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1.
Fluorine-containing nitrogen compounds—VI Sulfur tetrafluoride fluorination of aliphatic nitro acids
Sulfur tetrafluoride converts aliphatic nitro acids to the corresponding trifluoromethyl compounds. The yield is poor with primary nitro acids; but high yields of fluoronitrocarbons, otherwise difficult to obtain, are produced from certain γ-substituted butyric acids and from substituted acrylic acids. Eleven new fluoronitrocarbons are described. 相似文献
2.
The ab initio energies, nuclear and electron repulsions and charge distributions have been calculated using moderately large basis sets as a function of the RC N angle (R NH2, NF2 or PF2). The optimum RC N angles were calculated to be 178.9°, 176.6°, and 175° for NH2CN, NF2CN, and PF2CN, respectively. A rationalization of the differing bends is presented in terms of nuclear-nuclear and electron-electron repulsions. 相似文献
3.
Field compressing magnetothermal instability in laser plasmas 总被引:1,自引:0,他引:1
The mechanism for a new instability in magnetized plasmas is presented and a dispersion relation derived. Unstable behavior is shown to result purely from transport processes-feedback between the Nernst effect and the Righi-Leduc heat-flow phenomena in particular-neither hydrodynamic motion nor density gradients are required. Calculations based on a recent nanosecond laser gas-jet experiment [D. H. Froula, Phys. Rev. Lett. 98, 135001 (2007)] predict growth of magnetic field and temperature perturbations with typical wavelengths of order 50 μm and characteristic growth times of ~0.1 ns. The instability yields propagating magnetothermal waves whose direction depends on the magnitude of the Hall parameter. 相似文献
4.
The representation of the AC electrical data in the complex plane reveal two major classifications of the relaxation processes known as ideal (Debye) and non-ideal (non-Debye) types. The non-Debye relaxation has been empirically observed via Cole-Cole (C-C), Davidson-Cole (D-C), and Havriliak-Negami (H-N) responses. Each of these non-Debye relaxations is visualized with an equivalent circuit similar to the ideal relaxation. Both ideal and C-C relaxations reveal semicircular behavior in the complex plane while D-C and H-N relaxations deviate from the usual semicircular loci known as skewed behavior. The extracted equivalent circuit elements are essentially non-Debye for both D-C and H-N relaxations possessing complexity in the relaxation time. The analytical method of extracting these elements in conjunction with the empirical parameters of the D-C relaxation is described using conventional (real) domain and complex domain. The curve fitting procedure provided extremely small error for the complex domain analysis. The behavior of the D-C relaxation function and the depression parameter β are also discussed using ωτ=1 and ωτ≠1 corresponding to the maximum of the imaginary part of the impedance (Z*) or permittivity (ε*). 相似文献
5.
CM Silva MF Duarte ML Mira MH Florêncio K Versluis AJ Heck 《Rapid communications in mass spectrometry : RCM》1999,13(12):1098-1103
Fast atom bombardment, combined with high-energy collision-induced tandem mass spectrometry, has been used to investigate gas-phase metal-ion interactions with captopril, enalaprilat and lisinopril, all angiotensin-converting enzyme inhibitors.Suggestions for the location of metal-binding sites are presented. For captopril, metal binding occurs most likely at both the sulphur and the nitrogen atom. For enalaprilat and lisinopril, binding preferably occurs at the amine nitrogen. Copyright 1999 John Wiley & Sons, Ltd. 相似文献
6.
