Hexamethylcyclopentadiene: time-resolved photoelectron spectroscopy and ab initio multiple spawning simulations-Reference-Cited by-同舟云学术

Hexamethylcyclopentadiene: time-resolved photoelectron spectroscopy and ab initio multiple spawning simulations

Published:2014 Issue:23 Volume:16 Page:11770-11779
ISSN:1463-9076
Container-title:Phys. Chem. Chem. Phys.
language:en
Short-container-title:Phys. Chem. Chem. Phys.

Author:

Wolf T. J. A.¹²³⁴⁵,Kuhlman T. S.⁶⁷⁸,Schalk O.⁹¹⁰¹¹¹²¹³,Martínez T. J.⁴⁵⁶¹⁴¹⁵,Møller K. B.⁶⁷⁸,Stolow A.¹²¹³⁶¹⁶¹⁷,Unterreiner A.-N.¹²³

Affiliation:

1. Institut für Physikalische Chemie and Center for Functional Nanostructures (CFN)

2. Karlsruhe Institute of Technology (KIT)

3. 76131 Karlsruhe, Germany

4. Stanford PULSE Institute

5. Menlo Park, USA

6. Department of Chemistry

7. Technical University of Denmark

8. DK-2800 Kgs. Lyngby, Denmark

9. Stockholm University

10. AlbaNova University Center

11. , Sweden

12. National Research Council

13. , Canada

14. Stanford University

15. Stanford, USA

16. University of Ottawa

17. Canada

Abstract

Time-resolved photoelectron spectroscopy and ab initio multiple spawning dynamical simulations of hexamethylcyclopentadiene reveal wavepacket evolution in a distinct degree of freedom.

Publisher

Royal Society of Chemistry (RSC)

Subject

Physical and Theoretical Chemistry,General Physics and Astronomy

Link

http://pubs.rsc.org/en/content/articlepdf/2014/CP/C4CP00977K

Reference59 articles.

1. Ultrafast internal conversion and fragmentation in electronically excited C2H4 and C2H3Cl molecules

2. Ultrafast dynamics of the 11Bu-state of 1,3-butadiene after excitation at 204 nm

3. Dynamics of excited-state proton transfer systems via time-resolved photoelectron spectroscopy

4. Femtosecond time-resolved dynamics of the electronically excited ethylene molecule

5. Ultrafast photochemistry of cyclopentadiene: Competing hydrogen migration and electrocyclic ring closure

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