An expeditious,environment-friendly,and microwave-assisted synthesis of 5-isatinylidenerhodanine derivatives

A series of nine 5-arylidenerhodanine derivatives was prepared in good yields and purity without the use of a solvent or catalyst under microwave-assisted condensation with some substituted isatins. All 5-arylidenerhodanines were evaluated as possible inhibitors of the CK1α/β, CDK5/p25, and GSK-3α/β kinases. None of them showed substantive inhibitory activity against these kinases when evaluated at the concentration of 10 μM.     

A re-investigation of [Fe(L-cysteinate)2(CO)2]2-: an example of non-heme CO coordination of possible relevance to CO binding to ion channel receptors

[Fe(L-cysteinate)(2)(CO)(2)](2-) is a CO releasing molecule which has low cytotoxicity to RAW264.7 macrophages. It provides an example of CO binding using ligands available to ion channels which use CO as a signalling molecule in the absence of heme. Previous work has shown that this compound consists of five isomers and it was proposed that the two isomers with trans-dicarbonyls are dominant. In this work the isomers are re-assigned and shown to be capable of releasing CO, albeit too slowly to act as a signalling receptor. It is shown that by linking the two L-cysteines together to form [Fe(SCH(2)CH{CO(2)H}NHCH(2))(2)(CO)(2)], only one isomer is isolated.     

Infrared-induced reactivity of N2O on small gas-phase rhodium clusters

Far- and mid-infrared multiple photon dissociation spectroscopy has been employed to study both the structure and surface reactivity of isolated cationic rhodium clusters with surface-adsorbed nitrous oxide, Rh(n)N(2)O(+) (n = 4-8). Comparison of experimental spectra recorded using the argon atom tagging method with those calculated using density functional theory (DFT) reveals that the nitrous oxide is molecularly bound on the rhodium cluster via the terminal N-atom. Binding is thought to occur exclusively on atop sites with the rhodium clusters adopting close-packed structures. In related, but conceptually different experiments, infrared pumping of the vibrational modes corresponding with the normal modes of the adsorbed N(2)O has been observed to result in the decomposition of the N(2)O moiety and the production of oxide clusters. This cluster surface chemistry is observed for all cluster sizes studied except for n = 5. Plausible N(2)O decomposition mechanisms are given based on DFT calculations using exchange-correlation functionals. Similar experiments pumping the Rh-O stretch in Rh(n)ON(2)O(+) complexes, on which the same chemistry is observed, confirm the thermal nature of this reaction.     

Insight into the chiral induction in supramolecular stacks through preferential chiral solvation

Preferred handedness in the supramolecular chirality of self-assembled achiral oligo(p-phenylenevinylene) (OPV) derivatives is induced by chiral solvents and spectroscopic probing provides insight into the mechanistic aspects of this chiral induction through chiral solvation.     

Shadowgraphic imaging of material removal during laser drilling with a long pulse excimer laser

After the development of a novel XeCl excimer laser with a nearly diffraction-limited beam and 175 ns pulse length, research was done on different industrial applications of this laser. Hole drilling, one of these applications, was studied extensively. A better understanding of the drilling process is necessary to optimise the drilling efficiency and to control the quality of the holes. A shadowgraphic imaging technique was used for studying the removal of material from the hole and the absorption of the laser beam by this removed material. Images were made at successive times both during and after the laser pulse.In drilling of thin foils, it was shown that the material was ejected mainly after the laser pulse. A comparison of different materials showed that the drilling process should be optimised for each material independently. Furthermore, the plume was found to be not fully transparent for processing materials with a strong absorption line at or near the laser wavelength. The correlation between material and drilling speed suggests improved energy transfer and improved melt ejection for the materials with this absorption. PACS 42.62.Cf; 52.38.Dx; 52.38.Mf     

Radiation damage of mylar foils by a nuclear microprobe

Mylar foils have been irradiated under typicalPIXE conditions using the Bochum nuclear microprobe. The induced radiation damage was investigated with theHEIS technique for studies of the chemical composition and theSTIM technique for studies of the extent of axial and lateral damage. The data show that the current density of the microbeam influences the extent of axial and lateral damage in the foils, while the fluence of the microbeam causes changes in chemical composition: more than one-half of the originalH andO abundances are lost, while theC abundance — after a 15% drop within the first few seconds — increases slowly with fluence. Furthermore, the thickness of the foil affects the final chemical composition of the sample only at large fluences. The results indicate that some caution is necessary in the interpretation of PIXE analyses of trace elements in biological or medical samples using nuclear microprobes.     

Coulomb displacement energies and the structure of the low-lying negative-parity states in 2s-1d shell nuclei

Negative-parity states in A = 13–33 nuclei are described as two-component wave functions, one containing a hole in the 1p shell, the other a particle in the 1f–2p shell. The large difference in Coulomb displacement energy (CDE) for both components has been used to determine the relative intensities by fitting the experimental CDE. For the lowest-lying states these intensities are compared to experimental ones derived from spectroscopic factors for pick-up reactions. Strong binding-energy effects seem to play an important role for these states.