Connectivity pattern modifies excited state relaxation dynamics of fluorophore–photoswitch molecular dyads. Issue 5 (20th January 2017)

• Record Type: Journal Article
• Authors: Schweighöfer, F.; Moreno, J.; Bobone, S.; Chiantia, S.; Herrmann, A.; Hecht, S.; Wachtveitl, J.
• Is Part Of: Physical chemistry chemical physics. Volume 19:Issue 5(2017)
• Page Start: 4010
• Page End: 4018
• Publication Date: 2017-01-20
• Subjects: Chemistry, Physical and theoretical -- Periodicals; 541.3
• DOI: 10.1039/c6cp07112k
• Languages: English
• ISSNs: 1463-9076

Abstract

Abstract : Systematic variation of the orientation and distance in donor–bridge–acceptor compounds allows tuning of energy vs. electron transfer and provides a detailed view of the underlying molecular mechanisms. Abstract : In order to modulate the emission of BODIPY fluorophores, they were connected to a diarylethene (DAE) photoswitch via phenylene–ethynylene linkers of different lengths and orientations. The latter allowed for modulation of the electronic coupling in the prepared four BODIPY–DAE dyads, which were compared also to appropriate BODIPY and DAE model compounds by steady state as well as time-resolved spectroscopies. In their open isomers, all dyads show comparable luminescence behavior indicative of an unperturbed BODIPY fluorophore. In strong contrast, in the closed isomers the BODIPY emission is efficiently quenched but the deactivation mechanism depends on the nature of the linker. The most promising dyad was rendered water-soluble by means of micellar encapsulation and aqueous suspensions were investigated by fluorescence spectroscopy and microscopy. Our results (i) illustrate that the electronic communication between the BODIPY and DAE units can indeed be fine-tuned by the nature of the linker to achieve fluorescence modulation while maintaining photoswitchability and (ii) highlight potential applications to image and control biological processes with high spatio-temporal resolution.