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Distance Dependence (distance + dependence)
Selected AbstractsDistance dependence of long-range electron transfer through helical peptides,JOURNAL OF PEPTIDE SCIENCE, Issue 2 2008Minako Kai Abstract Helical peptides of 8mer, 16mer, and 24mer carrying a disulfide group at the N -terminal and a ferrocene moiety at the C -terminal were synthesized, and they were self-assembled on gold by a sulfur,gold linkage. Infrared reflection,absorption spectroscopy and ellipsometry confirmed that they formed a monolayer with upright orientation. Cyclic voltammetry showed that the electron transfer from the ferrocene moiety to gold occurred even with the longest 24mer peptide. Chronoamperometry and electrochemical impedance spectroscopy were carried out to determine the standard electron transfer rate constants. It was found that the dependence of the electron-transfer rates on the distance was significantly weak with the extension of the chain from 16mer to 24mer (decay constant , = 0.02,0.04). This dependence on distance cannot be explained by an electron tunneling mechanism even if increased hydrogen-bonding cooperativity or molecular dynamics is considered. It is thus concluded that this long-range electron transfer is operated by an electron hopping mechanism. Copyright © 2007 European Peptide Society and John Wiley & Sons, Ltd. [source] Scaling behavior of plasmon coupling in Au and ReO3 nanoparticles incorporated in polymer matricesPHYSICA STATUS SOLIDI - RAPID RESEARCH LETTERS, Issue 7 2010Urmimala Maitra Abstract Polymer nanocomposites containing different concentrations of Au nanoparticles have been investigated by small angle X-ray scattering and electronic absorption spectroscopy. The variation in the surface plasmon resonance (SPR) band of Au nanoparticles with concentration is described by a scaling law. The variation in the plasmon band of ReO3 nanoparticles embedded in polymers also follows a similar scaling law. Distance dependence of plasmon coupling in polymer composites of metal nanoparticles. (© 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Distance dependence and salt sensitivity of pairwise, coulombic interactions in a proteinPROTEIN SCIENCE, Issue 5 2002Kelly K. Lee Abstract Histidine pKa values were measured in charge-reversal (K78E, K97E, K127E, and K97E/K127E) and charge-neutralization (E10A, E101A, and R35A) mutants of staphylococcal nuclease (SNase) by 1H-NMR spectroscopy. Energies of interaction between pairs of charges (,Gij) were obtained from the shifts in pKa values relative to wild-type values. The data describe the distance dependence and salt sensitivity of pairwise coulombic interactions. Calculations with a continuum electrostatics method captured the experimental ,Gij when static structures were used and when the protein interior was treated empirically with a dielectric constant of 20. The ,Gij when rij , 10 Å were exaggerated slightly in the calculations. Coulomb's law with a dielectric constant near 80 and a Debye-Hückel term to account for screening by the ionic strength reproduced the salt sensitivity and distance dependence of ,Gij as well as the structure-based method. In their interactions with each other, surface charges behave as if immersed in water; the Debye length describes realistically the distance where interactions become negligible at a given ionic strength. On average, charges separated by distances (rij) ,5 Å interacted with ,Gij , 0.6 kcal/mole in 0.01 M KCl, but ,Gij decayed to ,0.10 kcal/mole when rij = 20 Å. In 0.10 M KCl, ,Gij , 0.10 kcal/mole when rij = 10 Å. In 1.5 M KCl, only short-range interactions with rij , 5 Å persisted. Although at physiological ionic strengths the interactions between charges separated by more than 10 Å are extremely weak, in situations where charge imbalance exists many weak interactions can cumulatively produce substantial effects. [source] A method for controlling the spins of atoms using optical near-fieldsJOURNAL OF MICROSCOPY, Issue 3 2003A. Shojiguchi Summary On the basis of the procedure for controlling the spins of atoms using circularly polarized evanescent light proposed by Hori et al.