4 quantum mechanical study of collision induced electronic-to-rotational energy transfer !n the fluorine-para-hydrogen system (F + Ha) is reported. The three potential energy surfaces of the system, constrained to lie in a fmed plane, are obtained by the diatomics-in-molecules approach, and close-co
Electronic Energy Transfer in a Multiporphyrin-Based Molecular Box
✍ Scribed by Anna Prodi; Claudio Chiorboli; Franco Scandola; Elisabetta Iengo; Enzo Alessio
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 134 KB
- Volume
- 7
- Category
- Article
- ISSN
- 1439-4235
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✦ Synopsis
Abstract
The molecular box 1 comprises of two zinc‐porphyrin metallacycles connected by two free‐base 4′‐trans‐dipyridylporphyrins, axially coordinated to the zinc centers. The photophysics of 1 were studied in chloroform by emission and ultrafast absorption spectroscopy. In the molecular box, fast singlet energy transfer (main component, τ=32 ps) is observed to occur from the zinc‐porphyrin metallacycles to the free‐base chromophores. From wavelength‐dependent spectrofluorimetric data, the efficiency of the energy‐transfer (ET) process is estimated as 0.5. The lower‐than‐unity value is tentatively attributed to the possibility of a competing electron‐transfer quenching pathway. Molecular box 1 can be considered to be a simple, self‐assembling, six‐chromophore antenna system. It has an inner cavity, 11.4 Å wide, that could be used, in principle, to host a variety of guest molecules and obtain higher‐order assemblies.
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