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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 89 (1988), S. 3929-3930 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , 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 86 (1987), S. 5882-5883 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The electronic structure of H4 in C3v symmetry has been studied by ab initio calculations. The ground state energy minimum found in these calculations is shown by vibrational analysis to be a saddle point rather than a stable bound state. The path of steepest descent from the C3v saddle point is found to lead monotonically to dissociation into two H2 molecules.
    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 87 (1987), S. 771-773 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The electronic structure of H+6 has been studied by ab initio calculations. It is found that there exist two stable structures, of Cs and D2d symmetries. Post-SCF calculations suggest that the ordering of these states is determined by electron correlation, with the D2d structure lying slightly lower than the Cs structure. It is suggested that the D2d structure is formed in the recent experiments of Kirchner and Bowers.
    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 93 (1990), S. 1805-1813 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: An ab initio study of the electronic structure of NF5 and PF5 has been carried out using Møller–Plesset perturbation theory. Optimized geometries were calculated at the SCF and MP2 levels of theory using several basis sets, ranging from 6-31G to 6-311G(2df). A vibrational analysis indicates that NF5, in D3h symmetry, has all real frequencies, even if d orbital contributions are set to zero. Dissimilar N–F bond lengths (req=1.38 A(ring), rax=1.58 A(ring)) are found, in contrast to PF5, which exhibits nearly equal equatorial and axial bond lengths. A topological analysis of the calculated charge distribution in NF5 indicates true pentavalent coordination. Spectroscopic data for NF5 have been calculated using a scaled MP2 force field based on the known NF3 molecule. A comparison of calculated thermochemistry between NF3 and NF5 yields a predicted standard state heat of formation for NF5(g) of ΔH0f (0 K)=+25.1 kJ/mol. Our results suggest that synthesis of NF5 and other hypervalent compounds of first row atoms may be possible.
    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 88 (1988), S. 7248-7249 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The electronic structure of asymmetric dinitrogen dioxide (a-N2O2) has been studied by ab initio calculations. A stable structure in Cs symmetry, of similar geometry to FN3, is predicted for the lowest 1A' state. This structure is characterized by an IR frequency of 1206 cm−1 for the N–O stretch and exhibits a significant activation barrier (65 kJ/mol) for decomposition into N2+singlet O2. This asymmetric form of N2O2 has a heat of formation of approximately +500 kJ/mol and is potentially explosive.
    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 103 (1995), S. 7844-7850 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The photochemical interconversion of BOH to the considerably more stable HBO isomer is evaluated. The BOH and HBO isomers, while differing considerably in energy, possess a significant barrier to interconversion on the ground 1A′ potential energy surface. However, by accessing the low-lying double minimum a 3A′ state, we define an interconversion pathway that facilitates the interconversion process, allowing a substantial energy release. Here, we calculate the potential surfaces for the X 1A′ and a 3A′ states of HBO–BOH and present limited evaluations for the b 3A″ and A 1A′ states. We outline means to distinguish the BOH and HBO isomers, following the progress of the isomerization process using optical, infrared, and mass spectrometric techniques. The energetics of this geometric isomerization process and the potential utilization of BOH as a storable high energy material are discussed. © 1995 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 98 (1994), S. 8952-8958 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 97 (1993), S. 6602-6606 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    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〉 94 (1990), S. 7507-7514 
    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 98 (1993), S. 7940-7950 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Hydroxide ion (HO−) reacts with nitric oxide by slow reactive electron detachment with a rate coefficient ∼4×10−12 cm3 s−1 at 298 K. The detachment process is presumably associative detachment forming nitrous acid and an electron. Observations, data analysis, and alternative explanations for these observations are discussed. The associative detachment reaction was also investigated theoretically through calculations of the geometries, relative energies, and normal-mode vibrational frequencies of the relevant species HO−, HO, NO, cis- and trans-HONO, and cis- and trans-HONO−. These calculations indicate that in the ion HONO−, the cis conformer is more stable, while in the neutral HONO, the trans conformer is more stable. The HO–NO bond in HONO, which is formed in this reaction, is much stronger than the HO−–NO bond in HONO− with an energy of 198.7±1.8 kJ mol−1 for cis-HONO [J. Phys. Chem. Ref. Data 14, 1 (1985)] and 52.2±5 kJ mol−1 for cis-HONO− at 0 K. HONO− is bound with respect to HONO. The adiabatic electron detachment energy resulting from detachment from cis-HONO− forming the same conformer of the neutral molecule cis-HONO is 0.29±0.05 eV. The HO–NO equilibrium bond distance in HONO− is considerably longer than that in HONO, with values of 1.750 and 1.640 A(ring) for trans- and cis-HONO−, respectively, and 1.429 and 1.392 A(ring) for trans- and cis-HONO, respectively. These geometric and energetic characteristics of HONO− and HONO are combined with calculations of relative energies of these species at nonequilibrium/distorted HO–NO bond lengths to give a qualitative picture of the potential energy curves for these species along the reaction coordinate. While no significant energy barrier to autodetachment of HONO− is present, the Franck–Condon wave function overlap for autodetachment is small and is likely the reason for the observed inefficiency. The maximum calculated rate constant for associative detachment is 4×10−12 cm3 s−1, in good agreement with the observed value.
    Type of Medium: Electronic Resource
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