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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 96 (1992), S. 1016-1029 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Results from new laser excitation spectra of 20Ne2 have been combined with previously published experimental and theoretical data to provide a consistent picture describing many of the Rydberg states observed below the first ionization limit. These states are found to fall mainly into Rydberg series converging on the ...3σu X 2Σ+u ground core of Ne+2. Spectral data for the npσ 3Σ+g←a 3Σ+u and npπ 3Πg←a 3Σ+u series support the current assignments of the upper states. Although (0–0) bands dominate these series, other vibronic transitions are observed. The 6–23pσ 3Σ+g–a(0–0) bands are more perturbed than the npπ 3Πg–a(0–0) series; hence, data for 4–17pπ 3Π+g–a(0–0) and 4–6fλ(3Σ+g,3Π+g)–a(0–0) were used to determine a value of 34 409±2 cm−1 for the lowest ionization limit of 20Ne2. Rotational constants for the v=0 levels of 4–17pπ 3Πg and 10–23pσ 3Σ+g also are presented.
    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 96 (1992), S. 6407-6422 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Extensive spectra attributable to transitions from the 4sσ a 3Σ+ metastable state of Ar2 to excited Rydberg states have been observed by intracavity absorption spectroscopy and by laser excitation spectroscopy in the afterglow of a pulsed corona discharge. Of these the most extensive and best resolved were the laser induced fluorescence spectra. Most of the spectra can be assigned to vibronic transitions in the nfλ (3Πg,3Σ+g) and npλ (3Πg,3Σ+g)←a 3Σ+u series. The 5pπ3Πg←a 3Σ+u and 7pσ 3Σ+g←a 3Σ+u transitions observed near 19 823 and 19 529 cm−1, respectively, exhibit many bands with v'≠0 in their (v'–v‘) vibrational band system developments. The higher n value members of these and other observed series are dominated by (0–0) transitions. Rotational structure is partially resolved in a few bands of the 7pσ 3Σ+g–a system, but most of the spectra observed appear to be either rotationally unresolved or made up of blended collections of rotational lines. Above the 7pσ, 5pπ pair, the (n+2)pσ 3Σ+g and npπ 3Πg members of the npλ series rapidly coalesce, indicating a rapid onset of decoupling of the electronic orbital angular momentum, Lˆ, from the internuclear axis.Such decoupling leads to np-complex formation at n values much lower than observed in the npλ series of the lighter dimers: He2 and Ne2. From the data for the observed series, the lowest ionization limit of Ar2 (relative to a 3Σ+u,v=0 ) was determined to be 29 373±3 cm−1. Vibrational intervals ΔG(v+1/2) for a 3Σ+u(v≤4) and 7pσ 3Σ+g(v≤2) yield the vibrational constants ωe=296 and 282 cm−1 and xωe=2.5 and 17 cm−1, respectively.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 77 (2000), S. 199-201 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Flexible microdischarge arrays have been fabricated in metal–polymer–metal structures having a total thickness of ∼30 μm (∼1.2 mils). Composed of individual cylindrical devices having a diameter of 150 μm, positive differential resistance (30–120 kΩ), and operating voltages as low as 114 V for a 5 μm thick dielectric layer, the arrays operate at pressures beyond 700 Torr of Ne and in 1 atm of air. For Ne pressures ≤ 200 Torr, emission is produced from Ne ion excited states lying more than 55 eV above the neutral ground state (2p6). The structures reported here are inexpensive to fabricate and have lifetimes beyond 50 h. Arrays that have been sealed by conventional lamination have also been operated successfully. © 2000 American Institute of 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 101 (1994), S. 4561-4571 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Rotationally resolved transitions from the metastable 4sσ a3Σ+u state of Ar2 to the 7pσ 3Σ+g state have been observed by laser excitation spectroscopy in a pulsed corona discharge. Laser induced fluorescence spectra for the 7pσ 3Σ+g←a3Σ+u transition observed near 19 530 cm−1 have led to the first resolved triplet splittings and rotational analyses for Rydberg–Rydberg transitions in Ar2. Analyses for the (0–0), (0–1), (1–0), and (1–1) bands of 7pσ←a are presented here. Bands with v'=2 are observed for this system but exhibit no rotational structure and bands with v'(approximately-greater-than)2 are not observed, indicating that the predissociation lifetimes of these upper levels fall rapidly for v'(approximately-greater-than)1. Data presented lead to rotational energies and molecular constants for the a3Σ+u and 7pσ 3Σ+g states, including the effective rotational constant Be which is determined to be 0.1412 cm−1 and 0.1345 cm−1 for the 4sσ a3Σ+u and 7pσ 3Σ+g states, respectively. Results are compared to ab initio and other calculations, and combined with existing data to produce experimental estimates of D0 and De for the a3Σ+u state of 5700±200 cm−1 and 5850±200 cm−1, respectively.
