4.7 Article

Oxidized Charcoal-Supported Thiol-Protected Palladium Nanoparticles for Cross Dehydrogenative Coupling of Heteroarenes

Journal

ACS APPLIED NANO MATERIALS
Volume 5, Issue 2, Pages -

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsanm.1c04341

Keywords

heterogeneous catalysis; palladium nanoparticles; oxidized charcoal; cross dehydrogenative coupling; mechanistic insights

Funding

  1. SERB [EEQ/2018/000348]
  2. SERB-DST [ECR/2018/000312, ECR/2017/001434]
  3. UGC, India
  4. CSIR, India
  5. Department of Science and Technology (DST) [DST/INSPIRE/04/2017/002162]
  6. SERB-New Delhi [SRG/2021/000075]
  7. DST-FIST [SR/FST/CSI-270/2015, SR/FST/CSI-257/2014 (C)]
  8. Central University of Rajasthan

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The synthesis of thiol-protected Pd nanoparticles supported on oxidized charcoal was described in this report. The nanoparticles showed a diameter range of 8-12 nm and the nanocomposites had a surface area of 138.449 m(2)/g. The catalyst exhibited high efficiency in activating heteroarenes under mild reaction conditions, with a low loading requirement and good reusability.
This report describes the synthesis of thiol-protected Pd nanoparticles (NPs) (Pd-MUA) (MUA = 11-mercaptoundeca-noic acid) supported on oxidized charcoal (OC-Pd-MUA) at room temperature. The Pd-MUA NPs and OC-Pd-MUA nanocomposites (NCs) were characterized with Fourier transform infrared (FTIR) spectroscopy, transmission electron microscopy (TEM), energy-dispersive X-ray spectrometry (EDX), X-ray photoelectron spectros-copy (XPS), and Brunauer-Emmett-Teller (BET) techniques. The size distribution curve revealed that the diameter of the nanoparticles was in the range of similar to 8-12 nm, and the surface area of the NCs was found to be 138.449 m(2)/g. The as-prepared OC-Pd-MUA NCs were used as a catalyst for the cross dehydrogenative coupling (CDC) of two different heteroarenes. Remarkably, the catalyst was found to be very efficient in activating various heteroarenes under mild reaction conditions. Most importantly, no homocoupled or other byproducts were observed during the heterocoupling reactions. Moreover, the catalyst can be potentially used for the homocoupling reaction of various heteroarenes. It is noteworthy that only 0.22 mol % catalyst loading was required to activate a broad substrate scope with large functional group tolerance. Notwithstanding, the efficacy of the catalyst was found to be retained even after six reaction cycles. The reusability and hot filtration tests validated the heterogeneous nature of the catalysis. In addition, the experimental and computational studies collectively suggested that thiophene derivatives react to produce energetically stable products compared with other heteroarenes during the reaction.

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