Mono- and binuclear palladacycles via regioselective C–H bond activation: syntheses, mechanistic insights and catalytic activity in direct arylation of azoles

RSC Advances ◽  
2015 ◽  
Vol 5 (99) ◽  
pp. 81502-81514 ◽  
Author(s):  
Dilip K. Pandey ◽  
Shrikant M. Khake ◽  
Rajesh G. Gonnade ◽  
Benudhar Punji

Hybrid “POCN”-ligated mono- and binuclear palladacycles have been synthesized via the base-assisted regioselective C–H bond activation, and their mechanistic aspects and catalytic application for the arylation of azoles have been described.

Catalysts ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 131 ◽  
Author(s):  
Rola Mohammad Al Soubaihi ◽  
Khaled Mohammad Saoud ◽  
Myo Tay Zar Myint ◽  
Mats A. Göthelid ◽  
Joydeep Dutta

Carbon monoxide (CO) oxidation is considered an important reaction in heterogeneous industrial catalysis and has been extensively studied. Pd supported on SiO2 aerogel catalysts exhibit good catalytic activity toward this reaction owing to their CO bond activation capability and thermal stability. Pd/SiO2 catalysts were investigated using carbon monoxide (CO) oxidation as a model reaction. The catalyst becomes active, and the conversion increases after the temperature reaches the ignition temperature (Tig). A normal hysteresis in carbon monoxide (CO) oxidation has been observed, where the catalysts continue to exhibit high catalytic activity (CO conversion remains at 100%) during the extinction even at temperatures lower than Tig. The catalyst was characterized using BET, TEM, XPS, TGA-DSC, and FTIR. In this work, the influence of pretreatment conditions and stability of the active sites on the catalytic activity and hysteresis is presented. The CO oxidation on the Pd/SiO2 catalyst has been attributed to the dissociative adsorption of molecular oxygen and the activation of the C-O bond, followed by diffusion of adsorbates at Tig to form CO2. Whereas, the hysteresis has been explained by the enhanced stability of the active site caused by thermal effects, pretreatment conditions, Pd-SiO2 support interaction, and PdO formation and decomposition.


Catalysts ◽  
2020 ◽  
Vol 10 (11) ◽  
pp. 1344
Author(s):  
Tim Van Everbroeck ◽  
Radu-George Ciocarlan ◽  
Wouter Van Hoey ◽  
Myrjam Mertens ◽  
Pegie Cool

Mixed oxides were synthesized by co-precipitation of a Cu source in combination with Al, Fe or Mn corresponding salts as precursors. The materials were calcined at 600 and 1000 °C in order to crystallize the phases and to mimic the reaction conditions of the catalytic application. At 600 °C a mixed spinel structure was only formed for the combination of Cu and Mn, while at 1000 °C all the materials showed mixed spinel formation. The catalysts were applied in three-way catalysis using a reactor with a gas mixture containing CO, NO and O2. All the materials calcined at 600 °C displayed the remarkable ability to oxidize CO with O2 but also to reduce NO with CO, while the pure oxides such as CuO and MnO2 were not able to. The high catalytic activity at 600 °C was attributed to small supported CuO particles present and imperfections in the spinel structure. Calcination at 1000 °C crystallized the structure further which led to a dramatic loss in catalytic activity, although CuAl2O4 and CuFe2O4 still converted some NO. The materials were characterized by X-ray diffraction (XRD), Raman spectroscopy, H2-Temperatrue Programmed Reduction (H2-TPR), N2-sorption and scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM-EDX).


2019 ◽  
Vol 34 (2) ◽  
Author(s):  
Murat Kaloğlu ◽  
Nevin Gürbüz ◽  
İlkay Yıldırım ◽  
Namık Özdemir ◽  
İsmail Özdemir

2011 ◽  
Vol 50 (48) ◽  
pp. 11400-11404 ◽  
Author(s):  
Mahesh K. Lakshman ◽  
Ashoke C. Deb ◽  
Raghu Ram Chamala ◽  
Padmanava Pradhan ◽  
Ramendra Pratap

2013 ◽  
Vol 15 (10) ◽  
pp. 2490-2493 ◽  
Author(s):  
Thomas Wesch ◽  
Anaïs Berthelot-Bréhier ◽  
Frédéric R. Leroux ◽  
Françoise Colobert

2014 ◽  
Vol 43 (38) ◽  
pp. 14450-14460 ◽  
Author(s):  
Dmitry M. Lyubov ◽  
Anton V. Cherkasov ◽  
Georgy K. Fukin ◽  
Sergey Yu. Ketkov ◽  
Andrey S. Shavyrin ◽  
...  

[(Ap9MeLu)3(μ2-H)3(μ3-H)2(CH2SiMe3)(thf)2] was synthesized. For Y and Yb C–Si bond activation occurs affording [(Ap9MeLu)3(μ2-H)3(μ3-H)2(CH2SiMe3)(thf)2] and [(Ap9MeLn)3(μ2-H)3(μ3-H)2(CH2SiH2Ph)(thf)2].


2019 ◽  
Vol 55 (96) ◽  
pp. 14414-14417 ◽  
Author(s):  
Ying Dong ◽  
Jing-Jing Jv ◽  
Xiao-Wei Wu ◽  
Jing-Lan Kan ◽  
Ting Lin ◽  
...  

A Pd–C-bond-connected organometallic framework and its catalytic activity for the Suzuki–Miyaura cross-coupling reaction were reported.


RSC Advances ◽  
2014 ◽  
Vol 4 (103) ◽  
pp. 59379-59386 ◽  
Author(s):  
Sabyasachi Patra ◽  
Debasis Sen ◽  
Ashok K. Pandey ◽  
J. Bahadur ◽  
S. Mazumder ◽  
...  

Growth kinetics of membrane stabilized silver nanoparticles have been studied for the first time with time resolved in situ SAXS. The catalytic application of nanocomposite membranes thus formed has also been explored.


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