Carbon Microspheres Co-decorated with Nanosized Iron Sulfide and Magnetite Nanoparticles as a Magnetically Separable Heterogeneous Catalyst for the Green Synthesis of 4,4′-(Arylmethylene)bis(1H-pyrazol-5-ols)

Carbon microspheres co-decorated with nanosized iron sulfide and magnetite nanoparticles were synthesized by carbonizing an iron(III) sulfate-loaded polystyrene–divinylbenzene-based iminodiacetate-type cation-exchange resin in an inert atmosphere at 600°C for 4 h. The synthesized material was successfully employed as a magnetically separable heterogeneous catalyst for the green synthesis of 4,4′-(arylmethylene)­bis(1H-pyrazol-5-ols) via a one-pot pseudo-three-component condensation of aldehydes and 3-methyl-5-pyrazolone. The developed protocol offers several advantages, including high yields, short reaction times, simple work-up procedure, and catalyst reusability. Hence, it represents a valuable contribution to green and sustainable chemistry.

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Publication Details

Journal
Russian Journal of Organic Chemistry
Published
2025-03-01
DOI
https://doi.org/10.1134/s1070428024604588
Citations
1
Primary Topic
Multicomponent Synthesis of Heterocycles
Type
article
Field-Weighted Citation Impact
0.94
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article

Carbon Microspheres Co-decorated with Nanosized Iron Sulfide and Magnetite Nanoparticles as a Magnetically Separable Heterogeneous Catalyst for the Green Synthesis of 4,4′-(Arylmethylene)bis(1H-pyrazol-5-ols)

Sunil U. Tekale, Tibor Pasinszki, Rajendra P. Pawar, Anand V. Dhirbassi et al.
1 citations
Russian Journal of Organic Chemistry
Multicomponent Synthesis of Heterocycles
0.94
article

Carbon Microspheres Co-decorated with Nanosized Iron Sulfide and Magnetite Nanoparticles as a Magnetically Separable Heterogeneous Catalyst for the Green Synthesis of 4,4′-(Arylmethylene)bis(1H-pyrazol-5-ols)

Sunil U. Tekale, Tibor Pasinszki, Rajendra P. Pawar, Anand V. Dhirbassi, László Kótai, Sushama S. Kauthale
article en
1 citations

Abstract

Carbon microspheres co-decorated with nanosized iron sulfide and magnetite nanoparticles were synthesized by carbonizing an iron(III) sulfate-loaded polystyrene–divinylbenzene-based iminodiacetate-type cation-exchange resin in an inert atmosphere at 600°C for 4 h. The synthesized material was successfully employed as a magnetically separable heterogeneous catalyst for the green synthesis of 4,4′-(arylmethylene)­bis(1H-pyrazol-5-ols) via a one-pot pseudo-three-component condensation of aldehydes and 3-methyl-5-pyrazolone. The developed protocol offers several advantages, including high yields, short reaction times, simple work-up procedure, and catalyst reusability. Hence, it represents a valuable contribution to green and sustainable chemistry.

Russian Journal of Organic ChemistryVol. 61(3)
Gauhati University (IN), Chhatrapati Shahu Ji Maharaj University (IN), Institute of Materials and Environmental Chemistry (HU), Seva Mandir (IN), Fiji National University (FJ)
Openalex Percentile: Top 26%
Multicomponent Synthesis of Heterocycles
0.94
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Carbon Microspheres Co-decorated with Nanosized Iron Sulfide and Magnetite Nanoparticles as a Magnetically Separable Heterogeneous Catalyst for the Green Synthesis of 4,4′-(Arylmethylene)bis(1H-pyrazol-5-ols) — Sunil U. Tekale, Tibor Pasinszki, et al. · Russian Journal of Organic Chemistry (2025) | TGRS Research Map | TGRS