Post-synthetic Modification Research Articles

Metal Imidazole-Modified Covalent Organic Frameworks as Electrocatalysts for Alkaline Oxygen Evolution Reaction

Since the product contains no carbon-based substances and can be driven by non-carbon-based electricity, electrocatalytic water splitting is considered to be among the most effective strategies for alleviating the energy crisis and environmental pollution. This process helps lower greenhouse gas emissions while also supporting the shift toward renewable energy sources. The anodic oxygen evolution reaction (OER) involves a more complex multi-electron transfer process, which is the principal limiting factor in overall water splitting. Extensive research has demonstrated that the controlled design of effective electrocatalysts can address this limitation. In this study, a previously unreported covalent organic framework material (COF-IM) was synthesized via a post-synthetic modification strategy. Notably, COF-IM contains imidazole nitrogen metal active sites. Transition metal-coordinated COF-IM@Co can function as a highly effective electrocatalyst, exhibiting a lower overpotential (403.8 mV@10 mA cm−2) in alkaline electrolytes, thereby highlighting its potential for practical applications in energy conversion technologies. This study offers new perspectives on the design and synthesis of COFs, while also making substantial contributions to the advancement and application of OER electrocatalysts.

Engineering designed functional covalent organic frameworks via pore surface modifications for effectively reducing the dielectric constant of polyimide-based electronic packaging materials

Polyimide (PI) is considered one of the most promising candidate materials for the microelectronics and wireless communication industries. Nevertheless, the relatively high dielectric constant of PI has become a significant obstacle, constraining its utilization in the realm of microelectronics. Herein, novel PI nanocomposite films were fabricated by incorporating covalent organic frameworks (COFs) and their functionalized counterparts (COF@POSS and COF@DTF) through post-synthetic modification. Among all PI nanocomposites films, PI/COF@POSS nanocomposite film including 2 wt% COF@POSS achieved the lowest dielectric constant (2.41) and dielectric loss (0.0076). These values represented a reduction of 22.5 % and 24 % compared to pure PI, respectively. The decrease in dielectric constant is ascribed to the combined influence of the porous structure of COF and the augmentation in free volume fraction caused by the steric hindrance of POSS. Additionally, the tensile strength of the PI/COF@POSS and PI/COF@DTF nanocomposite films increased up to 121.1 MPa and 112.0 MPa, representing a 95 % and 80 % improvement over pure PI, respectively. Furthermore, the introduction of COFs functionalized with POSS and DTF significantly enhanced the hydrophobicity of PI nanocomposite films. The combination of porous organic nanofillers with surface functionalization offers a feasible route to create low-k PI nanocomposite films with improved mechanical properties and hydrophobicity.

Post-synthetic modification of a MOF via Continuous Flow Methods for Gold E-Waste Recycling.

This study pioneers the use of continuous flow methods to modify the nanoporous metal-organic framework Fe-BTC (MIL-100(Fe)) with redox-active poly-p-phenylenediamine (PpPDA). The Fe-BTC/PpPDA composite, known for its gold extraction capabilities, was synthesized in continuous flow on a 250 g scale. Fe-BTC/PpPDA was then tested in eight industrial leachates (e.g., cyanide, thiourea, aqua regia) exhibiting varying effectiveness, pH, and gold speciation, which led to significant differences in the composite's performance for gold extraction. The composite performed best in solutions containing [AuCl4]- species. Structured into spherical beads using a novel continuous flow microdroplet technique, these adsorbents were tested for gold recovery from real e-waste solutions in a breakthrough epemriment. They achieved a capacity of ~600 mg of gold per gram before breakthrough and ~900 mg per gram at a 60% recovery rate. Selectivity ratios for Au/Ni, Au/Co, and Au/Fe were 972, 262, and 193, respectively. In situ X-ray absorption near edge spectroscopy (XANES) provided evidence of the reduction of Au³⁺ to Au⁰, facilitated by the redox-active oligomers. Outperforming several commercial resins, Fe-BTC/PpPDA shows great promise for scalable, selective metal recovery from waste streams. This study highlights the potential of MOF/polymer composites and continuous flow methods for large-scale production.

