The
modulator 2-fluorobenzoic acid (2-fba) is widely used to prepare
RE clusters in metal–organic frameworks (MOFs). In contrast
to known RE MOF structures containing hydroxide bridging groups, we
report for the first time the possible presence of fluoro bridging
groups in RE MOFs. In this report we discuss the synthesis of a holmium-UiO-66
analogue as well as a novel holmium MOF, where evidence of fluorinated
clusters is observed. The mechanism of fluorine extraction from 2-fba
is discussed as well as the implications that these results have for
previously reported RE MOF structures.
There is growing interest in Holmium carriers for radiotherapeutic applications. In this work, a holmium-based metal-organic framework (MOF) using the 4,4′-biphenyldicarboxylic acid (H2BPDC) linker was synthesized and characterized to explore its potential as a radiotherapeutic
carrier. The 3D MOF [Ho(BPDC)2]·(CH3)2NH2 was characterized by single crystal X-ray diffraction, FTIR, TGA and PXRD. A challenge to overcome in lanthanide-based MOFs is the deformation or collapse of the framework that can occur after evacuation
of the pores. This structure displays high thermal stability and no collapse was observed when the molecules confined in the pores were removed. The coordination around the holmium center (CN = 8) is the key to this stability since only the organic linker and no solvent molecules coordinate
to the metallic center. The porosity of the material was confirmed by high-pressure carbon dioxide (CO2) adsorption–desorption analysis. The stability of the MOF, its holmium content (28 wt%) and its porosity are features that make this material a potential holmium carrier
for radiotherapeutic applications.
A novel
copper(II) metal–organic framework (MOF) has been
synthesized by modifying the reaction conditions of a 1D coordination
polymer. The 1D polymer is built by the coordination between copper
and 2,2′-(1H-imidazole-4,5-diyl)di-1,4,5,6-tetrahydropyrimidine
(H-L1). The geometry of H-L1 precludes its ability to form extended
3D framework structures. By adding 1,4-benzenedicarboxylic acid (H2BDC), a well-studied linker in MOF synthesis, we achieved
the transition from a 1D polymer chain into porous 2D layered structures.
Hydrogen bonding between L1 and BDC directs the parallel stacking
of these layers, resulting in a 3D structure with one-dimensional
channels accessible by two different pore windows. The preferred growth
orientation of the crystal produces prolonged channels and a disparity
in pore size distribution. This in turn results in slow diffusion
processes in the material. Furthermore, an isoreticular MOF was prepared
by substituting the BDC linker by 2,6-naphthalenedicarboxylic acid
(H2NDC).
Four new isostructural 3d-4f mixed metal organic frameworks (MOFs) Cu Gd2 (BDC)4, compound 1, Cu Ho2 (BDC)4, compound 2, Cu Eu2 (BDC)4, compound 3, and Cu Dy2 (BDC)4, compound 4 were successfully synthesized. The structure, stability, and magnetic properties were analyzed. Each MOF has two lanthanide ions and one copper ion node with terephthalic acid as the organic linker. The lanthanide ions form a dimer with each having a capped trigonal prismatic geometry while the copper ion has a square planar geometry. Each of these MOFs shows varying degrees of antiferromagnetic interactions.
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