Cyanurate-Linked Covalent Organic Frameworks Enabled by Dynamic Nucleophilic Aromatic Substitution.
J Am Chem Soc
; 144(39): 17737-17742, 2022 10 05.
Article
in En
| MEDLINE
| ID: mdl-36165690
ABSTRACT
We report, for the first time, highly crystalline cyanurate-linked covalent organic frameworks synthesized via dynamic nucleophilic aromatic substitution. The high crystallinity is enabled by the bond exchange reaction (self-correction) between 2,4,6-triphenoxy-1,3,5-triazine and diphenols via reversible SNAr catalyzed by triazabicyclodecene. The CN-COFs contain flexible backbones that exhibit a unique AA'-stacking due to interlayer hydrogen bonding interactions. The isoreticular expansion study demonstrates the general applicability of this synthetic method. The resulting CN-COFs exhibited good stability, as well as high CO2/N2 selectivity.
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Metal-Organic Frameworks
Language:
En
Journal:
J Am Chem Soc
Year:
2022
Type:
Article
Affiliation country:
United States