In this work, we introduce a novel enantiopure chiral spiro bistriazolate linker molecule (H2-bibta) and the corresponding first enantiopure bistriazolate-based metal–organic framework, CFA-18 (Coordination Framework Augsburg-18).
In comparison to
the vast field of porous materials, research into
hydrogen-bonded organic frameworks (HOFs)and especially the
subclass of metal hydrogen-bonded organic frameworks (M-HOFs), with
only very few structures showing permanent porosity thus faris
still in its infancy. Herein, Kuratowski coordination units, which
are well-known from various complexes and metal–organic frameworks,
were applied to advance this field of research with the synthesis
and characterization of a novel series of M-HOFs. Synthesis of Kuratowski
complexes with the 1H-benzotriazole-5,6-diamine (H-btda) ligand resulted in molecular building blocks, which
initially assemble into CFA-20-Cl and CFA-20-Br M-HOFs ((2,6-lutidinium)+[Zn5X4(btda)6X]−·n(DMF);
X = Cl, Br; CFA-20 = Coordination Framework Augsburg University-20,
DMF = N,N-dimethylformamide). Both
frameworks are isostructurally stabilized via a unique hydrogen bond
framework between 12 amine functional groups of six btda ligands and a central 12-fold hydrogen bonded halogen anion, which
adapts the coordination of an irregular icosahedron. Postsynthetic
ligand exchange at the Kuratowski complex of CFA-20-Cl performed with Tp and Tp* ligands resulted in permanently porous CFA-20-Tp and CFA-20-Tp* M-HOFs ([Zn5Y4(btda)6]; Y = Tp (trispyrazolylborate), Tp*
(tris(3,5-dimethyl-1-pyrazolyl)borate)), which, thus, constitute an
important addition to the meager subclass of permanently porous M-HOFs.
Crystallization of the soluble complex of CFA-20-Tp* from
dimethylsulfoxide (DMSO) was additionally shown to result in a variant CFA-20-Tp*-DMSO M-HOF structure.
The cubic SBU Ni8X6L6 (X=OH-/H2O, L=ligand) is of great interest due to its stability and potential applications when integrated in MOFs. Here, we investigate by detailed DRIFTS measurements and exchange...
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