Lambda$ in some space R^d${\mathbb{R}}^d$ and whose group action is that of translation of these point sets by the vectors of R^d${\mathbb{R}}^d$. Steven Dworkin’s argument relates the diffraction of the typical point sets comprising X$X$ to the dynamical spectrum of X$X$. In this paper we look more deeply at this relationship, particularly in the context of point processes.     

Experimental generation and characterization of uniformly filled ellipsoidal electron-beam distributions

For 40 years, uniformly filled ellipsoidal beam distributions have been studied theoretically, as they hold the promise of generating self-fields linear in the coordinate offset in all three directions. Recently, a scheme for producing such distributions, based on the strong longitudinal expansion of an initially very short beam under its own space-charge forces, has been proposed. In this Letter we present the experimental demonstration of this scheme, obtained by illuminating the cathode in a rf photogun with an ultrashort laser pulse (approximately 35 fs rms) with an appropriate transverse profile. The resulting 4 MeV beam spatiotemporal (x,t) distribution is imaged using a rf deflecting cavity with 50 fs resolution. A temporal asymmetry in the ellipsoidal profile, due to image charge effects at the photocathode, is observed at higher charge operation. This distortion is also found to degrade the transverse beam quality.