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Title: Ultrafast Curve Crossing Dynamics through Conical Intersections in Methylated Cyclopentadienes

Journal Article · · Journal of Physical Chemistry A
DOI:https://doi.org/10.1021/jp910786s· OSTI ID:979315

We explored the curve crossing dynamics of 1,2,3,4-tetramethyl-cyclopentadiene (TMCPD) and 1,2,3,4,5-pentamethyl-cyclopentadiene (PMCPD) upon {pi} {yields} {pi}* excitation to the 1B{sub 2} state using time-resolved, resonance-enhanced multiphoton ionization mass and photoelectron spectroscopy. Upon excitation with a femtosecond laser pulse at 267 nm, the energy relaxation pathway is observed by a time-delayed probe pulse at 400 nm, which ionizes the molecule through Rydberg states that reveal the momentary state of the molecule in the photoelectron spectra. We observe that the initially populated 1B{sub 2} state decays to the 2A{sub 1} surface in 135 fs in TMCPD and 183 fs in PMCPD, followed by a crossing to the ground state 1A{sub 1} surface on 57 and 60 fs time scales for TMCPD and PMCPD, respectively. The spectroscopic signatures of the 2A{sub 1} states are clearly revealed in the two-photon ionization photoelectron spectra. In both systems we observe that the ground states are recovered completely, indicating that no new molecular structures are created on the time scale of the experiment.

Research Organization:
Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)
Sponsoring Organization:
USDOE Laboratory Directed Research and Development (LDRD) Program
DOE Contract Number:
DE-AC05-00OR22725
OSTI ID:
979315
Journal Information:
Journal of Physical Chemistry A, Vol. 114, Issue 13
Country of Publication:
United States
Language:
English

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