ChemInform Abstract: Amidation of Aryl Halides Catalyzed by Silica-Supported Bidentate Phosphine Palladium Complex.

ChemInform ◽  
2010 ◽  
Vol 28 (26) ◽  
pp. no-no
Author(s):  
M.-Z. CAI ◽  
C.-S. SONG ◽  
X. HUANG
1997 ◽  
Vol 27 (3) ◽  
pp. 361-366 ◽  
Author(s):  
Ming-Zhong Cai ◽  
Cai-Sheng Song ◽  
Xian Huang

2020 ◽  
Vol 43 (1) ◽  
pp. 184-199
Author(s):  
Mohammad Abdollahi-Alibeik ◽  
Najmeh Gharibpour ◽  
Zahra Ramazani

AbstractA palladium complex of a dendrimer type ligand of aminoethylacrylamide immobilized onto the mesoporous channels of MCM-41 with magnetic core was prepared and characterized using various techniques such as XRD, TEM, BET, FT-IR, TGA, and VSM. The prepared nanostructured material was found as a magnetically recoverable catalyst for Heck reaction of aryl halides and vinylic C–H. The catalyst is easily recoverable with an external magnet and is reusable with different leaching amounts depending to loading of Pd. A hot filtration test was also performed and gave evidence that Palladium in heterogeneous samples can dissolve and then redeposit on the surface of the support material.


2018 ◽  
Vol 31 (4) ◽  
pp. 425-437 ◽  
Author(s):  
Bin Huang ◽  
Pingping Wang ◽  
Xiaojun Zhu ◽  
Mingzhong Cai

A series of novel aromatic poly(ether ketone amide)s (PEKAs) were synthesized by the heterogeneous palladium-catalyzed carbonylative polycondensation of aromatic diiodides with ether ketone units, aromatic diamines, and carbon monoxide in N, N-dimethylacetamide (DMAc) at 120°C using 6 mol% of a magnetic nanoparticles–supported bidentate phosphine palladium complex (Fe3O4@SiO2-2P-PdCl2) as catalyst and 1,8-diazabicyclo[5,4,0]-7-undecene as base. The PEKAs had inherent viscosities ranging from 0.61 dl g−1 to 0.75 dl g−1. All the PEKAs were soluble in strong dipolar organic solvents. These PEKAs showed glass transition temperatures between 178°C and 232°C and 10% weight loss temperatures ranging from 443°C to 496°C in nitrogen. These PEKAs could be cast into transparent, flexible, and strong films from DMAc solutions with tensile strengths of 72.8–82.6 MPa, tensile moduli of 2.19–2.84 GPa, and elongations at break of 5.4–7.5%. Importantly, the heterogeneous palladium catalyst can be conveniently recovered from the reaction mixture by simply applying an external magnet and recycled up to eight times without significant loss of activity.


2020 ◽  
Vol 44 (11-12) ◽  
pp. 684-688
Author(s):  
Can Feng ◽  
Cheng-xin Liu ◽  
Yu-fang Wang ◽  
Jin Cui ◽  
Ming-jie Zhang

A new bis- N-heterocyclic carbene palladium complex, (C13H9N2F2)2PdCl2, is synthesized by a three-step reaction and characterized by 1H NMR and 13C NMR spectroscopy as well as by X-ray crystallography. This new bis- N-heterocyclic carbene palladium complex has excellent stability and is capable of efficiently catalyzing the Mizoroki–Heck coupling reaction of aryl halides with acrylates.


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