journal article·2021-05-14

Catalytic Amine Functionalization and Polymerization of Cyclic Alkenes Creates Adhesive and Self-Healing Materials

Damon J. Gilmour, Tanja Tomkovic, Nirmalendu Kuanr, Mitchell R. Perry, Hans Gildenast, Savvas G. Hatzikiriakos, Laurel L. Schafer

ACS Applied Polymer Materials· Volume 3· Issue 5
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Abstract

The chemical functionalization of polyolefins to access responsive materials is a long-standing challenge in materials science. Current protocols do not typically tolerate polar functional groups, and postpolymerization modification often leads to material defects. Here the catalytic synthesis of amine-functionalized polyolefins has been achieved using a two-step catalytic combination of hydroaminoalkylation and ring-opening metathesis polymerization (ROMP). Furthermore, reduction was used to obtain an aminated polyethylene analogue. This preparation transforms simple starting materials into polar-functionalized polymers with complete atom economy. Utilizing dynamic associative interactions, including hydrogen bonding, these materials demonstrate tunable rheological properties, autonomous self-healing, and unexpected adhesion to polytetrafluoroethylene (PTFE).
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Synthetic Organic Chemistry Methods · Polymer composites and self-healing · Carbon dioxide utilization in catalysis

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Chemistry, University of British Columbia, Vancouver, BC, Canada V6T 1Z4

Department of Chemical and Biological Engineering, University of British Columbia, Vancouver, BC, Canada V6T 1Z3

Funding

Studienstiftung des Deutschen Volkes · Canada Research Chairs · Natural Sciences and Engineering Research Council of Canada · University of British Columbia

References (41)

Show source-provided references
1. 10.1039/c3cs60032g10.1039/c3cs60032g ↗
2. 10.1351/PAC-CON-12-04-1310.1351/PAC-CON-12-04-13 ↗
3. 10.1002/pola.2399210.1002/pola.23992 ↗
4. 10.1021/cr990251u10.1021/cr990251u ↗
5. 10.1002/anie.20200006010.1002/anie.202000060 ↗
6. 10.1039/b311405h10.1039/b311405h ↗
7. 10.1021/ie102005q10.1021/ie102005q ↗
8. Schulz M. D. · 2015 · 31310.1002/9783527674107.ch39 ↗
9. 10.1007/s13203-014-0048-z10.1007/s13203-014-0048-z ↗
10. 10.1039/C2PY20883K10.1039/C2PY20883K ↗
11. 10.1002/anie.20140465510.1002/anie.201404655 ↗
12. 10.1021/acs.macromol.7b0084110.1021/acs.macromol.7b00841 ↗
13. 10.1021/acs.macromol.6b0030610.1021/acs.macromol.6b00306 ↗
14. 10.1021/ma100330u10.1021/ma100330u ↗
15. 10.1021/ma802243e10.1021/ma802243e ↗
16. 10.1002/pola.2295010.1002/pola.22950 ↗
17. 10.1021/acs.macromol.9b0215810.1021/acs.macromol.9b02158 ↗
18. 10.1055/s-0034-137921610.1055/s-0034-1379216 ↗
19. 10.1002/anie.20090365610.1002/anie.200903656 ↗
20. 10.1021/acscatal.7b0148610.1021/acscatal.7b01486 ↗
21. 10.1021/ja00711a03010.1021/ja00711a030 ↗
22. 10.1021/la902340z10.1021/la902340z ↗
23. 10.1016/j.polymer.2010.05.00210.1016/j.polymer.2010.05.002 ↗
24. 10.1002/pola.1992.08030030710.1002/pola.1992.080300307 ↗
25. 10.1021/ma001304910.1021/ma0013049 ↗
26. 10.1122/1.494223110.1122/1.4942231 ↗
27. 10.1021/ma402368s10.1021/ma402368s ↗
28. 10.1122/1.495543210.1122/1.4955432 ↗
29. 10.1016/j.progpolymsci.2008.02.00110.1016/j.progpolymsci.2008.02.001 ↗
30. 10.1002/adma.20100303610.1002/adma.201003036 ↗
31. 10.1038/nature0666910.1038/nature06669 ↗
32. 10.1002/adma.20170684610.1002/adma.201706846 ↗
33. 10.1038/nchem.131410.1038/nchem.1314 ↗
34. 10.1021/jacs.8b1331610.1021/jacs.8b13316 ↗
35. 10.1002/ange.20191000210.1002/ange.201910002 ↗
36. 10.1021/acs.macromol.5b0074710.1021/acs.macromol.5b00747 ↗
37. 10.1021/ma00016a03410.1021/ma00016a034 ↗
38. 10.1021/ma970617+10.1021/ma970617+ ↗
39. 10.1021/ma401111n10.1021/ma401111n ↗
40. Ebnesajjad S. · 2014
41. 10.1021/jacs.9b1335610.1021/jacs.9b13356 ↗