Amine–imine palladium catalysts for living polymerization of ethylene and copolymerization of ethylene with methyl acrylate: incorporation of acrylate units into the main chain and branch end

2016 ◽  
Vol 7 (3) ◽  
pp. 529-537 ◽  
Author(s):  
Haibin Hu ◽  
Darui Chen ◽  
Haiyang Gao ◽  
Liu Zhong ◽  
Qing Wu

A bulky amine–imine palladium catalyst can polymerize ethylene in a living fashion. Copolymerizations of ethylene and methyl acrylate afford branched copolymers with terminal and main chain acrylate units.

2021 ◽  
Author(s):  
Shu-Ming Kang ◽  
Xun-Hui Xu ◽  
Lei Xu ◽  
Li Zhou ◽  
Na Liu ◽  
...  

Polyallene is one of the most attractive synthetic precursors for constructing functional materials due to its unsaturated bonds on the main chain or pendants. Facile synthesis of high regioselectivity polyallenes...


2012 ◽  
Vol 31 (17) ◽  
pp. 6054-6062 ◽  
Author(s):  
Lihua Guo ◽  
Haiyang Gao ◽  
Qirui Guan ◽  
Haibin Hu ◽  
Juean Deng ◽  
...  

2016 ◽  
Vol 52 (63) ◽  
pp. 9777-9780 ◽  
Author(s):  
Xu Tian ◽  
Fanzhi Yang ◽  
Dace Rasina ◽  
Michaela Bauer ◽  
Svenja Warratz ◽  
...  

C–H arylations were accomplished with a user-friendly heterogeneous palladium catalyst in the biomass-derived γ-valerolactone (GVL) as an environmentally-benign reaction medium.


Catalysts ◽  
2020 ◽  
Vol 10 (2) ◽  
pp. 150 ◽  
Author(s):  
Vasco Corti ◽  
Enrico Marcantonio ◽  
Martina Mamone ◽  
Alessandro Giungi ◽  
Mariafrancesca Fochi ◽  
...  

The palladium-catalyzed (3 + 2) cycloaddition reaction between vinylcyclopropanes (VCPs) bearing geminal EWG’s and imines represents a straightforward and flexible entry to polysubstituted pyrrolidine derivatives. In this paper, we demonstrate that using a synergistic catalysis approach, based on the combination of phosphoric acid and palladium catalysts, it is possible to engage for the first time N-aryl and N-benzyl imines in this cycloaddition reaction. A range of polysubstituted pyrrolidines is obtained with moderate to good yields and diastereoselectivities, using a simple palladium species (Pd(PPh3)4) and an archetypical phosphoric acid as catalyst combination. A two-step scheme which exploits the same palladium catalyst for two consecutive and mechanistically distinct reactions (the cycloaddition and a Suzuki–Miyaura cross-coupling) is also presented. This synergistic catalysis approach is well posited for the development of the enantioselective version of this reaction. A screening of common BINOL-derived chiral phosphoric acids as catalyst component identified a species giving the product with moderate, yet promising, enantioselectivity (64% ee).


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