Search results for "absorption spectroscopy"
showing 10 items of 828 documents
Nonlinear optical susceptibilities of polysilanes: exciton effect
1992
Abstract Third-order nonlinear optical susceptibilities of σ-conjugated one-dimensional polymers have been calculated in a tight-binding model by taking account of the formation of excitons due to long-range Coulomb interactions. The spectrum of third-harmonic generation (THG) exhibits peaks due to excitons as well as unbound electron—hole states, in contrast to the linear absorption spectrum which is dominated by the lowest exciton state. The results are in excellent agreement with recent experiments in polysilanes not only for THG but also for linear absorption, two-photon absorption, and electroabsorption in a mutually consistent way.
Concave π-prismand hydrocarbon [2.2.2]cyclophanes and their crystalline Ag-triflate complexes
1999
New small concave hydrocarbon cyclophanes were prepared via the well-known HD-2SO2-method. The cyclophanes obtained are isomers of the very well-known [2.2.2]p,p,p-cyclophane, C24H24, a π-prismand efficiently complexing Ag+-ion. X-ray crystal structure determinations showed the bis-sulfide 7 (1,10-dithia[3.3.2]m,p,p-cyclophane) to be helically chiral and that the conformation of the parent hydrocarbon cyclophane 13 ([2.2.2]m,p,p-cyclophane) does not change dramatically upon complexation with the Ag+-ion. The 16- and 17-membered [2.2.2]m,m,p- and [2.2.2]m,p,p-cyclophane (15 and 16) also act as π-prismands and form surprisingly similar crystalline 1:1 Ag-triflate complexes (π-prismates) as th…
The abundance of Au, Pt, Pd, and the mode of heavy metal fixation in highly polluted sediments from the Rhine River near Mainz, West Germany
1984
The Au, Pt and Pd contents of the sediments of Ginsheimer‐Altrhine River, a channel of the Rhine river which drains one of the most industrialized regions of western Europe, have been determined by flameless atomic absorption spectrophotometry. The abundances of these noble metals range from 96–460 ppb Au; 734 ppb‐31 ppm Pt and 32 ppb‐4 ppm Pd. The extremely high concentrations, particulary those of Pt and Pd, are attributed to their use in industry and are due to the formation and concentration of metal‐organic complexes, mainly at the interface between an extremely reducing and an oxidizing aquatic environment. Differential thermal analyses of the polluted sediments in comparison to the p…
Synthesis and photophysical properties of hyperbranhced polyfluorenes containing 2,4,6-tris(tiophen-2-yl)-1,3,5-triazine as the core
2011
A series of new hyperbranched polymers containing a 2,4,6-tris(thiophen-2-yl)-1,3,5-triazine core unit and polyfluorene chain arms have been synthesized via Suzuki coupling, and characterized by NMR, IR and GPC. All the polymers exhibit good thermal stability with a high decomposition temperature. By changing the 2,4,6-tris(thiophen-2-yl)-1,3,5-triazine/fluorene ratio the UV-vis absorption and emission spectra can be partially tuned. It has been found that the polymers containing a low ratio of 2,4,6-tris(thiophen-2-yl)-1,3,5-triazine units (P1-P3) have an absorption maximum around 385 nm, localized in the polyfluorene chain, and a shoulder around 425 nm ascribable to a charge transfer stat…
<title>Iodine and mercury resonance lamps and their spectrum in far UV</title>
2001
Electrodeless iodine, mercury iodide, and mercury radio- frequency discharge lamps have been made to provide effective sources of atomic spectra for analytical spectroscopy providing powerful resonance radiation of iodine and mercury in the 120-253 nm region. The lamps are required and can be used for spectral calibration, resonance absorption, and fluorescence detection techniques, for investigation of atomic characteristics (e.g., branching ratios) and other purposes where intense monochromatic spectra are needed. Production technology, development, and investigation of the UV and VUV emission are described.© (2001) COPYRIGHT SPIE--The International Society for Optical Engineering. Downlo…
Structural characterization of frozen n-heptane solutions of metal-containing reverse micelles
2007
The microstructure of temperature-quenched solutions of reverse micelles formed by sodium, cobalt, ytterbium, and cobalt/ytterbium bis(2-ethylhexyl)sulfosuccinate in n-heptane has been investigated by SAXS and EXAFS. Some changes in the X-ray absorption spectra with respect to the same systems at room temperature have been observed. The analysis of the SAXS spectra leads to the hypothesis that at 77 K the closed spherical structure of reverse micelles is retained and that during the temperature quench they undergo a clustering process involving the transition from a quite random dispersion to the formation of more or less large clusters of strongly packed reverse micelles. This behavior is …
Infrared spectroscopy on lead silicate glass
1993
The reflectance spectra of some lead silicate glasses of general formula (PbO)x(SiO2)y have been measured in the infrared frequency range from 50 to 4000 cm−1. The dispersion and absorption spectra in the range 50–2000 cm−1 have been calculated from the reflectance data using the Kramers-Kronig relations. The band at ∼ 135 cm−1 is assigned to the stretching vibration of lead-oxygen bonds. The shoulder band of the silicon-oxygen stretching mode at ∼900 cm−1 shows a weak coupling of those bonds to the Pb2+ modifier. The vibration strength of those bands shows that the number of the Pb2+ modifier increases first up approximately to 50 Mol% with the increase of PbO content and then decreases ra…
Polymerization of mono- and multilayer forming diacetylenes
1977
Heptadeca-2,4-diine-1-ol and Heptadeca-2,4-diine-1-acid were synthesized and their polymerization behaviour in the solid state was investigated. Both compounds polymerize thermally below the melting point and photochemically under the action of uv-light to form polymers via 1,4-addition to the conjugated triple bonds with a backbone of conjugated double-and triple-bonds. The photoresponse spectra resemble the absorption spectra exhibiting maxima of photoreactivity in the absorption band of the conjugated triple bonds of the monomers.
Photoreactive Langmuir–Blodgett–Kuhn multilayer assemblies from functionalized liquid-crystalline side chain polymers, I. Homopolymers containing azo…
1991
Stable monomolecular layers of a liquid-crystalline homopolymer bearing azobenzene chromophores in the mesogenic side groups could be prepared at the water–air interface by slow compression at room temperature. From the area per monomer unit of A0≈0.25 nm2 a structural model with tightly packed azobenzene groups oriented nearly parallel to the surface normal was deduced. After transfer to a solid support in a Y-type mode the obtained Langmuir–Blodgett–Kuhn (LBK) multilayer assemblies of varying thicknesses (from a double layer to a thick film of d = 238 nm, capable of guiding optical modes) were prepared and analyzed by X-ray reflection and optical evanescent wave techniques. A monolayer th…
Shallow-donor impurities in indium selenide investigated by means of far-infrared spectroscopy.
1992
Shallow impurities in n-type indium selenide (InSe) have been investigated by means of Fourier-transform spectroscopy in the far-infrared region. Three electric dipole transitions have been identified: 1s-2${\mathit{p}}_{\ifmmode\pm\else\textpm\fi{}}$, 1s-2${\mathit{p}}_{0}$, and 1s-3${\mathit{p}}_{\ifmmode\pm\else\textpm\fi{}}$, corresponding to electrons bound to native donors and tin-, silicon-, and chlorine-related donors, whose ionization energies (17.6, 18.1, 18.8, and 19 meV, respectively) have been determined through the Guerlach-Pollmann model. That model was also used to calculate the oscillator strengths of those dipole transitions, and then to estimate the shallow-donor concentr…