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Heshmatollah Alinezhad

Heshmatollah Alinezhad

Academic rank: Professor
ORCID:
Education: PhD.
ScopusId:
HIndex:
Faculty: Faculty of Chemistry
Address:
Phone: 9111144735

Research

Title
MOF nano porous-supported C-S cross coupling through one-pot post-synthetic modification
Type
JournalPaper
Keywords
Metal−organic framework; Post-synthetic modification; Cross coupling; Thioethers; Nickel complex; Heterogeneous catalyst; Nanoporous
Year
2019
Journal JOURNAL OF ORGANOMETALLIC CHEMISTRY
DOI
Researchers Heshmatollah Alinezhad ، Shahram Ghasemi ، Mansoureh Cheraghian

Abstract

UIO-66-NH2-Fu@Ni has been synthesized by anchoring a molecular nickel furfural (Fu) complex into a functionalized nanoporous metal-organic framework (MOF) with the amine functional groups, using the one-pot post-synthetic modification. This new catalyst was identified via Fourier-transform infrared (FTIR) spectroscopy, proton-nuclear-magnetic-resonance (1HNMR) spectroscopy, nitrogen gas adsorptiondesorption method, thermogravimetric analyses (TGA), energy-dispersive X-ray- mapping spectroscopy (EDX-MAP), field emission scanning electron microscopy (FE-SEM), and X-ray diffraction (XRD). 1HNMR analysis showed that around 16% of the amine functional groups of the nanocrystalline UIO-66- NH2 framework were modified with nickel complex. Also, according to the inductive couple plasma atomic emission spectroscopy (ICP), around 2.98 w% of Ni was determined in the modified MOF. The Ni complex which was supported by UIO-66-NH2 nanocatalyst was effectively used as a heterogeneous catalyst for the formation of sulfur-containing molecules such as thioethers which are generally found in chemical biology, organic synthesis, and materials chemistry through the C-S bond cross-coupling of aryl iodides with thiols. UIO-66-NH2-Fu@Ni propagated the condensation reaction by different aryl iodides and aryl thiols in moderate conditions in the presence of K2CO3 as a base in high reaction yield during 8 e14 h. The Ni complex which was supported by UIO-66-NH2 nanocatalyst was simply recycled and reused thrice while its catalytic activity was maintained approximately.