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  • 11
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 93 (1990), S. 4485-4487 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The dissociation energy of N3 has been computed ab initio using coupled cluster techniques and large basis sets. Our best theoretical estimates (accuracy ±2 kcal/mol) are ∑De=234.0, ∑D0=228.4, ΔH0 f =109.3, and ΔH0 f,298=108.4 kcal/mol. These values are in excellent agreement with an ICR determination of ΔH0 f=112±5 kcal/mol. Very large basis set effects are observed.
    Type of Medium: Electronic Resource
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  • 12
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 93 (1990), S. 8850-8861 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The harmonic frequencies, infrared intensities, and isotopic substitution bands of C6 have been evaluated at the MP2/6-31G* level. They confirm previous assignments of the 1952 and 1197 cm−1 matrix IR bands to C6. Isotopic substitution spectra at the MP2/6-31G* and HF/4-21G levels, as well as those with a newly developed ad hoc modified neglect of diatomic overlap (MNDO) method are shown to be in good agreement with experiment for C4, C5, and C6. On the basis of RHF/4-21G, RHF/6-31G*, MP2/4-21G, MP2/6-31G*, and ad hoc MNDO data, including theoretical frequencies, IR intensities, and isotopic substitution spectra, it is shown with virtual certainty that the 2128 and 1893 cm−1 matrix IR bands belong to C7. A recent assignment of the very intense 1997 cm−1 matrix IR feature to C8 is contradicted on the same grounds, and an alternative assignment to C9 put forward.
    Type of Medium: Electronic Resource
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  • 13
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 92 (1990), S. 6655-6667 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The spectroscopic properties of the three lowest-lying states X 3Π, A 3∑−, and a 1∑+ of SiC have been computed accurately using augmented coupled cluster methods and different basis sets. Partition functions have been set up, accounting for anharmonicity, rotation–vibration coupling, centrifugal distortion, and isotope effects. Thermodynamic properties are tabulated in JANAF style from 100 to 6000 K. A critical analysis of the effects of the various contributions is made, as well as an error analysis.
    Type of Medium: Electronic Resource
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  • 14
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 98 (1993), S. 7951-7957 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The protonation of N2O and the intramolecular proton transfer in N2OH+ have been studied using large basis sets in conjunction with second-order many-body perturbation theory (MP2), singles and doubles coupled cluster (CCSD), the augmented coupled cluster method [CCSD(T)], and complete active space self-consistent field (CASSCF) methods. It is shown that MP2 is inadequate even for HNNO+, which has a minor nondynamical correlation effect; for the transition state only CCSD(T) produces a reliable geometry due to serious nondynamical correlation effects. Harmonic frequencies accurate to 50 cm−1 or better are predicted for both protonated species. The proton affinity at 298.15 K is found to be 137.6 kcal/mol, in excellent agreement with the recent experimental redetermination of 137.3±1 kcal/mol; the HNNO+ isomer is found to be 4.4 kcal/mol above the HONN+ isomer, with an interconversion barrier of ∼89 kcal/mol, herewith confirming recent experimental evidence that both species occur together with an energy difference of 6±1.5 kcal/mol. Comparison of the traditional double-zeta plus polarization (DZP) basis and the newer correlation consistent polarized valence double zeta (cc-pVDZ) basis set appears to indicate that the latter might lead to more accurate geometries and harmonic frequencies, although a more detailed investigation would be needed before any definitive conclusions.
    Type of Medium: Electronic Resource
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  • 15
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 97 (1992), S. 6549-6556 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The lowest 1Σ+ and 3Π states of the BN molecule have been studied using multireference configuration interaction (MRCI) and averaged coupled-pair functional (ACPF) methods and large atomic natural orbital (ANO) basis sets, as well as several coupled cluster methods. Our best calculations strongly support a 3Π ground state, but the a 1Σ+ state lies only 381±100 cm−1 higher. The a 1Σ+ state wave function exhibits strong multireference character and, consequently, the predictions of the perturbationally-based single-reference CCSD(T) coupled cluster method are not as reliable in this case as the multireference results. The best theoretical predictions for the spectroscopic constants of BN are in good agreement with experiment for the X 3Π state, but strongly suggest a misassignment of the fundamental vibrational frequency for the a 1Σ+ state.
    Type of Medium: Electronic Resource
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  • 16
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 97 (1992), S. 3530-3536 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The anharmonic potential surface of NH2 has been computed ab initio using the quadratic configuration interaction method and large basis sets. The all-electron augmented coupled cluster surface with the [5s4p2d1f,3s2p] basis set reproduces the experimental fundamentals to within a few cm−1. For this quantitative agreement with experiment, both f functions and core correlation seem to be prerequisite. From our best computed force field, a set of spectroscopic constants has been derived for all important isotopomers of NH2. Using a hybrid analytic/direct summation method recently developed by the present authors, the thermodynamic functions gef(T), hcf(T), S0, and Cp are computed including exact accounts for anharmonicity and rovibrational coupling, and very good analytical approximations to centrifugal distortion and quantum rotation effects. Thermodynamic tables in JANAF style from 100–3000 K, as well as a full set of rovibrational spectroscopic constants, are presented for NH2 and all important isotopomers. The effect of the A 2A1 state is found to become significant around 2000 K.
