Ag@FONPs nanohybrids derived from a sulfur-functionalized dicarbene ligand: efficient catalysts and selective azide-ion sensors

Abstract

A sulfur-bridged dibenzimidazolium-based pincer ligand was successfully synthesized and utilized to fabricate fluorescent organic nanoparticles (FONPs) via a simple, water-based re-precipitation method. FONPs exhibited a strong blue fluorescence, and upon interaction with Ag+ ions, they efficiently underwent in situ reduction to form Ag@FONPs nanohybrids. These nanohybrids demonstrated excellent chemical and oxidative stability, maintaining over 95% fluorescence intensity after exposure to H2O2 and NaCl environments. Ag@FONPs showed outstanding catalytic efficiency, achieving the complete reduction of 4-nitrophenol within 18 minutes and 80% degradation of methyl orange within 10 minutes under light irradiation. Furthermore, the nanohybrids exhibited high selectivity and sensitivity toward azide (N3) ions. These findings highlight the multifunctional nature of Ag@FONPs, positioning them as robust candidates for applications in environmental catalysis, pollutant degradation, and ion sensing.

Graphical abstract: Ag@FONPs nanohybrids derived from a sulfur-functionalized dicarbene ligand: efficient catalysts and selective azide-ion sensors

Supplementary files

Article information

Article type
Paper
Submitted
17 Mar 2026
Accepted
26 May 2026
First published
02 Jun 2026

New J. Chem., 2026, Advance Article

Ag@FONPs nanohybrids derived from a sulfur-functionalized dicarbene ligand: efficient catalysts and selective azide-ion sensors

R. Kumar, K. Garg, V. Yadav, Rishu and V. K. Bhardwaj, New J. Chem., 2026, Advance Article , DOI: 10.1039/D6NJ00999A

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