MOF modified with a Cu-complex as a novel MOF-based heterogeneous catalyst for the one-pot one-step synthesis of α-aminophosphonates directly from alcohols by a tandem oxidation process

A metal-organic framework functionalized with a copper complex, named Cu-ISA-MIL-Fe, was fabricated through post-synthetic modification of Fe-MIL-101-NH<sub>2</sub> <i>via</i> isatin Schiff-base formation followed by coordination with Cu(OAc)<sub>2</sub>. The newly synthesized Cu-ISA-MIL-Fe was characterized by analytical methods, including PXRD, FT-IR, XPS, FESEM, EDS elemental mapping, TEM, and elemental analysis. The similarity of its PXRD pattern with that of Fe-MIL-101-NH<sub>2</sub> indicated that the crystalline structure of the MOF in the post-synthetic modification remained intact. FT-IR analysis endorsed the successful construction and functionalization of the MOF. FESEM and TEM images showed that the octahedral morphology of the MOF with an edge length of ∼500 nm was well preserved. XPS elemental survey and EDS elemental mapping confirmed the existence of C, N, O, Cu and Fe, with a uniform distribution throughout the MOF structure. Cu-ISA-MIL-Fe was used as the first MOF-based catalyst for the one-pot one-step synthesis of dialkyl α-aminophosphonates directly from readily available alcohols <i>via</i> a tandem oxidation process. The catalyst showed an extremely high catalytic performance for the selective oxidation of different benzyl alcohols, followed by the condensation of the <i>in situ</i>-prepared benzaldehyde with anilines and alkyl phosphites (tri-ethyl/methyl/<i>iso</i>-propyl and di-<i>iso</i>-propyl phosphites) to produce a variety of dialkyl α-aminophosphonates. This methodology offers a number of merits, including cost-effective operational conditions, efficient and selective product formation in 75-95% yields, reduced reaction times, use of a green solvent, and facile catalyst separation and recyclability. Besides, conducting a simplified one-pot one-step synthetic procedure contributes to step saving, minimizes the procedural complexity and decreases waste production, further enhancing the overall efficiency of the method.

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Publication Details

Journal
RSC Advances
Published
2025-01-01
DOI
https://doi.org/10.1039/d5ra06341h
Citations
1
Primary Topic
Organophosphorus compounds synthesis
Type
article
Field-Weighted Citation Impact
0.94

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article

MOF modified with a Cu-complex as a novel MOF-based heterogeneous catalyst for the one-pot one-step synthesis of α-aminophosphonates directly from alcohols by a tandem oxidation process

Roya Jahanshahi, José M. Sansano, Sara Sobhani, Alireza Paseban
1 citations
RSC Advances
Organophosphorus compounds synthesis
0.94
article

MOF modified with a Cu-complex as a novel MOF-based heterogeneous catalyst for the one-pot one-step synthesis of α-aminophosphonates directly from alcohols by a tandem oxidation process

Roya Jahanshahi, José M. Sansano, Sara Sobhani, Alireza Paseban
article en
1 citations

Abstract

A metal-organic framework functionalized with a copper complex, named Cu-ISA-MIL-Fe, was fabricated through post-synthetic modification of Fe-MIL-101-NH<sub>2</sub> <i>via</i> isatin Schiff-base formation followed by coordination with Cu(OAc)<sub>2</sub>. The newly synthesized Cu-ISA-MIL-Fe was characterized by analytical methods, including PXRD, FT-IR, XPS, FESEM, EDS elemental mapping, TEM, and elemental analysis. The similarity of its PXRD pattern with that of Fe-MIL-101-NH<sub>2</sub> indicated that the crystalline structure of the MOF in the post-synthetic modification remained intact. FT-IR analysis endorsed the successful construction and functionalization of the MOF. FESEM and TEM images showed that the octahedral morphology of the MOF with an edge length of ∼500 nm was well preserved. XPS elemental survey and EDS elemental mapping confirmed the existence of C, N, O, Cu and Fe, with a uniform distribution throughout the MOF structure. Cu-ISA-MIL-Fe was used as the first MOF-based catalyst for the one-pot one-step synthesis of dialkyl α-aminophosphonates directly from readily available alcohols <i>via</i> a tandem oxidation process. The catalyst showed an extremely high catalytic performance for the selective oxidation of different benzyl alcohols, followed by the condensation of the <i>in situ</i>-prepared benzaldehyde with anilines and alkyl phosphites (tri-ethyl/methyl/<i>iso</i>-propyl and di-<i>iso</i>-propyl phosphites) to produce a variety of dialkyl α-aminophosphonates. This methodology offers a number of merits, including cost-effective operational conditions, efficient and selective product formation in 75-95% yields, reduced reaction times, use of a green solvent, and facile catalyst separation and recyclability. Besides, conducting a simplified one-pot one-step synthetic procedure contributes to step saving, minimizes the procedural complexity and decreases waste production, further enhancing the overall efficiency of the method.

RSC AdvancesVol. 15(44)
University of Alicante (ES), Shiraz University (IR), University of Birjand (IR)
Universidad de Alicante, University of Birjand
Openalex Percentile: Top 21%
Organophosphorus compounds synthesis
0.94
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