Post-synthetic modification of Zr-based metal organic framework by schiff base zinc complex for catalytic applications in a click reaction

A novel nanocatalyst, denoted as UiO-66/Sal-ZnCl2, has been synthesized and systematically characterized employing a range of analytical techniques, including Fourier-transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), thermogravimetric analysis (TGA), Brunauer–Emmett–Teller (BET) surface area analysis, and inductively coupled plasma (ICP) analysis. The comprehensive analyses collectively affirm the effective coordination of zinc chloride onto the functionalized UiO-66. Subsequently, the catalytic efficacy of UiO-66/Sal-ZnCl2 was assessed in a one-pot, three-component click reaction involving terminal alkynes, alkyl halides, and sodium azide, conducted in an aqueous medium. The catalyst demonstrated remarkable catalytic activity, showcasing the capability to facilitate the reaction with high yields and exceptional regioselectivity. Noteworthy attributes of this nanocatalyst and the method include its elevated efficiency, recyclability, convenient product workup, and, significantly, the utilization of a sustainable solvent medium. The synthesis, characterization, and catalytic performance of this catalyst collectively contribute to its potential as an innovative and reusable nanocatalyst for diverse synthetic transformations.

GQDs@SiO3Pr Schiff-base complexes Co (II); As an eco-friendly environmental nanocatalyst for the synthesis of the amino carbonitrile chromenes

An effective nanocomposite comprising functionalized graphene quantum dots has been developed for the rapid, one-step production of amino carbonitrile chromenes. To this end, the surface of graphene quantum dots (GQDs) was functionalized with a novel synthetic Schiff-base complex of cobalt (II) prepared by post-synthetic surface modification of the graphene quantum dot surface with a silane coupling agent (3-chloropropyl trimethoxysilane, SiO3PrCl) in order to synthesize GQDs@SiO3PrCl. Then, the Schiff base ligand synthesized from the condensation reaction of 4-aminoantipyrine with ortho-phenylenediamine was immobilized on the surface of the silane-linker grafted GQDs to synthesize the GQDs@SiO3Pr-Schiff base. Finally, the cobalt particles were stabilized on the surface of the graphene quanta functionalized with Schiff bases (GQDs@SiO3Pr-Schiff Base/Co (II)). The GQDs@SiO3Pr-Schiff Base/Co (II) nanocatalyst demonstrated exceptional performance in the synthesis of amino carbonitrile chromenes derivatives, facilitating high product yields using various aromatic aldehydes, 4‑hydroxy coumarin and malononitrile under mild conditions. Additionally, the catalyst exhibited reusability up to seven times without significant loss of productivity, showcasing its environmental friendliness and sustainability in organic synthesis. This versatile nanocatalyst holds promising for efficient and economically viable catalysis in diverse chemical applications.

Design and synthesis of pillared metal-organic frameworks featuring olefinic fragments.

While metal-organic frameworks (MOFs) are known primarily for their well-defined crystalline porous structures that make them desirable for a myriad of applications, they also distinguish themselves with their chemical tunability. One strategy for chemical tailoring of MOF structures is post-synthetic modification (PSM) targeting moieties present in their organic building blocks (linkers). In this context, alkene (olefinic) fragments are underrepresented in the realm of MOFs despite their extremely well-established and versatile chemistry. With the majority of reported olefinic MOFs falling into the microporous regime, the PSM opportunities involving bulkier reagents are severely limited. Herein, we report a family of UofT (University of Toronto) pillared MOFs constructed around olefinic 1,4-bis(2-(pyridin-4-yl)vinyl)benzene (BPVB) and tetrakis(4-carboxyphenyl)porphyrin (TCPP) linkers. By utilizing a variety of M(II) [M = Zn, Ni, Co] precursors, three structurally distinct frameworks were synthesized and characterized. Most notably, the nickel-based framework represents the first reported example of a stable mesoporous olefinic pillared MOF. In addition to the de novo formation of a stable pillared MOF, Ni(II) is also used in a cation exchange process to structurally reinforce zinc-based frameworks.

ZnH2P4N8: Case Study on Topochemical Imidonitridophosphate High-Pressure Synthesis.

Nitridophosphates are subject of current research, as they have a broad spectrum of properties and potential applications, such as ion conductors or luminescent materials. Yet, the subclass of imidonitridophosphates has been studied less extensively. The primary reason is that the controlled N-H functionalization of nitridophosphates is not straight forward, making targeted synthesis more challenging. Inspired by the high-pressure (HP) post-synthetic modification of nitridophosphates, we present the topochemical HP deprotonation of phosphorus nitride imides using the high-pressure polymorph β-PN(NH) as an example. Additional incorporation of Zn2+ results in the first quaternary transition metal imidonitridophosphate ZnH2P4N8. The crystal structure was elucidated by single-crystal X-ray diffraction (SCXRD), energy-dispersive X-ray spectroscopy (EDX), powder X-ray diffraction (PXRD) and solid-state magic angle spinning nuclear magnetic resonance spectroscopy (MAS NMR). In addition, the presence of H as part of an imide group was confirmed by IR spectroscopy. The potential of this defunctionalization approach for controlling the N-H content is demonstrated by the preparation of partially deprotonated intermediates ZnxH4-2xP4N8 (x≈0.5, 0.85). This topochemical high-pressure reaction represents a promising way to prepare, control and manipulate new imide-based materials without altering their overall anionic framework.

