ISSN:
1089-7690
Source:
AIP Digital Archive
Topics:
Physics
,
Chemistry and Pharmacology
Notes:
In this paper we explore the intramolecular relaxation processes within two long carotenoids, namely decapreno-β-carotene (M15) and dodecapreno-β-carotene (M19) with 15 and 19 conjugated double bonds (N), respectively. Amplified 200 fs pulses at 590 nm were used to excite the optically allowed S0→S2 (1 1Ag→1 1Bu) transition of the two carotenoids. The excited state dynamics were probed by continuum light between 400–890 nm in solvents with different polarizabilities. The transient absorption spectra consist of a bleaching region, due to loss of ground state absorption, and of an excited state absorption region at longer wavelengths, due to the S1→Sn transition. The Sn state was assigned to an n 1Bu state. The overall wavelength dependence of the measured kinetics could be well described by introducing three decay time constants. One reflects the S1 lifetime (τ1) and was determined to 1.1 and 0.5 ps for M15 and M19, respectively. A second lifetime, between 5 and 15 ps, was attributed to vibrational cooling in the ground state. A third decay time was in the subpicosecond range, and was ascribed to the vibrational redistribution and relaxation of the S1 potential surface after being populated by the subpicosecond S2–S1 internal conversion. No significant change of the decay constants was observed for M15 embedded in a 77 K matrix. This shows that the relaxation rates are only influenced by intramolecular processes.The S2 lifetime was shorter than the pulse duration and was estimated to be in the order of 100 fs. The S0→S2 transition of M15 in the liquid phase exhibits a 0.39 anisotropy at short times, while the S1→Sn transition has an initial value of only 0.31. This corresponds to an angle of 23° between the transition dipoles. The measured S1 rate constants were analyzed, together with decay constants of shorter carotenes, in terms of the energy gap law. When going from the shortest (N=5) to the longest (N=19) polyene, τ1 decreases about 6000 times, i.e., from 3 ns to 0.5 ps. By using an empirical form of the energy gap law the 0–0 transition of S1(2 1Ag)→S0 was estimated to be located at 11 300 and 10 200±1 000 cm−1 for M15 and M19, respectively. By fitting the excitation energies of all carotenes in the series (3≤N≤19) with a truncated two or three term expansion of a power series in 1/N the long-chain limit values were extrapolated to be 11 000 and 3 500 cm−1 for the 1 1Bu and 2 1Ag state, respectively. The implication of these limit values on the electronic structure of polyacetylene are discussed. © 1995 American Institute of Physics.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1063/1.469672
Permalink
