Analysis of mechanical vibrations through speckle interferometry: A phase-space approach

The goal of this paper is to determine hidden periodicities (spatial frequencies) into speckles patterns obtained in a diffuser after reflection of an unexpanded laser beam over an aluminum membrane by means of the so-called Wigner Distribution Function (WDF). These spatial frequencies are used to find the temporal frequencies at which the mechanic system is vibrating.     

Combined NMR and computational study for azide binding to human manganese superoxide dismutase

Human manganese superoxide dismutase (MnSOD) labeled with 3-fluorotyrosine (Tyf) was complexed with the (15)N-labeled inhibitor azide ([(15)N(3)(-)]). The sample was characterized by solid-state NMR (SSNMR) spectroscopy ((19)F-MAS and (15)N-CPMAS). Employing (19)F-(15)N-REDOR spectroscopy, we determined the distances between the fluorine label in Tyrosine-34 and the three (15)N-nuclei of the azide and the relative orientation of the azide in the binding pocket of the MnSOD. A distance of R(1)=4.85A between the (19)F-label of Tyf34 and the nearest (15)N of the azide and an azide-fluorotyrosine Tyf34 angle of 90 degrees were determined. These geometry data are employed as input for molecular modeling of the location of the inhibitor in the active site of the enzyme. In the computations, several possible binding geometries of the azide near the Mn-complex were assumed. Only when the azide replaces the water ligand at the Mn-complex we obtained a geometry of the azide-Mn-complex, which is consistent with the present NMR data. This indicates that the water molecule ligating to the Mn-complex is removed and the azide is placed at this position. As a consequence the azide forms an H bond with Gln143 instead with Tyf34, in contrast to non-(19)F-labeled MnSOD, where the azide is hydrogen bonded to the hydroxy group of Tyr34.     

Vibrational modes of rare‐earth formates

In this work we investigate the room‐temperature Raman spectra of several rare‐earth [RE(HCOO)₃; RE = La, Pr, Nd, Gd, Tb and Y] formates. Polarized measurements were carried out for La(HCOO)₃ yielding the observation of most of the Raman‐active phonons predicted by group theory analysis. The respective assignment is given based on the formate vibrations and correlations with previous results in other RE(HCOO)₃ systems. The wavenumber ‘softening’ observed when RE goes from Y to La is accounted for the lattice expansion. Copyright © 2009 John Wiley & Sons, Ltd.     

Boron doped carbon nanotubes via ceramic catalysts

A facile metal catalyst free route to synthesize boron doped (0.6%–1.0%) carbon nanotubes via ceramic nanowires in which the formation of the nanowires (probably serving as templates), the carbon nanotubes and their doping all occur unanimously in the reaction, is presented.

     

Inside polyMOFs: layered structures in polymer-based metal–organic frameworks

In this report, we explore the internal structural features of polyMOFs consisting of equal mass ratios of metal-coordinating poly(benzenedicarboxylic acid) blocks and non-coordinating poly(ethylene glycol) (PEG) blocks. The studies reveal alternating lamellae of metal-rich, crystalline regions and metal-deficient non-crystalline polymer, which span the length of hundreds of nanometers. Polymers consisting of random PEG blocks, PEG end-blocks, or non-coordinating poly(cyclooctadiene) (COD) show similar alternation of metal-rich and metal-deficient regions, indicating a universal self-assembly mechanism. A variety of techniques were employed to interrogate the internal structure of the polyMOFs, including transmission electron microscopy (TEM), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), and small-angle synchrotron X-ray scattering (SAXS). Independent of the copolymer architecture or composition, the internal structure of the polyMOF crystals showed similar lamellar self-assembly at single-nanometer length scales.

In this report, we explore the internal structural features of polyMOFs consisting of equal mass ratios of metal-coordinating poly(benzenedicarboxylic acid) blocks and non-coordinating poly(ethylene glycol) (PEG) blocks.     

The effects of an electric field on an autocatalytic ionic reaction in a system with high ionic strength

The effects of an applied electric field on an ionic autocatalyticreaction with a quadratic rate law are considered, where thereacting species, A⁺ and B⁺, are present in a system which alsoincludes non-reacting species C^- and D⁺. The conditions areestablished under which the general terms which describe theelectric field effects in the reaction-diffusion equations canbe simplified to those used in previous studies, where theseeffects are modelled by linear advection terms. The resultingequations are then studied in detail by first obtaining conditionsfor the existence of travelling waves of permanent form. Thisdiscussion shows that _B, the ratio of the diffusion coefficientsof B⁺ and A⁺, is a critical parameter, with different formsof behaviour arising for _B < 1 and _B > 1. This analysisis augmented by obtaining solutions valid for large times andlarge values of (the dirnensionless applied field). Numericalsolutions of initial-value problems are obtained for a rangeof values of and _B, guided by and interpreted through the analysispreviously obtained. These numerical integrations show the formationof reaction fronts, with the possibility of greatly increasedreaction rates caused by the applied electric field, as wellas propagating electrophoretic fronts in B⁺ being formed incases where a reaction front is also initiated. There is alsothe possibility of separate electrophoretic fronts in A⁺ andB⁺ being formed, which become increasingly separated as timeincreases with the reaction being completely inhibited.     

Resilience in reaction-diffusion systems

Reaction-diffusion systems with zero-flux Neumann boundariesare widely used to model various kinds of interaction in, forexample, the scientific fields of ecology, biology, chemistry,medicine and industry. The physical systems within these fieldsare often known to be (conditionally or unconditionally) resilientwith respect to shocks, disturbances or catastrophies in theimmediate environment. In order to be good mathematical modelsof such situations the reaction-diffusion systems must havethe same resilient or asymptotic behaviour as that of the physicalsituation. Three fundamentally different kinds of reaction termsare usually distinguished according to the entry signs of thereaction Jacobian: mutualism, mixed (predator-prey) interactionand competition. The asymptotic stability (in the Poincarésense) of mutualistic systems has already been studied extensively,but the results cannot be generalized (globally) to the othertwo fundamental types, which are not order-preserving. A partial(local) generalization is, however given here for these twotypes, involving simple Jacobian inequalities and knowledge(often prompted by the underlying physical situation) of invariantsets in solution space. The return time of resilient systemsand the approach rate of asymptotically stable solutions arealso estimated.     

Octopamine increases the excitability of neurons in the snail feeding system by modulation of inward sodium current but not outward potassium currents

Background  

Although octopamine has long been known to have major roles as both transmitter and modulator in arthropods, it has only recently been shown to be functionally important in molluscs, playing a role as a neurotransmitter in the feeding network of the snail Lymnaea stagnalis. The synaptic potentials cannot explain all the effects of octopamine-containing neurons on the feeding network, and here we test the hypothesis that octopamine is also a neuromodulator.     

Organotin hydride additions to E- And Z-trisubstituted ethylenes synthesis of some new functionally substituted organotin compounds

The syntheses of some new functionally substituted organotin compounds are reported. The results indicate that the additions of tri-n-butyltin and tri-phenyltin hydrides to trisubstituted ethylenes (where one substituent is either a carbomethoxy or a nitrile group) proceed smoothly to give high yields of organotin adducts and that the reactions are stereoselective. Evidence concerning the reversibility of the free radical forming step is presented.