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  • Electronic Resource  (8)
  • 1990-1994  (8)
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  • Electronic Resource  (8)
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Year
  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 100 (1994), S. 6240-6262 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The (0,0) band of the B 4Π–X 4Σ− transition of NbO, near 6600 A(ring), has been analyzed from spectra taken at sub-Doppler resolution. The transition is notable for the great width of its Nb nuclear hyperfine structure, which is caused principally by the unpaired 5sσ electron in the ground state interacting with the large magnetic moment of the 4193Nb nucleus (I=9/2). A fit to the ground-state combination differences, including four very precise microwave lines measured by Suenram et al. [J. Mol. Spectrosc. 148, 114 (1991)], has given a comprehensive set of rotational, spin, and hyperfine parameters. Prominent among these are the third-order spin–orbit distortions of the spin-rotation interaction and the Fermi contact interaction, which are large and well determined, reflecting different degrees of spin–orbit contamination of the the 4Σ1/2− and 4Σ3/2− components of the ground state.The δ 2π B 4Π state was hard to fit, for a number of reasons. First, its spin–orbit structure is asymmetric, because of strong perturbations by a 2Π state which has been identified in this work, from among the various weak bands in the NbO spectrum near 7000 A(ring); the result is that many high order centrifugal distortion terms are needed in an effective Hamiltonian model for the rotation. Second, the hyperfine structure is perturbed, not only by this 2Π state, but by distant Σ and Δ states at higher energy. The δ 2σ* C 4Σ− state at 21 350 cm−1 appears to be one of these. The distant states generate large apparent nuclear spin-rotation interactions, both within and between the Λ components of the Π state, as a result of cross terms between matrix elements of the operators −2BJ⋅L and aI⋅L. Similar cross terms arising from the operators AL⋅S and aI⋅L produce corrections to the Fermi contact matrix elements and are responsible for the unexpected negative sign of the magnetic hyperfine parameter d. The "off-diagonal'' quadrupole parameter e2Qq2 is very large, and causes some of the higher J line shapes of the B–X system to be noticeably asymmetric at Doppler limited resolution; its value is consistent with the electron configuration of the B 4Π state being δ 2π.
    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 101 (1994), S. 7300-7310 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: High-resolution intracavity dye laser spectroscopy has been used to obtain sub-Doppler spectra of transitions to 350 rotational levels in the 410 band of the A˜ 1A2–X˜ 1A1 electronic transition of thioformaldehyde. Ground state combination differences from the sub-Doppler spectra, combined with microwave and infrared data, have been used to improve the ground state rotational and centrifugal distortion constants of H2CS. The upper state shows a remarkable number of perturbations. The largest of these are caused by nearby triplet levels, with matrix elements of 0.05–0.15 cm−1. A particularly clear singlet–triplet avoided crossing in Ka' = 7 has been shown to be caused by interaction with the F1 component of the 3162 vibrational level of the a˜ 3A2 state. At least 53% of the S1 levels show evidence of very small perturbations by high rovibronic levels of the ground state. The number of such perturbations is small at low J, but increases rapidly beyond J=5 such that 40%–80% of the observed S1 levels of any given J are perturbed by ground state levels. Model calculations show that the density and J dependence of the number of perturbed levels can be explained if there is extensive rotation-induced mixing of the vibrational levels in the ground state.
    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 99 (1993), S. 6336-6344 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A detailed examination of the structure of the 4Δi ground state of gaseous CoO has been carried out from analysis of the electronic spectrum near 6300 A(ring), using intracavity dye laser and wavelength-resolved fluorescence methods. The intracavity experiments have given the details of the hyperfine structure of the two lowest spin–orbit components at sub-Doppler resolution, permitting the hyperfine parameters, a=0.02295 cm−1 and (b+c)=−0.01117 cm−1, to be derived; from the negative value of the contact interaction the electron configuration is established as (4sσ)2(3dδ)3(3dπ)2. The wavelength-resolved fluorescence experiments have given the relative positions of the four spin–orbit components of the X 4Δi state to ±0.3 cm−1. Based on these measurements, a pair of subbands sharing a common electronic upper level, but with the Ω=5/2 and 7/2 components of the ground state as lower levels, has been recognized. Rotational analysis of Doppler-limited intracavity spectra of these two subbands has given an accurate value for the Ω=5/2–7/2 separation as 304.321±0.007 cm−1.
    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 99 (1993), S. 3320-3328 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: An apparatus has been constructed to produce metal compounds using laser ablation and to investigate their rotational spectra with a microwave Fourier transform (MWFT) cavity spectrometer. The first three such compounds that have been studied are silver chloride, aluminum (I) chloride, and copper (I) chloride, produced by ablation of silver, aluminum, and copper rods in the presence of chlorine gas, using a Q-switched Nd:YAG laser (532 nm). The high resolution and sensitivity available with the MWFT cavity spectrometer have permitted the first determination of nuclear spin–rotation coupling constants for AlCl and CuCl. These constants have been used to examine the electronic structures of the molecules. Values of the rotational and nuclear quadrupole coupling constants have also been improved for the three metal chlorides.
