Fluorescence switching with subphthalocyanine-dihydroazulene dyads. Issue 1 (21st January 2019)

• Record Type: Journal Article
• Authors: Gotfredsen, Henrik; Kilde, Martin Drøhse; Santella, Marco; Kadziola, Anders; Nielsen, Mogens Brøndsted
• Is Part Of: Molecular Systems Design and Engineering. Volume 4:Issue 1(2019)
• Page Start: 199
• Page End: 205
• Publication Date: 2019-01-21
• Subjects: Chemistry -- Molecular aspects -- Periodicals; Chemical engineering -- Molecular aspects -- Periodicals; Nanotechnology -- Periodicals; 620.5
• DOI: 10.1039/c8me00075a
• Languages: English
• ISSNs: 2058-9689

Abstract

Abstract : The boron subphthalocyanine (SubPc) fluorescence is reversibly modulated by photoisomerization of a covalently attached dihydroazulene (DHA) photoswitch into a vinylheptafulvene (VHF). Abstract : One convenient way of reversibly modulating the emission properties of a fluorophore is by introducing a photochromic unit that upon irradiation is converted into an isomeric unit that can quench the fluorescence of the fluorophore. Here we present the synthesis of two dyads containing a boron subphthalocyanine (SubPc) fluorophore and the dihydroazulene (DHA) photoswitch. Upon photoisomerization, the DHA unit is converted to a vinylheptafulvene (VHF) unit that was found to efficiently quench the SubPc fluorescence when placed at the axial boron position of the SubPc. The original fluorescence was restored by thermal conversion of the VHF to DHA. Fluorescence was thereby turned off and on by successive light-heat cycles. The other dyad has the DHA unit placed at the periphery of the SubPc, and this dyad showed instead limited photostability.