Mixed ligand complexes of ruthenium(III), rhodium(III) and iridium(III) with dipicolinic acid and some monobasic bidentate nitrogen,oxygen donor ligands

The trivalent ruthenium, rhodium and iridium complexes of dipicolinic acid and its mixed ligand complexes with several nitrogen, oxygen donor molecules, of types: Na[M(dipic)₂]·2H₂O and [M(dipic)(N-O)]·nH₂O (where M = Ru(III), Rh(III) or Ir(III); dipicH₂ = dipicolinic acid; NOH represents different nitrogen, oxygen donor molecules, viz., picolinic acid, nicotinic acid, isonicotinic acid, glycine, aminophenol, o- or p-aminobenzoic acid), have been synthesized and characterised on the basis of elemental analyses, electrical conductance, magnetic susceptibility measurements and spectral (electronic and infrared) data. The parent dipicolinic acid complexes are found to have a six-coordinate pseudooctahedral structure, whereas for mixed ligand complexes, a polymeric six-coordinate structure has been assigned. Various ligand field and nephelauxetic parameters have also been evaluated.     

Radial motion of a solid spherical body in a magnetic field

The object of the present paper is to investigate the radial motion of a solid spherical body, assumed to be homogeneous, isotropic and elastic, in presence of a magnetic field in the azimuthal direction. The body is assumed to be in a state of initial stress which is hydrostatic in nature. This theory of radial motion of a solid spherical body in a magnetic field has been utilised to find the small radial motion of a solid Earth assumed to be homogeneous isotropic elastic sphere in presence of a magnetic field in the azimuthal direction. Considering the effect of gravity and the initial stress produced by slow process of creep due to extra masses over the surface of the Earth, the fundamental equations of motion are derived which are non-linear in character and are solved. The times of a desired radial displacement are calculated in presence of a magnetic field only and in presence of the same magnetic field, initial stress and gravitational field, which are compared and exhibited numerically.     

Laser-pulse-induced second-harmonic and hard x-ray emission: role of plasma-wave breaking

We report time resolved measurements of second-harmonic and hard x rays emitted during the interaction of an intense laser pulse (10(16) W cm(-2), 100 fs) with a preplasma generated on a solid target. We observe that for a particular length scale the second harmonic goes through a minimum, while hard x-ray emission on the contrary maximizes. Theoretical or numerical modeling of this anticorrelation in terms of wave breaking of strongly driven electron plasma waves clearly brings out hitherto unexplored links between the physical mechanisms of second-harmonic generation and hard x-ray emission.     

Supersolids versus phase separation in two-dimensional lattice bosons

We study the nature of the ground state of the two-dimensional extended boson Hubbard model on a square lattice by quantum Monte Carlo methods. We demonstrate that strong but finite on-site interaction U along with a comparable nearest-neighbor repulsion V result in a thermodynamically stable supersolid ground state for densities larger than 1/2, in contrast to fillings less than 1/2 or for very large U, where the checkerboard supersolid is unstable towards phase separation. We discuss the relevance of our results to realizations of supersolids using cold bosonic atoms in optical lattices.     

Medium-dependent electron and H atom transfer between 2'-deoxyadenosine and menadione: a magnetic field effect study

The interaction between 2'-deoxyadenosine and the model antitumor drug menadione has been studied in organic solvent and in micellar medium. The aim of the work is to elucidate the mechanism of this drug-nucleoside interaction and to determine the environmental effects. Laser flash photolysis and magnetic field effect are used to detect the transients and their spin states. The results indicate that H atom transfer and electron transfer are the operative mechanisms depending upon the medium.     

Role of tilt order in the asymmetric ripple phase of phospholipid bilayers

We present the electron density map of the asymmetric ripple phase of dilauroylphosphatidylcholine. We find that the primary feature characterizing the "asymmetry" of the rippled bilayers is the difference in the bilayer thickness in the two arms, and not the asymmetry of the bilayer height profile as is generally assumed. This difference in the bilayer thickness can be attributed to a mean tilt of the hydrocarbon chains of the lipid molecules along the direction of the ripple wave vector. We propose a Landau theory for this phase which takes into account the anisotropic elastic properties of a bilayer with tilt order.     

Nonvanishing of symmetric square -functions of cusp forms inside the critical strip

We shall give a certain nonvanishing result for the symmetric square -function of an elliptic cuspidal Hecke eigenform w.r.t. the full modular group inside the critical strip.

     

Elastic constants from microscopic strain fluctuations

Fluctuations of the instantaneous local Lagrangian strain epsilon(ij)(r,t), measured with respect to a static "reference" lattice, are used to obtain accurate estimates of the elastic constants of model solids from atomistic computer simulations. The measured strains are systematically coarse-grained by averaging them within subsystems (of size L(b)) of a system (of total size L) in the canonical ensemble. Using a simple finite size scaling theory we predict the behavior of the fluctuations as a function of L(b)/L and extract elastic constants of the system in the thermodynamic limit at nonzero temperature. Our method is simple to implement, efficient, and general enough to be able to handle a wide class of model systems, including those with singular potentials without any essential modification. We illustrate the technique by computing isothermal elastic constants of "hard" and "soft" disk triangular solids in two dimensions from Monte Carlo and molecular dynamics simulations. We compare our results with those from earlier simulations and theory.     

DNA Encapsulation of Ten Silver Atoms Produces a Bright, Modulatable, Near Infrared-Emitting Cluster

Photostability, inherent fluorescence brightness, and optical modulation of fluorescence are key attributes distinguishing silver nanoclusters as fluorophores. DNA plays a central role both by protecting the clusters in aqueous environments and by directing their formation. Herein, we characterize a new near infrared-emitting cluster with excitation and emission maxima at 750 and 810 nm, respectively that is stabilized within C(3)AC(3)AC(3)TC(3)A. Following chromatographic resolution of the near infrared species, a stoichiometry of 10 Ag/oligonucleotide was determined. Combined with excellent photostability, the cluster's 30% fluorescence quantum yield and 180,000 M(-1)cm(-1) extinction coefficient give it a fluorescence brightness that significantly improves on that of the organic dye Cy7. Fluorescence correlation analysis shows an optically accessible dark state that can be directly depopulated with longer wavelength co-illumination. The coupled increase in total fluorescence demonstrates that enhanced sensitivity can be realized through Synchronously Amplified Fluorescence Image Recovery (SAFIRe), which further differentiates this new fluorophore.