Synthesis and characterization of poly(4-vinylbenzyl-graft-ethylene glycol methyl ether) amphiphilic graft copolymer via free-radical polymerization and 'click' chemistry.
Saved in:
| Title: | Synthesis and characterization of poly(4-vinylbenzyl-graft-ethylene glycol methyl ether) amphiphilic graft copolymer via free-radical polymerization and 'click' chemistry. |
|---|---|
| Authors: | Savaş, Bedrettin1 (AUTHOR), Öztürk, Temel2 (AUTHOR) temelozturk@msn.com, Günaydin, Elif2 (AUTHOR), Akman, Murat Emre1 (AUTHOR) |
| Source: | Journal of Chemical Sciences. Jun2025, Vol. 137 Issue 2, p1-9. 9p. |
| Subjects: | Methoxyethanol, Addition polymerization, Physical & theoretical chemistry, Methyl ether, Polyethylene glycol, Graft copolymers |
| Abstract: | Poly(4-vinylbenzyl-graft-ethylene glycol methyl ether) (poly(VB-g-mPEG)) amphiphilic graft copolymer was obtained using 'click' chemistry of polyethylene glycol methyl ether propargyl (mPEG-propargyl) and terminal azido poly(4-vinylbenzyl chloride) (PVB-N3). Using 2,2′-azobis(2-methylpropionitrile) and 4-vinylbenzyl chloride, poly(4-vinylbenzyl chloride) (PVBC) was created by free-radical polymerization (FRP). PVB-N3 was obtained using PVBC and sodium azide. Propargyl chloride and polyethylene glycol methyl ether were reacted to form mPEG-propargyl. The 'click' chemical method created poly(VB-g-mPEG) amphiphilic graft copolymer by reacting PVB-N3 with mPEG-propargyl. 1H-NMR, DSC, FTIR and GPC characterized the products. The spectroscopic and thermal studies monitored that poly(VB-g-mPEG) was built via combining FRP and 'click' chemistry. The synthesis of poly(4-vinylbenzyl-graft-ethylene glycol methyl ether) amphiphilic graft copolymer was demonstrated in this study by using "click" chemistry and free radical polymerization. The synthesized products were characterized by using 1H-NMR, DSC, FT-IR, and GPC instruments. Here, we aimed to report on synthesizing the amphiphilic graft copolymer using "click" chemistry and free radical polymerization methods. [ABSTRACT FROM AUTHOR] |
| Copyright of Journal of Chemical Sciences is the property of Springer Nature and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) | |
| Database: | Engineering Source |
|
Full text is not displayed to guests.
Login for full access.
|
|
| Abstract: | Poly(4-vinylbenzyl-graft-ethylene glycol methyl ether) (poly(VB-g-mPEG)) amphiphilic graft copolymer was obtained using 'click' chemistry of polyethylene glycol methyl ether propargyl (mPEG-propargyl) and terminal azido poly(4-vinylbenzyl chloride) (PVB-N3). Using 2,2′-azobis(2-methylpropionitrile) and 4-vinylbenzyl chloride, poly(4-vinylbenzyl chloride) (PVBC) was created by free-radical polymerization (FRP). PVB-N3 was obtained using PVBC and sodium azide. Propargyl chloride and polyethylene glycol methyl ether were reacted to form mPEG-propargyl. The 'click' chemical method created poly(VB-g-mPEG) amphiphilic graft copolymer by reacting PVB-N3 with mPEG-propargyl. 1H-NMR, DSC, FTIR and GPC characterized the products. The spectroscopic and thermal studies monitored that poly(VB-g-mPEG) was built via combining FRP and 'click' chemistry. The synthesis of poly(4-vinylbenzyl-graft-ethylene glycol methyl ether) amphiphilic graft copolymer was demonstrated in this study by using "click" chemistry and free radical polymerization. The synthesized products were characterized by using 1H-NMR, DSC, FT-IR, and GPC instruments. Here, we aimed to report on synthesizing the amphiphilic graft copolymer using "click" chemistry and free radical polymerization methods. [ABSTRACT FROM AUTHOR] |
|---|---|
| ISSN: | 09743626 |
| DOI: | 10.1007/s12039-025-02368-9 |
