Issue 7, 2010

Sulfate encapsulation in three-fold interpenetrated metal–organic frameworks with bis(pyridylurea) ligands

Abstract

Self-assembly of two flexible bis-pyridylurea ligands, pentane-1,5-diylbis(3-pyridin-3-ylurea) (L5) and hexane-1,6-diylbis(3-pyridin-3-ylurea) (L6) with ZnSO4 or CdSO4 (metal-to-ligand molar ratio 1 : 2) results in three metal–organic frameworks with (4,4) net structures, {[ML2(H2O)2]SO4·2H2O}n (1: Zn, L5; 2: Cd, L5; and 3: Zn, L6). Single-crystal X-ray diffraction analyses reveal that all the compounds are characteristic of a 3-fold parallel interpenetrated framework with cavities suitable for encapsulating the sulfate anion despite the different spacer lengths ((CH2)5 and (CH2)6) of the two ligands and variation of the metal ions. The ligand adopts an antianti conformation and functions as a bridging bidentate linker, while the sulfate ion is selectively bound by four urea functionalities via multiple hydrogen bonds.

Graphical abstract: Sulfate encapsulation in three-fold interpenetrated metal–organic frameworks with bis(pyridylurea) ligands

Supplementary files

Article information

Article type
Paper
Submitted
05 Oct 2009
Accepted
26 Jan 2010
First published
24 Feb 2010

CrystEngComm, 2010,12, 2129-2134

Sulfate encapsulation in three-fold interpenetrated metal–organic frameworks with bis(pyridylurea) ligands

B. Wu, J. Liang, Y. Zhao, M. Li, S. Li, Y. Liu, Y. Zhang and X. Yang, CrystEngComm, 2010, 12, 2129 DOI: 10.1039/B920777E

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