A novel approach to RE–OR bond from in situ reaction of rare earth triflates and sodium alkoxides: A versatile catalyst for living ring-opening polymerization of ε-caprolactone

Polymer ◽  
2014 ◽  
Vol 55 (10) ◽  
pp. 2404-2410 ◽  
Author(s):  
Lixin You ◽  
Zhiquan Shen ◽  
Jie Kong ◽  
Jun Ling
2007 ◽  
Vol 26 (3) ◽  
pp. 651-657 ◽  
Author(s):  
Michael T. Gamer ◽  
Peter W. Roesky ◽  
Isabelle Palard ◽  
Maude Le Hellaye ◽  
Sophie M. Guillaume

2021 ◽  
Author(s):  
Guuanming Yang ◽  
Yanfang Zhai ◽  
Jianyao Yao ◽  
Shufeng Song ◽  
Liyang Lin ◽  
...  

We report rare-earth triflate catalyst Sc(OTf)3 for ring-opening polymerization of 1,3-dioxolane in-situ producing quasi-solid-state poly(1,3-dioxolane) electrolyte, which not only demonstrates superior ionic conductivity of 1.07 mS cm-1 at room temperature,...


Author(s):  
Seema Agarwal ◽  
Christian Mast ◽  
Kurt Dehnicke ◽  
Andreas Greiner

2004 ◽  
Vol 856 ◽  
Author(s):  
Alexandru D. Asandei ◽  
Isaac W. Moran ◽  
Gobinda Saha ◽  
Yanhui Chen

ABSTRACTTi(III)Cp2Cl-catalyzed radical ring opening (RRO) of epoxides or single electron transfer (SET) reduction of aldehydes generates Ti alkoxides and carbon centered radicals which add to styrene, initiating a radical polymerization. This polymerization is mediate in a living fashion by the reversible termination of growing chains with the TiCp2Cl metalloradical. In addition, polymers or monomers containing pendant epoxide groups (glycidyl methacrylate) can be used as substrates for radical grafting or branching reactions by self condensing vinyl polymerization. In addition, Ti alkoxides generated in situ by both epoxide RRO and aldehyde SET initiate the living ring opening polymerization of ε-caprolactone. Thus, new initiators and catalysts are introduced for the synthesis of complex polymer architectures.


2011 ◽  
Vol 49 (19) ◽  
pp. 4213-4220 ◽  
Author(s):  
Kubra Dogan Demir ◽  
Mehmet Atilla Tasdelen ◽  
Tamer Uyar ◽  
Asei William Kawaguchi ◽  
Atsushi Sudo ◽  
...  

2012 ◽  
Vol 184-185 ◽  
pp. 1302-1306
Author(s):  
Xi Zhu ◽  
Yao Rong Wang

A dianionic phenoxyamido ligand was the first to be used to stabilize organo-rare-earth mental amido complex. Amine elimination reaction of La[N(SiMe3)2]3(THF)2 with 3,5-But2-2-HO-C6H2CH-NH-C5H4N in a 1 : 1 molar-ratio gave the anionic phenoxyamido neodymium amide LLa[N(TMS)2]•DME (1) in a high isolated yield. Furthemore, the catalytic behavior of complex 1 for the ring-opening polymerization of rac-lactide was explored.


2008 ◽  
Vol 9 (2) ◽  
pp. 704-710 ◽  
Author(s):  
Mohamad Takwa ◽  
Yan Xiao ◽  
Neil Simpson ◽  
Eva Malmström ◽  
Karl Hult ◽  
...  

2011 ◽  
Vol 30 (20) ◽  
pp. 5509-5523 ◽  
Author(s):  
Mikhail Sinenkov ◽  
Evgeny Kirillov ◽  
Thierry Roisnel ◽  
Georgy Fukin ◽  
Alexander Trifonov ◽  
...  

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