Cu(II)-Doped ZIF-8 as a Sustainable Catalyst for the Dehydrogenative Coupling of 2-Aminobenzamide with Methanol

In this study, an effective and stable Cu<sup>2+</sup> incorporated within the lattice of ZIF-8 was hydrothermally synthesized and employed as a heterogeneous catalyst for the dehydrogenative coupling between 2-aminobenzamide and CH<sub>3</sub>OH. The Cu<sup>2+</sup>-doped ZIF-8 (Cu@ZIF-8) catalysts were firmly characterized using powder X-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, UV-visible diffuse reflectance spectra, and Brunauer-Emmett-Teller techniques to examine their structural, morphological, elemental, optical, and surface properties. The catalytic efficiency of Cu@ZIF-8 was investigated in the synthesis of quinazolinone from 2-aminobenzamide and CH<sub>3</sub>OH as a C1 source with Cs<sub>2</sub>CO<sub>3</sub> as a base under an oxygen atmosphere. Among the different catalysts, 30% Cu@ZIF-8 catalyst demonstrated superior activity in the formation of quinazolinone compared to pristine ZIF-8, indicating that the doping of the Cu<sup>2+</sup> ions provides a synergetic effect during the reaction. Furthermore, reusability experiments were carried out with a 30% Cu@ZIF-8 catalyst, and the observed findings show that the activity is maintained up to four cycles. The structural integrity along with the morphology and chemical structure of the reused solid were also verified, and no significant differences between the fresh and reused solids were observed in the dehydrogenative coupling reaction. Furthermore, a plausible reaction mechanism for this reaction is also proposed.

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Journal
Inorganic Chemistry
Published
2025-05-01
DOI
https://doi.org/10.1021/acs.inorgchem.5c00612
Citations
3
Primary Topic
Metal-Organic Frameworks: Synthesis and Applications
Type
article
Field-Weighted Citation Impact
1.61
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article

Cu(II)-Doped ZIF-8 as a Sustainable Catalyst for the Dehydrogenative Coupling of 2-Aminobenzamide with Methanol

Samuel Lalthazuala Rokhum, Amarajothi Dhakshinamoorthy, Veerappan Karthik, A. Shophia Lawrence et al.
3 citations
Inorganic Chemistry
Metal-Organic Frameworks: Synthesis and Applications
1.61
article

Cu(II)-Doped ZIF-8 as a Sustainable Catalyst for the Dehydrogenative Coupling of 2-Aminobenzamide with Methanol

Samuel Lalthazuala Rokhum, Amarajothi Dhakshinamoorthy, Veerappan Karthik, A. Shophia Lawrence, B. Sivakumar, Kalimuthu Abirami Sundari
article en
3 citations

Abstract

In this study, an effective and stable Cu<sup>2+</sup> incorporated within the lattice of ZIF-8 was hydrothermally synthesized and employed as a heterogeneous catalyst for the dehydrogenative coupling between 2-aminobenzamide and CH<sub>3</sub>OH. The Cu<sup>2+</sup>-doped ZIF-8 (Cu@ZIF-8) catalysts were firmly characterized using powder X-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, UV-visible diffuse reflectance spectra, and Brunauer-Emmett-Teller techniques to examine their structural, morphological, elemental, optical, and surface properties. The catalytic efficiency of Cu@ZIF-8 was investigated in the synthesis of quinazolinone from 2-aminobenzamide and CH<sub>3</sub>OH as a C1 source with Cs<sub>2</sub>CO<sub>3</sub> as a base under an oxygen atmosphere. Among the different catalysts, 30% Cu@ZIF-8 catalyst demonstrated superior activity in the formation of quinazolinone compared to pristine ZIF-8, indicating that the doping of the Cu<sup>2+</sup> ions provides a synergetic effect during the reaction. Furthermore, reusability experiments were carried out with a 30% Cu@ZIF-8 catalyst, and the observed findings show that the activity is maintained up to four cycles. The structural integrity along with the morphology and chemical structure of the reused solid were also verified, and no significant differences between the fresh and reused solids were observed in the dehydrogenative coupling reaction. Furthermore, a plausible reaction mechanism for this reaction is also proposed.

Inorganic ChemistryVol. 64(18)
Madurai Kamaraj University (IN), National Institute Of Technology Silchar (IN), Universitat Politècnica de València (ES)
Responsible consumption and production
Openalex Percentile: Top 17%
Metal-Organic Frameworks: Synthesis and Applications
1.61
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