TY - JOUR
T1 - Molecular Accessibility and Diffusion of Resorufin in Zeolite Crystals
AU - Maris, J J Erik
AU - Parker, Luke A
AU - Stanciakova, Katarina
AU - Nikolopoulos, Nikolaos
AU - Berendsen, Koen M H
AU - van Blaaderen, Alfons
AU - Meirer, Florian
AU - Rabouw, Freddy T
AU - Weckhuysen, Bert Marc
N1 - Publisher Copyright:
© 2023 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH.
PY - 2024/1/2
Y1 - 2024/1/2
N2 - 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.
AB - 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.
KW - aggregation
KW - fluorescence probes
KW - fluorescence spectroscopy
KW - host–guest chemistry
KW - zeolites
UR - http://www.scopus.com/inward/record.url?scp=85176267516&partnerID=8YFLogxK
U2 - 10.1002/chem.202302553
DO - 10.1002/chem.202302553
M3 - Article
C2 - 37815001
SN - 0947-6539
VL - 30
JO - Chemistry-A European Journal
JF - Chemistry-A European Journal
IS - 1
M1 - e202302553
ER -