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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 112 (1990), S. 8983-8984 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 113 (1991), S. 3619-3621 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 93 (1990), S. 7800-7802 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We have accumulated large pure carbon clusters (Fullerenes) on a surface. These clusters were produced by laser vaporization of graphite in a static rare-gas atmosphere. Their presence on the surface was confirmed by an isotope scrambling experiment using a laser-desorption/laser-ionization mass spectrometric detection scheme.
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  • 4
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 92 (1990), S. 7625-7635 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The technique of laser desorption followed by jet cooling allows wavelength-selective as well as mass-selective detection of molecules, desorbed from a surface without fragmentation. Resonance enhanced multi photon ionization (REMPI) spectra of the para-amino benzoic acid (PABA) molecule and its methyl and n-butyl ester were obtained in this way. The origin of the S1←S0 transition in PABA was found at 34173±2 cm−1. The adiabatic ionization potential of PABA was determined as 7.998±0.001 eV. In addition, jet-cooled REMPI spectra of the PABA dimer and its ring-deuterated isotopes were recorded. The dimer is formed by two identical hydrogen bonds between the carboxylic acid groups. The excitation in the dimer is found to be almost completely localized in one monomer unit. Clusters of PABA molecules with molecules seeded in the beam (argon, methanol, water) were resonantly detected as well, using PABA as the chromophore.
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  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 89 (1988), S. 2588-2589 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: CO molecules in their electronic and vibrational ground state were state selectively detected using a tunable ArF excimer laser. Rotational state selectivity is due to the one-photon resonance of the spin-forbidden a 3Π, v'=2←X 1∑+,v‘=0 transition. Subsequent absorption of two additional ArF laser photons yields, via a dissociative continuum, electronically excited C(3 1P) atoms, whose fluorescence is detected.
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 111 (1999), S. 10750-10753 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The infrared (IR) absorption spectra of the jet-cooled C6H6 and C6D6 cations, complexed with Ar, are measured throughout the 450–1500 cm−1 region via IR-laser-induced vibrational dissociation spectroscopy. The IR spectrum of the C6H6–Ar cation is dominated by a Fermi resonance between the IR active ν11 mode and two components of the combination mode of the lowest frequency modes ν6 and ν16. A stringent upper limit of 316 cm−1 is found for the value of the dissociation limit D0 of the neutral C6D6–Ar complex. © 1999 American Institute of Physics.
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  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 103 (1995), S. 5269-5274 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: In a laser desorption jet-cooling molecular beam spectrometer the concentration of translationally and internally cooled laser desorbed organic molecules that can be achieved is experimentally determined. Sensitive direct absorption detection of laser desorbed jet-cooled diphenylamine (DPA) via cavity ring down (CRD) spectroscopy on the S1←S0 transition around 308 nm is used to measure the line-integrated absolute absorption of the pulse of laser desorbed DPA molecules. The absolute cross section for the various vibrational bands of the electronic transition that is used, is determined in a separate two-color ionization experiment. It is concluded that the optimum beam intensity that is obtained with laser desorption is comparable to the beam intensity that is obtained in the same spectrometer by conventional seeding of the desired species at a partial pressure of 10−4. © 1995 American Institute of Physics.
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  • 8
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 102 (1995), S. 1925-1933 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Direct time and spatially resolved detection of metastable CO molecules, prepared in selected quantum states via pulsed laser excitation, is experimentally demonstrated in a molecular beam machine. Characterization of the molecular beam in terms of parallel and perpendicular velocity distributions and rotational temperatures is performed. A direct two-dimensional (2D) demonstration of the mass-focusing effect in binary gas mixtures is given. Two-dimensional imaging of the spatial distribution of the metastable a 3Π CO molecules in the beam after passage through a hexapole field is used to study hexapole focusing performance. Structured 2D images demonstrate the dependence of the focusing characteristics on the magnitude of the Λ-doubling and on the angular dependence of the focusing force in a hexapole consisting of cylindrical rods. © 1995 American Institute of Physics.
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  • 9
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 85 (1986), S. 6914-6922 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The first observation of (2+1)-REMPI of H2O and D2O is reported. With the use of a high power tunable excimer laser radiating at 248 nm, the H2O and D2O molecules are ionized after resonant two-photon absorption into the predissociated C˜ 1B1 state. The clearly observable peaks in the (2+1)-REMPI spectra are all identified and can be used for sensitive state selective detection. Parent molecular fluorescence excitation spectra (C˜ 1B1→A˜ 1B1) were remeasured over an increased spectral range, and are remarkably the same as the (2+1)-REMPI spectra. Furthermore the OH/OD (A 2Σ+, v'=0→X 2Π, v‘=0) photofragment fluorescence excitation spectra were measured, and these spectra do not show any nonresonant background as stated before. Additional fluorescence bands starting from the vibrationally excited A 2Σ+, v'=1 state were observed. Simulation of the observed REMPI and fluorescence excitation spectra yields the branching ratios for the predissociation, ionization, and fluorescence processes.
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  • 10
    Electronic Resource
    Electronic Resource
    [s.l.] : Macmillian Magazines Ltd.
    Nature 411 (2001), S. 174-176 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] The ability to cool and manipulate atoms with light has yielded atom interferometry, precision spectroscopy, Bose–Einstein condensates and atom lasers. The extension of controlled manipulation to molecules is expected to be similarly rewarding, but molecules are not as amenable to ...
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