2001
DOI: 10.1021/jp002424l
|View full text |Cite
|
Sign up to set email alerts
|

Use of Quantum Methods with Transition State Theory:  Application to H-Atom Metathesis Reactions

Abstract: The use of quantum chemical methods to determine rate constants for some H-atom metathesis reactions using transition state theory and tunneling corrections is explored. Comparisons are made among several methods (DFT, MP2, QCISD), all of which yield similar structures and frequencies for the transition states, but quite different barrier heights. Tunneling corrections are made using either the well-known Eckart method or one based on the WKB approach. We find that we can fit the extant data by varying the bar… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

1
28
1

Year Published

2001
2001
2017
2017

Publication Types

Select...
8
1

Relationship

1
8

Authors

Journals

citations
Cited by 29 publications
(30 citation statements)
references
References 40 publications
1
28
1
Order By: Relevance
“…2 and S- Table 2, the rate constants from MP2 calculations are about one order of magnitude underestimated as compared to the experiment rate constants. This underestimate rate constant is likely due to the overestimate energy barriers [39]. The rate constants from CCSD(T) calculations are in better agreement with the experimental values (shown as in Fig.…”
Section: Resultssupporting
confidence: 68%
“…2 and S- Table 2, the rate constants from MP2 calculations are about one order of magnitude underestimated as compared to the experiment rate constants. This underestimate rate constant is likely due to the overestimate energy barriers [39]. The rate constants from CCSD(T) calculations are in better agreement with the experimental values (shown as in Fig.…”
Section: Resultssupporting
confidence: 68%
“…The importance of including anharmonicity in the torsion mode for this reaction was emphasized earlier by Senosiain et al 56 and Sumathi et al 43 We will therefore pay special attention to the effect of torsional anharmonicity on the calculated reaction rates. A key difference between reaction ͑R1͒ and the reaction of H with CH 4 is that there is a torsional mode in reaction ͑R1͒ that is not present in the H + CH 4 system.…”
Section: Introductionmentioning
confidence: 93%
“…To extrapolate a rate coefficient over an extended temperature range or to compare calculated reaction barrier heights with experimentally derived ones, it is often useful to extract a "vibrationally adiabatic" reaction barrier (V a ) from experimental data, as delineated in Senosiain et al [18]. To obtain V a accurately, the effect of quantum tunneling needs to be accounted for.…”
Section: Theoreticalmentioning
confidence: 99%