Supramolecular complexation of porphyrin and quinone with two coordination bonds and intramolecular electron transfer
β Scribed by Hiroshi Imahori; Koji Yamada; Eiichi Yoshizawa; Kiyoshi Hagiwara; Tadashi Okada; Yoshiteru Sakata
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 266 KB
- Volume
- 01
- Category
- Article
- ISSN
- 1088-4246
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β¦ Synopsis
V-shaped zinc porphyrin dimer and quinone with two pyridyl groups have
been rationally designed and synthesized to assemble a porphyrin-quinone
supramolecule with two coordination bonds. Selective formation of the 1:1
bridging structure between the host-guest molecules was seen by
^1^ H NMR and UV-Vis absorption spectroscopy.
Molecular mechanics calculation suggests that the bridging structure has
rigidity as well as flexibility in geometry between the redox pair, which
supports the interpretation of ^1^ H NMR studies.
Intramolecular photoinduced electron transfer from the excited singlet state
of the porphyrin to the quinone was observed by steady-state fluorescence
spectra and picosecond fluorescence lifetime measurements.
π SIMILAR VOLUMES
## Abstract Scalar coupling constants have been computed using the EOMβCCSD method for equilibrium structures of complexes stabilized by Fο£ΏHβ¦P hydrogen bonds, as well as structures along the protonβtransfer coordinates of these complexes. Variations in the signs and absolute values of ^1^__J__(Fο£ΏH)
Figure 1. Components of a supramolecular assembly 1.
Figure 1. Components of a supramolecular assembly 1.
This review describes light induced energy or electron transfer reactions in self-assembled supramolecular zinc porphyrin/zinc phthalocyanine and fullerene bearing donor-acceptor systems. The self-assembled supramolecular dyads and triads are formed by using one or two types of the binding mechanism