Synthesis of a magnetic polystyrene-supported Cu(II)-containing heterocyclic complex as a magnetically separable and reusable catalyst for the preparation of N-sulfonyl-N-aryl tetrazoles

Publikation: Beitrag in FachzeitschriftForschungsartikelBeigetragenBegutachtung

Beitragende

  • Mahmoud Nasrollahzadeh - , University of Qom (Autor:in)
  • Narjes Motahharifar - , University of Qom (Autor:in)
  • Khatereh Pakzad - , University of Qom (Autor:in)
  • Zahra Khorsandi - , University of Qom, Iran Polymer and Petrochemical Institute (Autor:in)
  • Talat Baran - , Aksaray University (Autor:in)
  • Jinghan Wang - , Seoul National University (Autor:in)
  • Benjamin Kruppke - , Professur für Biomaterialien (Autor:in)
  • Hossein Ali Khonakdar - , Professur für Biomaterialien, Iran Polymer and Petrochemical Institute (Autor:in)

Abstract

In this work, a cost-effective, environmentally friendly, and convenient method for synthesizing a novel heterogeneous catalyst via modification of polystyrene using tetrazole-copper magnetic complex [Ps@Tet-Cu(II)@Fe3O4] has been successfully developed. The synthesized complex was analyzed using TEM (transmission electron microscopy), HRTEM (high resolution-transmission electron microscopy), STEM (scanning transmission electron microscopy), FFT (Fast Fourier transform), XRD (X-ray diffraction), FT-IR (Fourier transform-infrared spectroscopy), TG/DTG (Thermogravimetry and differential thermogravimetry), ICP-OES (Inductively coupled plasma-optical emission spectrometry), Vibrating sample magnetometer (VSM), EDS (energy dispersive X-ray spectroscopy), and elemental mapping. N-Sulfonyl-N-aryl tetrazoles were synthesized in high yields from N-sulfonyl-N-aryl cyanamides and sodium azide using Ps@Tet-Cu(II)@Fe3O4 nanocatalyst. The Ps@Tet-Cu(II)@Fe3O4 complex can be recycled and reused easily multiple times using an external magnet without significant loss of catalytic activity.

Details

OriginalspracheEnglisch
Aufsatznummer3214
Seitenumfang17
FachzeitschriftScientific reports
Jahrgang2023
Ausgabenummer13
PublikationsstatusVeröffentlicht - 24 Feb. 2023
Peer-Review-StatusJa

Externe IDs

PubMed 36828906
WOS 000942280900053

Schlagworte

ASJC Scopus Sachgebiete