Bright and Photostable TADF‐Emitting Zirconium(IV) Pyridinedipyrrolide Complexes: Efficient Dyes for Decay Time‐Based Temperature Sensing and Imaging

Author:

Russegger Andreas1,Debruyne Angela C.2,Berrio Daniel Carvajal3,Fuchs Stefanie1,Marzi Julia34,Schenke‐Layland Katja34,Dmitriev Ruslan I.25,Borisov Sergey M.1ORCID

Affiliation:

1. Institute of Analytical Chemistry and Food Chemistry Graz University of Technology Stremayrgasse 9 Graz 8010 Austria

2. Tissue Engineering and Biomaterials Group Department of Human Structure and Repair Faculty of Medical and Health Sciences Ghent University C. Heymanslaan 10 Ghent 9000 Belgium

3. Institute of Biomedical Engineering Department for Medical Technologies and Regenerative Medicine and Cluster of Excellence iFIT (EXC 2180) “Image‐Guided and Functionally Instructed Tumor Therapies” Eberhard Karls University Tübingen 72076 Tübingen Germany

4. NMI Natural and Medical Sciences Institute at the University of Tübingen 72770 Reutlingen Germany

5. Ghent Light Microscopy Core Ghent University Ghent 9000 Belgium

Abstract

AbstractLuminescence thermometry represents a technique of choice for measurements in small objects and imaging of temperature distribution. However, most state‐of‐the‐art luminescent probes are limited in spectral characteristics, brightness, photostability, and sensitivity. Molecular thermometers of the new generation utilizing air and moisture‐stable zirconium(IV) pyridinedipyrrolide complexes can address all these limitations. The dyes emit pure thermally activated delayed fluorescence without any prompt fluorescence and show a unique combination of attractive features: a) visible light excitation and emission in the orange/red region, b) high luminescence brightness (quantum yields ≈0.5 in toluene and 0.8–1.0 in polystyrene matrix), c) excellent photostability, d) suitability for two‐photon excitation and e) mono‐exponential decay on the order of tens to hundreds of microseconds with strongly temperature‐dependent lifetimes (between −2.5 and −2.9% K−1 in polystyrene at 25 °C). Immobilization in gas‐blocking polymers yields sensing materials for self‐referenced decay time read‐out that are manufactured in two common formats: planar optodes and water‐dispersible nanoparticles. Positively charged nanoparticles are demonstrated to be suitable for nanothermometry in live cells and multicellular spheroids. Negatively charged nanoparticles represent advanced analytical tools for imaging temperature gradients in samples of small volumes such as microfluidic devices.

Funder

Austrian Science Fund

Publisher

Wiley

Subject

Atomic and Molecular Physics, and Optics,Electronic, Optical and Magnetic Materials

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