Solvent‐Free Synthesis of Pd‐Modified Zeolitic Imidazolate Framework Nanocomposites for Competitive Arylation and Carbon–Carbon Coupling Reactions

ABSTRACT Over an extended period, identifying effective approaches for achieving versatile arylations has presented a notable synthetic challenge. In our research, we have successfully fabricated nanocomposites of zeolitic imidazole frameworks, specifically Pd‐ZIF‐8 and Pd‐ZIF‐67, using an in situ thermal (IST) approach. These compounds have exhibited high catalytic activity as heterogeneous catalysts in carbon–carbon coupling processes mediated by palladium, such as the Suzuki–Miyaura reaction (which involves aryl halides and aryl boronic acids) and the Mizoroki–Heck reaction (which involves aryl halides and olefins). In comparison to previously published research, the IST technique has a number of benefits; these features include the removal of solvents and additives, a low reaction temperature, a single‐step process, no need for activation, and the use of the smallest possible precursor ratio (M/L). This accomplishment was realized through the precise control of ligands and additives.

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Publication Details

Journal
Applied Organometallic Chemistry
Published
2025-05-19
DOI
https://doi.org/10.1002/aoc.70200
Citations
2
Primary Topic
Catalytic Cross-Coupling Reactions
Type
article
Field-Weighted Citation Impact
1.87

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article

Solvent‐Free Synthesis of Pd‐Modified Zeolitic Imidazolate Framework Nanocomposites for Competitive Arylation and Carbon–Carbon Coupling Reactions

Alireza Pourvahabi Anbari, Francis Verpoort, Alireza Ranjbari, Muhammad Kashif et al.
2 citations
Applied Organometallic Chemistry
Catalytic Cross-Coupling Reactions
1.87
article

Solvent‐Free Synthesis of Pd‐Modified Zeolitic Imidazolate Framework Nanocomposites for Competitive Arylation and Carbon–Carbon Coupling Reactions

Alireza Pourvahabi Anbari, Francis Verpoort, Alireza Ranjbari, Muhammad Kashif, Serge Zhuiykov, Philippe M. Heynderickx, Shima Rahmdel Delcheh, Tatwadhika Rangin Siddhartha
article en
2 citations

Abstract

ABSTRACT Over an extended period, identifying effective approaches for achieving versatile arylations has presented a notable synthetic challenge. In our research, we have successfully fabricated nanocomposites of zeolitic imidazole frameworks, specifically Pd‐ZIF‐8 and Pd‐ZIF‐67, using an in situ thermal (IST) approach. These compounds have exhibited high catalytic activity as heterogeneous catalysts in carbon–carbon coupling processes mediated by palladium, such as the Suzuki–Miyaura reaction (which involves aryl halides and aryl boronic acids) and the Mizoroki–Heck reaction (which involves aryl halides and olefins). In comparison to previously published research, the IST technique has a number of benefits; these features include the removal of solvents and additives, a low reaction temperature, a single‐step process, no need for activation, and the use of the smallest possible precursor ratio (M/L). This accomplishment was realized through the precise control of ligands and additives.

Applied Organometallic ChemistryVol. 39(6)
Peoples' Friendship University of Russia (RU), National Research Tomsk State University (RU), Wuhan University of Technology (CN), Tomsk Polytechnic University (RU), Ghent University (BE), Ghent University Global Campus (KR)
Universiteit Gent
Openalex Percentile: Top 16%
Catalytic Cross-Coupling Reactions
1.87
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Solvent‐Free Synthesis of Pd‐Modified Zeolitic Imidazolate Framework Nanocomposites for Competitive Arylation and Carbon–Carbon Coupling Reactions — Alireza Pourvahabi Anbari, Francis Verpoort, et al. · Applied Organometallic Chemistry (2025) | TGRS Research Map | TGRS