Switching of Adsorption Properties in a Zwitterionic Metal–Organic Framework Triggered by Photogenerated Radical Triplets
Carboxylate
Cationic polymerization
DOI:
10.1021/acs.chemmater.6b03224
Publication Date:
2016-10-17T14:40:13Z
AUTHORS (6)
ABSTRACT
A new metal–organic framework (MOF) that features photoreactive zwitterionic pyridinium 4-carboxylate units has been designed. Upon UV light irradiation, these form radical triplets permitted by intramolecular electron transfer between anionic carboxylate and cationic groups. This reversible light-responsive behavior creates on/off switchable charge gradients localized at the MOF's major adsorption sites and, thus, allows significant control of gas sorption process. It is shown this strategy offers design routes for accessing stimulus-responsive materials.
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