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  • 1
    ISSN: 1520-5827
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    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 82 (1985), S. 1115-1134 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The Rydberg spectrum of benzene is explored by means of linear and circular polarized ultraviolet two-photon absorption spectroscopy of the jet-cooled molecule. A strong gerade Rydberg series previously designated nRg and all its associated vibronic structure seen in linear polarization is shown to have symmetry A1g, but analysis of spectra obtained under circular polarization demonstrates that E2g origins lie just to lower energies. These combined facts give an unambiguous assignment of this series as nd1 (E2g, A1g, A2g). Four new Rydberg series, each having vibrational structure nearly identical to each other and to the ground state ion, are also identified and have E1g or E2g symmetry. The five Rydberg series converging to the first ionization potential have quantum defects 0.77, 0.06, 0.05, 0.02, and −0.11. Bandwidths indicative of ultrafast radiationless decay processes are observed for low-n vibronic states, but higher states are sharp. In addition, an Eg band system is observed at 68 980 cm−1 (69 330 for C6D6) whose term value, vibrational structure, bandwidth, and isotope shift on deuteration are all consistent with its assignment as the lowest Rydberg state converging to the first excited ionic state (second ionization potential).
    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 82 (1985), S. 1135-1146 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We report the observation of six gerade Rydberg series in benzene converging to the first ionization potential, seen in the region from 14 500–18 500 cm−1 as four-photon resonances in the five-photon ionization spectrum of the jet-cooled molecule. Polarization ratios measured for each transition in two- as well as four-photon resonance aid in determining excited state symmetries. We assign a Rydberg series with a quantum defect of 0.76 to higher members of the 3s Rydberg state first seen by Johnson in the near UV two-photon resonant three-photon ionization spectrum of benzene. The observed quantum defect, polarization ratios, and correlation with synchrotron absorption data all strongly support this assignment. Another series, with a quantum defect of 0.24, exhibits a polarization ratio of 4.5±0.5 signifying pure rank four activity. This is the first report of a purely rank four transition in a molecule. We assign this as an excitation to a d2 orbital which when converging to the first ionization potential (the 2E1g cation) gives rise to B1g and B2g Rydberg transitions. Within the D6h point group, these symmetries are allowed only in a four-photon transition. The number of gerade Rydberg series observed as four-photon resonances exceeds those available from the s-(1) and d-(3) bound members of a hydrogenic basis set. The participation of g(l=4) orbitals is indicated as the lowest members of two of the Rydberg series are at the n=5 level.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 63 (1993), S. 3550-3552 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: A hybrid near-field/fiber laser probe has been developed for high flux, reflection mode optical imaging of surfaces on a subwavelength scale. Spatial resolution of ∼100 nm (i.e., ∼λ/10 at λ=1060 nm) has been achieved simultaneously with signals of ∼1014–1015 photons/s, an improvement of ∼103–104 over earlier designs. The probe thus represents an important step in the development of advanced near-field transducers for high bandwidth applications such as high density data storage.
    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 84 (1986), S. 1080-1088 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The ν1 and ν12 ring breathing vibrational modes of pyridine in aqueous solution were studied as functions of concentration (up to 12 M) and pressure (up to 35 kbar) in a diamond anvil cell. The pyridine isotopes -h5 and -d5 exhibited marked differences. The pressure dependence of ν1 is quite linear for pyr-h5 but has pronounced curvature for pyr-d5 and this curvature increases as the concentration decreases. This unusual isotope effect is attributed to pyridine–water complexes involving both O–H ⋅ ⋅ ⋅N and C–H ⋅ ⋅ ⋅O hydrogen bonds. For ν12, the pressure dependence does not change with concentration, but it is at least five times more steep for pyr-h5 than pyr-d5. This may occur because the mass at all six ring vertices becomes equal for the -d5 isotope, making the volume change during vibration very small. At high concentrations, ν1 appears as two distinct peaks with different pressure dependence, indicative of uncomplexed and complexed pyridine. For certain combinations of solvent and concentration, a strong pressure dependent Fermi resonance between the ν1 and ν12 modes appears. Similar experiments were done with a weakly associating solvent, dimethylformamide, and nonassociating solvents, toluene and benzene. For these, the pressure dependence did not change with concentration; this and other features indicate which aspects of the aqueous solution results can be attributed to pyridine–water and pyridine–pyridine complexes.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 92 (1988), S. 1419-1425 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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