Highly emissive covalent organic frameworks

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Sasanka Dalapati - , Japan Advanced Institute of Science and Technology (Author)
  • Enquan Jin - , The Graduate University for Advanced Studies (Author)
  • Matthew Addicoat - , Leipzig University (Author)
  • Thomas Heine - , Leipzig University (Author)
  • Donglin Jiang - , Japan Advanced Institute of Science and Technology (Author)

Abstract

Highly luminescent covalent organic frameworks (COFs) are rarely achieved because of the aggregation-caused quenching (ACQ) of stacked layers. Here, we report a general strategy to design highly emissive COFs by introducing an aggregation-induced emission (AIE) mechanism. The integration of AIE-active units into the polygon vertices yields crystalline porous COFs with periodic stacked columnar AIE arrays. These columnar AIE arrays dominate the luminescence of the COFs, achieve exceptional quantum yield via a synergistic structural locking effect of intralayer covalent bonding and interlayer noncovalent interactions and serve as a highly sensitive sensor to report ammonia down to sub ppm level. Our strategy breaks through the ACQ-based mechanistic limitations of COFs and opens a way to explore highly emissive COF materials.

Details

Original languageEnglish
Pages (from-to)5797-5800
Number of pages4
JournalJournal of the American Chemical Society
Volume138
Issue number18
Publication statusPublished - 11 May 2016
Peer-reviewedYes
Externally publishedYes