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Green synthesis of thiourea derivatives from nitrobenzenes using Ni nanoparticles immobilized on triazine-aminopyridine-modified MIL-101(Cr) MOF

Sara HeidariDepartment of Organic Chemistry, Faculty of Chemistry, Bu-Ali Sina University, Hamadan, 6517838683, IranSedigheh AlaviniaDepartment of Organic Chemistry, Faculty of Chemistry, Bu-Ali Sina University, Hamadan, 6517838683, IranRamin Ghorbani‐VagheiDepartment of Organic Chemistry, Faculty of Chemistry, Bu-Ali Sina University, Hamadan, 6517838683, Iran. [email protected]
2023en
ABI

Abstract

Abstract Nanohybrid metal–organic frameworks (MOF) have recently been considered next-generation catalysts regarding their unique features like large surface-to-volume ratio, tailorable geometry, uniform pore sizes, and homogeneous distribution of active sites. In this report, we address the triazine-aminopyridine-modified 3D Cr-centred MOF MIL-101(Cr)-NH 2 following a post-synthetic modification approach. The excellent chelating ability of triazine-aminopyridine was applied to immobilize Ni ions over the host matrix MOF. The as-synthesized material was physicochemically characterized using various analytical techniques like FT-IR, electron microscopy, EDS, elemental mapping, XRD, and ICP-OES. Subsequently, the material has been catalytically employed in synthesizing new thiourea derivatives by reacting to nitrobenzene derivatives and phenyl isocyanate. The catalyst was isolated by centrifugation and recycled in 6 consecutive runs without momentous loss of its reactivity.

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