In the title coordination polymer, catena-poly[[[triaqua-europium(III)]-bis-(μ-1H,3H-benzimidazol-3-ium-5,6-dicarb-oxyl-ato-κ(3)O(5),O(5'):O(6))-[triaqua-europium(III)]-di-μ-sulfato-κ(3)O:O,O';κ(3)O,O':O'] hexahydrate], [Eu(2)(C(9)H(5)N(2)O(4))(2)(SO(4))(2)(H(2)O)(6)]·6H(2)O}(n), the 1H,3H-benzimidazol-3-ium-5,6-dicarb-oxy-l-ate ligand is protonated at the imidazole group (H(2)bdc). The Eu(III) ion is coordinated by nine O atoms from two H(2)bdc ligands, two sulfate anions and three water mol-ecules, displaying a bicapped trigonal prismatic geometry. The carboxyl-ate groups of the H(2)bdc ligands and the sulfate anions link the Eu(III) ions, forming a chain along [010]. These chains are further connected by N-H⋯O and O-H⋯O hydrogen bonds and π-π inter-actions between the imidazole and benzene rings [centroid-centroid distances = 3.997 (4), 3.829 (4) and 3.573 (4) Å] into a three-dimensional supra-molecular network.
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http://dx.doi.org/10.1107/S1600536811034337 | DOI Listing |
Chem Sci
December 2024
Department of Chemistry and Biochemistry, University of California, San Diego La Jolla California 92093 USA
Metal-organic frameworks (MOFs) can be prepared from oligomeric organic ligands to prepare materials referred to as oligoMOFs. Studies of oligoMOFs are relatively limited, with most existing reports focused on fundamental structure-property relationships. In this report, functional groups, such as terminal alkynes and pyridine groups, are installed on the tether between 1,4-benzene dicarboxylic acid (Hbdc) groups of the dimer ligands.
View Article and Find Full Text PDFChem Asian J
January 2025
Department of Chemistry, Aliah University, New Town, Kolkata, 700 160, India.
Chem Mater
October 2024
Department of Chemistry and Biochemistry, University of California, San Diego, La Jolla, California 92093, United States.
Polymeric linkers used to construct porous, crystalline polymer-metal-organic frameworks (polyMOFs) are predominantly based on macromolecules with metal-coordinating ligand units (e.g., 1,4-benzenedicarboxylic acid, Hbdc) included in the primary polymer backbone.
View Article and Find Full Text PDFLangmuir
October 2024
Key Laboratory of Nuclear Solid-State Physics Hubei Province, School of Physics and Technology, Wuhan University, Wuhan 430072, China.
A series of UiO-66 samples with various amino functional group ratios were prepared by modulating the proportion of terephthalic acid (HBDC) and aminoterephthalic acid (HBDC-NH) ligands, and the microstructure of the samples and dependence of methyl orange (MO) adsorption properties on the amino group content were investigated by X-ray diffraction, scanning electron microscopy, FTIR spectra, nitrogen adsorption, positron annihilation lifetime spectroscopy, and UV-vis spectra. The results showed that as the ratio of amino groups increased, the specific surface area and total porosity of the samples decreased, primarily due to decrement in the crystallinity as well as the bulky effect of amino groups in inherent pores. Interestingly, the amino-functionalized samples possessed considerable adsorption capacity of MO even in alkaline conditions due to the hydrogen bonding between the MO and -NH groups.
View Article and Find Full Text PDFInorg Chem
September 2024
Chemical and Environmental Engineering Group. ESCET, Universidad Rey Juan Carlos. c/Tulipán s/n, Móstoles 28933, Spain.
The catalytic activity and stability of sulfonic-based UiO-66(Zr) materials were tested in the Friedel-Crafts acylation of anisole with acetic anhydride. The materials were prepared using microwave-assisted synthesis, producing microporous materials with remarkable crystallinity and physicochemical features as acid catalysts. Different ratios between both organic ligands, terephthalic acid (HBDC) and monosodium 2-sulfoterephthalic acid (HBDC-SONa), were used for the synthesis to modulate the sulfonic content.
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