Catarina IV Ramos Flávio Figueira Marcelo D Polêto Francisco ML Amado Hugo Verli João PC Tomé M Graça PMS Neves 《Journal of mass spectrometry : JMS》2016,51(5):342-349
Electrospray mass spectrometry/mass spectrometry was used to investigate the gas‐phase properties of protonated expanded porphyrins, in order to correlate those with their structure and conformation. We have selected five expanded meso‐pentafluorophenyl porphyrins, respectively, a pair of oxidized/reduced fused pentaphyrins (22 and 24 π electrons), a pair of oxidized/reduced regular hexaphyrins (26 and 28 π electrons) and a regular doubly N‐fused hexaphyrin (28 π electrons). The gas‐phase behavior of the protonated species of oxidized and reduced expanded porphyrins is different. The oxidized species (aromatic Hückel systems) fragment more extensively, mainly by the loss of two HF molecules. The reduced species (Möbius aromatic or Möbius‐like aromatic systems) fragment less than their oxidized counterparts because of their increased flexibility. The protonated regular doubly fused hexaphyrin (non‐aromatic Hückel system) shows the least fragmentation even at higher collision energies. In general, cyclization through losses of HF molecules decreases from the aromatic Hückel systems to Möbius aromatic or Möbius‐like aromatic systems to non‐aromatic Hückel systems and is related to an increase in conformational distortion. Copyright © 2016 John Wiley & Sons, Ltd. 相似文献
7.
K. T. Flanagan J. Billowes M. L. Bissell I. Budinčević T. E. Cocolios R. P. de Groote S. De Schepper V. N. Fedosseev S. Franchoo R. F. Garcia Ruiz H. Heylen K. M. Lynch B. A. Marsh G. Neyens T. J. Procter R. E. Rossel S. Rothe I. Strashnov H. H. Stroke K. D. A. Wendt 《Hyperfine Interactions》2014,227(1-3):131-137
The ability to study rare isotopes with techniques such as mass spectrometry and laser spectroscopy is often prevented by low production rates and large isobaric contamination. This has necessitated the development of novel beam cleaning techniques that can efficiently isolate the isotope of interest. The Collinear Resonance Ionization Spectroscopy (CRIS) experiment at ISOLDE, achieves this by resonantly ionizing a bunched atom beam in a region of ultra high vacuum. This method is motivated by the need to measure the hyperfine structure and isotope shift at the extremes of isospin where typical production rates drop to 1 atom/s. The technique also offers the ability to purify an ion beam and even select long-lived isomeric states (> 1 ms) from the ground state, which can be subsequently studied by decay spectroscopy or mass spectrometry experiments. This paper will report on the successful commissioning of the CRIS beam line and the recent laser spectroscopy results and laser assisted nuclear decay spectroscopy on the neutron deficient francium isotopes. 相似文献
8.
Y. Gangrsky K. Marinova S. Zemlyanoi M. Avgoulea J. Billowes P. Campbell B. Cheal B. Tordoff M. Bissell D. H. Forest M. Gardner G. Tungate J. Huikari H. Penttilä J. Äystö 《Hyperfine Interactions》2006,171(1-3):209-215
Collinear laser spectroscopy experiments on the ScII transition 3d4s
3D2→3d4p
3F3 at λ ≈ 363.1 nm were performed on the 42–46Sc isotopic chain using an ion guide isotope separator with a cooler–buncher. Isotope and isomer shifts and hyperfine structures
of five ground states and two isomers were measured. Preliminary results on the nuclear moments and charge radii changes deduced
from these measurements are reported. 相似文献
9.
The potassium disulphate-potassium sulphate, silver chloride-potassium chloride electrochemical cell
The fused salt electrochemical cell: Ag; AgCl, KC1; K(2)S(2),O(7),K(2)SO(4); O(2), Pt has been studied. Exact thermodynamic treatment of the chemical reaction, which occurs when current is drawn from the cell, is possible because K(2)S(2)O(7)(1) and AgCl(1) are immiscible, so that no junction potential occurs. Potentials observed at temperatures ranging from 700-800 degrees K for six different mixtures are reported. The Nernst equation is obeyed if it is assumed that the potassium disulphate-potassium sulphate system behaves ideally and that the silver chloride-potassium chloride system deviates slightly, negatively, from ideality. The thermodynamic functions, DeltaG degrees , DeltaH degrees and DeltaS degrees have been calculated from the corrected values of E degrees obtained. The free energy change follows the equation: DeltaG(700-800 degrees K) degrees = -71,680-29.50 T cal mole . 相似文献
10.