Full description
Attached file provides supplementary data for linked article. The excited-state dynamics of two molecular dyads, consisting of zinc (1) and free-base (2) porphyrin connected via a peptide linker to a core-substituted naphthalenediimide (NDI) have been investigated using optical spectroscopy. These dyads exhibit rich photophysics because of the large number of electronic excited states below 3 eV. In the case of 1 in apolar solvents, excitation energy transfer from the vibrationally hot singlet excited porphyrin to the NDI takes place with a 500 fs time constant. Electronic energy ends up in the NDI-localized triplet state, which decays to the ground state on a microsecond timescale. In polar solvents, ground-state recovery is faster by 5 orders of magnitude because of the occurrence of charge separation followed by recombination. On the other hand, excitation energy transfer in 2 takes place in the opposite direction, namely from the NDI to the porphyrin, which then undergoes intersystem crossing to the triplet state, followed by triplet energy transfer back to the NDI. Therefore, four distinct local electronic excited states are consecutively populated after excitation of the NDI unit of 2, with the energy shuttling between the two ends of the dyad. Subjects
Chemical Sciences |
Charge separation pathways |
Excitation energy |
Excited-state dynamics |
Light harvesting arrays |
Molecular electronics |
Multiporphyrin arrays |
Organic Chemistry |
Organic Chemical Synthesis |
Photoinduced electron |
Photosynthetic antenna |
Reaction center complex |
Ultrafast dynamics |
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- Local : feb0a2a76bf4f40deca4b5c771c2b2c9
