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681.
D. Ajò M. Casarin G. Granozzi U. Croatto M. G. Bettoli 《Journal of chemical crystallography》1984,14(4):349-357
The He(I)- and He(II)-excited photoelectron spectra of theN-phenyl derivatives of succinimide, maleimide, phthalimide, and urazole are presented and discussed. The spectra are assigned by comparison with related molecules and by analysis of the relative band intensities under different radiation sources. The effects ofN-phenyl substitution are discussed in relation toN-methyl-substituted corresponding system. 相似文献
682.
V. Busetti J. A. Mayoral C. Cativiela D. Ajò M. Casarin 《Journal of chemical crystallography》1988,18(1):75-85
The crystal and molecular structure of the methyl ester of (Z)-N-acetyl-(3-pyridyl)-dehydroalanine [methylZ-2-acetamido-3(3-pyridyl) propenoate] have been determined from three-dimensional X-ray data. Crystals are monoclinic, space groupP21]. The molecular [=–51.5(5),=157.0(4)°] conformation is discussed making reference to previous experimental results of analogous amino acid derivatives (in particular, ethyl (Z)-N-acetyldehydrophenylalaninate) and theoretical predictions. On the basis of He(I) and He(II) photoelectron spectra, a similar conformation is proposed for the title molecule in the vapor phase also. 相似文献
683.
G. Alonzo N. Bertazzi G. Bombieri G. Bruno F. Nicolò 《Journal of chemical crystallography》1991,21(5):635-640
The compound has been characterized by X-ray crystal structure determination, Mössbauer and i.r. spectroscopy. It crystallizes in the monoclinic space groupP2
1
/c (No. 14) witha=24.228(4),b=8.335(2),c=23.975(4) Å,=117.83(3)° andZ=8. Least-squares refinement on 3749 observed reflections gave finalR=0.034 (R
w=0.037). The compound is constituted by [(C6H5)SbCl4OMe]– anions andphenH+cations. The coordination polyhedron about Sb is an octahedron (Sb-Cl 2.416(3), Sb-O 1.962(7) and Sb-C 2.138(9) Å). The whole structure is characterized by two short contacts (O(1)N(2) 2.76(1) O(2)N(4) 2.75(1) Å) involving the methoxy oxygens of the two independent anionic units [(C6H5)SbCl4OMe]– and two nitrogens of the two independent phenanthrolinium moieties. 相似文献
684.
A method based on microchip electrophoresis with electrochemical (EC) detection has been developed for the simultaneous determination of Yellow AB, Red 2G, Sunset Yellow, New Coccine, and Amaranth which are azo-dyes frequently added to foodstuffs. Factors affecting both separation and detection processes were examined and optimized, with best performance achieved by using a 10 mM phosphate buffer (pH 11) as BGE solution and applying a voltage of 2500 V both in the separation and in the electrokinetic injection (duration 4 s). Under these optimal conditions, the target dye analytes could be separated and detected within 300 s by applying a detection potential of -1.0 V (vs. Ag/AgCl) to the glassy carbon (GC) working electrode. The recorded peaks were characterized by a good repeatability (RSD=1.8-3.2%), high sensitivity, and a wide linear range. Detection limits of 3.8, 3.4, 3.6, 9.1, 15.1 microM were obtained for Yellow AB, Red 2G, Sunset Yellow, New Coccine, and Amaranth, respectively. Fast, sensitive, and selective response makes the new microchip protocol very attractive for the quantitative analysis of commercial soft drinks and candies. 相似文献
685.
Simon Federico Spanò Giuseppe Isgrò Paola Russo Maria Elena Fragalà Giuseppe Compagnini 《Applied Physics A: Materials Science & Processing》2014,115(1):19-23
The authors present a nano-plasmonic disk resonator with a gap structure using the multi-mode interference effect coupling. The coupling intensity of the multi-mode interference effect coupling is 1.5 times greater than that of the conventional side coupling. The multi-mode interference effect is adopted as the coupling between the input bus waveguide and the nano-plasmonic disk resonator. The thickness of the dielectric layer, the width of the bus waveguide, and the length of the coupling portion are designed by theoretical calculations. 相似文献
686.
We report on the nanometer scale morphology of CoO thin films grown on top of Fe(001) substrates from the early stages of interface formation (few atomic layers), and on the surface topography of Fe/CoO/Fe(001) layered structures. The growth of the CoO films is dominated by formation of islands up to about 5 nominal atomic layers, then it proceeds in the layer-plus-island regime. The surface topography of thin Fe films grown on top of the CoO/Fe systems is strongly influenced by the morphology of the latter. Moreover, we observe a strong relationship between the growth mode and the chemical interactions at the CoO/Fe interface, since thick layers of iron oxides develop only below the CoO islands, as an effect of the proximity between Fe and Co atoms. We finally discuss possible implications of our observations on the magnetic properties of these layered magnetic structures. 相似文献
687.