Sequential Linker Installation in Metal-Organic Frameworks.

ConspectusMetal-organic frameworks (MOFs) represent a sophisticated blend of inorganic and organic components, promoting the development of coordination chemistry greatly and offering a versatile platform for tailored functionalities. By combining various metal nodes, organic linkers, and functional guests, MOFs provide numerous pathways for their design, synthesis, and customization. Among these, sequential linker installation (SLI) stands out as a novel and crucial strategy, enabling the precise integration of desired properties and functions at the atomic scale. SLI enhances structural diversity and stability while facilitating the meticulous construction of robust frameworks by leveraging open metal sites and functional organic linkers at targeted locations. Compared to the direct synthesis of MOFs, postsynthetic modification methods allow for precise regulation of their structures and corresponding properties. While unlike conventional postsynthetic modification methods, SLI requires the careful selection of linkers and framework design to ensure precise positioning for installation, which gives rise to the well-designed and ordered positions for the installed linkers, confirmed directly by X-ray diffraction technology.Recent advancements in MOF synthesis have led to the creation of increasingly tailored flexible matrix structures, particularly due to the diverse connection modes of multicore metal clusters, especially for the Zr6 cluster. The spatial hindrance of certain ligands has resulted in the formation of unsaturated metal clusters and various missing linker pockets. Examples of these advanced MOFs include PCN-606, PCN-608, PCN-609, PCN-700, and PCN-808, which feature specific open metal sites and certain framework flexibility conducive to SLI. Strategically positioned open metal sites within these frameworks serve as predetermined anchor points for desired functional molecules, while the frameworks' flexibility can accommodate molecules of varying sizes to a certain extent, enlarging the scopes of application greatly. This precise positioning of functional groups enables the creation of tailored sites for enhanced applications, such as adsorption, catalysis, and recognition.In this Account, we delve into the intricate process of designing and synthesizing MOFs with appropriate missing-linker pockets for the aforementioned applications. We discuss the meticulous selection of functional linkers and the methods used to insert them into the corresponding missing-linker pockets within the MOFs. Additionally, we explore the diverse properties and functionalities of the resulting MOFs, focusing on their adsorptive, catalytic, and recognition performance. Furthermore, we provide insights into the future trajectory of SLI methods, complemented by our recent works. This Account not only reviews the evolution of the SLI method but also underscores its practical applications across various functional domains, paving a rational pathway for the future development of advanced multifunctional MOFs through this method.

Regulating the Hydrophilicity of Hyper-Cross-Linked Polymers via Thermal Oxidation for Atmospheric Water Harvesting.

We explore the thermal oxidation of hyper-cross-linked polymers to enhance their hydrophilicity and efficacy in atmospheric water harvesting. Comprehensive chemical and physical characterizations are used to confirm the successful incorporation of polar oxygen moieties and the preservation of porosity upon thermal treatment. Newly introduced oxygen-based functional groups significantly improve water sorption properties, increasing total water uptake capacities by up to 400% and shifting water uptake onsets to significantly lower relative humidity. We also investigate the regeneration of oxidized hyper-cross-linked polymers after water sorption to probe their potential for multiple water harvesting cycles and reuse. Our findings outline a simple and cost-effective postsynthetic modification route for optimizing porous organic polymers for more sustainable and efficient atmospheric water harvesting.

Post-Synthetic Modification of Porous Organic Cages for Enhanced Iodine Adsorption Performance.