    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 92 (1990), S. 2848-2861 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A detailed re-investigation of the (0,0) and 211 bands of the A˜ 2Πu–X˜ 2Πg transition of 11BO2, near 545 nm, has been carried out from spectra taken at sub-Doppler resolution. Avoided crossings are found to occur between the 2Σ and 2Δ vibronic components of the v2=1 level of the A˜ 2Πu state. These perturbations are the first known examples of K-resonance crossings, which result from an interplay of the electronic Λ-type doubling and the vibrational l-type doubling in a state where the electrostatic parameter ε is small. It turns out that perturbations of this type must always occur in a 2Π electronic state if the ratio A/εω2 is large enough, but have not been seen until now for lack of suitable data. Their existence allows an unusually complete description of the orbital angular momentum effects in both the A˜ 2Πu and X˜ 2Πg states. It has been necessary to fit the avoided crossings by a full matrix treatment of the K resonance. In addition the A˜ 2Πu state, although it appears to be unperturbed at lower resolution, shows an astonishing number of very small random rotational perturbations. These arise from vibronic coupling between the A˜ 2Πu and X˜ 2Πg states of BO2 through the ν3 vibration, which has species σ+u; their presence is consistent with the explanation given by Kawaguchi et al. [Mol. Phys. 44, 509 (1981)] for the sizable negative anharmonicity of the ground state ν3 vibration. About 20% of the available ground state energy levels at 18 300 cm−1 appear to be active in causing level shifts and splittings in the A˜ 2Πu state. The matrix elements are quite small, ranging up to about 600 MHz, but the great number of perturbations indicates the onset of chaotic behavior.
    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 97 (1992), S. 1630-1637 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Intracavity dye laser spectroscopy has been used to obtain sub-Doppler spectra of selected rotational lines in the A˜ 1A2–X˜ 1A1 410 band of thioformaldehyde with very high resolution and sensitivity. Many of the spectra show extra lines due to perturbations involving high vibrational levels of the ground state. Most of the perturbations observed for K'a = 0 and 4 are found to correlate well with previous observations of anomalously long single rotational level fluorescence lifetimes and reduced quantum yields [J. Dunlop and D. J. Clouthier, J. Chem. Phys. 93, 6371 (1990)]. S1–S0 interaction matrix elements of 0.001–0.006 cm−1 are found for levels involved in simple two level perturbations. The large number of small random perturbations by levels of the ground state is indicative of the first stages of the onset of quantum chaos in a small molecule. Some larger perturbations in the rotational structure are also observed; these are caused by additional local interactions with levels of the nearby triplet state.
    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 101 (1994), S. 31-38 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The ν2 infrared fundamental of the transient molecule formyl chloride, HCOCl, has been recorded at high resolution. Detailed assignments of the rotational structure have been made for both HCO 35Cl and HCO 37Cl. The ν2 band, whose origin is at 1784.1377 cm−1 in HCO 35Cl, is predominantly A type with a very weak B-type component. Numerous excited state perturbations occur throughout the band, caused mainly by ||ΔKa||=2 Fermi resonance and ||ΔKa||=1 Coriolis interactions with the 3151 vibrational state. Even though no "extra'' lines resulting from the perturbations could be assigned, a complete analysis of the perturbed rotational structure has been possible. Accurate molecular constants for both the "bright'' perturbed 21 state and the "dark'' 3151 perturbing state have been obtained, using a Hamiltonian which includes both the Fermi and Coriolis interactions; only two interaction parameters are needed, one for each mechanism. Further perturbations at high Ka are assigned to Coriolis interactions with the 5261 level.
    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 100 (1994), S. 4138-4155 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Rotational and hyperfine analyses have been carried out for the (0,0) bands of the C 3Π–X 3Δ, e 1Π–X 3Δ, and f 1Φ–a 1Δ transitions of gaseous NbN from laser excitation spectra taken at sub-Doppler resolution. The δπ C 3Π and e 1Π states lie only 102 cm−1 apart in zero order but the spin–orbit matrix element between them, which is the sum of the spin–orbit constants for the δ and π electrons, is 698 cm−1; as a result the 3Π1 spin component lies below both the 3Π0 and 3Π2 components, and its hyperfine structure is highly irregular. This irregularity is an extreme example of how cross terms between the spin–orbit interaction and the Fermi contact hyperfine operator alter the apparent value of the hyperfine a constant, the coefficient of I⋅L in the magnetic hyperfine Hamiltonian. Molecular parameters for the C 3Π and e 1Π states have been obtained from a combined fit to the two of them. Including data for the B 3Φ state recorded earlier [Azuma et al., J. Chem. Phys. 91, 1 (1989)], detailed information is now available for all six of the electronic states from the electron configurations σδ and δπ. It has been verified that the spin–orbit/Fermi contact cross terms cause roughly equal and opposite shifts in the hyperfine a constants for the singlet states and the Σ=0 components of the triplet states. After allowing for this effect, it has been possible to interpret the hyperfine a constants in terms of one-electron parameters for the δ and π electrons, in similar fashion to spin–orbit parameters. Wavelength resolved fluorescence, following selective laser excitation of the C 3Π, e 1Π, and f 1Φ states, has led to the discovery of three new electronic states, δ2 c 1Γ, δ2 A 3Σ−, and σ2 b 1Σ+, besides giving the absolute position of a 1Δ. Strong configuration interaction mixing is found to occur between the σ2 b 1Σ+ and δ2 d 1Σ+ states. The low-lying electronic states of NbN are now well understood.
    Type of Medium: Electronic Resource
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