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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 112 (1990), S. 5763-5772 
    ISSN: 1520-5126
    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 91 (1989), S. 3340-3359 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The electronic spectra of silyl radicals, SiH3 and SiD3, were observed between 310 and 430 nm (46 000–64 000 cm−1) by resonance enhanced multiphoton ionization (REMPI) mass spectroscopy. The spectra were generated through a 2+1 REMPI mechanism. Two Rydberg series originating from planar, D3h point group states were observed. One series, of quantum defect δ=1.45(2), is comprised of the E˜ 2A‘2(4p), J˜ 2A‘2(5p), and M˜ 2A‘2(6p) Rydberg states which have origins at ν0–0 =48 438, 56 929, and 60 341 cm−1 in SiH3 and at ν0–0 =48 391, 56 874, and 60 267 cm−1 in SiD3. In SiD3 theP˜ 2A‘2(7p) Rydberg origin was observed at ν0–0 =62 002 cm−1. The H˜, K˜, and N˜ states observed in the SiD3 spectrum comprise the second Rydberg series, δ=2.09, and were tentatively assigned as ns 2A'1 Rydberg states (n=5, 6, 7). The K˜ and N˜ origins were observed at ν0–0 =58 417 and 61 005 cm−1. A fit of the Rydberg formula to the np 2A‘2(n≥5) origins found the adiabatic ionization potential of the SiH3 and SiD3 radicals to be IPa=8.135(+5,−2) eV and IPa=8.128(1) eV, respectively. Detailed vibrational analyses of these Rydberg states are presented. Analysis showed that in the E˜ 2A‘2 (4p) state of the SiH3 radical ω2 (a‘2 symmetric bend)=796(7) and 2ω4 /2(e' degenerate bend)=870(5) cm−1 and that in SiD3 radical ω'1 (a1 SiH3 symmetric stretch)=1576(3), ω'2 =589(3), and 2ω4 /2=635(6) cm−1. The REMPI spectra exhibited ν‘2 hot bands from vibrational levels as high as Ev =2073 cm−1 in the X˜ 2A1state. Modeling calculations, which fit the numerous ν‘2 hot bands, predicted barriers to inversion of Binv=1935 cm−1 and Binv =1925 cm−1 for SiH3 and SiD3 X˜ 2A1 radicals, respectively.
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 89 (1988), S. 4558-4563 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The germyl (GeH3) radical has been observed by resonance enhanced multiphoton ionization (REMPI) spectroscopy in the region of 370–430 nm. The spectrum arises from two-photon resonances with the 5p 2A‘2 (D3h) Rydberg state that possesses an origin at 419.1 nm (ν0–0 =47 705 cm−1). A vibrational progression of 756 cm−1 was assigned to the "umbrella'' mode, ν2. The observed X˜ 2A1 (C3v) v‘2=2 to v‘2=0 vibrational interval is 663 cm−1 which leads to an estimated barrier to inversion of 1530 cm−1.
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  • 4
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 89 (1988), S. 6064-6068 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The resonance enhanced multiphoton ionization spectra from 400 to 500 nm of the GeF and GeCl radicals are reported. In GeF bands involving transitions to the A 2Σ+, C' 2Π, D' 2Π, E 2Σ+, and G 2Δ states were observed. The bands involving transitions to the valence A 2Σ+ state were accounted for by 1+2 and 1+1+1 resonance enhanced multiphoton ionization (REMPI) mechanisms. Bands associated with the other Rydberg states were generated by a 2+1 REMPI mechanism. The spectrum of the GeCl radical arose from 2+1 REMPI excitation through the C' 2Πr (5pπ) and C 2Πr (4pπ) Rydberg states. The C' 2Πr state spin–orbit coupling constant was determined by direct measurement of C' 2Π1/2←←X 2Π1/2 transitions and "one photon forbidden'' C' 2Π3/2←←X 2Π1/2 transitions. A least-squares fit determined the spectroscopic constants of the C' 2Πr 5pπ Rydberg state of GeCl: Te=42 190±5 cm−1, Ae=81.0±3.5 cm−1, ωe=509.2±5.3 cm−1, and ωexe=3.3±1.1 cm−1.