    Type of Medium: Electronic Resource
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  • 17
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 97 (1992), S. 8361-8371 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The quartic force field of ammonia is computed using basis sets of spdf/spd and spdfg/spdf quality and an augmented coupled cluster method. After correcting for Fermi resonance, the computed fundamentals and ν4 overtones agree on average to better than 3 cm−1 with the experimental ones except for ν2. The discrepancy for ν2 is principally due to higher-order anharmonicity effects. The computed ω1, ω3, and ω4 confirm the recent experimental determination by Lehmann and Coy but are associated with smaller error bars. The discrepancy between the computed and experimental ω2 is far outside the expected error range, which is also attributed to higher-order anharmonicity effects not accounted for in the experimental determination. Spectroscopic constants are predicted for a number of symmetric and asymmetric top isotopomers of NH3.
    Type of Medium: Electronic Resource
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  • 18
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 96 (1992), S. 7633-7645 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The anharmonic potential energy surface of water has been computed ab initio using an augmented coupled cluster method and various basis sets. Whereas the Pople 6–311 G family is manifestly unsatisfactory, Huzinaga–Dunning basis sets perform quite well. The [5s4p2d1f,3s2p] surface reproduces harmonic frequencies and anharmonicity constants to better than about 2 and 1 cm−1, respectively. For quantitative agreement with experiment, both f functions on oxygen and inclusion of core correlation seem to be prerequisite. Comparison with various experimentally derived force fields reveals that the ab initio force field is of comparable quality. From the best computed force field, a set of spectroscopic constants has been derived for all important isotopomers of water. Using a hybrid analytic/direct summation method recently developed by the present authors, the thermodynamic functions gef(T), hcf(T), S0, and Cp are computed including exact account of anharmonicity and rovibrational coupling, and very good analytical approximations to centrifugal distortion and quantum rotation effects. The computed functions substantially revise previous literature results at high temperatures. Differences between thermodynamic functions from various computed force fields are an order of magnitude smaller than these errors. Thermodynamic tables in JANAF style from 100 to 3000 K, as well as a full set of rovibrational spectroscopic constants, are presented. It is concluded that obtaining force fields of near-spectroscopic accuracy, and thermodynamic tables of very high accuracy, is presently feasible for small polyatomic molecules.
    Type of Medium: Electronic Resource
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  • 19
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 93 (1990), S. 5037-5045 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The potential energy surface of the C+3 cation has been investigated using coupled cluster techniques and large basis sets. The results are particularly sensitive towards the level of electron correlation. Spin contamination even produces a "false stationary point'' at the UHF/6-31G* level. C+3 has a cyclic 2B2 ground state with predicted geometry r=1.3242 A(ring), θ=73.06° (MP2/6-311G*, empirically corrected bond distance). At the highest level of theory considered, the linear structure (2Σ+u state) lies about 2 kcal/mol above the ground state: this might imply quasilinearity. There is also a low barrier towards degenerate isomerization: at high temperatures, C+3 will be extremely floppy. Harmonic frequencies (UHF/6-31G*) as well as double-harmonic IR and Raman intensities are given for various structures of C+3. Interesting analogies of C+3 with B3 and B2N are pointed out. The heat of formation at 298.15 K, vertical and adiabatic ionization potentials of C3 are predicted as 194.9±2 kcal/mol, 11.92±0.1 eV, and 11.84±0.1 eV, respectively.
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  • 20
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 90 (1989), S. 6469-6485 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: For a number of different structures and states of B3, B2N, BN2, and N3, optimum geometries and harmonic spectra were obtained at the HF/6-31G* level. The relative stability of the isomers was determined using full fourth-order Møller–Plesset theory, both with and without spin projection, as well as coupled cluster methods. Estimates for the dissociation energies are based on scaled CCD+ST(CCD) binding energies. Koopmans' vertical ionization potentials and Mulliken charge distributions, both at the UHF/6-31G* level, are quoted for the most stable isomers. B3 is found to be an equilateral triangle in its 2A'1 ground state. B2N has a symmetric linear arrangement in its 2Σ+u ground state with an extremely low bending frequency (73 cm−1), and an unusually low vertical ionization potential (6.75 eV). Its asymmetric stretching (2021 cm−1) is found to be extremely intense (8782 km mol−1). BN2 has four rather closely spaced states, of which an isosceles triangle is the absolute minimum (2A1 state). However, at high temperatures, an asymmetric linear arrangement (2Π state) is found to have equal importance, whereas a 4Σ− state plays a role there too. The same theoretical methods correctly predict for N3 a symmetric linear arrangement in the 2Πg ground state; the spectroscopic constants are found to be in reasonable agreement with experiment. Estimated dissociation energies (expected accuracy ±4 kcal mol−1) are: B3 197.9, B2N 265.0, BN2 224.9, N3 210.1 kcal mol−1. From a statistical thermodynamical analysis, B3 is stable against dissociation to B2 and B up to very high temperatures, B2N is extraordinarily stable, whereas BN2 and N3 dissociate spontaneously to B+N2 and N+N2 at all temperatures. From these results, the presence of B2N+ and B+3, the high abundance of B2N+, as well as the absence of BN+2 and N+3 in laser mass spectra of boron nitride is explained.
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