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Ultrafast Dynamics of Porphyrins in the Condensed Phase: II. Zinc Tetraphenylporphyrin

Yu, Hua-Zhong and Baskin, J. Spencer and Zewail, Ahmed H. (2002) Ultrafast Dynamics of Porphyrins in the Condensed Phase: II. Zinc Tetraphenylporphyrin. Journal of Physical Chemistry A, 106 (42). pp. 9845-9854. ISSN 1089-5639. doi:10.1021/jp0203999.

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Femtosecond spectroscopic studies of zinc tetraphenylporphyrin (ZnTPP) in benzene and dichloromethane are reported, combining both fluorescence up-conversion and transient absorption measurements. The purpose is to investigate the initial electronic and vibrational relaxation of the S_1 and S_2 excited states, in a system in which interference from solvent rearrangement is insignificant as evidenced by the small Stokes shift in the fluorescence. Excitation of the low-lying singlet excited state (S_1) results in nanosecond relaxation, while excitation to S_2, the Soret band, leads to multiple electronic and vibrational relaxation time scales of S_2 and S_1 populations, from hundreds of femtoseconds to tens of picoseconds. The systematic and detailed studies reported here reveal that the Soret fluorescence band decays with a lifetime in benzene of 1.45 ps for excitation at 397 nm, while emission monitored at the same wavelength, but for two-photon 550 nm excitation, decays biexponentially with 200 fs and 1.0 ps time constants. In addition, the Soret fluorescence decay lifetime for 397 nm excitation is distinctly longer than the rise time of S_1 fluorescence for the same excitation, which varies with wavelength. These observations are consistent with the model presented here in which the Soret band structure consists of absorption from S_0 to two manifolds of states with distinct electronic and vibrational couplings to S_1 and higher electronic states. To compare with literature, we also measured the S_2 lifetime in dichloromethane and found it to be 1.9 ps, a lengthening from its value in benzene. However, the transient fluorescence intensity is greatly reduced. These observations in dichloromethane provide evidence of an ultrafast (<100 fs) channel for electron transfer from ZnTPP to dichloromethane for a subset of excited molecules in favorably oriented contact with the solvent, that is, a bifurcation of population. Finally, solvent-induced vibrational relaxation of the S_1 population following internal conversion from S_2 occurs over a range of time scales (picoseconds to tens of picoseconds) depending on the wavelength (fluorescence or transient absorption), and the observed rate indeed changes with solvent.

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Additional Information:© 2002 American Chemical Society. Received: February 11, 2002; In Final Form: April 17, 2002. Publication Date (Web): August 3, 2002. This work was supported by the National Science Foundation (Laboratory for Molecular Sciences). We thank Prof. Fred Anson for discussions that we had in this and related collaborative research.
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Issue or Number:42
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Official Citation:Ultrafast Dynamics of Porphyrins in the Condensed Phase:  II. Zinc Tetraphenylporphyrin Hua-Zhong Yu, J. Spencer Baskin, and Ahmed H. Zewail The Journal of Physical Chemistry A 2002 106 (42), 9845-9854 DOI: 10.1021/jp0203999
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:69745
Deposited By: Ruth Sustaita
Deposited On:18 Aug 2016 19:11
Last Modified:11 Nov 2021 04:19

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