A triazine-based covalent organic framework/palladium hybrid for one-pot silicon-based cross-coupling of silanes and aryl iodides

RSC Advances ◽  
2015 ◽  
Vol 5 (51) ◽  
pp. 41017-41024 ◽  
Author(s):  
Sha Lin ◽  
Yuxia Hou ◽  
Xiao Deng ◽  
Haoliang Wang ◽  
Shuzhuang Sun ◽  
...  
Keyword(s):  
Hybrid Material ◽  
Coupling Reaction ◽  
Cross Coupling ◽  
One Pot ◽  
Covalent Organic Framework ◽  
Aryl Iodides ◽  
Cross Coupling Reaction ◽  
Silicon Based ◽  
Excellent Selectivity ◽  
Organic Framework

A palladium/COF hybrid material could efficiently catalyze the silicon-based one-pot cross-coupling reaction of silanes and aryl iodides with excellent selectivity.

Nanoporous palladium catalyzed silicon-based one-pot cross-coupling reaction of aryl iodides with organosilanes

2014 ◽  
Vol 4 (6) ◽  
pp. 1734-1737 ◽  
Author(s):  
Zhiwen Li ◽  
Sha Lin ◽  
Lisha Ji ◽  
Zhonghua Zhang ◽  
Xiaomei Zhang ◽  
...  
Keyword(s):  
Heterogeneous Catalyst ◽  
Coupling Reaction ◽  
Cross Coupling ◽  
One Pot ◽  
Aryl Iodides ◽  
Cross Coupling Reaction ◽  
Palladium Catalyzed ◽  
Silicon Based

One-pot cross-coupling of aryl iodides with organosilanes is realized using dealloyed nanoporous palladium as a sustainable and heterogeneous catalyst.

An N-heterocyclic carbene-functionalised covalent organic framework with atomically dispersed palladium for coupling reactions under mild conditions

2019 ◽  
Vol 21 (19) ◽  
pp. 5267-5273 ◽  
Author(s):  
Junjuan Yang ◽  
Yuanyuan Wu ◽  
Xiaowei Wu ◽  
Wenjing Liu ◽  
Yaofang Wang ◽  
...  
Keyword(s):  
Room Temperature ◽  
Coupling Reaction ◽  
Cross Coupling ◽  
Coupling Reactions ◽  
Pure Ethanol ◽  
Covalent Organic Framework ◽  
Mild Conditions ◽  
Cross Coupling Reaction ◽  
Aqueous Solvent ◽  
Organic Framework

We report a heterogeneous catalyst based on N-heterocyclic carbene-functionalized covalent organic framework, which shows high activity in the C–C cross coupling reaction at room temperature in pure/ethanol aqueous solvent even with multiple reuse.

One-Pot Palladium-Catalyzed Cross-Coupling Reaction of Aryl Iodides with Stannylarsanes and Stannylstibanes

2003 ◽  
Vol 5 (15) ◽  
pp. 2731-2734 ◽  
Author(s):  
Mariana Bonaterra ◽  
Sandra E. Martín ◽  
Roberto A. Rossi
Keyword(s):  
Coupling Reaction ◽  
Cross Coupling ◽  
One Pot ◽  
Aryl Iodides ◽  
Cross Coupling Reaction ◽  
Palladium Catalyzed

Synthesis of Shape-Persistent Macrocycles by a One-Pot Suzuki-Miyaura Cross-Coupling Reaction

2010 ◽  
Vol 17 (2) ◽  
pp. 440-444 ◽  
Author(s):  
Weiguo Huang ◽  
Ming Wang ◽  
Chun Du ◽  
Yulan Chen ◽  
Ruiping Qin ◽  
...  
Keyword(s):  
Coupling Reaction ◽  
Cross Coupling ◽  
One Pot ◽  
Cross Coupling Reaction

An Efficient Copper-Catalyzed Cross-Coupling Reaction of Thiols with Aryl Iodides

2011 ◽  
Vol 2011 (9) ◽  
pp. 1776-1781 ◽  
Author(s):  
Hsin-Lun Kao ◽  
Chin-Keng Chen ◽  
Yu-Jen Wang ◽  
Chin-Fa Lee
Keyword(s):  
Coupling Reaction ◽  
Cross Coupling ◽  
Aryl Iodides ◽  
Cross Coupling Reaction

A robust, catalytic metal–organic framework with open 2,2′-bipyridine sites

2014 ◽  
Vol 50 (37) ◽  
pp. 4810-4812 ◽  
Author(s):  
Honghan Fei ◽  
Seth M. Cohen
Keyword(s):  
Metal Organic Framework ◽  
Coupling Reaction ◽  
Cross Coupling ◽  
Cross Coupling Reaction ◽  
Metal Organic ◽  
Catalytic Metal ◽  
Organic Framework

A highly crystalline Zr(iv)-based metal–organic framework (MOF) containing open 2,2′-bipyridine (bpy) chelating sites has been realized using two synthetic strategies, and readily forms complexes with PdCl2 to produce a MOF that exhibits efficient and recyclable catalysis for the Suzuki–Miyaura cross-coupling reaction.

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