Porous glasses from metal−organic frameworks (MOFs) represent a new class of functional inorganic−organic materials, which have been proposed for applications ranging from solid electrolytes to radioactive waste storage. So far, just a few zeolitic imidazolate frameworks (ZIFs), a subset of MOFs, have been reported to melt and the structural and compositional requirements for MOF melting and glass formation are poorly understood. Here, we show how the melting point of the prototypical ZIF-4/ZIF-62(M) frameworks (composition M(im) 2−x (bim) x ; M 2+ = Co 2+ , Zn 2+ ; im − = imidazolate; bim − = benzimidazolate) can be controlled systematically by adjusting the molar ratio of the two imidazolate-type linkers im − and bim − . By covering the entire range from x = 0 to 0.35, we unveil a delicate transition from ZIF materials showing sequential amorphization/recrystallization to derivatives exhibiting coherent melting and a liquid phase that is stable over a large temperature window. The melting point of this ZIF system is a direct function of x and can be lowered from ca. 430 °C to only 370 °C, by far the lowest melting point reported for a three-dimensional porous MOF. On the basis of our results, we postulate compositional requirements for ZIF melting and glass formation, which may guide the search for other meltable ZIFs. Moreover, gas physisorption experiments establish that the ZIF glasses adsorb technologically relevant C 3 and C 4 hydrocarbons. Importantly, the adsorption kinetics are much faster for propylene compared to propane and are also dependent on the im − :bim − ratio, thus demonstrating the potential of these ZIF glasses for applications in gas separation.

We report the first microporous cobalt imidazolate glass obtained from a meltable cobalt-based zeolitic imidazolate framework, ZIF-62(Co).

Stimuli-responsive flexible metal-organic frameworks (MOFs) remain at the forefront of porous materials research due to their enormous potential for various technological applications. Here, we introduce the concept of frustrated flexibility in MOFs, which arises from an incompatibility of intra-framework dispersion forces with the geometrical constraints of the inorganic building units. Controlled by appropriate linker functionalization with dispersion energy donating alkoxy groups, this approach results in a series of MOFs exhibiting a new type of guest- and temperature-responsive structural flexibility characterized by reversible loss and recovery of crystalline order under full retention of framework connectivity and topology. The stimuli-dependent phase change of the frustrated MOFs involves non-correlated deformations of their inorganic building unit, as probed by a combination of global and local structure techniques together with computer simulations. Frustrated flexibility may be a common phenomenon in MOF structures, which are commonly regarded as rigid, and thus may be of crucial importance for the performance of these materials in various applications.

<div><div><div><p>Stimuli-responsive flexible metal-organic frameworks (MOFs) remain at the forefront of porous materials research due to their enormous potential for various technological applications. Here, we introduce the concept of frustrated flexibility in MOFs, which arises from an incompatibility of intra-framework dispersion forces with the geometrical constraints of the inorganic building units. Controlled by appropriate linker functionalization with dispersion energy donating alkoxy groups, this approach results in a series of MOFs exhibiting a new type of guest- and temperature-responsive structural flexibility characterized by reversible loss and recovery of crystalline order under full retention of framework connectivity and topology. The stimuli-dependent phase change of the frustrated MOFs involves non-correlated deformations of their inorganic building unit, as probed by a combination of global and local structure techniques together with computer simulations. Frustrated flexibility may be a common phenomenon in MOF structures, which are commonly regarded as rigid, and thus may be of crucial importance for the performance of these materials in various applications.</p></div></div></div>

A series of seven homoleptic CuI complexes based on hetero‐bidentate P^N ligands was synthesized and comprehensively characterized. In order to study structure–property relationships, the type, size, number and configuration of substituents at the phosphinooxazoline (phox) ligands were systematically varied. To this end, a combination of X‐ray diffraction, NMR spectroscopy, steady‐state absorption and emission spectroscopy, time‐resolved emission spectroscopy, quenching experiments and cyclic voltammetry was used to assess the photophysical and electrochemical properties. Furthermore, time‐dependent density functional theory calculations were applied to also analyze the excited state structures and characteristics. Surprisingly, a strong dependency on the chirality of the respective P^N ligand was found, whereas the specific kind and size of the different substituents has only a minor impact on the properties in solution. Most importantly, all complexes except C3 are photostable in solution and show fully reversible redox processes. Sacrificial reductants were applied to demonstrate a successful electron transfer upon light irradiation. These properties render this class of photosensitizers as potential candidates for solar energy conversion issues.