Time-resolved imaging of hydrogel printing via laser-induced forward transfer

In this work, the printing mechanism of an alginate-based hydrogel via laser-induced forward transfer (LIFT) is investigated by spatial and temporal high-resolved stroboscopic imaging. First, the generation of the liquid jet is studied at two different laser fluences in a process without collector slide. Furthermore, the impingement process onto the collector slide at the same fluence levels is observed. With the help of these images the development of the jet is explained. Besides the influences of the collector slide as well as the applied laser fluence on the transfer are demonstrated.     

Physical processes during development of upward leaders from tall structures

The objective of our study was to identify and interpret the various processes during development of upward positive leaders from tall structures. We provide a physical interpretation for the varying luminosity of the leader channel during its initial ascent and the pulsing luminosity during much later stages of the established leader. Our analysis confirms that pulsed luminosity is a result of recoil leaders intercepting the current-carrying channel connected to ground. This interception produces an M-component. Applying the bidirectional leader concept and a simplified electrostatic approximation, we introduce physical models of the dart leader-return stroke sequence and the M-component.     

Relativistic calculations for two- and three-nucleon systems

The relativistic theory for few-nucleon systems developed by Glöckle and Müller is evaluated numerically for a model of scalar particles exchanging scalar mesons to lowest order in the coupling constant. 2-nucleon binding energies and scattering phases and 3-nucleon binding energies are compared with the usual non-relativistic calculation for different choices of the potential. The relativistic treatment gives a weaker binding. The mechanism of this is studied in more detail. We compare our results with the relativistic correction in the 1/c² expansion of Foldy and Krajcik.     

13C solid state NMR investigation of structural relaxation of the polymer backbone in poly (ethylmethacrylate)

Geometry and time scale of structural relaxation of poly(n-alkylmethacrylates) above the glass transition is studied by temperature dependent one- and two-dimensional 13C-NMR spectroscopy. The geometry of the isotropization of the polymer backbone as deduced from detailed analysis of spectral line shapes is identified as random angular jumps. Analysis of echo decays confirms that at a given temperature this isotropization can adequately be described with a single correlation time. The results are discussed in terms of conformational memory and local structure recently identified in these polymeric glasses.     

Richness of isomerism in labile octahedral Werner-type cobalt(II) complexes demonstrated by 19F NMR spectroscopy: structure and stability

The cobalt(II) complexes [CoL2(R2-Py)2] (1-4) where HLA = 1,1,1-trifluoro-5,5-dimethyl-2,4-hexanedione, R2-Py = 4-methylpyridine (1), HLB = 4,4,4-trifluoro-1-(2-thienyl)-1,3-butanedione, R2-Py = 4-methylpyridine (2), 4-phenylpyridine (3) and S-(-)-1-(4-pyridyl)ethanol (4) were prepared by two-step reactions. X-ray structure analysis of [CoLA2(CH3-Py)2] revealed the {trans(N)-trans(CF3)-trans} configuration for the complex obtained by crystallization from ethanol. A dynamic equilibrium between the five possible stereoisomers was observed for each complex 1-4 in solution by 19F NMR spectroscopy. The criteria used for full NMR assignment (180-265 K) include comparison of integral ratios, cis(N) and trans(N) differentiation in presence of the chiral amine [S-(-)-1-(4-pyridyl)ethanol], effect of solvent polarity on the relative stabilities of the five isomers and observation of trans influences in a mixture of complexes. Thermodynamic parameters for the equilibria between the isomers of 2 in CD2Cl2 (DeltaHi,j, DeltaSi,j and Ki,j) were obtained from signal integrals. The two trans(N) isomers are slightly more stable than the three cis(N) isomers at low temperature [DeltaGdegreesi,j (max) = 2.8 kJ mol(-1) at 179.8 K], but this stability difference almost vanishes with increasing temperature [DeltaGdegreesi,j (max) = 1.0 kJ mol(-1) at 265.0 K]. The values found for DeltaHdegreesi,j are relatively small and largely entropy compensated.