The capture of radioactive iodine species from nuclear waste is crucial for environmental protection and human health. Porous organic cages (POCs), an emerging porous material, have showed potential in iodine adsorption due to the advantages of tunable pores and processibility. However, integrating multiple desirable characteristics into a single POC through bottom-up assembly of pre-designed building blocks remains challenging. Post-synthetic modification (PSM) offers an alternative approach, enabling the introduction of various functions into a single POC. Herein, a viable and highly efficient three-step PSM strategy to modify a representative POC (CC3), is presented. The modified POC, OFT-RCC36+6Br-, features a charged confined space, electron-rich heteroatom, and halide ions, exhibiting significantly enhanced iodine vapor uptake compared to the parental cage. The universality of the PSM strategy has been verified by successfully modifying two other POCs. The iodine adsorption behaviors of three modified cage adsorbents in organic solvent and aqueous solution have also been investigated, all of which exhibited improved performance, especially in comparison to ionic cages modified through direct protonation. This work provides an effective PSM strategy for POCs to facilitate iodine adsorption. More importantly, the introduction of a new PSM strategy enriches the functional diversity of POCs, potentially broadening their future applications.

Halogen-Driven Single-Crystal to Single-Crystal Transformation Engineering the Cluster-based Spin Crossover Frameworks.

Cluster-based spin crossover (SCO) frameworks are a new class of smart metal-organic frameworks (MOFs) with diverse structures and topologies and unique bistable physicochemical properties. Here, we report a cluster-based SCO framework [Fe3{Ag4(CN)6(H2O)}2(TPBA)3](ClO4)2·7DMF (1) with an extremely rare 3,4,6-T108 topology, in which the tripodal [Ag{Ag(CN)2}3(H2O)]2- clusters axially link the Fe2+ ions to form 2D→3D n-fold Borromean entangled networks. Under the guidance of reticular chemistry, the post-synthetic modification (PSM) from 1 with 3,4,6-T108 topology to [Fe3{Ag8X8(CN)6}(TPBA)3] (2_X, X = Cl, Br, I) with urk topology is firstly achieved via single-crystal to single-crystal (SCSC) transformation. Moreover, the successive SCSC transformations from 2_Cl to 2_Br and then to 2_I are realized for the first time. Their SCO behaviors are also modified by halogen-driven stepwise cluster transformations. Hence, these findings provide new strategies for the development of cluster-based SCO MOFs towards the smart functional porous materials.

Halogen‐Driven Single‐Crystal to Single‐Crystal Transformation Engineering the Cluster‐based Spin Crossover Frameworks

Cluster‐based spin crossover (SCO) frameworks are a new class of smart metal‐organic frameworks (MOFs) with diverse structures and topologies and unique bistable physicochemical properties. Here, we report a cluster‐based SCO framework [Fe3{Ag4(CN)6(H2O)}2(TPBA)3](ClO4)2·7DMF (1) with an extremely rare 3,4,6‐T108 topology, in which the tripodal [Ag{Ag(CN)2}3(H2O)]2− clusters axially link the Fe2+ ions to form 2D→3D n‐fold Borromean entangled networks. Under the guidance of reticular chemistry, the post‐synthetic modification (PSM) from 1 with 3,4,6‐T108 topology to [Fe3{Ag8X8(CN)6}(TPBA)3] (2_X, X = Cl, Br, I) with urk topology is firstly achieved via single‐crystal to single‐crystal (SCSC) transformation. Moreover, the successive SCSC transformations from 2_Cl to 2_Br and then to 2_I are realized for the first time. Their SCO behaviors are also modified by halogen‐driven stepwise cluster transformations. Hence, these findings provide new strategies for the development of cluster‐based SCO MOFs towards the smart functional porous materials.

Tandem Solid‐Solution Phase Post‐Synthetic Modification of Porous Molecular Crystals for In‐Situ Generation of Fluorophores

AbstractConventional synthetic methods of organic luminescent molecules often involve labor‐intensive solution‐phase organic synthesis, which violate the principles of atom‐economic transformation. Post‐synthetic modification (PSM) offers a promising alternative, allowing direct transformation from one fluorophore to another. Although PSM is commonly implemented in extended frameworks, its application in porous molecular crystals remains challenging. Herein, we focus on utilizing porous molecular crystals, specifically tetraphenylethylene‐cored frameworks, as versatile platforms for tandem PSM reactions to customize organic fluorophores. The tailored skeleton design ensures both the formation of porous structures and the occurrence of tandem solid‐solution phase reactions while maintaining the solid state of reactants and products in each step. The inherent non‐covalent bonding nature of the frameworks facilitates processing and characterization, offering unparalleled advantages for porous networks. The accompanying solid‐state fluorescence transition from green to blue and then to green (or yellow) enables real‐time monitoring of tandem reactions and provides intuitive mechanistic insights. This phenomenon is exploited for the facile construction of a dynamic information encryption system using fluorescent quick response codes.