[(1996) Abstracts of the 1st Asia-Pacific Workshop on Near-field Optics] we discuss the influence of boundary conditions on the probability of spontaneous emission and thus on the spin polarization efficiency, which was not considered in the Hori et al. study. Using the Carniglia,Mandel mode expansion of electromagnetic fields, we derive the spontaneous emission and spin polarization probabilities of atoms near a dielectric surface, and show the atom,surface distance dependence and refractive index dependence. Numerical evaluation for the 6P1/2,6S1/2 transition of a Cs atom indicates an increase in the efficiency of spin polarization by 30%. [source] SERS-active sites on various copper substratesJOURNAL OF RAMAN SPECTROSCOPY, Issue 4 2001C. Siemes The wavenumbers of the Raman bands of ethylene adsorbed on Cu in ultra-high vacuum depend on the surface structure of the copper substrate. Thus it is possible to differentiate between ethylene adsorbed at Cu(110) sites, Cu(111) sites and surface defect sites of unknown configuration. These latter are the ,SERS-active sites.' Only when these sites are annealed does the distance dependence of SERS follow the expectations from the electromagnetic model of SERS. In the presence of the SERS-active sites, also the signal of ethylene at (111) sites shows a ,first layer effect.' Ethylene adsorbed on cold-deposited copper films shows strong infrared absorption at the same wavenumber as the ethylene at SERS-active sites in Raman scattering, irrespective of the Raman,infrared exclusion rule for the free centrosymmetric ethylene molecule. This raises the possibility that SERS-active sites are also infrared-active sites. The SERS-active sites at stepped Cu surfaces decorated by 3 nm of cold-deposited copper anneal below 200 K, whereas they prevail beyond 400 K on Cu island films. Copyright © 2001 John Wiley & Sons, Ltd. [source] Effects of dilution and disorder on magnetism in diluted spin systemsPHYSICA STATUS SOLIDI (B) BASIC SOLID STATE PHYSICS, Issue 2 2007Guixin Tang Abstract The influence of configurational disorder on the magnetic properties of diluted Heisenberg spin systems is studied with regard to the ferromagnetic stability of diluted magnetic semiconductors. The equation of motion of the magnon Green's function is decoupled by Tyablikov approximation. With supercell approach, the concentrations of magnetic ions are determined by the size of the supercell in which there is only one magnetic ion per supercell in our method. In order to distinguish the influence of dilution and disorder, there are two kinds of supercells being used: the diluted and ordered case and the diluted and disordered case. The configurational averaging of magnon Green function due to disorder is treated in the augmented space formalism. The random exchange integrals between two supercells are treated as a matrix. The obtained magnon spectral densities are used to calculate the temperature dependence of magnetization and Curie temperature. The results are shown as following: (i) dilution leads to increasing the averaged distance of two magnetic ions, further decreases the effective exchange integrals and is main reason to reduce Curie temperature; (ii) spatial position disorder of magnetic ions results in the dispersions of the exchange integrals between two supercells and slightly changes ferromagnetic transition temperature; (iii) the exponential damping of distance dependence obviously reduces Curie temperature and should be set carefully in any phenomenological model. (© 2007 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Distance dependence and salt sensitivity of pairwise, coulombic interactions in a proteinPROTEIN SCIENCE, Issue 5 2002Kelly K. Lee Abstract Histidine pKa values were measured in charge-reversal (K78E, K97E, K127E, and K97E/K127E) and charge-neutralization (E10A, E101A, and R35A) mutants of staphylococcal nuclease (SNase) by 1H-NMR spectroscopy. Energies of interaction between pairs of charges (,Gij) were obtained from the shifts in pKa values relative to wild-type values. The data describe the distance dependence and salt sensitivity of pairwise coulombic interactions. Calculations with a continuum electrostatics method captured the experimental ,Gij when static structures were used and when the protein interior was treated empirically with a dielectric constant of 20. The ,Gij when rij , 10 Å were exaggerated slightly in the calculations. Coulomb's law with a dielectric constant near 80 and a Debye-Hückel term to account for screening by the ionic strength reproduced the salt sensitivity and distance dependence of ,Gij as well as the structure-based method. In their interactions with each other, surface charges behave as if immersed in water; the Debye length describes realistically the distance where interactions become negligible at a given ionic strength. On average, charges separated by distances (rij) ,5 Å interacted with ,Gij , 0.6 kcal/mole in 0.01 M KCl, but ,Gij decayed to ,0.10 kcal/mole when rij = 20 Å. In 0.10 M KCl, ,Gij , 0.10 kcal/mole when rij = 10 Å. In 1.5 M KCl, only short-range interactions with rij , 5 Å persisted. Although at physiological ionic strengths the interactions between charges separated by more than 10 Å are extremely weak, in situations where charge imbalance exists many weak interactions can cumulatively produce substantial effects. [source] | |||||||||||||