scholarly journals Metal-Free Catalysts for the Polymerization of Alkynyl-Based Monomers

Catalysts ◽  
2020 ◽  
Vol 11 (1) ◽  
pp. 1 ◽  
Author(s):  
Jie Zhang ◽  
Zhiming Zhang ◽  
Fulin Yang ◽  
Haoke Zhang ◽  
Jingzhi Sun ◽  
...  

Novel polymerizations based on alkyne monomers are becoming a powerful tool to construct polymers with unique structures and advanced functions in the areas of polymer and material sciences, and scientists have been attracted to develop a variety of novel polymerizations in recent decades. Therein, catalytic systems play an indispensable role in the influence of polymerization efficiencies and the performances of the resultant polymers. Concerning the shortcomings of metallic catalysts, much of the recent research focus has been on metal-free polymerization systems. In this paper, metal-free catalysts are classified and the corresponding polymerizations are reviewed, including organobase-catalyzed polymerizations, Lewis-acid-catalyzed polymerizations, as well as catalyst-free polymerizations. Moreover, the challenges and perspectives in this area are also briefly discussed.

2019 ◽  
Vol 4 (31) ◽  
pp. 8973-8977 ◽  
Author(s):  
Gullapalli Kumaraswamy ◽  
Maram Gangadhar
Keyword(s):  

ChemInform ◽  
2010 ◽  
Vol 41 (47) ◽  
pp. no-no
Author(s):  
Stephen J. Geier ◽  
Preston A. Chase ◽  
Douglas W. Stephan
Keyword(s):  

2010 ◽  
Vol 46 (27) ◽  
pp. 4884 ◽  
Author(s):  
Stephen J. Geier ◽  
Preston A. Chase ◽  
Douglas W. Stephan
Keyword(s):  

RSC Advances ◽  
2019 ◽  
Vol 9 (64) ◽  
pp. 37675-37685
Author(s):  
Pan Du ◽  
Jiyang Zhao

We investigated the mechanism of the dehydrosilylation of (hetero)arenes and extended the scope of the silylation catalysts and substrates.


Synthesis ◽  
2021 ◽  
Author(s):  
Zhao-Ying Yang ◽  
Ming Zhang ◽  
Xiao-Chen Wang

The development of chiral borane Lewis acid catalysts opened the door for transition-metal-free catalyzed asymmetric organic reactions. Herein, we have summarized our work on the preparation of two classes of novel chiral bicyclic bisborane Lewis acid catalysts derived from C2-symmetric [3.3.0] dienes and [4.4] dienes, respectively. These catalysts not only form frustrated Lewis pairs with Lewis bases to catalyze asymmetric hydrogenation reactions but also activate Lewis basic functional groups in traditional Lewis acid catalyzed asymmetric reactions.


2016 ◽  
Vol 18 (21) ◽  
pp. 5773-5776 ◽  
Author(s):  
Xiufang Cheng ◽  
Huamin Wang ◽  
Fuhong Xiao ◽  
Guo-Jun Deng

An efficient procedure for the synthesis of 2-arylquinazolines from N′-arylbenzimidamides has been developed under transition-metal-free conditions.


Author(s):  
Dan Song ◽  
Changfeng Huang ◽  
Peishi Liang ◽  
Baofu Zhu ◽  
Xiang Liu ◽  
...  
Keyword(s):  

An efficient, direct, and novel Lewis acid-catalyzed regioselective C–H carboxamidation of indolizines with dioxazolones via an acyl nitrene type rearrangement under metal-free conditions has been documented.


2020 ◽  
Author(s):  
José Tiago Menezes Correia ◽  
Gustavo Piva da Silva ◽  
Camila Menezes Kisukuri ◽  
Elias André ◽  
Bruno Pires ◽  
...  

A metal- and catalyst-free photoinduced radical cascade hydroalkylation of 1,7-enynes has been disclosed. The process is triggered by a SET event involving a photoexcited electron-donor-aceptor complex between NHPI ester and Hantzsch ester, which decomposes to afford a tertiary radical that is readily trapped by the enyne. <a>The method provides an operationally simple, robust and step-economical approach to the construction of diversely functionalized dihydroquinolinones bearing quaternary-centers. A sequential one-pot hydroalkylation-isomerization approach is also allowed giving access to a family of quinolinones. A wide substrate scope and high functional group tolerance was observed in both approaches</a>.


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