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Updated: Jan 13, 2026

Synthesis of High Purity Nonsymmetric Dialkylphosphinic Acid Extractants
Published on: October 19, 2017
Extractante de pinza modificado con tioamida para la recuperación selectiva de Pd(II)
Manabu Yamada1, Yuri Matsuba2, Riko Matsuba3
1Department of Materials Science, Graduate School of Engineering Science, Akita University, 1-1 Tegatagakuen-Machi, Akita 010-8502, Japan.
Abstract:
Solvent extraction is an important method for recovering Pd(II) from secondary resources; however, conventional Pd(II) extractants often exhibit limited efficiency and selectivity. In this study, a new pincer extractant was synthesized by incorporating two thioamide groups as polar moieties at the 1,3-positions of the benzene ring. Its Pd(II) extraction performance was evaluated as a function of the shaking time and HCl concentration. Optimal stripping reagents for the back-extraction of Pd(II) were also investigated. The extractant effectively extracted Pd(II) from a simulated mixed-metal solution containing platinum group metals and base metals as well as from a leach liquor of a spent automotive catalyst. Mechanistic studies using 1H nuclear magnetic resonance (1H NMR) spectroscopy, Fourier transform infrared (FT-IR) spectroscopy, single-crystal X-ray diffraction (SCXRD), and X-ray absorption spectroscopy (XAS) revealed distinct coordination behaviors: in solution, Pd(II) bound only to the two sulfur atoms of the thioamide groups, behaving like a bidentate ligand, whereas in the crystalline state, the Pd(II) complex displayed typical features of pincer ligands, that is, tridentate binding involving two sulfur atoms and a central donor atom that together "clamp" the Pd center. This study provides a foundation for the molecular design of novel pincer extractants for enhanced Pd(II) recovery and organometallic catalyst development.
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