Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 108 (1986), S. 1698-1699 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    ISSN: 1432-072X
    Keywords: Erythrobacter ; Photosynthetic bacteria ; Aerobic bacteria ; Bacteriochlorophyll-protein complex
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Bacteriochlorophyll(Bchl)-protein complexes were isolated from obligate aerobic bacteria, Erythrobacter longus and Erythrobacter species OCh 114. The apparent molecular weights, absorption spectra and polypeptide compositions of the light-harvesting complexes were, in general, similar to those of the light-harvesting Bchl-protein complexes of purple photosynthetic bacteria. The reaction center complexes of these bacteria also showed similar properties to those of the purple bacteria except for slightly altered polypeptides. However, the following characteristic features of the light-harvesting systems were found in these aerobic bacteria. Major carotenoids were not bound to the Bchl-protein complex in E. longus. In Erythrobacter sp. OCh 114, a new type of Bchl-protein complex which showed a single absorption band in the near infrared region at 806 nm was obtained. The reaction center of strain OCh 114 was associated with a c-type cytochrome.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 93 (1990), S. 1054-1060 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We have performed model calculations on the vibrational relaxation (including population relaxation and dephasing) induced by intermolecular interactions in the liquid phase. Taking into account the points that (1) intermolecular interactions are primarily of atom–atom origin, and (2) the relaxation resulting from quasielastic collisions are considered to be dominant, we have calculated how the eigenvector (on the Cartesian coordinate basis) of an initially excited normal mode is transformed when the three components corresponding to one atom are displaced without change in the vibrational energy. On this basis, the relative efficiency of intramolecular energy flow from the initial state has been estimated. Calculations on the CH stretches of dichloromethane and the OH stretch of methanol are compared with existing experimental results.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 6
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Vibrational mode assignments of S1 trans-stilbene (tSB) in a jet, particularly those for fundamental vibrational levels above the isomerization barrier, are reported with three partially isotope-substituted analogues (C6 H5 –13CH=13CH–C6 H5 , C6 H5 –CD=CD–C6 H5 , and C6 D5 –CH=CH–C6 D5 ). Vibrational levels are assigned on the basis of the frequency shifts due to isotopic substitution. The established mode assignments then enable us to discuss the individual band intensities in the fluorescence excitation spectra which bear mode specific information on the isomerization dynamics in isolated tSB molecules. Upon deuteration, the intensities of several CH deformation modes increase drastically as their frequencies become lower than the isomerization barrier. Intensities of several fundamental bands are found much smaller than those of nearby combination bands, contrary to what is expected from ordinary absorption spectra in condensed phases. The intensity ratio of the 71 (C=C stretch) to the 00 band is semiquantitatively studied with reference to a molecular-orbital calculation, the resonance Raman intensity, and the absorption intensity in a low-temperature crystal. The unusually low fluorescence excitation intensities are ascribable to large isomerization rates specific to certain kinds of fundamental vibrational levels.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 89 (1988), S. 3945-3950 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Dependence of the inverse Raman band shape on the probe frequency was observed in detail in the region of a single photon resonance with a structured electronic absorption band of rhodamine 640 (a highly fluorescent molecule). Three parameters were introduced to represent an inverse Raman band shape which is strongly dependent on the probe frequency. The band-shape parameters derived from the observed data could be simulated using a vibronic treatment based on a Herzberg–Teller expansion. The simulation is shown to be potentially useful for obtaining information on the excited electronic states of fluorescent molecules whose spontaneous Raman spectra are difficult to observe.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 8
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 103 (1995), S. 8964-8979 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Structures and vibrational force fields of all-trans-oligoenes of various chain lengths are studied by ab initio molecular orbital (MO) calculations at the second-order Møller–Plesset perturbation (MP2) level with the 3-21G and 6-31G* basis sets. Dependencies of the structure parameters and the force constants of trans-oligoenes on the chain length and the position in the chain are analyzed quantitatively. The structure and the force field of trans-polyacetylene are extrapolated from those of trans-oligoenes. Normal coordinate calculations are performed for trans-polyacetylene on this basis. The following results show the reliability of the structure and the vibrational force field of trans-polyacetylene obtained in the present study. (1) The calculated C=C and C–C bond lengths of trans-polyacetylene are in satisfactory agreement with the observed. (2) The calculated δ=0 (null phase difference) frequencies are in good agreement with the observed infrared and Raman frequencies. (3) The calculated phonon dispersion curves are consistent with some criteria obtained experimentally. (4) Most of the observed infrared bands which do not correspond to the δ=0 frequencies of trans-polyacetylene are assignable to peaks in the profile of the calculated density of vibrational states. (5) The calculated hydrogen-amplitude-weighted density of states is in reasonable agreement with the observed inelastic neutron scattering spectrum. © 1995 American Institute of Physics.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 9
