The vacuum ultraviolet spectra of fluorine chlorine substituted trivalent phosphorus

The vapor phase absorption spectra of PF₃, PF₂Cl, PFCl₂, and PCl₃ are reported in the vacuum ultraviolet spectral region 2400—1200 A. These results are compared with information obtained from photoelectron spectra. A brief discussion of the spectra in terms of analogous absorption regions and results from CNDO/2 calculations are given.     

Photoelectron and vacuum ultraviolet spectra of a series of fluoroethers

Fluoroethers of the F(CF(CF₃)CF₂O)_nCHFCF₃ (n = 1-4) type have their lowest ionization potentials about 3.5 eV higher than ordinary ethers. Their ultraviolet absorption spectra also begin at high frequencies, at about 80000 cm^-1 or 10 eV. Both spectra are complex indicating the existence of several close lying molecular orbitals in these compounds.     

The vacuum ultraviolet spectrum of bromosilane

The vacuum ultraviolet absorption spectrum of bromisilane in the vapor phase is reported. Assignments are made using photoelectron data and oscillator strengths. The absorptions of this compound are related to absorptions of chlorosilane, methyl bromide and methyl chloride. The results of this work indicate the presence of dπ-pπ (SiBr) delocalizations and concomitant stabilization of halogen nonbonding electrons.     

Absorption spectra of volatile aromatic hydrocarbon films in the vacuum ultraviolet region

Absorption spectra of volatile aromatic hydrocarbon films, p-terphenyl, chrysene, benzanthracene and triphenylene, in the near and vacuum ultraviolet region down to 130 nm were measured under an atmosphere of Ar gas to suppress their sublimation. The spectrum of p-terphenyl is different from the spectra reported for other phases. This difference is explained in terms of the change of dihedral angles among the three benzene rings. The peak positions in the spectra of chrysene and bezanthracene agree with those in the solution spectra. The differences in the peak intensities are discussed in terms of the orientation of the films with the aid of MO calculations. The result of triphenylene suggests the presence of Davydov splitting.     

The vacuum ultraviolet spectrum of stannane

The vacuum UV spectrum of SnH₄ has been recorded up to 110nm (12.26 eV). This spectrum has been interpreted by ab initio calculations (SCF + CI), using a relativistic pseudopotential to describe the core electrons of the tin atom. The spectrum consists of a broad band composed of three maxima (at 8.73, 9.53 and 11.33 eV). The transition below 9.50 eV have been attributed to transitions to diffuse Rydberg states (6s and 6p). The other bands are due essentially to valence transitions.     

The ultraviolet spectra of silocyclobutanes

The UV spectra of Si-substituted silocyclobutanes in vacuum were studied. The bathochromic shift of the absorption band, disclosed by comparison with bands of the corresponding acyclic compounds, can be explained by the highly strained state of the four-membered ring. This same principle in disilocyclobutanes leads to the reduction of the barrier effect of the methylene group, disrupting the interaction of the silicon atoms in the unstrained molecule.     

Absorption spectra in the vacuum ultraviolet region of small molecules in condensed phases

With radiation from a synchrotron we measured the spectra of several small molecular species, in the solid phase at 10K, either pure--O2, NO, CO2, N2O, H2O and NH3--or, for NH3, also dispersed in Ar at molar ratio 1/250, from the onset of absorption in the ultraviolet region until the limits of transmission by crystalline LiF or solid Ar. In a quantitative treatment of spectral data, we fitted the total absorption profile divided by wavenumber to Gaussian curves of minimal number, and made tentative assignments of electronic transitions and vibrational structure by comparison with spectra of gaseous species. These results illuminate the nature of electronic spectra of samples in solid phases in the vacuum ultraviolet region.     

The vacuum ultraviolet photoelectron spectrum of difluoramine

The HeI photoelectron spectrum of difluoramine is reported. The seven ionization potentials within the Hel region have been assigned. Extensive vibrational structure on the first band of both HNF₂ and DNF₂, and ab initio calculations of the ionic geometry, indicate that the ground ionic state is planar.     

Emission spectra of an argon inductively coupled plasma in the vacuum ultraviolet: background spectra from 85 to 200 nm

The background spectra emitted from an argon ICP discharge have been recorded over the spectral range 85 to 200 nm. These vacuum ultraviolet spectra were acquired by coupling the ICP to a 0.5-m Seya-Namioka vacuum monochromator, through a helium purged side-arm. Background features observed include emission from the resonance lines of ArI, and emission from gas impurities such as oxygen, nitrogen, carbon and hydrogen.     

