期刊
PHYSICAL CHEMISTRY CHEMICAL PHYSICS
卷 19, 期 43, 页码 29146-29152出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c7cp06292c
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资金
- National Natural Science Foundation of China [21573228]
- National Basic Research Program of China (973 Program) [2013CB922202]
- Ministry of Science and Technology of China [2012YQ12004704]
The ultrafast excited-state dynamics of 2,4-dimethylpyrrole following excitation at wavelengths in the range of 255.8-199.7 nm are studied using the time-resolved photoelectron imaging method. It is found that excitation at longer wavelengths (255.8, 250.0, 246.0 and 242.0 nm) results in population of the S-1((1)pi sigma*) state, which decays out of the photoionization window in less than 30 fs. At 237.7 nm, the second 1 ps* state is excited, which decays in about 130 fs. At shorter pump wavelengths (231.8, 224.8, 217.5 and 199.7 nm), the assignments are less clear-cut. We tentatively assign the initially photoexcited states to the (1)pi 3p Rydberg states, which decay in about 60 fs, with internal conversion to the S1(1 ps*) state as one of the decay channels. The lifetimes of these (1)pi 3p Rydberg states vary little with the pump wavelengths in this wavelength range.
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