Evidence map›Paper›PMID 42321271›Full record

ArticleScientific reports2026

Functionalization of magnetic TMU-17-NH

Roghayeh Vahedian, Heshmatollah Alinezhad, Ameneh Kiani

Abstract read
In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Roghayeh VahedianDepartment of Organic Chemistry, Faculty of Chemistry, University of Mazandaran, Babolsar, Iran.
Heshmatollah AlinezhadDepartment of Organic Chemistry, Faculty of Chemistry, University of Mazandaran, Babolsar, Iran. heshmat@umz.ac.ir.
Ameneh KianiDepartment of Organic Chemistry, Faculty of Chemistry, University of Mazandaran, Babolsar, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A novel magnetic nanocatalyst, Cu@M-TMU-17-NH₂-Gly-Met, was successfully prepared through a multi-step post-synthetic modification strategy. Initially, the TMU-17-NH₂ framework was functionalized with glyoxal, followed by immobilization of metformin to introduce nitrogen-rich coordination sites for copper incorporation. The composition and structural integrity of the resulting nanocomposite were confirmed by FT-IR, TGA, XRD, FE-SEM, EDX, BET, ICP-MS, and VSM analyses. The catalytic performance of the prepared nanocomposite was evaluated in the synthesis of dihydropyrimidinone derivatives via the Biginelli reaction, as well as in the synthesis of 2-amino-4H-pyran derivatives through a multicomponent reaction strategy. The results demonstrated that the catalyst efficiently promoted both reactions under mild conditions, affording high yields (73-92% and 79-98%, respectively) within short reaction times. The catalyst exhibited excellent reusability and stability over several cycles with a gradual and acceptable decrease in yield (from 89% to 74% for the Biginelli reaction, and from 96% to 84% for the pyran synthesis) over seven consecutive cycles for model reaction The combination of high efficiency, ease of separation, and environmental compatibility highlights the potential of this nanocatalyst for practical applications in organic synthesis.

Indexed as

2-amino-4H-pyranBiginelli reactionCopper catalystHeterogeneous nanocatalystMetal–organic frameworks

Identifiers

PMID42321271
PMCPMC13554157

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