From SmOF to SmH0.78OF0.22: H/F Substitution in Oxide Fluorides as a Synthesis Route to Heteroanionic Compounds

Author(s):  
Nicolas Zapp ◽  
Henry E. Fischer ◽  
Holger Kohlmann
2016 ◽  
Vol 42 (6) ◽  
pp. 6782-6790 ◽  
Author(s):  
Linggen Kong ◽  
Inna Karatchevtseva ◽  
Rohan Holmes ◽  
Joel Davis ◽  
Yingjie Zhang ◽  
...  

Molecules ◽  
2021 ◽  
Vol 26 (14) ◽  
pp. 4158
Author(s):  
Patrycja Glińska ◽  
Andrzej Wolan ◽  
Wojciech Kujawski ◽  
Edyta Rynkowska ◽  
Joanna Kujawa

There has been an ongoing need to develop polymer materials with increased performance as proton exchange membranes (PEMs) for middle- and high-temperature fuel cells. Poly(vinyl alcohol) (PVA) is a highly hydrophilic and chemically stable polymer bearing hydroxyl groups, which can be further altered. Protic ionic liquids (proticILs) have been found to be an effective modifying polymer agent used as a proton carrier providing PEMs’ desirable proton conductivity at high temperatures and under anhydrous conditions. In this study, the novel synthesis route of PVA grafted with fluorinated protic ionic liquids bearing sulfo groups (–SO3H) was elaborated. The polymer functionalization with fluorinated proticILs was achieved by the following approaches: (i) the PVA acylation and subsequent reaction with fluorinated sultones and (ii) free-radical polymerization reaction of vinyl acetate derivatives modified with 1-methylimidazole and sultones. These modifications resulted in the PVA being chemically modified with ionic liquids of protic character. The successfully grafted PVA has been characterized using 1H, 19F, and 13C-NMR and FTIR-ATR. The presented synthesis route is a novel approach to PVA functionalization with imidazole-based fluorinated ionic liquids with sulfo groups.


Author(s):  
Youyu Xie ◽  
Feng Xu ◽  
Lin Yang ◽  
He Liu ◽  
Xiangyang Xu ◽  
...  

Amine transaminases offer an environmentally benign chiral amine asymmetric synthesis route.


Author(s):  
Tamás Hergert ◽  
Béla Mátravölgyi ◽  
Róbert Örkényi ◽  
János Éles ◽  
Ferenc Faigl

AbstractA three-step batch-flow hybrid process has been developed for an expeditious synthesis of the enynol key intermediate of antifungal terbinafine. This procedure involves consecutive organometallic steps without the necessity of any in-line purification: after a metalation by n-butyllithium, a selective addition of the lithium salt was elaborated followed by a Grignard reaction resulting in a high yield of 6,6-dimethylhept-1-en-4-yn-3-ol. Moreover, as an alternative to tetrahydrofuran, cyclopentyl methyl ether was used as solvent implementing a safe, sustainable, yet selective synthetic process. Even on a laboratory-scale, the optimized batch-flow hybrid process had a theoretical throughput of 41 g/h. Furthermore, the newly developed process provides an efficient synthesis route to the key-intermediate, while making acrolein obsolete, minimizing side-products, and enabling safe and convenient scale-up.


2014 ◽  
Vol 43 (39) ◽  
pp. 14644-14652 ◽  
Author(s):  
E. García-González ◽  
M. D. Soriano ◽  
E. Urones-Garrote ◽  
J. M. López Nieto

The synthesis route followed to prepare h-WO3 type oxides results in the production of nanostructured crystals by the spontaneous formation of self-assembled and regular nano-cavities on their surface.


1998 ◽  
Vol 33 (2) ◽  
pp. 237-252 ◽  
Author(s):  
Sylvie Even-Boudjada ◽  
Laurence Burel ◽  
Roger Chevrel ◽  
Marcel Sergent

2015 ◽  
Vol 504 ◽  
pp. 81-91 ◽  
Author(s):  
A. Dragu ◽  
S. Kinayyigit ◽  
E.J. García-Suárez ◽  
M. Florea ◽  
E. Stepan ◽  
...  

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