Click chemistry-driven heteromolecular integration into layered zeolite frameworks for photochemical upconversion applications

Abstract

Organic–inorganic hybrid layered porous materials enabling triplet–triplet annihilation upconversion (TTA-UC) were developed by integrating anthracene-based emitters and metal–complex sensitizers within zeolitic nanospace. Diphenylanthracene (DPA) units were covalently anchored between MWW-type layers via thiol–ene click chemistry, forming organic pillars that generated ordered interlayer micropores, confirmed by XRD and N2 adsorption. Incorporation of cationic chromophores and Pt(octaethylporphyrin) [Pt(OEP)] enabled efficient intermolecular energy transfer. Upon 535 nm excitation, Pt(OEP)-loaded samples exhibited phosphorescence at 650 nm and upconverted emission at 400–500 nm. This work highlights a rational strategy for tuning nanoscale photochemical behavior via host–guest engineering in layered hybrid systems.

Graphical abstract: Click chemistry-driven heteromolecular integration into layered zeolite frameworks for photochemical upconversion applications

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Article information

Article type
Communication
Submitted
04 Nov 2025
Accepted
09 Feb 2026
First published
18 Feb 2026
This article is Open Access
Creative Commons BY-NC license

Chem. Commun., 2026, Advance Article

Click chemistry-driven heteromolecular integration into layered zeolite frameworks for photochemical upconversion applications

F. Kishimoto, K. Hisano, T. Wakihara and T. Okubo, Chem. Commun., 2026, Advance Article , DOI: 10.1039/D5CC06270E

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