This work is supported by King Abdullah University of Science and Technology (FIC/2010/06). The microcrystal diffraction of porph(Cl−)@MOM-11(Mn2+) was carried at the Advanced Photon Source on beamline 15ID-B at ChemMatCARS Sector 15 (NSF/CHE-0822838 and DE-AC02-06CH11357).
Communication
Post-Synthetic Modification of Porphyrin-Encapsulating Metal–Organic Materials by Cooperative Addition of Inorganic Salts to Enhance CO2/CH4 Selectivity†
Article first published online: 21 AUG 2012
DOI: 10.1002/anie.201203594
Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Issue

Angewandte Chemie International Edition
Volume 51, Issue 37, pages 9330–9334, September 10, 2012
Additional Information
How to Cite
Zhang, Z., Gao, W.-Y., Wojtas, L., Ma, S., Eddaoudi, M. and Zaworotko, M. J. (2012), Post-Synthetic Modification of Porphyrin-Encapsulating Metal–Organic Materials by Cooperative Addition of Inorganic Salts to Enhance CO2/CH4 Selectivity . Angew. Chem. Int. Ed., 51: 9330–9334. doi: 10.1002/anie.201203594
- †
Publication History
- Issue published online: 5 SEP 2012
- Article first published online: 21 AUG 2012
- Manuscript Revised: 28 JUN 2012
- Manuscript Received: 9 MAY 2012
Funded by
- King Abdullah University of Science and Technology. Grant Number: FIC/2010/06
Keywords:
- CO2/CH4 selectivity;
- encapsulation;
- metal salts;
- metal–organic frameworks;
- porphyrinoids
Keeping MOM: Reaction of biphenyl-3,4′,5-tricarboxylate and Cd(NO3)2 in the presence of meso-tetra(N-methyl-4-pyridyl)porphine tetratosylate afforded porph@MOM-11, a microporous metal–organic material (MOM) that encapsulates cationic porphyrins and solvent in alternating open channels. Porph@MOM-11 has cation and anion binding sites that facilitate cooperative addition of inorganic salts (such as M+Cl−) in a stoichiometric fashion.

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