Controlling the mechanism of fulvene S/S decay: Switching off the stepwise population transfer
Physical Chemistry Chemical Physics, ISSN: 1463-9076, Vol: 12, Issue: 48, Page: 15725-15733
2010
- 50Citations
- 36Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations50
- Citation Indexes50
- CrossRef50
- 47
- Captures36
- Readers36
- 36
Article Description
Direct quantum dynamics simulations were performed to model the radiationless decay of the first excited state S of fulvene. The full space of thirty normal mode nuclear coordinates was explicitly considered. By default, ultrafast internal conversion takes place centred on the higher-energy planar region of the S/S conical intersection seam, giving the stepwise population transfer characteristic of a sloped surface crossing, and leading back to the ground state reactant. Two possible schemes for controlling whether stepwise population transfer occurs or not - either altering the initial geometry distribution or the initial momentum composition of the photo-excited wavepacket - were explored. In both cases, decay was successfully induced to occur in the lower-energy twisted/peaked region of the crossing seam, switching off the stepwise population transfer. This absence of re-crossing is a direct consequence of the change in the position on the intersection at which decay occurs (our target for control), and its consequences should provide an experimentally observable fingerprint of this system. © 2010 the Owner Societies.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=78649709208&origin=inward; http://dx.doi.org/10.1039/c0cp01757d; http://www.ncbi.nlm.nih.gov/pubmed/21082138; https://xlink.rsc.org/?DOI=c0cp01757d; https://dx.doi.org/10.1039/c0cp01757d; https://pubs.rsc.org/en/content/articlelanding/2010/cp/c0cp01757d
Royal Society of Chemistry (RSC)
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