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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 94 (1991), S. 7319-7334 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The Hamiltonian based on curvilinear normal modes and local modes (CNLM) is discussed using Wilson's exact vibrational Hamiltonian as basis, the CNLM representation diagonalizing only the normal mode block of FG matrix in curvilinear internal coordinates. Using CNLM the kinetic and potential energy operators for benzene are given, including cubic and quartic anharmonicity in the potential energy and cubic and quartic terms in the kinetic energy expansion in curvilinear coordinates. Using symmetrized coordinates and cubic and higher force constants the number and identity of the independent symmetry allowed (A1g) such force constants are obtained. The relation to conventional anharmonic force constants is then given and the allowed contributions of the latter are obtained. The results are applied to CH overtone spectra and intramolecular vibrational dynamics in Part III of this series.
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 97 (1992), S. 5283-5295 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The CH overtone spectra for vCH=1, 2, and 3 for an intermediate sized molecule, benzene, and the related intramolecular vibrational dynamics are treated theoretically. For this purpose, an artificial intelligence (AI) search technique is employed, using the evaluation function developed in Part II. The curvilinear local-normal mode coordinate system discussed in Part I is also used. The main features of the theoretical spectra are in reasonable accord with those of the experimental ones. Results reflecting the important role of the symmetry of molecules even in their high energy states are described.
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 95 (1991), S. 872-888 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Avoided crossings between quasidegenerate rovibrational states in the Doppler-free two-photon excitation of the 141 mode in the S1 excited state of benzene are treated theoretically. Two sets of avoided crossings in plots of spectral line frequency vs J at a given K and ΔK have been reported experimentally between an initially prepared "light'' state (141 in zeroth order) and dark states, namely, one which in zeroth order is a 51101161 state, the other being in zeroth order a 62111 and/or possibly a 31161 state, implicated earlier by Neusser et al. The identification of these states makes the phenomenon an excellent candidate for treatment of the avoided crossing via a Van Vleck transformation, no other basis set states being needed for the diagonalization in order to extract the important features. Two successive transformations are used for handling direct coupling and coupling via virtual states. The dominant calculated contribution to the coupling is, jointly, Coriolis plus cubic–cubic anharmonic interactions between vibrational modes.Playing less of a role are Coriolis terms in which the inverse moment of inertia tensor is expanded up to quadratic terms in the coordinates. There results a 5×5 (for coupling to 51101161 ) and a 3×3 (for coupling to 62111 or 31161 ) matrix of the transformed Hamiltonian, each of which can also be described, if desired, to a very good approximation by a 2×2 matrix. The coupling element V0 and the difference of the rotational constants for the light and dark states (ΔB) are obtained from the plots of line position vs J(J+1) obtained. For the 141 to 51101161 and for the 141 to 62111 couplings the theoretical results are in reasonable agreement with the experimental results, no adjustable parameters being employed. For a coupling of 141 to 31161 the calculated V0 would be much too high compared with experiment (a factor of 10), the coupling involving the exchange of only three instead of four vibrational quanta. A situation in which the 141 state is coupled to the 62111 state to yield an avoided crossing and off-resonantly coupled to the 31161 state would be consistent with some experimental results and not affect the reasonable agreement of the slope difference and splitting for the avoided crossing plots.
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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. 4761-4770 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A recently described method for implementing RRKM theory for unimolecular reactions with highly flexible transition states is applied to the calculation of energy and angular momentum resolved rate constants and rotational–vibrational energy distributions for the reaction NCNO→hν NCNO*→NCNO(vib. hot)→NC+NO. The dissociation rate results are compared to the recent experimental results of Khundkar et al., and the vibrational and rotational distribution results are compared to the experimental values of Nadler et al. Comparison is also made with phase space theory calculations. The calculated rotational distributions at energies below the vibrational threshold of the products are the same as those of PST. At energies (2348, 2875 cm−1) above this threshold energy the rovibrational distribution is in better agreement with the data than is that of PST. The need for obtaining more accurate ab initio potential energy surfaces is noted, particularly for treating reactions at still higher energies.
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  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 96 (1992), S. 6065-6072 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The role of resonance centers in obtaining large size matrices via an artificial intelligence (AI) search is discussed. The results are used to develop for an AI search an evaluation function which takes cognizance of isolated internal resonances in these many-state systems. The effect of later-accepted states on resonance centers is included. This evaluation function and one without a resonance factor are used in Part III of this series. A search is made there to select zeroth-order vibrational states of benzene that are used in a diagonalization treatment of CH overtone spectra. When there are many overlapping resonances, as in that case, a comparison of results obtained with those two types of evaluation function is of particular interest.