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 101 (1994), S. 4496-4504 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The electronic absorption spectrum, the relative Raman intensities upon 0-0 excitation, and the resonance Raman excitation profiles of trans-1,3,5-hexatriene in the region of the 1 1Bu←1 1Ag transition are analyzed on the basis of the structures and vibrational force fields obtained from ab initio molecular orbital (MO) calculations. The second-order Møller–Plesset perturbation (MP2) and the configuration interaction singles (CIS) methods are employed to describe the 1 1Ag and 1 1Bu states, respectively. The vibrational force fields obtained from ab initio MO calculations are scaled in order to fit the calculated frequencies to the observed. The Duschinsky rotation among all the modes of ag symmetry is fully taken into account. Both the calculated absorption spectrum and resonance Raman intensities are in agreement with the observed. This shows the usefulness of the CIS method for estimating the structure and vibrational force field in the 1 1Bu state of trans-1,3,5-hexatriene. On this basis, some refinements are made on the structure and force field in the 1 1Bu state in order to obtain a better fit between the observed and calculated results for the absorption spectrum and resonance Raman intensities. Effects of the frequency changes and Duschinsky rotation upon the electronic excitation are significant in the resonance Raman excitation profiles of some bands. The structure and vibrational force field obtained for the ground electronic state by the simple Hartree–Fock method do not give an appropriate set of parameters for calculating the absorption spectrum and resonance Raman intensities.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 10
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Electronic structures in metallic and insulating phases of the Li, Cu, and Ba complexes of 2,5-R1,R2-DCNQI [R1=R2=Br (abbreviated as DBr) or R1=R2=CH3 (abbreviated as DMe); DCNQI=N,N'-dicyanoquinonediimine; 2,5- is usually omitted] have been studied by observing temperature dependencies of their infrared absorption bands between 295 and 23 K. At room temperature, the wave numbers (ν˜i) of infrared absorption bands of R1,R2-DCNQI and its Li and Ba complexes are linearly correlated with the degrees of charge transfer (ρ) (ρ=−0.5 and −1.0e for the Li and Ba complexes, respectively). The ν˜i–ρ relationships indicate that the ρ value for the Cu complexes is −0.67e. This result is consistent with the previously established view that the Cu cations in the Cu complexes at room temperature are in a mixed-valence state of Cu1.33+. In the infrared spectrum of Cu(DBr–DCNQI)2 at room temperature, no electron–molecular vibration (EMV) coupling bands are observed.Below the metal–insulator (M–I) transition temperature (TMI), EMV bands grow continuously and the ordinary infrared bands observed at room temperature gradually split into three bands with decreasing temperature. Similarly, the infrared bands of Li(DBr–DCNQI)2 split into two bands. These splittings are due to an inhomogeneous charge distribution in the DCNQI columns produced by the freezing of charge-density wave (CDW). The peak-to-peak amplitudes of CDWs in the DCNQI columns estimated by use of the ν˜i–ρ relationships are 0.08±0.04 and 0.40±0.04e, respectively, for the Li and Cu complexes of DBr–DCNQI. The state of the frozen CDW is inferred from the number of split bands. Based on the observed continuous change of the infrared spectra of Cu(DBr–DCNQI)2 and the discontinuous changes of other quantities such as x-ray satellite reflections, lattice parameters, and magnetic susceptibilities, the M–I transition in Cu(DBr–DCNQI)2 may be described as follows: (1) above TMI the charges on Cu cations (two Cu1+'s: one Cu2+) are dynamically averaged to +1.33e through the Cu...N≡C bridge. (2) At TMI the charges abruptly localize in the order of (Cu1+...Cu2+...Cu1+...)n. At the same time, the CDWs begin to be frozen in the DCNQI columns. (3) As temperature decreases below TMI, the order of the frozen CDW develops gradually. In contrast to these changes in Cu(DBr–DCNQI)2, neither EMV bands nor band splittings are observed in the infrared spectra of Cu(DMe–DCNQI)2 at low temperatures. Instead, almost all bands show negative absorption lobes on their low-wave number sides and become asymmetric. This asymmetrization is due to interactions between the vibrational levels and low-lying continuous electronic levels responsible for a broad band observed in the 1600–800 cm−1 region.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...