    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 111 (1999), S. 931-937 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The dissociation energy of the InI ground state (X 1Σ+(O+)) and the relative yield of In(6s 2S1/2) from the photodissociation of InI by sequential two-photon absorption have been measured by laser-induced fluorescence and excitation spectroscopy in the 390–431 nm region. Laser excitation spectroscopy and photoionization experiments demonstrate that the XO+ dissociation energy is 25 340±90 cm−1, which agrees with the value suggested by Vempati and Jones [J. Mol. Spectrosc. 127, 232 (1988)] if the InI ground state is covalent. Seven previously unreported vibrational bands of the InI(B←X) transition have been observed and the molecular emission spectra indicate that the B 3Π1(1) state is predissociated above v=6. Splitting between the fine structure levels of the In np 2P1/2,3/2 (15≤n≤17) states has also been measured by fluorescence suppression spectroscopy, following the three photon excitation of InI in the 450–470 nm interval. © 1999 American Institute of Physics.
    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 108 (1998), S. 5426-5431 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Rotationally resolved transitions of the 5fπ 3Πg←4sσ a 3Σu+ and 5fσ 3Σg+←4sσ a 3Σu+ systems of Ar2 have been observed by laser excitation spectroscopy in a pulsed corona discharge. These systems were previously observed at lower resolution [D. J. Kane et al., J. Chem. Phys. 96, 6407 (1992)] with the system tentatively labeled nlλΠg–a and subsequently assigned as 5fπ 3Πg–a on the basis of theoretical considerations [P. Duplàa and F. Spiegelmann, J. Chem. Phys. 105, 1500 (1996)]. Rotational analyses for the (0–0) and (0–1) bands of both systems are presented and the upper states characterized. The (0–2) bands of the 5fπ–a and 5fσ–a transitions are observed also, as are the (0–0) band of 4fδ 3Δg–a 3Σu+ and the (1–0) and (2–0) bands of 5fπ–a, but with rotational structures insufficiently developed to permit analysis. The linewidths of the rotational lines of the above bands are much broader than are the lines of the 7pσ 3Σu+–a system previously analyzed [C. M. Herring et al., J. Chem. Phys. 101, 4561 (1994)], presumably because of increased lifetime broadening. Several spectral features observed in the 5fπ 3Πg←4sσ a 3Σu+ band structures that are not apparently compatible with this upper state assignment are discussed. © 1998 American Institute of Physics.
    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 115 (2001), S. 5126-5131 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Excitation spectra for the 4pπ 3Πg–a 3Σu〈sup ARRANGE="STAGGER"〉+ system in 20Ne2 and 22Ne2 have been used to characterize the v=0 through v=3 levels in both electronic states. This is the first time levels with v〉1 have been characterized experimentally in either dimer. Rotational analyses lead to Be- and αe-values of 0.5638 cm−1 and −0.9000×10−2 cm−1 and of 0.5113 cm−1 and −0.6651×10−2 cm−1 for the a 3Σu〈sup ARRANGE="STAGGER"〉+ states in 20Ne2 and 22Ne2, respectively. The Be- and αe-values are, respectively, 0.5716 cm−1 and −0.6429×10−2 cm−1 (20Ne2) and 0.5201 cm−1 and −0.4172×10−2 cm−1 (22Ne2) for the 4pπ 3Πg state. The vibrational parameters ωe, xωe are found to be 556.2, 10.2 cm−1, and 593.2, 7.5 cm−1 for the a 3Σu〈sup ARRANGE="STAGGER"〉+ state and 4pπ 3Πg state, respectively, in 20Ne2 with corresponding values of 529.5, 9.75 cm−1, and 567, 7.5 cm−1 in 22Ne2. The observed vibrational level differences [ΔG(v+1/2)-values] for the 4pπ 3Πg state are within 0.5% of analogous spacings for the ground electronic state (X 2Σu〈sup ARRANGE="STAGGER"〉+) of Ne2〈sup ARRANGE="STAGGER"〉+ reported by Kim et al. [Phys. Rev. Lett. 68, 1311 (1992)]. © 2001 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1573-0832
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Penicillium corylophilum Dierckx was isolated from sludge collected at the interface of an aqueous, copper-bearing leachate and an organic, kerosene based, ion exchange solvent. The organism assimilated kerosene and various straight chain and cyclic hydrocarbons including dodecane, hexadecane, octadecane, toluene, benzene, and cyclohexane. Assimilation of kerosene and hexadecane was optimal at pH 2 and was stimulated by yeast extract.
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