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  • 6
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Results on vibrationally-excited ketene photofragment excitation (PHOFEX) spectra of Moore and co-workers are interpreted in terms of a previously described variational implementation of Rice–Ramsberger–Kassel–Marcus (RRKM) theory. At subvibrational excitations, the predictions of this theory reduce to those of phase space theory (PST). However, for excess energies just above the threshold of excitation of a particular vibrational mode of the products, the present theory predicts a significantly greater probability for vibrational excitation, compared with PST, in closer agreement with the experimental results, and predicts an energy dependence of the PHOFEX spectrum that is closer to the observed one. A key feature, to which the present calculations lead, is a two-transition state (TS) description for each vibrational excitation of the products, the PST TS region dominating at the threshold for that excitation and an inner TS region dominating at somewhat higher (∼200 cm−1) energies. The behavior contrasts partly with that of the unimolecular dissociation rate constant kEJ (except at the threshold for kEJ), because of the different focus of the two types of measurements. The theory provides a consistent interpretation of both properties.
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  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 91 (1989), S. 2280-2292 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A previously described implementation of Rice–Ramsberger–Kassel–Marcus (RRKM) theory for unimolecular dissociation processes involving a highly flexible transition state is applied to the dissociation of CH2CO into CH2 and CO. Results of theoretical calculations for the energy and angular momentum resolved rate constants are presented. Using an added dynamical approximation, the product vibrational–rotational distributions are also calculated. The calculated rate constants are compared with the corresponding experimentally determined quantities where possible. Comparison is also made with phase space theory (PST). The RRKM-based calculations are in good agreement with both the experimentally determined rate constants of Zewail and co-workers and the experimentally determined photofragment excitation spectra of Moore and co-workers. The results on rates are in contrast to the corresponding results from PST calculations. The RRKM-based theory for the product vibrational–rotational distributions predicts a moderately greater probability for vibrational excitations than does PST (particularly for excess energies just above the threshold for excitation of a particular vibrational mode of the products). In other respects the RRKM-based predictions of the ro-vibrational product state distributions are quite similar to those of PST.
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  • 8
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 98 (1993), S. 7405-7411 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A semi-infinite approach (rather than a slab method or finite number of layers) is used to treat surface properties such as wave functions, energy levels, and Fermi surfaces of semi-infinite solids within the tight-binding (TB) approximation. Previous single-band results for the face-centered cubic lattice with a (111) surface and for the simple cubic lattice with a (001) surface are extended to semi-infinite layers, while the extension to calculations of other surfaces is straightforward. Treatment of more complicated systems is illustrated in the calculation of the graphite (0001) surface. Four interacting bands are considered in the determination of the wave functions, energies, and Fermi surface of the graphite (0001) surface. For the TB model used, the matrix elements in the secular determinants for the semi-infinite solid and for the infinite bulk solid obey the same expressions, and the wave functions are closely related. Accordingly, the results for the bulk system can then be directly applied to the semi-infinite one. The main purpose of the present paper is to provide wave functions and other properties used elsewhere to treat phenomena such as scanning tunneling microscopy and electron transfer rates at electrodes.
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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. 7565-7573 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: An expression for the scanning tunneling microscopy (STM) current between the tip and sample is presented using first-order perturbation theory for a two-Hamiltonian formalism ("reactants'' and "products''). The calculated STM current depends on the square of the sample-tip matrix elements, averaged over a selection of random points in wave vector space. In the limit of low voltage and temperature, this averaging is over the Fermi surface of the sample. The model is applied to the graphite (0001) and Au(111) surfaces using a simple model (chain) of a tungsten tip and the tight-binding approximation. Comparisons with experiments and with the result for graphite obtained by Tersoff and Lang using a molybdenum tip are given. The theory is applied elsewhere to STM of adsorbates.
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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. 6044-6061 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Quantum calculations are reported for the intramolecular vibrational energy redistribution and absorption spectra of the first two excited states of the acetylenic CH stretch vibration in the polyatomic molecules (CX3)3YCCH, where X=H or D and Y=C or Si. Using approximate potential energy surfaces, comparison is made with the corresponding recent experimental spectra. It is found that a model of intramolecular vibrational relaxation based on the assumption of sequential off-resonance transitions via third and fourth order vibrational couplings (as opposed to direct high order couplings) is in agreement with experimental results on spectral linewidths. In a semiclassical limit this type of relaxation corresponds to a dynamic tunneling in phase space. It is shown that the local density of resonances of third and fourth order, rather than the total density of states, plays a central role for the relaxation. It is found that in the Si molecule an accidental absence of appropriate resonances results in a bottleneck in the initial stages of relaxation. As a result, an almost complete localization of the initially prepared excitation occurs. It is shown that an increase of the mass alone of the central atom from C to Si cannot explain the observed difference in the C and Si molecules. The spectral linewidths were calculated with the Golden Rule formula after prediagonalization of the relevant vibrational states which are coupled in the molecule to the CH vibration, directly or indirectly. For the spectral calculations, in addition to the direct diagonalization, a modified recursive residue generation method was used, allowing one to avoid diagonalization of the transformed Lanczos Hamiltonian. With this method up to 30 000 coupled states could be analyzed on a computer with relatively small memory. The efficiency of C programming language for the problem is discussed.
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