Ballistic phonon studies in the lowest Landau level

We report time-resolved studies of ballistic phonon absorption in the fractional quantum Hall regime at Landau level filling factors of and . The technique used can resolve the interaction of the two-dimensional electron system with LA and TA phonons and has been used to measure the temperature variation of the heat capacity of a single layer of electrons at . The energy gaps at have also been measured and found to be in good agreement with theory. The roles of compressible and incompressible regions in the phonon absorption process are discussed. Angle resolved measurements at are also in good agreement with theory.     

Improving Our Knowledge on the 229mThorium Isomer: Toward a Test Bench for Time Variations of Fundamental Constants

For more than four decades, the lowest excitation in the whole landscape of atomic nuclei, the low‐lying, isomeric state of ²²⁹Th, the so‐called thorium isomer, has challenged physicists of various disciplines. Being a solitaire with its uniquely low excitation energy of <10 eV, its predicted lifetime of a few hours results in an extremely sharp relative linewidth ΔE/E as low as 10^–20. While until recently the indication of its existence was based only on indirect evidence, its unique properties inspired a multitude of potential applications, like the use of the thorium isomer as a nuclear frequency standard, potentially able to outperform even the best atomic clocks and a sensitivity‐enhanced access to potential temporal variations of fundamental constants. The various proposals to exploit the unique properties of ^229mTh are presented herein, in particular focusing on its ability to serve as a test bench for time variations of fundamental constants like the fine structure constant.     

The RATIO method for time‐resolved Laue crystallography

A RATIO method for analysis of intensity changes in time‐resolved pump–probe Laue diffraction experiments is described. The method eliminates the need for scaling the data with a wavelength curve representing the spectral distribution of the source and removes the effect of possible anisotropic absorption. It does not require relative scaling of series of frames and removes errors due to all but very short term fluctuations in the synchrotron beam.     

Cyclotomic factors of Coxeter polynomials

In this paper we show that the cyclotomic factors of the En Coxeter polynomials depend only on the value of nmod360, and come exclusively from spherical subdiagrams.     

What is syncrystallization? States of the pH indicator methyl red in crystals of phthalic acid

The concept of syncrystallization was reinvestigated by focusing on phthalic acid (PA) grown with methyl red (MR). Crystals are alternately red and yellow in adjacent growth sectors. X-ray structures of MR and its cocrystals, revealing MR in the neutral, zwitterionic, and protonated states, as well as measurements of linear birefringence and linear dichroism of mixed crystals, were used to investigate mechanisms of PA coloring. These experiments were complemented by force field calculations of the lowest energy stable surfaces of expressed facets and energies of MR on and in crystals, as well as molecular orbital calculations of MR. Two MR species were detected in PA having distinct energies, polarizations, and face selectivities. Assignments of structures to these MRs, previously thought to be neutral and protonated, required a nuanced analysis of hydrogen bonds. The essential difference between yellow and red species is whether the MR carboxylic acid proton is inter- or intramolecularly hydrogen bound. Inferences about mixed crystal structure drawn from an examination of cocrystals of PA and MR are inconsistent with polarization spectroscopy signaling caution when using stoichiometric compounds as models of dilute solid solutions. Upon heating mixed crystals, linear dichroism diminishes and oriented, elongated pools of MR separate and pass through the bulk in directions perpendicular to the direction of elongation. These batonnets subsequently crystallize leaving macroscopic oriented crystals of a MR-rich phase within PA. No evidence was found for the simultaneous crystallization of MR and PA; however, the MR reorientation on heating as well as the separation and recrystallization of a MR-rich phase are distinct processes that could be embraced by the literal meaning of syncrystallization.     

Magnetic resonance imaging of velocity fields, the void fraction and gas dynamics in a cavitating liquid

In acoustic cavitation, the relationship between the bubble dynamics on the microscale and the flow properties on the macroscale is critical in determining sonochemical reaction kinetics. A new technique was developed to measure the void fraction and estimate water mobility in the vicinity of cavitating bubbles using phase-encoded magnetic resonance imaging with short characteristic measurement timescales (0.1–1 ms). The exponential behavior of the NMR signal decay indicated the fast diffusion regime, with the relationship between local mechanical dispersion D _mix and the average bubble radius R, D_mix >> \frac2R²10^-4s, D_{\rm mix}\gg \frac{2R^2}{10^{-4}\hbox{s}}, resulting in dispersion of orders of magnitude greater than diffusion in quiescent water. For two different samples (water and a surfactant solution), the independent measurements of three-dimensional void fraction and velocity fields permitted the calculation of compressibility, divergence and vorticity of the cavitating medium. The measured dynamics of the dissolved gas, compared with that of the surrounding liquid, reflected the difference in the bubble coalescence and lifetimes and correlated with the macroscopic flow parameters.     

Novel carotenoids genetically engineered in a heterologous host

Carotenoids are commercially important pigments that are essential for human health. Diverse carotenoids have been identified, but availability has impeded evaluation of their pharmaceutical potential. Molecular techniques have been developed to produce specific and novel carotenoids with improved biological activities.     

Restricted photochemistry in the molecular solid state: structural changes on photoexcitation of Cu(I) phenanthroline metal-to-ligand charge transfer (MLCT) complexes by time-resolved diffraction

The excited-state structure of [Cu(I)[(1,10-phenanthroline-N,N') bis(triphenylphosphine)] cations in their crystalline [BF(4)] salt has been determined at both 180 and 90 K by single-pulse time-resolved synchrotron experiments with the modified polychromatic Laue method. The two independent molecules in the crystal show distortions on MLCT excitation that differ in magnitude and direction, a difference attributed to a pronounced difference in the molecular environment of the two complexes. As the excited states differ, the decay of the emission is biexponential with two strongly different lifetimes, the longer lifetime, assigned to the more restricted molecule, becoming more prevalent as the temperature increases. Standard deviations in the current Laue study are very much lower than those achieved in a previous monochromatic study of a Cu(I) 2,9-dimethylphenanthroline substituted complex ( J. Am. Chem. Soc. 2009 , 131 , 6566 ), but the magnitudes of the shifts on excitation are similar, indicating that lattice restrictions dominate over the steric effect of the methyl substitution. Above all, the study illustrates emphatically that molecules in solids have physical properties different from those of isolated molecules and that their properties depend on the specific molecular environment. This conclusion is relevant for the understanding of the properties of molecular solid-state devices, which are increasingly used in current technology.     

Gradings of positive rank on simple Lie algebras

We complete the classification of positive rank gradings on Lie algebras of simple algebraic groups over an algebraically closed field k whose characteristic is zero or not too small, and we determine the little Weyl groups in each case. We also classify the stable gradings and prove Popov’s conjecture on the existence of a Kostant section.     

Enhancing the Photo and Thermal Stability of Nicotine through Crystal Engineering with Gentisic Acid

The use of crystal engineering to convert liquids into crystalline solids remains a powerful method for inhibiting undesired degradation pathways. When nicotine, a liquid sensitive to both light and air, is combined with the GRAS-listed compound, gentisic acid, the resulting crystalline solid, exhibits enhanced photo and thermal stability. Despite a modest ΔT_m of 42.7 °C, the melting point of 155.9 °C for the nicotinium gentisate salt is the highest reported for nicotine-containing crystalline solids. An analysis of the crystal packing and thermodynamic properties provides context for the observed properties.