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  • 1990-1994  (12)
  • 1980-1984  (3)
  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 88 (1984), S. 5513-5519 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 87 (1983), S. 2121-2127 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 88 (1984), S. 2250-2255 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 96 (1992), S. 5857-5877 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The 1Σ+(0+) and 3Σ−(0+) Rydberg states as well as the V 1Σ+(0+) valence state of hydrogen chloride isotopomers are studied using (2+1) resonance enhanced multiphoton ionization (REMPI) and time-of-flight mass spectrometry (TOFMS). Pulsed supersonic expansion provides sufficient rotational cooling to facilitate rotational analysis. Polarization selection in conjunction with fragment and isotope discrimination provide the first unambiguous identification of all vibrational bands from v'=3 to 32 of the V 1Σ+(0+) state. REMPI excitation spectra from the v‘=0 level of the X 1Σ+(0+) state through vibrational levels of the broad V 1Σ+(0+) state suggest non-Franck–Condon transitions. Perturbations in intensity, line position, and rotational constants are consistent with the near-adiabatic nature of the short-range E 1Σ+(0+) Rydberg state and long-range V 1Σ+(0+)state. Evidence for Rydberg∼valence interaction and repulsive superexcited states is provided by the detection of strong H+ and Cl+ ion yields. The onset of a distinct Cl+ channel is detected for the first time and confirms the presence of at least two dissociation pathways at the three-photon energy and at large internuclear distance.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 95 (1991), S. 2336-2351 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The optical spectrum of N2O in the region from 80 000 to 87 000 cm−1 has been investigated by two- and three-photon resonant multiphoton ionization mass spectrometry. State symmetry identification has been performed by the use of linearly and circularly polarized light in both two- and three-photon absorption, conclusively confirming the assignment of the spectrum as that of the 3pσ 1Π Rydberg state of N2O. The new spectra and polarization experiments also permit observation and analysis of previously unreported vibronic coupling effects in this state. Mass spectral data reveal significant variation in the degrees of fragmentation into NO+ and N+2 as a function of vibrational and rotational excitation in the intermediate state. An apparent progression of a previously unreported second electronic band is also observed and for which a possible assignment is discussed.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 95 (1991), S. 6261-6270 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The excited state dynamics of the indole(Ar)1, indole(d1)(Ar)1, indole(Ar)2, and indole(CH4)1 van der Waals clusters have been investigated in a free jet expansion. Excited state vibrational frequencies were determined using multiphoton ionization and fluorescence excitation spectroscopy. Time resolved emission spectroscopic techniques were used to determine vibrational predissociation rates and product state distributions. All of the clusters were found to predissociate when excited with sufficient vibrational energy in the S1 state. The predissociation dynamics were found to be consistent with a serial model in which energy transfer from the indole skeletal modes to the van der Waals modes precedes the dissociation step. The density of van der Waals vibrational states was found to be the most important factor in determining the predissociation dynamics.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 99 (1993), S. 67-79 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We have undertaken an extensive study of the spectroscopy and dynamics of the S1–S0 transition in jet-cooled 1-methylindole and 1-methyl(d3)indole. The energy-resolved fluorescence decays resulting from picosecond excitation of S1 vibrational modes display unusual quantum interference effects which have been attributed to the excitation of a large number of quasidegenerate states even at relatively low levels of vibrational excitation. This has been attributed to rovibrational coupling in which the selection rules are much less restrictive than is normally the case with rigid planar molecules. A significant rotational temperature dependence of the vibrational dynamics has been measured which serves to corroborate this model.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 99 (1993), S. 80-90 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The excited state dynamics of the 1-methylindole(Ar)1, 1-methyl(d3)indole(Ar)1, 1-methylindole(CH4)1, and 1-methyl(d3)indole(CH4)1 van der Waals clusters have been investigated in a free jet expansion. Time and energy resolved emission spectroscopic techniques were used to determine intramolecular vibrational redistribution rates and vibrational predissociation rates. All of the clusters were found to predissociate when excited with sufficient vibrational energy in the S1 state. The predissociation dynamics were found to be consistent with a serial model in which energy transfer from the 1-methylindole skeletal modes to the van der Waals modes precedes the dissociation step. These results are compared with earlier results on indole clusters. The density of vibrational states in the van der Waals clusters was found to be the most important factor in determining the vibrational dynamics. The role of the chromophore skeletal vibrations is also discussed.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 98 (1994), S. 12834-12843 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 100 (1994), S. 6129-6136 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The two-photon resonant, three-photon (2+1) ionization spectra of jet-cooled mXenXe, at energies near the Xe* 5d[5/2]03 state, are reported. A new progression has been observed and is attributed to transitions from the van der Waals ground state, X 1Σ+g(0+g), through bound vibrational levels of an excited state of gerade symmetry. The analysis of some 26 closely spaced vibronic bands and isotope effects provides information on the excited and ground state potential energy curves. The vibrational quantum number of the lowest frequency band near 82 539.1 cm−1 is assigned to v'=6±1. For v'=6 this leads to molecular constants Te' (approximately-equal-to) 82 514.9 cm−1, ωe' (approximately-equal-to) 5.7955 cm−1, and ωexe' (approximately-equal-to) 0.07491 cm−1. The upper state can be described by a Morse potential with dissociation energy De' (approximately-equal-to) 112.10 ± 0.05 cm−1 and internuclear separation Re' (approximately-equal-to) 5.51 ± 0.03 A(ring). This is consistent with assignment to a Rydberg molecular state of either the B 2Π1/2g or D 2Σ+1/2g ion core. At the Xe 1S0+Xe* 5d[5/2]03 threshold the molecular spectrum terminates and continuum absorption is evidenced by a rise and fall in the fragment ion yield. The direct determination of the dissociation limit for the excited state is used to derive the ground state dissociation energy De‘(approximately-equal-to) 196.32 ± 0.05 cm−1.
    Type of Medium: Electronic Resource
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