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W.E. Falconer G.R. Jones W.A. Sunder M.J. Vasile Annabel A. Muenter T.R. Dyke W. Klemperer 《Journal of fluorine chemistry》1974,4(2):213-234
Most known non-radioactive pentafluorides have been examined by molecular-beam mass spectrometry and by the deflection of molecular beams in inhomogeneous electric fields. Extensive association of the vapors occurs for all but the lighter pentafluorides and the interhalogens. The interhalogen pentafluorides are strongly polar, consistent with the accepted C4v symmetry. The transition-metal and Group V pentafluorides are all non-polar, except VF5 and CrF5 for which temperature-dependent polarity is observed. However, uncertainty exists as to whether these observations are applicable to monomeric pentafluorides in all cases. Mass-spectral cracking patterns are presented for all species. 相似文献
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Direct observations of infrared absorption in the weakly bound dimer of carbonyl sulphide, produced in pulsed molecular beams, have been made. Diode laser spectra in the 5 micron, carbonyl stretching, wavelength region were recorded with FWHM linewidths of approximately 100 MHz. All of the observations are consistent with OCS dimer having a C 2h , centrosymmetric geometry, with the centres of mass of the monomers nearly opposite one another. This essentially perpendicular structure places the S atoms close to the centre of the complex. The perpendicular distance between the monomer axes is 3·64 Å. Intermolecular potential functions containing dispersion and electrostatic contributions are discussed. 相似文献
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The fate of DCl molecules striking pure glycerol and a 2.6 M NaI-glycerol solution is investigated using scattering, uptake, and residence time measurements. We find that dissolved Na+ and I- ions alter every gas-liquid pathway from the moment of contact of DCl with the surface to its eventual emergence as HCl. In particular, the salt enhances both trapping-desorption of DCl and interfacial DCl --> HCl exchange at the expense of DCl entry into the bulk solution. The reduced entry and enhanced desorption of thermalized DCl molecules are interpreted by assuming that Na+ and I- ions bind to interfacial OH groups and tie up surface sites that would otherwise capture incoming DCl molecules. These ion-glycerol interactions may also be responsible for enhancing interfacial D --> H exchange by disrupting the interfacial hydrogen bond network that carries the newly formed H+ ion away from its Cl- pair. This disruption may increase the fraction of interfacial Cl- and H+ that recombine and desorb immediately as HCl before the ions separate and diffuse deeply into the bulk. 相似文献
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Molecular beam electric resonance spectroscopy has been used to measure the l-type doubling transitions in carbonyl sulfide. Transitions in J = 4 to J = 20 have been observed for the (0220) vibrational state and for J = 1 and J = 2 for the (0310) state. The data has been analyzed to give the v = 2 energy separation , and the vibrational dependence of q to be 86.52(9)(v2 + 1) KHz. The dipole moment of the (0220) vibrational state is 0.6936(3) D. 相似文献
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It is proposed that the Zeeman effect of the 202 → 111 transition in sulfur dioxide be used as a magnetic field calibration standard. The recent accurate beam maser measurements on this transition by Ellenbroek and Dymanus have been confirmed by electric resonance measurements in the 111 level. The Zeeman splittings most useful for calibration purposes depend linearly on the magnetic field. For perpendicular selection rules the Zeeman coefficient is 0.5282(3) MHz/kG while parallel transitions have a 0.3722(3) MHz/kG Zeeman coefficient. The sign of the rotational magnetic moment of SO2 has been determined to be negative. 相似文献