Facile access to 1,2-disubstituted benzimidazoles and 2,3-dihydro-1H-perimidines using a biogenically synthesized single phase δ-MnO2 NP catalyst and its dye removal study

R. Nandini, T. Thrilokraj, Umesh A. Kshirsagar, Rajeev V. Hegde, Arnab Ghosh, Siddappa A. Patil, Jan Grzegorz Malecki, Ramesh B. Dateer

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

A cost-effective and step-economic synthesis of pharmaceutically important 1,2-disubstituted benzimidazoles and 2,3-dihydro-1H-perimidine derivatives is accomplished without the assistance of external ligands. An environmentally friendly biogenic strategy for the synthesis of single phase δ-MnO2 NPs using the Pongamia pinnata leaf extract was adopted. The phytochemicals detected in the extract of Pongamia pinnata leaves might be responsible for the reduction of Mn(vii) to Mn(iv), which provides stability to the metal centre. The synthesized catalyst was tested for the synthesis of pharmaceutically important benzimidazole and perimidine analogues. In addition, mechanistic experiments and the plausible mechanism were discussed. The δ-MnO2 NP catalyst exhibited superior catalytic activity and high durability in the dye removal study.

Original languageEnglish
Pages (from-to)1327-1335
Number of pages9
JournalNew Journal of Chemistry
Volume48
Issue number3
DOIs
StatePublished - 8 Dec 2023
Externally publishedYes

ASJC Scopus subject areas

  • Catalysis
  • General Chemistry
  • Materials Chemistry

Fingerprint

Dive into the research topics of 'Facile access to 1,2-disubstituted benzimidazoles and 2,3-dihydro-1H-perimidines using a biogenically synthesized single phase δ-MnO2 NP catalyst and its dye removal study'. Together they form a unique fingerprint.

Cite this