Laser fluorescence on radio-active isotopes produced in very low yield

East particle-photon coincidence techniques, developed at Daresbury with strontium isotopes, allow ultrasensitive laser fluorescence spectroscopy of beams of radio-active isotopes which can only be produced in very low yields. The technique has now been applied to neutron-deficient barium isotopes down to¹²⁰Ba. From measured hyperfine splittings and isotope shifts, nuclear moments and changes in mean square radii have been determined. The work has revealed an abrupt increase in the mean square radius for¹²¹Ba large enough to disrupt the systematic staggering of nuclear size seen for the series. In a recent experiment an isomeric state of¹²⁷Ba with a half-life of about 2 seconds has been produced in a very low yield; nevertheless we have succeeded in obtaining a fluorescence spectrum.     

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On-line nuclear orientation and relaxation studies of Cs isotopes

The hyperfine field of CsFe has been measured to be (+)40.8(0.7)T, using the technique of on-line low temperature nuclear orientation. The time dependent relaxation of¹²¹Cs^m Fe has also been investigated using a new technique, giving a Korringa constant C_k of 0.059 (15) sK. From this, an effective relaxation time of 3.0 (0.8)s can be deduced for the short lived¹¹⁸Cs^m(T_1/2=17s). This value has then been used to extract the magnetic moment of¹¹⁸Cs^m to be |μ|=5.4 (1.1) nm.     

Magnetic field-controlled microfluidic transport.

Several new forms of magnetohydrodynamic (MHD) flow occurring in the solution gap between two 250-microm-diameter Pt microdisk electrodes, oriented in a face-to-face geometry and immersed in a uniform magnetic field (1 T), are described. The MHD flow results from the Lorentz force generated by diffusion of electrochemically generated molecular ions through the magnetic field. Individual microscopic flow tubes ( approximately 50-microm radius) spanning the gap between the face-to-face electrodes are observed during the 1-e(-) reduction of nitrobenzene in acetonitrile solutions. The flow tubes extend up to approximately 2 cm in length and are stable for indefinite periods. Directional transport of the electrogenerated nitrobenzene radical anion over macroscopic distances within the flow tubes, with minimal diffusional broadening, is demonstrated using an ultramicroelectrode probe to map the convective flux of redox species. Pulsed MHD transport of small packets of molecules and the formation of large area (approximately 3 cm(2)), microscopically thin (25 microm) rotating sheets of solution are also demonstrated. The results suggest that electrochemical methods, in combination with magnetohydrodynamic principles, may be useful for external field-controlled microfluidic systems.     

Schoolyard Shade and Sun Exposure: Assessment of Personal Monitoring During Children's Physical Activity

Childhood exposure to ultraviolet radiation (UVR) is a major risk factor for the development of melanoma later in life. However, it is challenging to accurately determine personal outdoor exposure to UVR, specifically erythemally weighted UVR (UV_Ery), due to technological constraints, variable time–activity patterns, and the influence of outdoor environmental design. To address this challenge, this study utilized mobile and stationary techniques to examine the UV_Ery exposures of 14 children in a schoolyard in Lubbock, TX, in spring 2016. The aims of the study were to examine the influence of artificial shade on personal UV_Ery exposures and to assess full sun exposure ratios (ERs) within the same playground microenvironment. On average, personal wrist dosimeters worn during play in the sun measured 18% of the total onsite UV_Ery measured by a stationary UV pyranometer. Shade was found to significantly reduce the personal UV_Ery exposures by 55%, UVB_{280–315 nm} exposures by 91%, and the overall solar radiation by 84%. Substantial benefits can be garnered through focused design of children's recreational space to utilize shade—both natural and artificial—to reduce UVR exposures during play, and to extend safe outdoor stays. Finally, although the wrist is a practical location for a dosimeter, it often underestimates full exposures, particularly during physical activity.     

Diversification of a β-Lactam Pharmacophore via Allylic C-H Amination: Accelerating Effect of Lewis Acid Co-Catalyst

This report describes the use of Pd(II)/bis-sulfoxide 1 catalyzed intra- and intermolecular allylic C-H amination reactions to rapidly diversify structures containing a sensitive β-lactam core similar to that found in the monobactam antibiotic Aztreonam. Pharmacologically interesting oxazolidinone, oxazinanone, and linear amine motifs are rapidly installed with predictable and high selectivities under conditions that use limiting amounts of substrate. Additionally, we demonstrate for the first time that intramolecular C-H amination processes may be accelerated using catalytic amounts of a Lewis acid co-catalyst [Cr(III)(salen)Cl 2].     

Antimony-Carbon bond activation in a Pt(II) complex: The crystal structure of [Pt(9S3)(SbPh3)(Ph)](PF6)·CH3NO2

The complex [Pt(9S3)(SbPh₃)(Ph)](PF₆) forms directly from [Pt(9S3)(SbPh₃)₂](PF₆)₂ during the room temperature crystallization of the latter in nitromethane. The crystal structure shows a five-coordinate Pt(II) center containing the tridentate thiacrown ligand, a Sb donor from the triphenylstibine ligand, and a σ-coordinating phenyl group. The phenyl group forms via Sb-C bond cleavage from one of the SbPh₃ ligands in the bis complex.