scholarly journals Facile Green Preparation of Rhodium Nanoclusters Supported Nano-Scaled Graphene Platelets for Sonogashira Coupling Reaction and Reduction of p-Nitrophenol

Catalysts ◽  
2019 ◽  
Vol 9 (11) ◽  
pp. 908 ◽  
Author(s):  
Gopiraman Mayakrishnan ◽  
Saravanamoorthy Somasundaram ◽  
Sana Ullah ◽  
Ilangovan Andivelu ◽  
Kim Ick Soo ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Electron Microscope ◽  
Inductively Coupled Plasma ◽  
Coupling Reaction ◽  
Significant Loss ◽  
Sonogashira Coupling ◽  
Inductively Coupled ◽  
Sonogashira Coupling Reaction ◽  
Graphene Platelets ◽  
Means Of Transmission

Rhodium nanoclusters were uniformly dispersed on nano-scaled graphene platelets by a simple ‘mix and heat’ method without using any toxic reagents. Distilled water was used to obtain the homogenous dispersion of Rh-nanoclusters on graphene platelets. The morphology of the resultant catalyst (Rh(0)NCs/GNPs) was studied by means of transmission electron microscope (TEM) and atomic force microscope (AFM) analyses. The X-ray photoemission spectroscope (XPS) result confirmed the metallic form of Rh-nanoclusters in Rh(0)NCs/GNPs. The crystalline property and the interaction between Rh-nanoclusters and graphene platelets (GNPs) were studied by means of XRD and Raman analysis. The Rh-loading in Rh(0)NCs/GNPs was confirmed by scanning electron microscope and energy dispersive spectroscope (SEM-EDS) and inductively coupled plasma-mass spectroscope (ICP-MS) analysis. After being optimized, the Rh(0)NCs/GNPs used as catalyst for the reduction of 4-nitrophenol with NaBH4 and the Sonogashira coupling reaction between iodobenzene with phenylacetylene. To our delight, the Rh(0)NCs/GNPs showed excellent catalytic activity towards the reduction of 4-nitrophenol with an excellent turnover frequency (TOF) value of 112.5 min−1. The kapp and k’ values were calculated to be 62.07 × 10−3 min−1(0.002 mg of Rh(0)NCs/GNPs) and 31035 × 10−3 mg−1 min−1,respectively. Alike, under the optimal conditions, the Rh(0)NCs/GNPs gave the desired product, diphenylacetylene, in a good yield of 87% with 91% selectivity. The Rh(0)NCs/GNPs can be reused without significant loss in its catalytic activity.

scholarly journals Pd Nanoparticles Stabilized on the Cross-Linked Melamine-Based SBA-15 as a Catalyst for the Mizoroki–Heck Reaction

2021 ◽  
Author(s):  
Ayat Nuri ◽  
Abolfazl Bezaatpour ◽  
Mandana Amiri ◽  
Nemanja Vucetic ◽  
Jyri-Pekka Mikkola ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Inductively Coupled Plasma ◽  
High Surface ◽  
High Surface Area ◽  
Coupling Reaction ◽  
Pd Nanoparticles ◽  
Significant Activity ◽  
Inductively Coupled ◽  
Transmission Electron ◽  
Ft Ir

AbstractMesoporous SBA-15 silicate with a high surface area was prepared by a hydrothermal method, successively modified by organic melamine ligands and then used for deposition of Pd nanoparticles onto it. The synthesized materials were characterized with infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA), nitrogen physisorption, scanning electron microscopy (SEM) coupled with energy dispersive X-ray analysis (EDX), transmission electron microscopy (TEM), nuclear magnetic resonance (NMR) and inductively coupled plasma (ICP-OES). The catalyst was effectively used in the Mizoroki–Heck coupling reaction of various reactants in the presence of an organic base giving the desired products in a short reaction time and with small catalysts loadings. The reaction parameters such as the base type, amounts of catalyst, solvents, and the temperature were optimized. The catalyst was easily recovered and reused at least seven times without significant activity losses. Graphic Abstract

ChemInform Abstract: 2,5-Bis(2-(diphenylphosphino)phenyl)-1,3,4-oxadiazole Ligands and Their Cu(I) Complexes for Sonogashira Coupling Reaction.

ChemInform ◽  
2014 ◽  
Vol 45 (35) ◽  
pp. no-no
Author(s):  
Cai-Xia Lin ◽  
Jia-Fang Zhu ◽  
Qing-Shan Li ◽  
Li-Hua Ao ◽  
Yan-Juan Jin ◽  
...  
Keyword(s):  
Coupling Reaction ◽  
Sonogashira Coupling ◽  
Sonogashira Coupling Reaction

scholarly journals The Utility of Sonogashira Coupling Reaction for the Derivatization of Aryl Halides with Fluorescent Alkyne

2018 ◽  
Vol 34 (10) ◽  
pp. 1183-1188 ◽  
Author(s):  
Naoyuki YASAKA ◽  
Naoya KISHIKAWA ◽  
Takumi HIGASHIJIMA ◽  
Kaname OHYAMA ◽  
Naotaka KURODA
Keyword(s):  
Coupling Reaction ◽  
Aryl Halides ◽  
Sonogashira Coupling ◽  
Sonogashira Coupling Reaction
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