Fabrication of thermo-responsive polymer-MOF@cellulase composites withimprovedcatlytic performancefor hydrolysis of cellulose.

Metal-organic frameworks (MOFs) are considered as an ideal enzyme support because of their porous structural superiority. However, MOFs@enzyme composites have usually compromised their hydrolysis efficiency due to the narrow space inducing unfavourable enzyme conformations. Herein, a thermo-responsive poly(N,N-dimethylacrylamide) (PD) was fixed onto the surface of UiO-66-NH2 (UiO) through a post-synthetic modification protocol. Using poly(2-vinyl-4,4 dimethylazlactone) (V) as a linker, PVD-UiO@cellulase composites were fabricated after cellulase was immobilized onto the UiO surface through covalent bonding. The composites conferred favorable cellulose conformations, boosting hydrolysis efficiency and stability, which relied on the soft PVD shell and confinement effect yielded by the curled PVD chains at high temperatures. Compared with free cellulase, the proposed composites exhibited a 33.1-fold enhancement of the Kcat values at 50 °C. The PVD-UiO@cellulase composites were applied to the hydrolysis of cellulose in the stalks and leaves of Epipremnum aureum. The results highlight the potential of smart PVD-UiO@cellulase composites in the hydrolysis of cellulose, affording a valuable platform for the preparation of unique MOFs@enzyme composites and their industrial applications.

Hydrogen-Bonded Organic Frameworks for Antibiotic Fluorescent Sensing Artificial Intelligence-Enhanced Anticounterfeiting.

The paramount importance of anticounterfeiting measures in safeguarding consumers from counterfeit products lies in their ability to ensure product safety and reliability. Advanced luminescent anticounterfeiting materials, particularly those responsive to multiple stimuli, afford a dynamic and multilayered security assurance. This study presents the synthesis of a novel material, Eu/Tb@GC-3, via postsynthetic modification, which exhibits notable photoluminescent properties with emission at 544 and 614 nm. The material demonstrates high selectivity and sensitivity in detecting Nitrofural and Enrofloxacin, with limits of detection at 0.0122 and 0.0280 μM, respectively. Furthermore, multistimulus responsive luminescent fibers and inks were developed, facilitating intelligent anticounterfeiting labels. The integration of these labels with back-propagation neural networks (BPNNs) significantly enhances pattern recognition and authentication capabilities, providing an efficacious strategy to combat counterfeit products and ensure consumer safety.

Macromorphological Control of Zr-Based Metal-Organic Frameworks for Hydrolysis of a Nerve Agent Simulant.

Zirconium-based metal-organic frameworks (MOFs) have become one of the most promising materials for the adsorption and destruction of chemical warfare agents. While numerous studies have shown differences in reactivity based on MOF topology and postsynthetic modification, the understanding of how modifying MOF macromorphology is less understood. MOF xerogels demonstrate modified defect levels and larger porosity, which increase the number of and access to potential active sites. Indeed, UiO-66 and NU-901 xerogels display reaction rates 2 and 3 times higher, respectively, for the hydrolysis of DMNP relative to their powder morphologies. Upon recycling, MOF-808 xerogel outperforms MOF-808 powder, previously noted as the fastest Zr6 MOF for hydrolysis of organophosphate nerve agents. The increase in reactivity is largely driven by a higher external surface area and the introduction of mesoporosity to previously microporous materials.

Thiatruxene-Based Conductive MOF: Harnessing Sulfur Chemistry for Enhanced Proton Transport.

Functionalizing the organic building blocks of electrically conductive MOFs (EC-MOFs) can be a powerful method for adjusting the electronic structure and introducing a specific chemistry. However, designing EC-MOF linkers with reactive functional groups for postsynthetic modification is challenging due to the requirements of d-p conjugation. This work addresses such design limitations by synthesizing an EC-MOF, Cu-thiatruxene (Cu-thiaTRX). This conductive framework incorporated a truxene-based linker with heterocyclic sulfur, allowing for efficient conjugation and an electrical conductivity of 2.2 × 10-2 S cm-1. Harnessing sulfur chemistry in Cu-thiaTRX involves a two-step postsynthetic modification: oxidation and SNAr. The sulfinic groups introduced in the framework enabled tunable proton conductivity, leading to a 200-fold improvement. These results highlight the importance of a rational linker design for functionalization.

