English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Journal Article

Electron transfer in porphyrin—quinone cyclophanes

MPS-Authors
/persons/resource/persons92994

Futscher,  Michael
Department of Organic Chemistry, Max Planck Institute for Medical Research, Max Planck Society;

/persons/resource/persons123617

Voit,  Guido
Department of Organic Chemistry, Max Planck Institute for Medical Research, Max Planck Society;

/persons/resource/persons197299

Weiser,  Jürgen
Department of Organic Chemistry, Max Planck Institute for Medical Research, Max Planck Society;

/persons/resource/persons95446

Staab,  Heinz A.
Department of Organic Chemistry, Max Planck Institute for Medical Research, Max Planck Society;

Fulltext (restricted access)
There are currently no full texts shared for your IP range.
Fulltext (public)
There are no public fulltexts stored in PuRe
Supplementary Material (public)
There is no public supplementary material available
Citation

Heitele, H., Pöllinger, F., Kremer, R. K., Michel-Beyerle, M. E., Futscher, M., Voit, G., et al. (1992). Electron transfer in porphyrin—quinone cyclophanes. Chemical Physics Letters, 188(3), 270-278. doi:10.1016/0009-2614(92)90021-E.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0019-ABAD-5
Abstract
We have measured the fluorescence properties of five cyclophanes containing, in a vertical face-to-face arrangement, a porphyrin as electron donor and one of several substituted quinones as electron acceptor with varying acceptor strength in a series of solvents covering a wide range of polarity. The results of time-resolved fluorescence decay measurements are interpreted in terms of a very fast intramolecular charge separation within 1–10 ps with driving forces decreasing from −ΔGcs = 0.7 to about 0 eV and a charge recombination in the order of 10–200 ps.