Coproducts in the category $${{\mathcal {S}}}(B)$$ S ( B ) of Segal topological algebras,revisited

Periodica Mathematica Hungarica - In this paper we generalize the result (obtained by the author earlier in the paper titled “Products and coproducts in the category $${{\mathcal {S}}}(B)$$...     

Solvent effects on oxygen-17 chemical shifts in methyl formate: linear solvation shift relationships

A multiple linear regression analysis has been carried out using the Kamlet-Abboud-Taft solvatochromic parameters in order to quantify the solvent effects on the (17)O chemical shifts of methyl formate (MF). The influence of the solvents upon the carbonyl oxygen chemical shifts is smaller for MF than for N-methylformamide (NMF). The influence (in parts per million) of the solvent polarity-polarizability reduces from -21.9pi* in amides to -9.6pi* in MF. The influence of the solvent hydrogen-bond-donor acidities reduces from -42.0alpha in formamides to -16.9alpha in MF. The solvent effects upon the dicoordinated oxygen chemical shifts of MF are smaller in magnitude and opposite in direction, i.e., 4.8pi* and 2.6alpha, than those for the carbonyl oxygen. (17)O hydration shifts have been calculated for the NMF + (H(2)O)(6) and MF + (H(2)O)(5) complexes by the ab initio GIAO method at the 6-311 + G** level. The hydration shifts calculated for the carbonyl oxygens of NMF and MF and for the dicoordinated oxygen of MF, -102.4, -64.7, and 17.6 ppm, respectively, show the same trend as the corresponding empirical hydration shifts, -101.7, -42.0, and 14.2 ppm.     

Electrochemical de-intercalation, oxygen non-stoichiometry, and crystal growth of NaxCoO2−δ

We report a detailed study of de-intercalation of Na from the compound Na_xCoO_2−δ using an electrochemical technique. We find evidence for stable phases with Na contents near the fractions x?1/3, 1/2, 5/8, 2/3, and 3/4. Details regarding the floating-zone crystal growth of Na_0.75CoO₂ single crystals are discussed as well as results from magnetic susceptibility measurements. We observe the presence of significant oxygen deficiencies in powder samples of Na_0.75CoO_2−δ prepared in air, but not in single crystal samples prepared in an oxygen atmosphere. The oxygen deficiencies in a Na_0.75CoO_2−δ sample with δ∼0.08 remain even after electrochemically de-intercalating to Na_0.3CoO_2−δ.     

Ionization phase-match gating for wavelength-tunable isolated attosecond pulse generation

High-order harmonic emission can be confined to the leading edge of an 800 nm driver laser pulse under moderately intense focusing conditions (7×10¹⁴ W/cm²) (Pfeifer et al. in Opt. Express 15:17120, 2007). Here, the experimentally observed curtailment of harmonic production on the leading edge of the driver pulse is shown to be controlled by an ionization-induced phase-matching condition. The transient plasma density inherent to the process of high-harmonic generation terminates the harmonic emission by an ultrafast loss of phase matching on the leading edge of the laser pulse. The analysis is supported by a reconstruction of the in situ intensity envelope of the driver pulse with attosecond temporal resolution, performed by measurements of the carrier-envelope phase dependence of individual half-cycle harmonic cutoffs. The method opens the way to wavelength-tunable isolated attosecond pulse generation.     

Single attosecond pulse generation in the multicycle-driver regime by adding a weak second-harmonic field

We present a method of producing single attosecond pulses by high-harmonic generation with multicycle driver laser pulses. This can be achieved by tailoring the driving pulse so that attosecond pulses are produced only every full cycle of the oscillating laser field rather than every half-cycle. It is shown by classical and quantum-mechanical model calculations that even a minor addition (1%) of phase-locked second-harmonic light to the 800 nm fundamental driver pulse for high-harmonic generation leads to a major (15%) difference in the maximum kinetic energies of the recombining electrons in adjacent half-cycles.     

Structure‐Making Effects of Metal Nanoparticles in Amyloid Peptide Fibrillation

There is growing concern that nanoparticles (NPs) may accelerate amyloid protein aggregation and thus cause amyloid‐related diseases. Here, the potential of silver and gold NPs is explored (diameter 20 nm) on the aggregation of the amyloid peptide sequences NNFGAIL from human islet amyloid polypeptide and the yeast prion protein sequence GNNQQNY, which are both the sequences of the full systems, which are able to aggregate into characteristic amyloid cross‐beta sheet fibrillar structures. Here, it is shown that silver and gold NPs in physiological aqueous solution at ambient temperatures accelerate the aggregation kinetics of both peptides significantly (in vitro). Scanning electron microscopy and X‐ray diffraction provide solid evidence for a “structure‐making” effect of the NPs. In particular, we are able to image the initial peptide corona and measure its structural reorganization in time‐resolved kinetic experiments. After a conversion time Δt, the coated NPs appear to act as templates or seeds for rapid fibrillation. Interestingly, cross‐fibrillation experiments with different peptide‐coated NPs (pcNPs) reveal that they can efficiently induce aggregation of similar peptides once the pcNPs are structurally converted. It is discussed that these structurally converted pcNPs may display similar kinetic features as toxic and aggregation inducing oligomers/protofibrils in normal amyloid aggregation, without being transient and very low‐concentration species. Finally, we suggest and discuss a simple mechanistic picture with the biomolecule corona of NPs being central to the function of the coated NPs in amyloid fibrillation.     

Application of Mössbauer spectroscopy to physical metallurgy: The role of light interstitial elements

Hyperfine Interactions - Light elements like hydrogen, nitrogen, and carbon, residing on interstitial sites of the host lattice, are capable of inducing noticeable changes in the physical...     

Oscillatory motion of a viscoelastic fluid past a stretching sheet

Summary The boundary layer flow of a viscoelastic fluid (Walters' B model) past a stretching sheet is considered for investigation. The solution of the equation of motion is obtained using the power series method. The effects of the viscoelastic parameterk ₁ on the flow have been investigated. It is also found that the effects of unsteadiness in the wall velocity and skin-friction are appreciable.