CO2-Responsive graft copolymers: synthesis and characterization. Issue 7 (17th January 2017)
- Record Type:
- Journal Article
- Title:
- CO2-Responsive graft copolymers: synthesis and characterization. Issue 7 (17th January 2017)
- Main Title:
- CO2-Responsive graft copolymers: synthesis and characterization
- Authors:
- Lin, Shaojian
Das, Anindita
Theato, Patrick - Abstract:
- Abstract : The synthesis and self-assembly study of CO2 -responsive graft copolymers fabricated from a "graft-to" strategy based on pentafluorophenyl esters as grafting sites. Abstract : A facile and versatile approach for preparing CO2 -responsive graft copolymers via a grafting-to strategy that combines controlled radical polymerization with post-polymerization modification has been demonstrated. A well-defined poly( N, N -dimethylacrylamide- co -pentafluorophenyl acrylate) (P(DMA- co -PFPA)) was synthesized by reversible addition fragmentation chain transfer (RAFT) polymerization bearing reactive pentafluorophenyl esters as grafting sites on a hydrophilic backbone. Then, amino end-functionalized poly(2-(diethylamino)ethyl methacrylate) (PDEAEMA) known for its CO2 responsiveness and hydrophobic poly(methyl methacrylate) (PMMA) were prepared via atom transfer radical polymerization (ATRP) as side blocks, respectively. Subsequently, post-polymerization modification via active-ester amine chemistry, resulted in CO2 -responsive graft copolymers with either homo-side chains or discrete multi-functional hetero side chains. Importantly, this grafting-to strategy utilizing active-ester amine chemistry appeared to be a facile and efficient method to fabricate graft copolymers. Interestingly, both prepared CO2 -responsive graft copolymers – due to their amphiphilic nature – could self-assemble into vesicles in aqueous solution and displayed CO2 -responsive expansion owing to theAbstract : The synthesis and self-assembly study of CO2 -responsive graft copolymers fabricated from a "graft-to" strategy based on pentafluorophenyl esters as grafting sites. Abstract : A facile and versatile approach for preparing CO2 -responsive graft copolymers via a grafting-to strategy that combines controlled radical polymerization with post-polymerization modification has been demonstrated. A well-defined poly( N, N -dimethylacrylamide- co -pentafluorophenyl acrylate) (P(DMA- co -PFPA)) was synthesized by reversible addition fragmentation chain transfer (RAFT) polymerization bearing reactive pentafluorophenyl esters as grafting sites on a hydrophilic backbone. Then, amino end-functionalized poly(2-(diethylamino)ethyl methacrylate) (PDEAEMA) known for its CO2 responsiveness and hydrophobic poly(methyl methacrylate) (PMMA) were prepared via atom transfer radical polymerization (ATRP) as side blocks, respectively. Subsequently, post-polymerization modification via active-ester amine chemistry, resulted in CO2 -responsive graft copolymers with either homo-side chains or discrete multi-functional hetero side chains. Importantly, this grafting-to strategy utilizing active-ester amine chemistry appeared to be a facile and efficient method to fabricate graft copolymers. Interestingly, both prepared CO2 -responsive graft copolymers – due to their amphiphilic nature – could self-assemble into vesicles in aqueous solution and displayed CO2 -responsive expansion owing to the protonation of tertiary amine groups of PDEAEMA side chains under CO2 stimulation. … (more)
- Is Part Of:
- Polymer chemistry. Volume 8:Issue 7(2017)
- Journal:
- Polymer chemistry
- Issue:
- Volume 8:Issue 7(2017)
- Issue Display:
- Volume 8, Issue 7 (2017)
- Year:
- 2017
- Volume:
- 8
- Issue:
- 7
- Issue Sort Value:
- 2017-0008-0007-0000
- Page Start:
- 1206
- Page End:
- 1216
- Publication Date:
- 2017-01-17
- Subjects:
- Polymers -- Periodicals
Macromolecules -- Periodicals
Polymerization -- Periodicals
547.705 - Journal URLs:
- http://www.rsc.org/Publishing/Journals/PY/Index.asp ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c6py01996j ↗
- Languages:
- English
- ISSNs:
- 1759-9954
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6547.703400
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 720.xml