Coupled-cluster studies of the electronic excitation spectra of silanes

The electronic excitation spectra of unsubstituted linear silanes (n-Si(m)H(2m+2), m = 1-6), cyclopentasilane (c-Si5H10), and neopentasilane (neo-Si5H12) have been studied at the coupled-cluster approximate singles and doubles (CC2) level using Dunning's quadruple-zeta basis sets augmented with diffuse functions (aug-cc-pVQZ). Comparisons with measured ultraviolet spectra for Si2H6 and n-Si3H8 show that CC2 calculations using these basis sets yield excitation energies in good agreement with experiment. The calculated excitation thresholds for Si2H6 and n-Si3H8 of 7.61 and 6.68 eV are only 0.05 eV larger than the gas-phase values of 7.56 and 6.63 eV, respectively. For n-Si4H10, n-Si5H12, and neo-Si5H12, the calculated excitation thresholds of 6.51, 6.14, and 6.87 eV for the lowest dipole-allowed transitions are about 0.4 eV larger than the corresponding liquid-phase data of 6.05, 5.77, and 6.53 eV; the discrepancy can mainly be attributed to solvent effects. The obtained excitation thresholds for n-Si6H14 is 5.85 eV, whereas no experimental data are available for its optical gap. Calculations using the Karlsruhe triple-zeta valence basis sets augmented with single and double sets of polarization functions show that very large basis sets augmented with diffuse functions are needed for obtaining accurate excitation energies. The optical gaps for silanes obtained using the triple-zeta polarization basis sets were found to be 0.4 and 0.2 eV larger than those obtained using Dunning's quadruple-zeta basis sets. Excitation thresholds calculated at density functional theory levels using generalized gradient approximation are 0.7-1.0 eV smaller than the experimental values and by employing hybrid functionals they are 0.3-0.4 eV below the experimental thresholds. By adding the present basis-set correction and environmental effects to the previously calculated CC2 value for the excitation threshold of the Si29H36 silicon nanocluster, the extrapolated absorption threshold is 4.0 eV as compared to the recently reported experimental value of 3.7 eV.     

Negative-ion mass spectra of methylated diuretics.

The negative-ion mass spectra of 19 methylated diuretics are presented and correlations between these spectra and the chemical structures of the compounds are indicated. The spectra are of interest as the basis of an analytical method for the identification of small quantities of diuretics in the urine of hypokalemic patients.     

The Raman and near ultraviolet spectra of thioanisole

The liquid Raman and vapour phase u.v. absorption spectra of thioanisole have been recorded and vibrational analyses performed. The vibrational structure accompanying the π* ← π electronic transition is similar to that in related monosubstituted benzenes and shows activity in the in-plane ring vibrations 1, 7a, 6a, 6b, 12 and 18b.     

Vibrational spectra of 1,3,5-hexatriene and methylated derivatives

The ground state vibrational spectra of E-hexatriene, Z-hexatriene, E,E-heptatriene, E,E,E-octatriene, and E-2,5-dimethyl-hexatriene are reported. For E- and Z-hexatriene complete vibrational assignments, and for heptatriene, octatriene, and dimethyl-hexatriene near-complete assignments are obtained. The effects of terminal and lateral methyl-substitution are compared.     

The vacuum ultraviolet absorption spectrum of 1,1-dichloro-2,2-difluoroethylene

The vacuum ultraviolet absorption spectrum of 1,1-dichloro-2,2-difluoroethylene is reported. Two Rydberg progressions converging on an ionization potential of 9.69 ± 0.01 eV are described. The π* ← π (V ← N) transition energy (57471 cm⁻¹) and ionization potential are discussed in terms of data for similar compounds.     

Transparent perfluoropolyethers for vacuum ultraviolet applications

After a broad scouting based on quantum chemical calculations, optical absorption measurements in the vacuum ultraviolet (VUV) wavelength region between 140 and 190 nm were performed on a narrower series of commercial and experimental liquids. By elimination of sources of external contamination, mainly due to atmospheric gases, the analysis of the contributions to the absorption related to the backbone structure and to the chain end composition allowed the synthesis of a novel family of linear perfluoropolyethers (PFPEs) with optical absorbance at 157 nm between 0.3 and 0.6 cm(-1) in a broad range of compositions and molecular weights. The dependence of the optical threshold on the PFPE composition demonstrates that -OCF2- is the most transparent segmental unit in the VUV region.