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Issue 3, 2020
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A zinc-responsive fluorophore based on 5′-(p-hydroxyphenyl)-pyridylthiazole

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Abstract

The synthesis and photophysical properties of an ion-sensitive fluorescent compound are described, featuring 5′-(p-hydroxyphenyl)pyridylthiazole (HPPT) as a highly emissive fluorophore. Density functional theory (DFT) calculations indicate that HPPT is capable of intramolecular charge transfer (ICT), with further polarization upon complexation with Zn(II). A 4′-picolyloxy–HPPT derivative was prepared and determined to form a 1 : 1 complex with Zn(NO3)2 in acetonitrile, with a Stokes shift of 137 nm (6323 cm−1) and a 67 nm bathochromic shift in emission relative to the neutral ligand, and a fluorescence quantum yield (ΦPL) of 92%. An X-ray crystal structure of the HPPT–Zn(II) complex confirmed a tridentate structure with a seven-membered chelate ring, and the picolyloxy unit rotated out of plane.

Graphical abstract: A zinc-responsive fluorophore based on 5′-(p-hydroxyphenyl)-pyridylthiazole

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Article information


Submitted
23 Oct 2019
Accepted
18 Jan 2020
First published
20 Jan 2020

Mater. Chem. Front., 2020,4, 899-904
Article type
Research Article

A zinc-responsive fluorophore based on 5′-(p-hydroxyphenyl)-pyridylthiazole

Y. Watanabe, W. Sungnoi, A. O. Sartorio, M. Zeller and A. Wei, Mater. Chem. Front., 2020, 4, 899
DOI: 10.1039/C9QM00648F

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