Issue 36, 2025

Synergistic catalysis: Ce(iv)-driven oxidation reactions facilitated by micellar composites

Abstract

The catalytic behaviour of polymer–surfactant (PS) composites has attracted significant interest due to their ability to influence reaction kinetics through microenvironmental modulation. In this study, we explore the Ce(IV)-governed oxidative transformation of organic substrates in the presence of a polymer–surfactant composite composed of sodium dodecyl sulphate (SDS, 6 mM) and polyethylene glycol (PEG-600, 5 mM). Notably, the PS composite promotes the formation of premicellar aggregates at surfactant concentrations well below the critical micelle concentration (CMC), leading to enhanced reaction rates compared to systems involving the surfactant alone. The kinetics of the oxidation reaction were monitored via UV-Vis spectroscopy, revealing a pronounced rate enhancement attributed to the synergistic interaction between PEG-600 and SDS. The physicochemical characteristics and nature of the PS interaction were systematically investigated through tensiometry, dynamic light scattering (DLS), zeta potential measurements, nuclear magnetic resonance (NMR) spectroscopy, and field emission scanning electron microscopy (FESEM). These complementary techniques provide insight into the structural and dynamic aspects of the PS composites, elucidating their role in modulating the kinetics of the Ce(IV)-catalysed oxidation pathway. This study underscores the potential of polymer–surfactant systems as tunable platforms for catalytic applications in aqueous media.

Graphical abstract: Synergistic catalysis: Ce(iv)-driven oxidation reactions facilitated by micellar composites

Supplementary files

Article information

Article type
Paper
Submitted
07 Jul 2025
Accepted
19 Aug 2025
First published
19 Aug 2025

New J. Chem., 2025,49, 15846-15857

Synergistic catalysis: Ce(IV)-driven oxidation reactions facilitated by micellar composites

S. Kundu, P. Karmakar, M. Layek, P. Pal, S. M. Rahaman, M. Nandi, P. Sar and B. Saha, New J. Chem., 2025, 49, 15846 DOI: 10.1039/D5NJ02761F

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