Fabrication of a novel Eu3+-functionalized Mn-MOF based on the X-type tetracarboxylate ligand for efficient temperature sensing

In this work, by utilizing an X-type tetracarboxylate ligand (1,2,4,5-tetrakis(4-carboxyphenyl)benzene, H4TCPB), a novel Mn-organic framework, namely, [(CH3CH2)2NH2]2[Mn(TCPB)(H2O)2] (SQNU-25, SQNU = Shangqiu Normal University), was prepared under a DEF/HAc solm. Due to the structural advantage of SQNU-25, the Ln3+ ions (Eu3+ and Gd3+) have been successfully introduced into the framework by post-synthetic modification. The result of the energy levels of the H4TCPB ligand and Eu3+ ion shows that the H4TCPB ligand as a chromophore can effectively sensitize Eu3+ ions. Moreover, the Eu@SQNU-25 not only shows a typical Eu3+ ion red emission but also exhibits good temperature sensing in the wide temperature range (80 to 300 K).

Structural Landscape and Proton Conduction of Lanthanide 5-(Dihydroxyphosphoryl)isophthalates.

Metal phosphonate-carboxylate compounds represent a promising class of materials for proton conduction applications. This study investigates the structural, thermal, and proton conduction properties of three groups of lanthanide-based compounds derived from 5-(dihydroxyphosphoryl)isophthalic acid (PiPhtA). The crystal structures, solved ab initio from X-ray powder diffraction data, reveal that groups Ln-I, Ln[O3P-C6H3(COO)(COOH)(H2O)2] (Ln = La, Pr), and Ln-II, Ln2{[O3P-C6H3(COO)(COOH)]2(H2O)4}·2H2O (Ln = La, Pr, Eu), exhibit three-dimensional frameworks, while group Ln-III, Ln[O3P-C6H3(COO)(COOH)(H2O)] (Ln = Yb), adopts a layered structure with unbonded carboxylic groups oriented toward the interlayer region. All compounds feature carboxylic groups and coordinating water molecules. Impedance measurements demonstrate that these materials exhibit water-mediated proton conductivity, initially following a vehicle-type proton-transfer mechanism. Upon exposure to ammonia vapors from a 14 or 28% aqueous solution, compounds from groups II and III adsorb ammonia and water, leading to an enhancement in proton conductivity consistent with a Grotthuss-type proton-transfer mechanism. Notably, group II of the studied compounds undergoes the formation of a new expanded phase through the internal reaction of carboxylic groups with ammonia, coexisting with the as-synthesized phase. This postsynthetic modification results in a significant increase in proton conductivity, from approximately ∼5 × 10-6 to ∼10-4 S·cm-1 at 80 °C and 95% relative humidity (RH), attributed to a mixed intrinsic/extrinsic contribution. Remarkably, the NH3(28%)-exposed Yb-III compound achieves an enhancement in proton conductivity, reaching ∼ 5 × 10-3 S·cm-1 at 80 °C and 95% RH, primarily through an extrinsic contribution.

Post-synthetic modification fluorescence UiO-66-Eu immunochromatography for high-performance detection of sodium pentachlorophenoate

Sodium pentachlorophenate (PCP) is widely used as a herbicide, fungicide, or molluscicide. It is highly toxic, easily soluble in water, making it highly prone to diffusion and causing water and soil pollution. Through the food chain, it enters animal bodies and remains in food, causing toxicity to humans and animals. Therefore, establishing a rapid and simple detection method for PCP is crucial for human health and environmental protection. Herein, lanthanide metal Eu3+ was introduced into UiO-66-(COOH)2 by post-synthesis modification, and the nanomaterials prepared based on this method have the advantages of both UiO-66-(COOH)2 and Eu3+. The rigid skeleton structure of UiO-66-(COOH)2 can protect the activity of antibody, the detection environment pH tolerance range of UiO-66-Eu is 3–11. While Eu3+ has long fluorescence lifetime, high fluorescence intensity, high signal-to-noise ratio, and low photobleaching rate. UiO-66-Eu-based immunochromatography assay was successfully applied in PCP detection with the detection limits of 0.84, 0.98, and 0.37 μg/kg for pork, chicken, and shrimp, respectively, which was up to 10-fold more sensitive than the reported ICAs. The recoveries ranged from 79.7 %−113.1 %, with the coefficient of variation from 6.6 %−17.1 %. Parallel detection of 30 samples by LC-MS/MS showed a good correlation with that of our proposed method (R2 >0.98). This work not only provides a creative attempt for UiO-66-Eu based highly sensitive and strongly tolerant ICAs, but also guarantees human health and environmental protection.