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  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 89 (1988), S. 3930-3930 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 87 (1987), S. 4546-4558 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The reactions of F(2P)+ketene and F(2P)+ketene-d2 were studied in a flow reactor. Spectra of the radical products CH2F, CD2F, CH, CF, and atomic carbon were detected between 292–395 nm by resonance enhanced multiphoton ionization (REMPI) mass spectrometry. Fluoromethyl radicals were identified as a major product of the F+ketene elementary reaction. REMPI spectra of fluoromethyl radicals originated from two-photon preparation of 3p, 4p, and 5p Rydberg states (quantum defect ∼0.6). Absorption of a third laser photon ionized the radicals, a 2+1 REMPI mechanism. Rydberg band origins were observed in CH2F at ν00=52 863, 63 275, and 67 265 cm−1 and in CD2F at ν00=52 786, 63 195, and 67 186 cm−1. A normal mode analysis revealed the vibrational frequencies of the C–F stretch, CH2 scissors, and out-of-plane bending modes in the Rydberg states. The ground state out-of-plane bending frequency in CH2F is 260(30) cm−1 and in CD2F it is 170(30) cm−1. CH radicals were generated by the photolysis of ketene and observed at ∼311 nm by two-photon excitation through the D 2Π(v′=2) ←←X 2Πr band. The reaction mechanism that generated the CF radicals was not determined. The REMPI CF radical spectrum generated by a 2+1 photon mechanism appeared as a series of bandheads described by the constants ν00=∼52 572 cm−1, ωe =1820 cm−1, and ωexe =−18.2 cm−1.
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  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 92 (1990), S. 6420-6425 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Three new electronic states of NH and ND (imidogen radical) have been observed by REMPI (resonance enhanced multiphoton ionization) spectroscopy in the region of 258 through 288 nm and assigned. The NH (ND) was produced by the photolysis of HN3 (DN3) (hydrazoic acid) in the same wavelength region. The observed two-photon transitions are from the a 1Δ state to 3p Rydberg states. Transitions were also observed from the a 1Δ state to the d 1Σ+ state. The new state assignments are: f 1Π (3pσ) at 86 378 cm−1, g 1Δ (3pπ) at 88 140 cm−1, and h 1Σ (3pπ) at 89 531 cm−1. Rotational constants (B and D) and, where possible, vibrational spacings for the thirteen observed bands are also determined.
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  • 8
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 87 (1987), S. 1977-1981 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The resonance enhanced multiphoton ionization (REMPI) spectrum of O2 a 1Δg between 305 and 350 nm is reported. The spectrum is compared to the REMPI spectrum of ground state molecular oxygen in the same electronic energy region, and a number of differences in the respective spectra are observed. Detection limits for O2 a 1Δg by REMPI is calculated to be 5×109 molecule cm−3 in the ion source of the mass spectrometer.
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  • 9
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 82 (1985), S. 4426-4433 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We report the resonance enhanced multiphoton ionization spectra of ClO and BrO free radicals between 415 and 475 nm. The observed electronic states were prepared by simultaneous absorption of three identical photons from a dye laser. Absorption of at least one additional photon induced ionization. ClO showed spectra originating from the D, E, and F states previously reported by N. Basco and R. D. Morse. The origin of the F 2Σ←X 2Πi bands were reassigned to ν00=70 183 cm−1 and ν00=69 868 cm−1. BrO showed three new vibrational progressions originating from transitions between the X 2Π3/2 state to Rydberg states with assignments of E 2Σ (ν00=65 003 cm−1), F 2Σ (ν00=67 470 cm−1), and an apparently inverted state, designated G (ν00=70 504 cm−1), that possesses orbital angular momentum greater than zero. The G-state bands were separated by 139(±3) cm−1 which should approximate the magnitude of the spin-orbit coupling constant of this excited state if it is of 2Πi symmetry.
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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. 3422-3428 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We report resonance enhanced multiphoton ionization (REMPI) spectra of gas-phase indium monochloride (InCl) between 330 and 490 nm. The spectra originate from one-, two-, and three-photon resonances with electronic states that reside between 27 000 and 75 000 cm−1. We assign 12 new Rydberg states. From these Rydberg origins we can extrapolate the adiabatic ionization potential IPa=77 460±600 cm−1 (9.60±0.08 eV). The Rydberg states exhibit vibrational frequencies ranging between 307 and 355 cm−1.
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