Fluorescence switching with subphthalocyanine-dihydroazulene dyads

Henrik Gotfredsen, Martin Drøhse Kilde, Marco Santella, Anders Kadziola, Mogens Brøndsted Nielsen

6 Citations (Scopus)

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.

Original languageEnglish
JournalMolecular Systems Design and Engineering
Volume4
Issue number1
Pages (from-to)199-205
ISSN2058-9689
DOIs
Publication statusPublished - Feb 2019

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