Depolymerizable semi-fluorinated polymers for sustainable functional materials. Issue 18 (13th April 2022)
- Record Type:
- Journal Article
- Title:
- Depolymerizable semi-fluorinated polymers for sustainable functional materials. Issue 18 (13th April 2022)
- Main Title:
- Depolymerizable semi-fluorinated polymers for sustainable functional materials
- Authors:
- Sathe, Devavrat
Zhou, Junfeng
Chen, Hanlin
Schrage, Briana R.
Yoon, Seiyoung
Wang, Zeyu
Ziegler, Christopher J.
Wang, Junpeng - Abstract:
- Abstract : Chemically recyclable semi-fluorinated polymers are demonstrated for the first time, and the hydrophobicity, self-assembly, and post-polymerization functionalization of these polymers are explored. Abstract : Fluorinated polymers are important functional materials for a broad range of applications, but the recycling of current fluorinated polymers is challenging. We present the first example of semi-fluorinated polymers that can undergo chemical recycling to form the corresponding monomers under ambient conditions. Prepared through ring-opening metathesis polymerization of functionalized trans -cyclobutane fused cyclooctene ( t CBCO) monomers, these polymers show tunable glass transition temperatures (−2 °C to 88 °C), excellent thermal stability (decomposition onset temperatures >280 °C) and hydrophobicity (water contact angles >90°). The hydrophobicity of the semi-fluorinated polymers was further utilized in an amphiphilic diblock copolymer, which forms self-assembled micelles with a size of ∼88 nm in an aqueous solution. Finally, through an efficient, regioselective para -fluoro-thiol substitution reaction, post-polymerization functionalization of a polymer with a pentafluorophenyl imide substituent was achieved. The ease of preparation, functionalization, and recycling, along with the diverse thermomechanical properties and demonstrated hydrophobicity make the t CBCO-based depolymerizable semi-fluorinated polymers promising candidates for sustainable functionalAbstract : Chemically recyclable semi-fluorinated polymers are demonstrated for the first time, and the hydrophobicity, self-assembly, and post-polymerization functionalization of these polymers are explored. Abstract : Fluorinated polymers are important functional materials for a broad range of applications, but the recycling of current fluorinated polymers is challenging. We present the first example of semi-fluorinated polymers that can undergo chemical recycling to form the corresponding monomers under ambient conditions. Prepared through ring-opening metathesis polymerization of functionalized trans -cyclobutane fused cyclooctene ( t CBCO) monomers, these polymers show tunable glass transition temperatures (−2 °C to 88 °C), excellent thermal stability (decomposition onset temperatures >280 °C) and hydrophobicity (water contact angles >90°). The hydrophobicity of the semi-fluorinated polymers was further utilized in an amphiphilic diblock copolymer, which forms self-assembled micelles with a size of ∼88 nm in an aqueous solution. Finally, through an efficient, regioselective para -fluoro-thiol substitution reaction, post-polymerization functionalization of a polymer with a pentafluorophenyl imide substituent was achieved. The ease of preparation, functionalization, and recycling, along with the diverse thermomechanical properties and demonstrated hydrophobicity make the t CBCO-based depolymerizable semi-fluorinated polymers promising candidates for sustainable functional materials that can offer a solution to a circular economy. … (more)
- Is Part Of:
- Polymer chemistry. Volume 13:Issue 18(2022)
- Journal:
- Polymer chemistry
- Issue:
- Volume 13:Issue 18(2022)
- Issue Display:
- Volume 13, Issue 18 (2022)
- Year:
- 2022
- Volume:
- 13
- Issue:
- 18
- Issue Sort Value:
- 2022-0013-0018-0000
- Page Start:
- 2608
- Page End:
- 2614
- Publication Date:
- 2022-04-13
- 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/d2py00240j ↗
- 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:
- 21600.xml