Molecular Accessibility and Diffusion of Resorufin in Zeolite Crystals

J J Erik Maris, Luke A Parker, Katarina Stanciakova, Nikolaos Nikolopoulos, Koen M H Berendsen, Alfons van Blaaderen, Florian Meirer, Freddy T Rabouw, Bert Marc Weckhuysen*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

We have used confocal laser scanning microscopy on the small, fluorescent resorufin dye molecule to visualize molecular accessibility and diffusion in the hierarchical, anisotropic pore structure of large (~10 μm-sized) zeolite-β crystals. The resorufin dye is widely used in life and materials science, but only in its deprotonated form because the protonated molecule is barely fluorescent in aqueous solution. In this work, we show that protonated resorufin is in fact strongly fluorescent when confined within zeolite micropores, thus enabling fluorescence microimaging experiments. We find that J-aggregation guest–guest interactions lead to a decrease in the measured fluorescence intensity that can be prevented by using non-fluorescent spacer molecules. We characterized the pore space by introducing resorufin from the outside solution and following its diffusion into zeolite-β crystals. The eventual homogeneous distribution of resorufin molecules throughout the zeolite indicates a fully accessible pore network. This enables the quantification of the diffusion coefficient in the straight pores of zeolite-β without the need for complex analysis, and we found a value of 3×10−15 m2 s−1. Furthermore, we saw that diffusion through the straight pores of zeolite-β is impeded when crossing the boundaries between zeolite subunits.

Original languageEnglish
Article numbere202302553
JournalChemistry-A European Journal
Volume30
Issue number1
Early online date10 Oct 2023
DOIs
Publication statusPublished - 2 Jan 2024

Bibliographical note

Publisher Copyright:
© 2023 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH.

Funding

B.M.W. is thankful for funding provided by the Netherlands Center for Multiscale Catalytic Energy Conversion (MCEC), an NWO Gravitation Program funded by the Ministry of Education, Culture and Science of the Government of the Netherlands and the US Army Research Office (ARO, with reference no. W911NF‐18‐1‐0284). F.M. acknowledges funding from the Netherlands Organization for Scientific Research (NWO) VIDI grant (no. 723.015.007). Andries Meijerink (Utrecht University, UU) is thanked for making available the Edinburgh Instruments FLS920 fluorescence spectrometer used for excited‐state lifetime and photoluminescence emission measurements. Remco Dalebout (UU) is thanked for the N‐physisorption measurements, while Yadolah Ganjkhanlou (UU) is thanked for X‐ray diffraction measurements and Sophie H. van Vreeswijk (UU) and Bill Gresnigt (UU) are thanked for fruitful discussions. 2

FundersFunder number
MCEC
Netherlands Center for Multiscale Catalytic Energy Conversion
Army Research OfficeW911NF‐18‐1‐0284
Ministerie van onderwijs, cultuur en wetenschap
Nederlandse Organisatie voor Wetenschappelijk Onderzoek723.015.007

    Keywords

    • aggregation
    • fluorescence probes
    • fluorescence spectroscopy
    • host–guest chemistry
    • zeolites

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