Festa C De Marino S Sepe V D'Auria MV Bifulco G Débitus C Bucci M Vellecco V Zampella A 《Organic letters》2011,13(6):1532-1535
Two unprecedented cyclic peptides, solomonamides A and B, were isolated from the marine sponge Theonella swinhoei. The structures were elucidated on the basis of comprehensive 1D and 2D NMR analysis and high-resolution mass spectrometry. A combined approach, involving Marfey's method, QM J based analysis, and DFT J/(13)C calculations, was used for establishing the absolute configuration of the entire molecule. Solomonamide A showed in vivo anti-inflammatory activity. 相似文献
688.
Anna Maria Cardinale Daniele Macciò Stefano Delfino Adriana Saccone 《Journal of Thermal Analysis and Calorimetry》2011,103(1):103-109
The isothermal section of the Nd–Al–Si ternary system at 500 °C has been investigated using differential thermal analysis,
X-ray diffraction analysis, scanning electron microscopy and electron micro-probe analysis. Four ternary intermetallic compounds
were confirmed: NdAl2Si2 (τ1), hP5-CaLa2O2 structure type, Nd2Al3Si (τ2), hP3-AlB2 structure type, NdAl1−x
Si1+x
, 0.25 ≤ x ≤ 0.3 (τ3), tI12-αThSi2 structure type and Nd2Al1−x
Si1+x
, 0 ≤ x ≤ 0.2, (τ5), oS8-CrB structure type. A new ternary intermetallic phase (τ4) was found: Nd4Al3Si3, orthorhombic oS20, isotypic with Pr4Al3Ge3. 相似文献
689.
Five peptide sequences corresponding to the E1 protein of GBV-C [NCCAPEDIGFCLEGGCLV (P7), APEDIGFCLEGGCLVALG (P8), FCLEGGCLVALGCTICTD (P10), QAGLAVRPGKSAAQLVGE (P18), and AQLVGELGSLYGPLSVSA (P22)] were synthesized because they were capable of interfering with the HIV-1 fusion peptide (HIV-1 FP)-vesicle interaction. In this work the interaction of these peptides with the HIV-1 FP, as well as with membrane models, was analyzed to corroborate their inhibition ability and to understand if the interaction with the fusion peptide takes place in solution or at the membrane level. Several studies were carried out on aggregation and membrane fusion, surface Plasmon resonance, and conformational analysis by circular dichroism. Moreover, in vitro toxicity assays, including cytotoxicity studies in 3T3 fibroblasts and hemolysis assays in human red blood cells, were performed to evaluate if these peptides could be potentially used in anti-HIV-1 therapy. Results show that P10 is not capable of inhibiting membrane fusion caused by HIV-1 and it aggregates liposomes and fuses membranes, thus we decided to discard it for futures studies. P18 and P22 do not inhibit membrane fusion, but they inhibit the ability of HIV-1 FP to form pores in bilayers, thus we have not discarded them yet. P7 and P8 were selected as the best candidates for future studies because they are capable of inhibiting membrane fusion and the interaction of HIV-1 FP with bilayers. Therefore, these peptides could be potentially used in future anti-HIV-1 research. 相似文献
690.
Dr. Simona Rizzo Prof. Tiziana Benincori Dr. Valentina Bonometti Dr. Roberto Cirilli Prof. Patrizia R. Mussini Prof. Marco Pierini Dr. Tullio Pilati Prof. Francesco Sannicolò 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(1):182-194
A series of tris‐aryl phosphanes, structurally designed to exist as residual enantiomers or diastereoisomers, bearing substituents differing in size and electronic properties on the aryl rings, were synthesized and characterized. Their electronic properties were evaluated on the basis of their electrochemical oxidation potential determined by voltammetry. The configurational stability of residual phosphanes, evaluated by dynamic HPLC on a chiral stationary phase or/and by dynamic 1H and 31P NMR spectroscopy, was found to be rather modest (barriers of about 18–20 kcal mol?1), much lower than that shown by the corresponding phosphane oxides (barriers of about 25–29 kcal mol?1). For the first time, the residual antipodes of a tris‐aryl phosphane were isolated in enantiopure state and the absolute configuration assigned to them by single‐crystal anomalous X‐ray diffraction analysis. In this case, the racemization barrier could be calculated also by CD signal decay kinetics. A detailed computational investigation was carried out to clarify the helix reversal mechanism. Calculations indicated that the low configurational stability of tris‐aryl phosphanes can be attributed to an unexpectedly easy phosphorus pyramidal inversion which, depending upon the substituents present on the blades, can occur even on the most stable of the four conformers constituting a single residual stereoisomer. 相似文献