Search results for "angle"
showing 10 items of 1921 documents
The oligomerisation of 3-hydroxy-1-alkynes with palladium(II) diketonates and phosphorus ligands as the catalytic system
1993
Abstract 3-Methylhex-1-yne-3-ol has been oligomerised by use of Pd(II) acetylacetonate with 31 different phosphorus ligands as catalyst, yielding a dimer (2,4-disubstituted but-1-en-3-yne) and a linear trimer (1,4,6-trisubstituted hexa-1,3-dien-5-yne) as the two main products. By input-output relations a variation of the diketonate and the P ligand, as weil as an alteration of the phosphorus/palladium ratio, has been connected with product ratios as dependent variables. Phosphines produced three association steps up to a cone angle of 170°; the third step representing a stop complex. For the first association the activity of the catalytic system and the portion of the 2,4-dimer increased wi…
Spectroscopic and conformational properties of size-fractions separated from a lignite humic acid
2007
Abstract A lignite humic acid (HA) was fractionated by preparative high performance size-exclusion chromatography (HPSEC) in seven different size-fractions. The size-fractions were characterized by cross polarization (CP) magic angle spinning (MAS) 13 C NMR spectroscopy and a further analytical HPSEC elution under UV and fluorescence detection. The alkyl hydrophobic components mainly distributed in the largest molecular-size-fraction, whereas the amount of oxidized carbons increased with decreasing size of fractions. Cross polarization time ( T CH ) and proton spin-lattice relaxation time in the rotating frame ( T 1 ρ (H)) were measured from variable contact time (VCT) experiments. The bulk…
Studies of Molecular Orientation and Order in Self-Assembled Semifluorinated n-Alkanethiols: Single and Dual Component Mixtures
1997
The structure, orientation and morphology of self-assembled monolayers of a semifluorinated n-alkanethiol, F(CF2)8(CH2)11SH (F8H11SH), have been investigated by polarized IR, angular dependent XPS, ToF-SIMS, contact angle, and ellipsometric measurements. The orientation of the all trans hydrocarbon segment was found to be tilted much less from the surface normal than the 30° tilt found for octadecanethiol. This has been attributed to the steric constraints imposed by the larger cross section fluorocarbon helices that subsequently are tilted from the surface normal. In addition, studies of dual component mixtures of F8H11SH/F8SH and F8SH/F8H2SH have revealed that competitive adsorption occur…
Self-assembly in surfactant-based mixtures driven by acid–base reactions: bis(2-ethylhexyl) phosphoric acid–n-octylamine systems
2013
Structural and dynamic features of bis(2-ethylhexyl) phosphoric acid (HDEHP)-n-octylamine (NOA) mixtures as a function of the NOA mole fraction (X-NOA) have been investigated by SAXS, WAXS, IR, dielectric spectroscopy and polarized optical microscopy. In the 0 <= X-NOA < 0.5 range, mixtures are transparent liquids, while the abrupt formation of a waxy solid characterized by an hexagonal bidimensional structure occurs at X-NOA = 0.5. Such a composition-induced phase transition results from the synergetic effect of the progressive increase in number density of ordered HDEHP-NOA nanodomains with X-NOA. Mainly driven by an HDEHP to NOA proton transfer, the increase of structural order with X-NO…
Polarization Force Fields for Peptides Implemented in ECEPP2 and MM2
2000
Abstract The empirical conformational energy program for peptides (ECEPP2) and molecular mechanics (MM2) have been used for the simulation of the For-Gly-NH2 backbone. I propose two different methods for the calculation of the polarization energy term: the polarization procedure by non-interacting induced dipoles (NID) which assumes scalar isotropic point polarizabilities and the polarization scheme by interacting induced dipoles (ID) which calculates tensor effective anisotropic point polarizabilities (method of Applequist). I present a comparative study of ECEPP2 and MM2 + polarization. I discuss molecular mechanics results including the total energy differences, partitional analyses of t…
Performances of symmetrical achiral ferrocenylphosphine ligands in palladium-catalyzed cross-coupling reactions: A review of syntheses, catalytic app…
2007
Abstract Ferrocene derivatives bearing donor atoms led to the generation of several classes of metallo-ligands, which collectively show an impressive diversity of applications, especially in metal-catalyzed modern organic reactions. Based on the impetus provided by the use of the diphosphine 1,1′-bis(diphenylphosphino)ferrocene (dppf) the investigations directed towards the synthesis of new ferrocenylphosphines remain of fundamental and industrial interest. The present review aims to describe the performances in palladium-catalyzed cross-coupling reactions of symmetrical achiral ferrocenylphosphine ligands, mainly diphosphines. We specifically choose to restrict our review efforts to these …
EV-Scale Sterile Neutrino Search Using Eight Years of Atmospheric Muon Neutrino Data from the IceCube Neutrino Observatory
2020
Physical review letters 125(14), 141801 (1-11) (2020). doi:10.1103/PhysRevLett.125.141801
FIRST MEASUREMENT OF THE STRANGE QUARK ASYMMETRY AT THE Z(0) PEAK
1995
A measurement of the strange quark forward-backward asymmetry at the Z0 peak was performed using 718,000 multihadronic Z0 decays collected by the DELPHI detector at LEP in 1992. The s-quark was tagged by the presence of high momentum charged kaons identified by the Ring Imaging Cherenkov detector and by Λ0;s decaying into pπ-. The s-quark purity obtained was estimated for the two hadrons to be 43%. The average s-quark asymmetry was found to be 0.131±0.035 (stat.) ±0.013 (syst.). The forward-backward asymmetry was measured for unresolved d-and s-quarks, tagged by the detection of a high energy neutron or neutral kaon in the Hadron Calorimeter. The combined d-and s-quark purity was 69% and th…
Bundlet Model of Single- Wall Carbon, BC2N and BN Nanotubes, Cones and Horns in Organic Solvents
2013
Bundlet Model of Single- Wall Carbon, BC2N and BN Nanotubes, Cones and Horns in Organic Solvents The existence of Single-wall C-nanocones (SWNCs), especially nanohorns (SWNHs) and BC2N/Boron Nitride (BN) analogues is discussed in organic solvents in cluster form. A theory is developed based on the bundlet model, describing distribution function by size. The phenomena present unified explanation in the model, in which free energy of (BC2N/BN )SWNCs involved in cluster, is combined from two components: volume one proportional to the number of molecules n in cluster and surface one, to n1/2. The model enables describing distribution function of (BC2N/BN )SWNC clusters by size. From geometrical…
Structural and morphological rearrangements in quenched poly(ethylene) by simultaneous SAXS/WAXS
2000
Structure formation by crystallization from the melt in a wide range of cooling rates (0.08-1 000°C/s) in low-density polyethylene has been studied by simultaneous small- and wide-angle X-ray scattering at the synchroton radiation source of DESY. The occurrence of two periodicities, characterized by different angular position of Bragg's maxima, was observed, pointing to the existence of two types of lamellar stacks, associated with two different long period values L 1 and L 2 (L 1 > L 2 ). L 1 depends on the cooling rate, whereas L 2 is almost constant. A comparison with isotactic polypropylene is performed, where a similar phenomenon takes place. While in the case of i-PP a definite correl…