Document Type
Article
Publication Date
2019
Digital Object Identifier (DOI)
https://doi.org/10.1063/1.5122674
Abstract
The strong coordination between metal ions and binding moieties in functional porous materials is central to the design and advancement of heterogeneous catalysis. In this study, we have successfully immobilized catalytically active iridium ions on a two-dimensional covalent organic framework (COF) having bipyridine moieties using a programmed synthetic procedure. The iridium immobilized framework, Ircod(I)@Py-2,2′-BPyPh COF, had high porosity, good stability, and exhibited excellent catalytic activity for C—H borylation, as compared with the pristine framework. Additionally, Ircod(I)@Py-2,2′-BPyPh COF was found to be an efficient catalyst for a series of electronically and sterically substituted substrates. The immobilized COF possessed excellent reusability, recyclability, and retention of crystallinity. This report highlights the role of porous materials as an ideal decorating platform for conducting a wide range of potent chemical conversions.
Rights Information
This work is licensed under a Creative Commons Attribution 4.0 License.
Was this content written or created while at USF?
Yes
Citation / Publisher Attribution
APL Materials, v. 7, issue 10, art. 101111
Scholar Commons Citation
Vardhan, Harsh; Pan, Yanxiong; Yang, Zhongyu; Verma, Gaurav; Nafady, Ayman; Al-Enizi, Abdullah M.; Alotaibi, Tawfiq M.; Almaghrabi, Omar A.; and Ma, Shengqian, "Iridium Complex Immobilization on Covalent Organic Framework for Effective C—H Borylation" (2019). Chemistry Faculty Publications. 107.
https://digitalcommons.usf.edu/chm_facpub/107
