A mild protocol for the development of an innovative green heterogeneous catalyst for the Hilbert-Johnson reaction
Recently, graphitic carbon nitride (g-C 3 N 4 ) has attracted great attention among the most promising materials in heterogeneous catalysis. Herein, we describe an application of ammonium iodide-coated g-C 3 N 4 (NH 4 I@g-C 3 N 4 ) as a new and sustainable heterogeneous catalyst for the selective N...
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Veröffentlicht in: | New journal of chemistry 2024-01, Vol.48 (24), p.1852-1862 |
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Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Recently, graphitic carbon nitride (g-C
3
N
4
) has attracted great attention among the most promising materials in heterogeneous catalysis. Herein, we describe an application of ammonium iodide-coated g-C
3
N
4
(NH
4
I@g-C
3
N
4
) as a new and sustainable heterogeneous catalyst for the selective
N
1-alkylation of pyrimidines. Structural, morphological, and spectroscopic analyses of NH
4
I@g-C
3
N
4
were carried out through X-ray diffraction (XRD), scanning electronic microscopy (SEM), ultra-violet visible spectroscopy (UV-visible) and Fourier-transform infrared spectroscopy (FTIR). The obtained results prove that the NH
4
I@g-C
3
N
4
is well prepared. Moreover, it was applied as an efficient catalyst in the synthesis of nucleoside analogs through the
N
1-alkylation reaction of pyrimidine nucleobases. Several alkylating agents were tested with various parameters to achieve excellent selectivity and high yields. This novel eco-friendly catalyst showed a catalytic activity and good selectivity in the synthesis of nucleoside analogs without noticeable changes in the morphology.
Ammonium iodide-coated g-C
3
N
4
(NH
4
I@g-C
3
N
4
) is investigated as a new and sustainable heterogeneous catalyst for the selective
N
1-alkylation of pyrimidines. |
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ISSN: | 1144-0546 1369-9261 1369-9261 |
DOI: | 10.1039/d4nj01358a |