Photopolymerized and acetylene-functionlized polyacrylates for photoclickable elastomers. (3rd January 2022)
- Record Type:
- Journal Article
- Title:
- Photopolymerized and acetylene-functionlized polyacrylates for photoclickable elastomers. (3rd January 2022)
- Main Title:
- Photopolymerized and acetylene-functionlized polyacrylates for photoclickable elastomers
- Authors:
- Zhang, Zhengyuan
Yan, Hongyu
Yin, Zejun
Wang, Yuechuan - Abstract:
- Abstract: The acetylene functional groups on polymer chains provide a photochemical access to modulate or actuate the properties of the polymer. We report here a photochemical way to actuate a polyacrylate to elastomers. High molecular weight acetylene functionalized homo- and copolymers of are prepared with a novel monomer, 2-(dimethylpropargyloxy)ethyl methacrylate, DMPOEMA, by photo-initiated free-radical polymerization (FRP) in solution at room temperature. The acetylene groups are tolerant of the solution photo FRP at 50 wt% concentration, but not tolerant to thermal FRP and photo FRP at 80 wt% concentration. Copolymers P(DMPOEMA- co -EA) with‾Mn in 12, 500–15, 100 g/mol were prepared with conversion up to 90% at 50% concentration and three monomer feed ratios. The feed ratio of DMPOEMA had slight effects on the polymerization rate, but effects on PDI at higher monomer conversion with prolonged photo-irradiation. The acetylene functionalized polyacrylates become photo-sensitive and are photo cross-linkable or photo clickable after solvent is removed. Real-time FT-IR study reveals that the photo cross-linking with a tri-thiol compound follows the normal thiol-yne photochemistry, and the photo cross-linking catalyzed with only photoinitiator results in diene units in the cross-linked polymer networks. These photo-treated polyacrylate exhibited designable elastomer properties: with T g in −24 to −11 °C, more than 10 times increase of relative cross-linking density andAbstract: The acetylene functional groups on polymer chains provide a photochemical access to modulate or actuate the properties of the polymer. We report here a photochemical way to actuate a polyacrylate to elastomers. High molecular weight acetylene functionalized homo- and copolymers of are prepared with a novel monomer, 2-(dimethylpropargyloxy)ethyl methacrylate, DMPOEMA, by photo-initiated free-radical polymerization (FRP) in solution at room temperature. The acetylene groups are tolerant of the solution photo FRP at 50 wt% concentration, but not tolerant to thermal FRP and photo FRP at 80 wt% concentration. Copolymers P(DMPOEMA- co -EA) with‾Mn in 12, 500–15, 100 g/mol were prepared with conversion up to 90% at 50% concentration and three monomer feed ratios. The feed ratio of DMPOEMA had slight effects on the polymerization rate, but effects on PDI at higher monomer conversion with prolonged photo-irradiation. The acetylene functionalized polyacrylates become photo-sensitive and are photo cross-linkable or photo clickable after solvent is removed. Real-time FT-IR study reveals that the photo cross-linking with a tri-thiol compound follows the normal thiol-yne photochemistry, and the photo cross-linking catalyzed with only photoinitiator results in diene units in the cross-linked polymer networks. These photo-treated polyacrylate exhibited designable elastomer properties: with T g in −24 to −11 °C, more than 10 times increase of relative cross-linking density and resistant to solvents, improved stress, strain and elongation properties. This work paves a way for the acetylene functionalized (meth)acrylates as advanced photo-reactive material. Graphical abstract: Image 1 Highlights: Acetylene functionalized polyacrylates (AFP) were synthesized by photo polymerization. AFP can be photo-crosslinked via thiol-yne or coupling reaction. The photo-crosslinked polyacrylate elastomers exhibited designable properties. … (more)
- Is Part Of:
- Polymer. Volume 238(2022)
- Journal:
- Polymer
- Issue:
- Volume 238(2022)
- Issue Display:
- Volume 238, Issue 2022 (2022)
- Year:
- 2022
- Volume:
- 238
- Issue:
- 2022
- Issue Sort Value:
- 2022-0238-2022-0000
- Page Start:
- Page End:
- Publication Date:
- 2022-01-03
- Subjects:
- Elastomer -- Polyacrylate -- Pohotopolymerization
Polymers -- Periodicals
Polymerization -- Periodicals
Polymères -- Périodiques
Polymérisation -- Périodiques
547.7 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00323861 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.polymer.2021.124415 ↗
- Languages:
- English
- ISSNs:
- 0032-3861
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6547.700000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 20273.xml