Conventional Oxyanionic versus Monomer-Activated Anionic Copolymerization of Ethylene Oxide with Glycidyl Ethers: Striking Differences in Reactivity Ratios

2016 ◽  
Vol 5 (11) ◽  
pp. 1206-1211 ◽  
Author(s):  
Jana Herzberger ◽  
Daniel Leibig ◽  
Johannes C. Liermann ◽  
Holger Frey
1993 ◽  
Vol 29 (2-3) ◽  
pp. 281-286 ◽  
Author(s):  
Stewart Dickson ◽  
Ga-Er Yu ◽  
Frank Heatley ◽  
Colin Booth

1991 ◽  
Vol 27 (7) ◽  
pp. 573-579 ◽  
Author(s):  
Frank Heatley ◽  
Ga-er Yu ◽  
Colin Booth ◽  
Trevor G. Blease

Polymers ◽  
2021 ◽  
Vol 13 (5) ◽  
pp. 838
Author(s):  
David Hermann Lamparelli ◽  
Magdalena Maria Kleybolte ◽  
Malte Winnacker ◽  
Carmine Capacchione

Soluble heterocomplexes consisting of sodium hydride in combination with trialkylaluminum derivatives have been used as anionic initiating systems at 100 °C in toluene for convenient homo-, co- and ter-polymerization of myrcene with styrene and isoprene. In this way it has been possible to obtain elastomeric materials in a wide range of compositions with interesting thermal profiles and different polymeric architectures by simply modulating the alimentation feed and the (monomers)/(initiator systems) ratio. Especially, a complete study of the myrcene-styrene copolymers (PMS) was carried out, highlighting their tapered microstructures with high molecular weights (up to 159.8 KDa) and a single glass transition temperature. For PMS copolymer reactivity ratios, rmyr = 0.12 ± 0.003 and rsty = 3.18 ± 0.65 and rmyr = 0.10 ± 0.004 and rsty = 3.32 ± 0.68 were determined according to the Kelen–Tudos (KT) and extended Kelen–Tudos (exKT) methods, respectively. Finally, this study showed an easy accessible approach for the production of various elastomers by anionic copolymerization of renewable terpenes, such as myrcene, with commodities.


2018 ◽  
Vol 140 (41) ◽  
pp. 13407-13412 ◽  
Author(s):  
Tassilo Gleede ◽  
Elisabeth Rieger ◽  
Jan Blankenburg ◽  
Katja Klein ◽  
Frederik R. Wurm

2020 ◽  
Vol 21 (8) ◽  
pp. 3152-3162
Author(s):  
Patrick Verkoyen ◽  
Philip Dreier ◽  
Matthias Bros ◽  
Christian Hils ◽  
Holger Schmalz ◽  
...  

2020 ◽  
Vol 93 (7) ◽  
pp. 1009-1018
Author(s):  
A. E. Tarasov ◽  
A. A. Grishchuk ◽  
S. V. Karpov ◽  
Yu. V. Podval’naya ◽  
A. V. Chernyak ◽  
...  

2021 ◽  
Vol 899 ◽  
pp. 226-231
Author(s):  
Yulia V. Podvalnaya ◽  
Aleksandr E. Tarasov ◽  
Alexander A. Grishchuk ◽  
Dmitry A. Chernyayev ◽  
Elmira R. Badamshina

It was found, studying acrylonitrile copolymerization with ethyl acrylate in dimethyl sulfoxide under the action of anionic initiating system of 1,4-diazabicyclo [2.2.2] octane – ethylene oxide, that the obtained copolymers have a branched structure. An increase in the molar fraction of ethyl acrylate in the reaction medium leads to a decrease in the initial rate of acrylonitrile polymerization. Thermal behavior of copolymer samples was investigated; it was found that ethyl acrylate, being introduced into the polyacrylonitrile structure, both reduces thermal effects related to the reactions taking place during heat treatment of copolymers, and increases the half-width of the heat release peak.


2017 ◽  
Vol 8 (12) ◽  
pp. 1882-1887 ◽  
Author(s):  
Jana Herzberger ◽  
Daniel Leibig ◽  
Jens Langhanki ◽  
Christian Moers ◽  
Till Opatz ◽  
...  

First one-step synthesis of poly(ethylene glycol) bearing multiple alkyne-groups along the polyether backbone and subsequent generation of PEG-glycopolymers by CuAAC.


2019 ◽  
Vol 10 (22) ◽  
pp. 2863-2871 ◽  
Author(s):  
Jan Blankenburg ◽  
Erik Kersten ◽  
Kamil Maciol ◽  
Manfred Wagner ◽  
Sirus Zarbakhsh ◽  
...  

An investigation of the copolymerization of EO and PO by in situ1H NMR spectroscopy reveals striking differences in the monomer gradient, depending on the polymerization method.


1994 ◽  
Vol 31 (1) ◽  
pp. 9-11
Author(s):  
M. Adal ◽  
P. Flodin ◽  
E. Gottberg-Klingskog ◽  
K. Holmberg

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