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- W2000896591 abstract "Lifetimes of long-lived collision complexes of H+ + H2 and some isotopic variants have been determined from classical trajectory calculations. A lifetime range of 0.1–50 ps could be covered, while a typical vibrational period of the complex is 10 fs. The results in agree with the expectation from RRKM theory: independence of τ of the origin of the energy of the complex (translation, vibration, or rotation), and a power law dependence of τ on E/(E + D) with exponent 2. A closer look shows a dependence of τ on total angular momentum J, which is also the main reason for non-exponential decay curves of samples for which J is not specified, and for much of the apparent dependence of τ on mass distributions. Our data show that an induction time is needed before the complex obtains its (statistical) properties." @default.
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- W2000896591 date "1985-05-01" @default.
- W2000896591 modified "2023-09-27" @default.
- W2000896591 title "Lifetimes of triatomic collision complexes" @default.
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- W2000896591 doi "https://doi.org/10.1016/0301-0104(85)80163-4" @default.
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