Cationic quaternary ammonium salt-catalyzed LED-induced living radical polymerization with in situ halogen exchange

2020 ◽  
Vol 11 (23) ◽  
pp. 3876-3883
Author(s):  
Feifei Li ◽  
Wanting Yang ◽  
Mengmeng Li ◽  
Lin Zhou ◽  
Lin Lei

Cationic quaternary ammonium salts were employed as organocatalysts for light-emitting diode (LED)-induced living radical polymerization (LRP) with the in situ halogen exchange of methacrylate monomers.

2019 ◽  
Vol 7 (2) ◽  
pp. 346-353 ◽  
Author(s):  
Hui Chang ◽  
Wenting Mao ◽  
Yingying Duan ◽  
Wanning Zhang ◽  
Chao Zhou ◽  
...  

Mesostructured fluorescent silica hybrids (MFSHs) were synthesized by using tetraphenylethylene (TPE)-based quaternary ammonium salts as surfactants with typical aggregation-induced emission (AIE) behaviours.


RSC Advances ◽  
2017 ◽  
Vol 7 (5) ◽  
pp. 2836-2841 ◽  
Author(s):  
Tao Wang ◽  
Wenlong Wang ◽  
Yuan Lyu ◽  
Xingkun Chen ◽  
Cunyao Li ◽  
...  

A series of cross-linked polymer supported ionic liquids based on quaternary ammonium salts have been prepared using a facile method of radical polymerization.


Molecules ◽  
2020 ◽  
Vol 25 (10) ◽  
pp. 2463
Author(s):  
Jacqueline Bitai ◽  
Alexandra M. Z. Slawin ◽  
David B. Cordes ◽  
Andrew D. Smith

The scope and limitations of a tandem N-allylation/[2,3]-rearrangement protocol are investigated through the incorporation of a variety of functional groups within an allylic phosphate precursor. This method uses readily accessible N,N-dimethylglycine aryl esters and functionalized allylic phosphates, forming quaternary ammonium salts in situ in the presence of a palladium catalyst. Subsequent enantioselective [2,3]-sigmatropic rearrangement, promoted by the chiral isothiourea tetramisole, generates α-amino acid derivatives with two contiguous stereocenters. The incorporation of electron-withdrawing ester and amide groups gave the best results, furnishing the desired products in moderate to good yields (29–70%), with low diastereocontrol (typically 60:40 dr) but high enantioselectivity (up to 90:10 er). These results indicate that substrate–catalyst interactions in the proposed transition state are sensitive to the substitution pattern of the substrates.


2017 ◽  
Vol 50 (5) ◽  
pp. 1882-1891 ◽  
Author(s):  
Longqiang Xiao ◽  
Keita Sakakibara ◽  
Yoshinobu Tsujii ◽  
Atsushi Goto

Synthesis ◽  
2020 ◽  
Author(s):  
Roberto Sole ◽  
Vanessa Gatto ◽  
Silvia Conca ◽  
Lodovico Agostinis ◽  
Noemi Bardella ◽  
...  

Nowadays, the development of new approaches which smartly bypass the use of harsh reaction conditions and hazardous chemicals covers a pivotal role. In this research paper the synthesis, characterization and application of novel libraries of triazine bis-quaternary ammonium salts, employed as coupling agents to produce amides, is reported. Full characterization of the novel compounds by 1H and 13C NMR, FT-IR spectroscopy, ESI-HRMS and elemental analysis (EA) is provided. Furthermore, a comparison in terms of activity of the preformed triazine compounds versus in situ formulations has been evaluated for the formation of amides in the presence of phenylethylamine and different aliphatic or aromatic acids. A possible correlation between the chemical structure of the triazine and their reactivity for the formation of the triazine bis-quaternary ammonium salts is also reported. Moreover, best performing condensation agents have been further tested for the cross-linking of collagen powder as possible wet white tanning systems, for sustainable and environmentally friendly leather tanning.


2015 ◽  
Vol 3 (18) ◽  
pp. 3704-3713 ◽  
Author(s):  
Man He ◽  
Huining Xiao ◽  
Yuming Zhou ◽  
Peng Lu

Novel water-soluble amphiphilic copolymers with ciprofloxacin are prepared by copolymerization of methacrylate monomers containing ciprofloxacin and quaternary ammonium salt monomers.


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