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).

Metal-organic framework (MOF) glasses are a new class of glass materials with immense potential for applications ranging from gas separation to optics and solid electrolytes. Due to the inherent difficulty to determine the atomistic structure of amorphous glasses, the intrinsic structural porosity of MOF glasses is only poorly understood. Here, we investigate the porosity features (pore size and pore limiting diameter) of a series of prototypical MOF glass formers from the family of zeolitic imidazolate frameworks (ZIFs) and their corresponding glasses. CO2 sorption at 195 K allows quantifying the microporosity of these materials in their crystalline and glassy states, also providing excess to the micropore volume and the apparent density of the ZIF glasses. Additional hydrocarbon sorption data together with X-ray total scattering experiments prove that the porosity features of the ZIF glasses depend on the types of organic linkers. This allows formulating design principles for a targeted tuning of the intrinsic microporosity of MOF glasses. These principles are counterintuitive and contrary to those established for crystalline MOFs but show similarities to strategies previously developed for porous polymers.

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.

Metal-organic framework (MOF) glasses are a new class of microporous glass materials with immense potential for applications ranging from gas separation to optics and solid electrolytes. Due to the inherent difficulty to determine the atomistic structure of amorphous glasses, the intrinsic structural porosity of MOF glasses is only poorly understood. In this work, the porosity features of a series of prototypical MOF glass formers from the family of zeolitic imidazolate frameworks (ZIFs) and their corresponding glasses is investigated comprehensively. CO2 gas sorption at 195 K allows to follow the evolution of microporosity when transforming from the crystalline to the glassy state of these materials. Based on these data, the pore volume and the real density of the ZIF glasses is quantified for the first time. Additional hydrocarbon sorption data (n-butane, propane and propylene) together with X-ray total scattering experiments prove that the porosity features (in particular the pore size and the pore limiting diameter) of the ZIF glasses depend on the types of organic linkers present in the glass network. This allows formulating first design principles for a targeted tuning of the intrinsic microporosity of MOF glasses. Importantly, these principles are counterintuitive and contrary to established porosity design concepts for crystalline MOFs but show similarities to strategies previously developed for porous polymers.