Lipid chain mobility in interdigitated DPPC systems

The segmental lipid chain mobility in the gel phase of dipalmitoylphosphatidylcholine (DPPC) multilayers dispersed in buffer and in the interdigitated gel phase induced by glycerol, ethylene glycol, ethanol and chaotropic salt NaClO₄ was compared by using conventional electron spin resonance (ESR) spectroscopy. The stearic acids bearing the nitroxide moiety at different positions down the acyl chain (n-NSA,n-5, 7, 10, 12 and 16) were used to characterized the chain motion, and the outer hyperfine splittings of the spectra, 2A _max, were taken as indices of the rotational mobility of the chain in the gel phase. The ESR measurements revealed a gradient of increased mobility on proceeding towards the terminal methyl end in the fully hydrated gel phase of DPPC bilayers. This gradient was reduced in the interdigitated gel phase induced by ethanol and chaotropic salt NaClO₄, whereas the rotational mobility throughout the length of the chain was comparable to that near the polar/apolar interface in the interdigitated gel phase in glycerol and ethylene glycol. Moreover, the motional anisotropy was much less affected by temperature in the interdigitated gel state of DPPC in glycerol and ethylene glycol as compared both to normal bilayer gel phase and to the other interdigitated DPPC systems. Finally, there was no evidence for chain interdigitation in the fluid phase of DPPC dispersions in any medium.     

A positron annihilation study in some amorphous scintillators

Two organic scintillators — NE104 and a liquid solution of 2,5 diphenyloxazole (PPO) — were investigated through positron annihilation spectroscopy to study the influence of the structural order on the magnetic quenching effect on positron bound systems in solids.Preliminary note in [11]     

Synthesis of 4H-pyrans by O-cyclization of 1,5-diketones

Substituted 4H-pyrans were obtained in high preparative yields by the reaction of 1,5-diketones with acetic anhydride and boron trifluoride etherate in diethyl ether. It is assumed that the heterocyclization of 1,5-diketones includes a step involving the formation and transformations of an acyloxy carbonium ion.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 320–322, March, 1992.     

On the strong monotonicity of power indices

The problem of choosing a power index which better describes a control situation could be solved by the property of strong monotonicity. We prove this property for some of the best known power indices.sponsored by Committee 10 of C.N.R.     

Acoustic effect of pulsed high-energy proton beams

Experimental data on the generation of acoustic radiation in solid targets by pulsed high-energy proton beams are outlined. The features of ultrasound generation in solids by beams of heavy charged particles are analyzed, and the possibility of using the acoustic effect of heavy charged particles to investigate the interaction between radiation and condensed media and to determine particle energies is shown.Translated from Izvestiya Vysshikh Uchebnykh Zavedenii, Fizika, No. 8, pp. 95–99, August, 1991.     

Magnetopause plasma transients: mapping into the auroral ionosphere

Attention is focused on a specific category of auroral event occurring predominantly during a southward directed interplanetary magnetic field (IMF). Coordinated observations from the ground and satellites in polar orbit have been used to study the temporal/spatial development of the events in relation to the background patterns of particle precipitation and ionospheric convection as well as the field-aligned current and ion drift characteristics of the individual events. Both prenoon and postnoon sector events are reported. In one case the auroral event was observed near the zero point potential line separating the morning and postnoon convection cells. The available data indicate that this auroral event sequence is a signature of quasi-periodic bursts of particle entry from the magnetosheath along flux tubes convecting into the polar cap, representing structures of enhanced IMF B_Y-related convection poleward of the persistent cleft aurora. Such events may be initiated by localized patches of enhanced merging rate at the dayside magnetopause     

Rotational Spectra of Argon Acetone: A Two-Top Internally Rotating Complex

The rotational spectra of the argon acetone weakly bound complex was studied by pulsed jet Fabry-Perot Fourier transform microwave spectroscopy. Over 500 transitions of the complex were measured between 5.5 and 26 GHz from J=2-1 to J=12-11. The two methyl groups undergo hindered internal rotation resulting in four or five internal rotation states. The microwave transitions are within these states, resulting in a splitting of each rotational transition into four and sometimes five distinct transitions. The three-fold barrier to internal rotation is determined to be 260 cm⁻¹, 2% less than the 266 cm⁻¹ barrier in acetone itself. The structure of the complex has the argon atom above the heavy atom plane of the acetone, 3.52 Å from the CO bond and approximately in the C_s plane, which is perpendicular to the CCC plane of acetone.     

A novel derivatization method for peptides to increase sensitivity and backbone fragmentation in liquid secondary-ion mass spectra.

Derivatization is used to increase both negative-ion sensitivity and positive-ion sequence information in the liquid secondary-ion mass spectra (LSIMS) of a series of peptides. The derivatization method involves acylation with pentafluorobenzoyl fluoride in a single-step reaction, and the reaction mixture is applied directly to the probe tip for analysis. Acylation takes place at the unprotected N-terminus, tyrosine, and lysine. The derivatives exhibit increased signal-to-noise ratio for [M-H]- ions, especially where there is not already an acidic amino acid residue in the peptide. In positive-ion LSIMS, the N-terminal group acts to retain the charge at the N-terminus, simplifying the fragmentation by producing N-terminal fragment ions. It also increases positive-ion fragmentation, sometimes very dramatically, making sequence determination more straightforward. The simplicity of the process, together with the enhancements it provides, make this a generally useful method for obtaining peptide structural information.