Acid–base directed supramolecular isomers of isophthalate based MOFs for CO2 adsorption and transformation. Issue 29 (5th June 2017)

• Record Type: Journal Article
• Authors: Perman, Jason A.; Chen, Meng; Mikhail, Antony A.; Niu, Zheng; Ma, Shengqian
• Is Part Of: CrystEngComm. Volume 19:Issue 29(2017)
• Page Start: 4171
• Page End: 4174
• Publication Date: 2017-06-05
• Subjects: Crystals -- Periodicals; Crystal growth -- Periodicals; Crystallography -- Periodicals; Cristaux -- Périodiques; Cristaux -- Croissance -- Périodiques; Cristallographie -- Périodiques; 548
• DOI: 10.1039/c7ce00405b
• Languages: English
• ISSNs: 1466-8033

Abstract

Abstract : Directing supramolecular isomers using an acid versus a base, two MOFs with the same composition yet different topologies show differences in their catalytic efficacy to transform CO2 and epoxides into cyclic carbonates. Abstract : The ubiquitous [Cu(O2 CR)4 ] paddlewheel molecular building block (MBB) is renowned for producing highly porous metal–organic frameworks (MOFs), yet some carboxylate based ligands can result in supramolecular isomers. We show that it is possible to manipulate the synthesis conditions to favor one isomer over another yielding MOFs with either an lvt or nbo topology. These isomers exist because the 4-connected paddlewheel MBB and isophthalate based ligand can form either a square grid or a Kagomé lattice, where layers can join to give their respective framework topologies. Topology differences and accessible Cu(ii ) centers in isomers of [Cu2 L] n were evaluated for their porous properties towards CO2 and their abilities to transform CO2 into value added chemicals under ambient conditions.