Abstract
Excited state dynamics, particularly intersystem crossing, of a set of meso-substituted porphyrins bearing different electron-donor and acceptor groups was studied by pulse train fluorescence technique. Triplet quantum yield was found to be critically dependent on the nature of meso-substituents in the porphyrin system. Porphyrins with meso methoxyphenyl groups were found to show high triplet quantum yields (T between 0.70 and 0.81). Moreover, the quantity of methoxyphenyl groups and the substitution pattern directly influence T. Alternatively, porphyrins attached to nitrophenyl group possess low triplet quantum yield values (∼0.3). The observed structure-properties relationships suggest new ways for tuning the optical properties of porphyrins via chemical modification.
Original language | English |
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Pages (from-to) | 282-291 |
Number of pages | 10 |
Journal | Journal of Porphyrins and Phthalocyanines |
Volume | 20 |
Issue number | 1-4 |
DOIs | |
Publication status | Published - 1 Apr 2016 |
Externally published | Yes |
Keywords
- donor/acceptor groups
- excited state spectroscopy
- porphyrins
- quantum yields
- relaxation times
- triplet state