Structural aspects of the product from glyoxal and tetrakis(ethoxycarbonylamino)ethane

The base-promoted addition of glyoxal to 1,1,2,2-tetrakis(ethoxycarbonylamino)ethane in DMF gives a product mixture containing mostly 1,1′,3,3′-tetrakis(ethoxycarbonyl)-4,4′,5,5,'-tetrahydroxy-2,2′-biimidazolidyl. An alternate structure containing a tetraazadecalin system was considered less likely, since the most significant peak in the mass spectrum of this product and a tetraacetate derivative corresponded to half the mass of the parent ion. Two-dimensional nmr spectra on the major hplc fraction are more consistent with the biimidazolidinyl structure (very low J_vic and lack of NOE enhancement). A HETCOSY spectrum on the mixture allowed assignment of ¹H nmr shifts.     

Simple methods for dead-time and pile-up corrections in analytical gamma-ray spectrometry

In the paper the mathematical methods for dead-time and pile-up corrections are discussed. The dead-time correction formulae for a system of two short-lived isotopes and constant component (background) are reported which mathematical problem has not been solved so far. The new electronic circuit for simultaneous measurements of clock- and live- (or dead-) times is described. It is shown that using this circuit one can correct the counting loss for both effects simultaneously. Finally, the advantages and disadvantages of mathematical methods for dead-time and pile-up corrections are discussed based on the authors' several-year laboratory practice.     

Der Zerfall des84Rb und die Fluoreszenzausbeute von Krypton

The electron capture decay and the positron decay of⁸⁴Rb were investigated using NaJ (Tl)-detectors and a Ge (Li)-detector. Measurements of all intensities and of some informative double and triple coincidences were performed. From coincidence measurements betweenK-X-radiation and the following γ-radiation we got theK-fluorescence yield of Krypton Ω_itK=0.653 ± 0.004. Taking in consideration former measurements¹ one concludes a continuous behaviour of Ω_itK(Z) forZ=36, 37 and 38 within an uncertainty of 1%. For the branching ratios of the decay of⁸⁴Rb we obtained The half-life of⁸⁴Rb was determined to beT _1/2=(34.5 ± 0.2) d.     

Experimentelle Untersuchungen am Elektroneneinfang des85Strontium und88Yttrium

The electron capture decay of⁸⁵Sr and⁵⁵Y has been investigated using NaI(Tl)-detectors. Spectroscopic-coincidence techniques have been employed to examine theK-electron capture rates. The experimental results areP _K ω _K (Sr)=.5959 ± 0.0035 andP _K ω _K (Y)=0.6340± 0.0032. Using theK-capture probabilities, derived from the capture ratios ofBrysk andRose with the exchange correction ofBahcall:P _K (Sr)=0.880± 0.008 andP _K (Y)=0.883 ± 0.008, one can derive from these results the fluorescence yieldsω _K (Rb)=0.677± 0.009 andω _K (Sr)=0.712± 0.010. Functions ofω _K (Z) were fitted to recent experimental data and tabulated forZ=5–90. In addition to these results the half life of the 514 keV state of⁸⁵Rb and the branching ratios and the positron rate of the⁸⁸Y-decay have been measured with the same techniques. The data obtained partly disagree from measurements of other authors.     

Coverage-mediated suppression of blinking in solid state quantum dot conjugated organic composite nanostructures

Size-correlated single-molecule fluorescence measurements on CdSe quantum dots functionalized with oligo(phenylene vinylene) (OPV) ligands exhibit modified fluorescence intermittency (blinking) statistics that are highly sensitive to the degree of ligand coverage on the quantum dot surface. As evidenced by a distinct surface height signature, fully covered CdSe-OPV nanostructures (approximately 25 ligands) show complete suppression of blinking in the solid state on an integration time scale of 1 s. Some access to dark states is observed on finer time scales (100 ms) with average persistence times significantly shorter than those from ZnS-capped CdSe quantum dots. This effect is interpreted as resulting from charge transport from photoexcited OPV into vacant trap sites on the quantum dot surface. These results suggest exciting new applications of composite quantum dot/organic systems in optoelectronic systems.     

Role of Au(+) in supporting and activating Au(7) on TiO(2)(110)

The adhesion properties and catalytic activity of rutile TiO(2)(110)-supported Au(7) nanoclusters in different oxidation states are investigated by means of density functional theory. The calculations cover both surface science conditions of reduced TiO(2) and real catalyst conditions of oxidized (alkaline) TiO(2) supports. Large adhesion energies of Au(7) are found only when modeling real catalysts where the cluster becomes cationic with Au(+) ions in Au-O or Au-OH bonds. The full catalytic cycle for oxidation of CO by O(2) over Au(7) on alkaline TiO(2)(110) is calculated and found to involve only small activation barriers. In the presence of the CO reductant, the Au(+) sites are capable of cycling between bonding of atomic and molecular oxygen. We confirm our findings by comparison of calculated and experimental infrared stretch frequency data for adsorbed CO.     

Threshold neutral pion photoproduction off the tri-nucleon to O(q4)

We calculate the electromagnetic neutral pion production off tri-nucleon bound states (³H, ³He) at threshold in chiral nuclear effective field theory to fourth order in the standard heavy baryon counting. We show that the fourth-order two-nucleon corrections to the S-wave multipoles at threshold are very small. This implies that a precise measurement of the S-wave cross section for neutral pion production off ³He allows for a stringent test of the chiral perturbation theory prediction for the S-wave electric multipole $E_{0+}^{\pi^0 n}$ .