Title |
Depolymerizable semi-fluorinated polymers for sustainable functional materials |
ID_Doc |
29763 |
Authors |
Sathe, D; Zhou, JF; Chen, HL; Schrage, BR; Yoon, S; Wang, ZY; Ziegler, CJ; Wang, JP |
Title |
Depolymerizable semi-fluorinated polymers for sustainable functional materials |
Year |
2022 |
Published |
Polymer Chemistry, 13.0, 18 |
DOI |
10.1039/d2py00240j |
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 (tCBCO) monomers, these polymers show tunable glass transition temperatures (-2 degrees C to 88 degrees C), excellent thermal stability (decomposition onset temperatures >280 degrees C) and hydrophobicity (water contact angles >90 degrees). The hydrophobicity of the semi-fluorinated polymers was further utilized in an amphiphilic diblock copolymer, which forms self-assembled micelles with a size of similar to 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 tCBCO-based depolymerizable semi-fluorinated polymers promising candidates for sustainable functional materials that can offer a solution to a circular economy. |
Author Keywords |
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Index Keywords |
Index Keywords |
Document Type |
Other |
Open Access |
Open Access |
Source |
Science Citation Index Expanded (SCI-EXPANDED) |
EID |
WOS:000783481200001 |
WoS Category |
Polymer Science |
Research Area |
Polymer Science |
PDF |
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