Modal spectra extracted from nonequilibrium fluid patterns in laboratory experiments on Rayleigh-Bénard convection

We describe a method to extract from experimental data the important dynamical modes in spatiotemporal patterns in a system driven out of thermodynamic equilibrium. Using a novel optical technique for controlling fluid flow, we create an experimental ensemble of Rayleigh-Bénard convection patterns with nearby initial conditions close to the onset of secondary instability. An analysis of the ensemble evolution reveals the spatial structure of the dominant modes of the system as well as the corresponding growth rates. The extracted modes are related to localized versions of instabilities found in the ideal unbounded system. The approach may prove useful in describing instability in experimental systems as a step toward prediction and control.     

Time-of-flight mass measurements for nuclear processes in neutron star crusts

We present results from time-of-flight nuclear mass measurements at the National Superconducting Cyclotron Laboratory that are relevant for neutron star crust models. The masses of 16 neutron-rich nuclei in the scandium-nickel range were determined simultaneously, with the masses of (61)V, (63)Cr, (66)Mn, and (74)Ni measured for the first time with mass excesses of -30.510(890) MeV, -35.280(650) MeV, -36.900(790) MeV, and -49.210(990) MeV, respectively. With these results the locations of the dominant electron capture heat sources in the outer crust of accreting neutron stars that exhibit super bursts are now experimentally constrained. We find the experimental Q value for the (66)Fe→(66)Mn electron capture to be 2.1 MeV (2.6σ) smaller than predicted, resulting in the transition occurring significantly closer to the neutron star surface.     

Near-field spectroscopy of surface plasmons in flat gold nanoparticles

We use near-field interference spectroscopy with a broadband femtosecond, white-light probe to study local surface plasmon resonances in flat gold nanoparticles (FGNPs). Depending on nanoparticle dimensions, local near-field extinction spectra exhibit none, one, or two resonances in the range of visible wavelengths (1.6-2.6 eV). The measured spectra can be accurately described in terms of interference between the field emitted by the probe aperture and the field reradiated by driven FGNP surface plasmon oscillations. The measured resonances are in good agreement with those predicted by calculations using discrete dipole approximation. We observe that the amplitudes of these resonances are dependent upon the spatial position of the near-field probe, which indicates the possibility of spatially selective excitation of specific plasmon modes.     

Synthesis and properties of nicked dumbbell and dumbbell DNA conjugates having stilbenedicarboxamide linkers

The synthesis and properties of nicked dumbbell and dumbbell DNA conjugates having A-tract base pair domains connected by rod-like stilbenedicarboxamide linkers are reported. The nicked dumbbells have one to eight dA-dT base pairs and are missing a sugar-phosphate bond either between the linker and a thymine nucleoside residue or between two thymine residues. Chemical ligation of all of the nicked dumbbells with cyanogen bromide affords the dumbbell conjugates in good yield, providing the smallest mini-dumbbells prepared to date. The dumbbells have exceptionally high thermal stability, whereas the nicked dumbbells are only marginally more stable than the hairpin structures on either side of the nick. The structures of the nicked dumbbells and dumbbells have been investigated using a combination of circular dichroism spectroscopy and molecular modeling. The base pair domains are found to adopt normal B'-DNA geometry and thus provide a helical ruler for studies of the distance and angular dependence of electronic interactions between the chromophore linkers.     

Sharp melting transitions in DNA hybrids without aggregate dissolution: proof of neighboring-duplex cooperativity

Similar to DNA-modified gold nanoparticles, comb polymer-DNA hybrids exhibit very sharp melting transitions that can be utilized in highly selective DNA detection systems. Current theories suggest that such sharp melting results from either a phase transition caused by the macroscopic dissolution of the aggregate or neighboring-duplex interactions in the close-packed environment between adjacent DNA duplexes. To delineate the contributions of each of these effects, an aggregate system based on polymer-DNA hybrids was designed to include both polymer-linked and partially untethered duplexes. When this hybridized system was subjected to thermal analysis, both types of duplexes exhibited sharp melting transitions. The very sharp melting transition displayed by the partially untethered DNA duplexes offers proof that neighboring-duplex interactions can indeed induce cooperativity. Contributions of this neighboring-duplex effect, as well as the enhanced stabilization observed in polymer-DNA:polymer-DNA aggregates, can be quantitatively assessed using a simple thermodynamic model. While neighboring-duplex interactions alone can lead to cooperative melting, the enhanced stabilization observed in polymer-DNA aggregates is a function of both neighboring-duplex interactions and multivalent or aggregate properties.     

A Square‐Planar Tetracoordinate Oxygen‐Containing Ti4O17 Cluster Stabilized by Two 1,1′‐Ferrocenedicarboxylato Ligands

By introducing steric constraints into molecular compounds, it is possible to achieve atypical coordination geometries for the elements. Herein, we demonstrate that a titanium‐oxo cluster [{Ti₄(μ₄‐O)(μ₂‐O)₂}(OPrⁱ)₆(fdc)₂], which possesses a unique edge‐sharing Ti₄O₁₇ octahedron tetramer core, is stabilized by the constraints produced by two orthogonal 1,1′‐ferrocenedicarboxylato (fdc) ligands. As a result, a square‐planar tetracoordinate oxygen (ptO) can be generated. The bonding pattern of this unusual anti‐van’t Hoff/Le Bel oxygen, which has been probed by theoretical calculations, can be described by two horizontally σ‐bonded 2p_x and 2p_y orbitals along with one perpendicular nonbonded 2p_z orbital. While the two ferrocene units are separated spatially by the ptO with an Fe???Fe separation of 10.4 Å, electronic communication between them still takes place as revealed by the cluster’s two distinct one‐electron electrochemical oxidation processes.     

1,4‐Diketones from Cross‐Conjugated Dienones: Potassium Permanganate‐Interrupted Nazarov Reaction

A domino potassium permanganate‐interrupted Nazarov reaction to yield syn‐2,3‐disubstituted 1,4‐diketones via a decarbonylative cleavage of the Nazarov oxyallyl intermediate, believed to be without precedent, is presented. This process allows syn substituents to be established stereospecifically on the 2‐carbon bridge connecting the ketone carbonyl carbons, and the formation of one carbon–carbon and two carbon–oxygen bonds. Two carbon–carbon bonds are cleaved in this process.     

Über die Geometrie von Laguerre. IX. Begleitende Dupinsche Zykliden bei Streifen.W-Kugelscharen undW-Streifen

Ohne Zusammenfassung