Exploiting negative photochromism to harness a four-photon-like fluorescence response with two-photon excitation

C Carlos Benitez-Martin (Department of Chemistry and Molecular Biology) J Jean Rouillon E Eduard Fron (Department of Chemistry, KU Leuven, Celestijnenlaan 200F, B-3001 Leuven, Belgium) F Flip de Jong (Department of Chemistry, Molecular Imaging and Photonics, KU Leuven, Leuven Chem&Tech, Celestijnenlaan 200F, Leuven 3001, Belgium) M Morten Grøtli (Department of Chemistry and Molecular Biology) J Johan Hofkens (Department of Chemistry, KU Leuven, Celestijnenlaan 200F, B-3001 Leuven, Belgium) U Uwe Pischel (CIQSO─Center for Research in Sustainable Chemistry and Department of Chemistry, University of Huelva, Campus de El Carmen s/n, E-21071 Huelva, Spain) J Joakim Andréasson (Chemistry and Chemical Engineering, Chemistry and Biochemistry)

Abstract

Abstract Combining nonlinear optical processes and photoswitching transcends the limitations of conventional and even standalone super-resolution imaging. While photoswitching enables resolution improvement, it is typically constrained by limited imaging depth, potential phototoxicity and the low number of inherently fluorescent photoswitches. Nonlinear excitation, such as two-photon absorption, addresses some of these challenges. Here, we present a molecular design strategy that unites the molecular control of T-type negative photoswitches (PS) and two-photon absorption. In these designs, two-photon absorbing push-pull fluorophores that function as FRET-donors are linked to T-type negative PS FRET-acceptors, e.g., donor-acceptor Stenhouse adducts (DASA) or 1,1′-binaphthyl-bridged imidazole dimers. FRET-sensitized isomerization of PS is delicately balanced by reverse thermal isomerization and results in nonlinearly potentiated fluorescence with a quartic fluorescence response upon two-photon excitation, implying enhanced spatial resolution potential. The use of T-type PS is instrumental to this approach, as it ensures temporally stable photonic responses and recyclability without incurring irreversible saturation effects.

Article Details

Volume / Issue Vol. 16, Issue 1
Published December 03, 2025
ISSN 2041-1723
Publisher Nature Portfolio

Journal Info

Nature Communications

Nature Portfolio

ISSN: 2041-1723 Open Access Life Sciences

Authors (8)

C

Carlos Benitez-Martin

Department of Chemistry and Molecular Biology

J

Jean Rouillon

E

Eduard Fron

Department of Chemistry, KU Leuven, Celestijnenlaan 200F, B-3001 Leuven, Belgium

F

Flip de Jong

Department of Chemistry, Molecular Imaging and Photonics, KU Leuven, Leuven Chem&Tech, Celestijnenlaan 200F, Leuven 3001, Belgium

M

Morten Grøtli

Department of Chemistry and Molecular Biology

J

Johan Hofkens

Department of Chemistry, KU Leuven, Celestijnenlaan 200F, B-3001 Leuven, Belgium

U

Uwe Pischel

CIQSO─Center for Research in Sustainable Chemistry and Department of Chemistry, University of Huelva, Campus de El Carmen s/n, E-21071 Huelva, Spain

J

Joakim Andréasson

Chemistry and Chemical Engineering, Chemistry and Biochemistry