Transfer Hydrogenative Cleavage of N═N Bond of Azoarenes to Aminoarenes Using Ruthenium Catalyst

Abstract Textile industry contaminants cause significant pollution of water resources, making them a major worry in the modern age. Azo dyes, one of the most harmful synthetic colors generated in textile industry pollutants, are particularly persistent in water bodies due to their chemical composition. In this study, an efficient transfer hydrogenative cleavage of the ─N═N─ moiety containing azoarene to their corresponding aminoarenes is accomplished using a terpyridine‐based ruthenium complex. This report depicts the suitable transformations from the azoarene by adopting a minimal base and catalyst loading. The preliminary mechanistic studies disclosed the selective conversion of azoarenes to its complete ─N═N─ cleavage products, aminoarenes, through the hydrazoarenes intermediate.

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Publication Details

Journal
ChemCatChem
Published
2024-11-19
DOI
https://doi.org/10.1002/cctc.202401459
Citations
2
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
0.32
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article

Transfer Hydrogenative Cleavage of N═N Bond of Azoarenes to Aminoarenes Using Ruthenium Catalyst

Prosenjit Daw, Aisa Mohanty, Rambabu Dandela, A. Sinha et al.
2 citations
ChemCatChem
Asymmetric Hydrogenation and Catalysis
0.32
article

Transfer Hydrogenative Cleavage of N═N Bond of Azoarenes to Aminoarenes Using Ruthenium Catalyst

Prosenjit Daw, Aisa Mohanty, Rambabu Dandela, A. Sinha, Gowtham Kenguva
article en
2 citations

Abstract

Abstract Textile industry contaminants cause significant pollution of water resources, making them a major worry in the modern age. Azo dyes, one of the most harmful synthetic colors generated in textile industry pollutants, are particularly persistent in water bodies due to their chemical composition. In this study, an efficient transfer hydrogenative cleavage of the ─N═N─ moiety containing azoarene to their corresponding aminoarenes is accomplished using a terpyridine‐based ruthenium complex. This report depicts the suitable transformations from the azoarene by adopting a minimal base and catalyst loading. The preliminary mechanistic studies disclosed the selective conversion of azoarenes to its complete ─N═N─ cleavage products, aminoarenes, through the hydrazoarenes intermediate.

ChemCatChemVol. 17(4)
Institute of Chemical Technology (IN), Indian Institute of Science Education and Research Berhampur (IN), Indian Institute of Technology Bhubaneswar (IN)
Clean water and sanitation
Openalex Percentile: Top 48%
Asymmetric Hydrogenation and Catalysis
0.32
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