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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 95 (1991), S. 6530-6534 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    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 95 (1991), S. 9420-9421 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The heat of formation of C5 has been computed ab initio using a variation on G1 theory. The computed ΔH0f = 251.7 ± 4 kcal/mol disagrees quite appreciably with the third-law measurements of Drowart et al.; however, the cause of this is shown to be in the use of very approximate free energy functions by these authors. Using better free energy functions leads to a revised experimental value of 253.3±5.8 kcal/mol, in excellent agreement with our ab initio value. A revision of previous estimates for C6 to C10 by Raghavachari and Binkley is presented.
    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 97 (1992), S. 5012-5018 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The total atomization energies of a number of molecules have been computed using an augmented coupled-cluster method and [5s4p3d2 f1g] and [4s3p2d1f] atomic natural orbital (ANO) basis sets, as well as the correlation consistent valence triple zeta plus polarization (cc-pVTZ) and correlation consistent valence quadrupole zeta plus polarization (cc-pVQZ) basis sets. The performance of ANO and correlation consistent basis sets is comparable throughout, although the latter can result in significant CPU time savings. Whereas the inclusion of g functions has significant effects on the computed ΣDe values, chemical accuracy is still not reached for molecules involving multiple bonds. A Gaussian-1 (G1) type correction lowers the error, but not much beyond the accuracy of the G1 model itself. Using separate corrections for σ bonds, π bonds, and valence pairs brings down the mean absolute error to less than 1 kcal/mol for the spdf basis sets, and about 0.5 kcal/mol for the spdfg basis sets. Some conclusions on the success of the Gaussian-1 and Gaussian-2 models are drawn.
    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 95 (1991), S. 8374-8389 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Correction terms (up to third order in temperature) for the effect of centrifugal distortion on the rotational partition function of linear molecules, spherical, symmetric, and asymmetric tops are evaluated by means of the classical partition function. It is shown that for the linear, spherical, and symmetric cases, the expressions thus obtained differ from the exact quantum expressions only in the absence of a very small constant correction term. It is then proposed that the partition function for a nonrigid asymmetric top, for which no exact expression has as yet been derived, be evaluated as the product of Watson's asymptotic expansion for the rigid rotor and the centrifugal correction factor derived in the present work. Numerical comparison with direct numerical summation shows that, even for troublesome cases, this approximation holds very well even at 2000 K. Similar performance is observed for the heat content function, except for pathological cases at high temperatures. In the rigid-rotor case, Watson's asymptotic series holds very well. As an example application, pilot calculations have been performed on the thermodynamic functions of water and formaldehyde. The present method yields functions in excellent agreement with those obtained by direct rovibrational summation, whereas computer-time requirements are reduced by 3 or 4 orders of magnitude.
    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 94 (1991), S. 3753-3761 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The lowest-lying 1Ag and 3Σ−g states of C4 have been studied using basis sets including f functions, quadratic configuration interaction, and full fourth-order Møller–Plesset perturbation theory with multiple spin projection. Basis set effects on the linear-cyclic separation have been found to be fairly significant. Use of the 6-311G* and [5s3p1d] basis sets leads to qualitatively different conclusions; this problem is remedied by expansion of the polarization space. At the highest level of theory considered, the cyclic structure lies about 1 kcal/mol below the linear structure. A G1-type estimate of its heat of formation at 0 K of 249.6 kcal/mol is proposed. This value is in disagreement with the generally quoted experimental values, but in good agreement with third-law values by Drowart et al. [J. Chem. Phys. 31, 1131 (1959)] corrected for improved partition functions. Geometries and harmonic frequencies are reported. It is tentatively suggested that a matrix ir band at 1284 cm−1 may belong to cyclic C4; to aid experimentalists in confirming or rejecting this assignment, theoretical isotope shifts are reported.
    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 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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  • 7
    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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  • 8
    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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  • 9
    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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  • 10
    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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