Time evolution of very high Rydberg states of large aromatic molecules. A kinetic analysis

U. Even; M. Ben-Nun; R. D. Levine

doi:10.1016/0009-2614(93)87047-7

Time evolution of very high Rydberg states of large aromatic molecules. A kinetic analysis

U. Even^*, M. Ben-Nun, R. D. Levine

^*Corresponding author for this work

Institute of Chemistry

Research output: Contribution to journal › Article › peer-review

39 Scopus citations

Abstract

A long (microseconds) and shorter ( ∼ 1 μs) decay channel are resolved in the time evolution of very high Rydberg states of large aromatic molecules. A simple kinetic analysis is presented and applied to the very detailed results available for tetracene. It is concluded that under our experimental conditions the time evolution is due to intramolecular processes. The various possible decay channels are discussed.

Original language	English
Pages (from-to)	416-422
Number of pages	7
Journal	Chemical Physics Letters
Volume	210
Issue number	4-6
DOIs	https://doi.org/10.1016/0009-2614(93)87047-7
State	Published - 30 Jul 1993

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title = "Time evolution of very high Rydberg states of large aromatic molecules. A kinetic analysis",

abstract = "A long (microseconds) and shorter ( ∼ 1 μs) decay channel are resolved in the time evolution of very high Rydberg states of large aromatic molecules. A simple kinetic analysis is presented and applied to the very detailed results available for tetracene. It is concluded that under our experimental conditions the time evolution is due to intramolecular processes. The various possible decay channels are discussed.",

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AU - Ben-Nun, M.

AU - Levine, R. D.

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Y1 - 1993/7/30

N2 - A long (microseconds) and shorter ( ∼ 1 μs) decay channel are resolved in the time evolution of very high Rydberg states of large aromatic molecules. A simple kinetic analysis is presented and applied to the very detailed results available for tetracene. It is concluded that under our experimental conditions the time evolution is due to intramolecular processes. The various possible decay channels are discussed.

AB - A long (microseconds) and shorter ( ∼ 1 μs) decay channel are resolved in the time evolution of very high Rydberg states of large aromatic molecules. A simple kinetic analysis is presented and applied to the very detailed results available for tetracene. It is concluded that under our experimental conditions the time evolution is due to intramolecular processes. The various possible decay channels are discussed.

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Time evolution of very high Rydberg states of large aromatic molecules. A kinetic analysis

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