Photoproduction of Proton Gradients with
-Stacked Fluorophore Scaffolds in Lipid Bilayers
Sheshanath Bhosale,1
Adam L. Sisson,1
Pinaki Talukdar,1
Alexandre Fürstenberg,2
Natalie Banerji,2
Eric Vauthey,2
Guillaume Bollot,1
Jiri Mareda,1
Cornelia Röger,3
Frank Würthner,3
Naomi Sakai,1
Stefan Matile1*
Rigid
p-octiphenyl rods were used to create helical tetrameric

-stacks of blue, red-fluorescent naphthalene diimides that can
span lipid bilayer membranes. In lipid vesicles containing quinone
as electron acceptors and surrounded by ethylenediaminetetraacetic
acid as hole acceptors, transmembrane proton gradients arose
through quinone reduction upon excitation with visible light.
Quantitative ultrafast and relatively long-lived charge separation
was confirmed as the origin of photosynthetic activity by femtosecond
fluorescence and transient absorption spectroscopy. Supramolecular
self-organization was essential in that photoactivity was lost
upon rod shortening (from
p-octiphenyl to biphenyl) and chromophore
expansion (from naphthalene diimide to perylene diimide). Ligand
intercalation transformed the photoactive scaffolds into ion
channels.
1 Department of Organic Chemistry, University of Geneva, Geneva, Switzerland.
2 Department of Physical Chemistry, University of Geneva, Geneva, Switzerland.
3 Institut für Organische Chemie, Universität Würzburg, Am Hubland, D-97074 Würzburg, Germany.
* To whom correspondence should be addressed. E-mail: stefan.matile{at}chiorg.unige.ch