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  • American Institute of Physics (AIP)  (6)
  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 111 (1999), S. 10747-10749 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The study of the phenol–(NH3)3 cluster with two-color two-photon ionization shows that the main ion observed with delays between the lasers up to a few hundred nanoseconds is the (NH4)+(NH3)2 fragment, resulting from direct ionization of the (NH4)(NH3)2 product coming from the reaction: PhOH(S1)–(NH3)3→PhO•+(NH4)(NH3)2. © 1999 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 117 (2002), S. 2120-2130 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Fe+-(CO2)n ion-molecule complexes are produced by laser vaporization in a pulsed-nozzle cluster source. These species are analyzed and mass-selected using a specially designed reflectron time-of-flight mass spectrometer. Infrared photodissociation of these complexes is investigated with an optical parametric oscillator/amplifier system using wavelengths near the CO2 asymmetric stretch vibration (2349 cm−1). Dissociation occurs by successive elimination of CO2 molecules. Tunable laser experiments obtain infrared resonance-enhanced photodissociation spectra for these complexes. Small complexes have CO2 asymmetric stretch resonances shifted to higher frequency than the free CO2 mode. The blueshift decreases initially with cluster size, but becomes nearly constant after the n=4 cluster. Argon-tagged complexes, e.g., Fe+-(CO2)n⋅Arm, photodissociate via the same CO2 resonances by elimination of argon. Except for the n=1 complex, bands for the tagged complexes occur at the same frequency as those for the corresponding CO2 complex without argon. Larger complexes exhibit additional resonances near the free CO2 asymmetric stretch indicating "surface" molecules not attached to the metal. Blueshifted resonances also persist in these complexes attributed to "core" ligands attached to the metal ion. In the largest clusters studied (n=9–14), additional resonances with an intermediate blueshift are measured associated with "caged" CO2 molecules not attached to the metal. These measurements demonstrate that infrared photodissociation spectroscopy has exciting potential to study clustering structures and dynamics around metal ions. © 2002 American Institute of Physics.
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 112 (2000), S. 8794-8805 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Femtosecond pump–probe ionization experiments on small NaI–Sn=1–7 clusters, S:NH3,H2O, are reported. The excitation of the clusters by the pump laser induces the NaI bond breaking within the cluster as well as evaporation of solvent molecules both in the excited and ionic states. Depending on the detection scheme used, namely one-photon or resonant two-photon ionization, the resulting Na+–Sn time-dependent signals are not similar. This reflects the major role of the ionization process in the nature of the dynamics probed. Furthermore, a solvent-selective behavior evidenced on the Na+–Sn signals has been related to different cluster structures according to the solvent nature: NaI seems to be embedded within ammonia clusters while it sticks on the surface of water clusters, when they are larger than four molecules. © 2000 American Institute of Physics.
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  • 4
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Review of Scientific Instruments 71 (2000), S. 1097-1099 
    ISSN: 1089-7623
    Source: AIP Digital Archive
    Topics: Physics , Electrical Engineering, Measurement and Control Technology
    Notes: At the output of a laser ion source, a high current of highly charged ions with a large range of charge states is available. The focusing of such a beam by magnetic elements causes a nonlinear space-charge field to develop which can induce large aberrations and emittance growth in the beam. Simulation of the beam from the CERN laser ion source will be presented for an ideal magnetic and electrostatic system using a radially symmetric model. In addition, the three dimensional software KOBRA3 is used for the simulation of the solenoid line. The results of these simulations will be compared with experiments performed on the CERN laser ion source with solenoids (resulting in a hollow beam) and a series of gridded electrostatic lenses. © 2000 American Institute of Physics.
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  • 5
    ISSN: 1089-7623
    Source: AIP Digital Archive
    Topics: Physics , Electrical Engineering, Measurement and Control Technology
    Notes: A laser ion source using a CO2 laser focused onto a solid target is under study at CERN for the production of high currents of highly charged heavy ions, for possible use in the preinjector for the large hadron collider. A new expansion and extraction layout was installed in this test facility, improving the alignment and making the target to extraction distance more flexible. A two solenoid beam transport system was studied for providing the matching of the beam to a radio-frequency quadrupole. An electrostatic beam transport using gridded electrostatic lenses was designed and constructed as an alternative to a magnetic system. Results show an increased overall current transmission for the electrostatic case. Investigation of the laser parameters required for the production of 1.4×1010 Pb25+ ions in a 5 μs pulse, has been performed using the TIR-1 laser facility at power densities up to 1014 W cm−2 for a focal spot size of 65 μm. The results of the latest scaling are presented. © 2000 American Institute of Physics.
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 110 (1999), S. 1521-1525 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The picosecond evaporation dynamics of ammonia molecules from Na(NH3)n clusters produced via the dissociation of NaI within an ammonia cluster is studied experimentally. A time dependence of the mass selected ion signal is observed only for one cluster size and not for larger clusters nor for smaller ones. It will be shown that evaporation in the ionic state is responsible for the absence of an observation of the evaporation in the neutral state. The variation of the ionization cross section with cluster size is the key point for the interpretation of the results. © 1999 American Institute of Physics.
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