Amandine Cadiau

A metal-organic framework–based splitter for separating propylene from propane

Separating one organic from another Separating closely related organic molecules is a challenge (see the Perspective by Lin).The separation of acetylene from ethylene is needed in high-purity polymer production. Cui et al. developed a copper-based metal-organic framework with hexafluorosilicate and organic linkers designed to have a high affinity for acetylene. These materials, which capture four acetylene molecules in each pore, successfully separated acetylene from mixtures with ethylene. Propane and propylene are both important feedstock chemicals. Their physical and chemical similarity, however, requires energy-intense processes to separate them. Cadiau et al. designed a fluorinated porous metal-organic framework material that selectively adsorbed propylene, with the complete exclusion of propane. Science, this issue pp. 141 and 137; see also p. 121 A tailored metal-organic framework material is able to separate propane from propylene. The chemical industry is dependent on the olefin/paraffin separation, which is mainly accomplished by using energy-intensive processes. We report the use of reticular chemistry for the fabrication of a chemically stable fluorinated metal-organic framework (MOF) material (NbOFFIVE-1-Ni, also referred to as KAUST-7). The bridging of Ni(II)-pyrazine square-grid layers with (NbOF5)2– pillars afforded the construction of a three-dimensional MOF, enclosing a periodic array of fluoride anions in contracted square-shaped channels. The judiciously selected bulkier (NbOF5)2– caused the looked-for hindrance of the previously free-rotating pyrazine moieties, delimiting the pore system and dictating the pore aperture size and its maximum opening. The restricted MOF window resulted in the selective molecular exclusion of propane from propylene at atmospheric pressure, as evidenced through multiple cyclic mixed-gas adsorption and calorimetric studies.

A Fine-Tuned Fluorinated MOF Addresses the Needs for Trace CO2 Removal and Air Capture Using Physisorption

The development of functional solid-state materials for carbon capture at low carbon dioxide (CO2) concentrations, namely, from confined spaces (<0.5%) and in particular from air (400 ppm), is of prime importance with respect to energy and environment sustainability. Herein, we report the deliberate construction of a hydrolytically stable fluorinated metal-organic framework (MOF), NbOFFIVE-1-Ni, with the appropriate pore system (size, shape, and functionality), ideal for the effective and energy-efficient removal of trace carbon dioxide. Markedly, the CO2-selective NbOFFIVE-1-Ni exhibits the highest CO2 gravimetric and volumetric uptake (ca. 1.3 mmol/g and 51.4 cm(3) (STP) cm(-3)) for a physical adsorbent at 400 ppm of CO2 and 298 K. Practically, NbOFFIVE-1-Ni offers the complete CO2 desorption at 328 K under vacuum with an associated moderate energy input of 54 kJ/mol, typical for the full CO2 desorption in conventional physical adsorbents but considerably lower than chemical sorbents. Noticeably, the contracted square-like channels, affording the close proximity of the fluorine centers, permitted the enhancement of the CO2-framework interactions and subsequently the attainment of an unprecedented CO2 selectivity at very low CO2 concentrations. The precise localization of the adsorbed CO2 at the vicinity of the periodically aligned fluorine centers, promoting the selective adsorption of CO2, is evidenced by the single-crystal X-ray diffraction study on NbOFFIVE-1-Ni hosting CO2 molecules. Cyclic CO2/N2 mixed-gas column breakthrough experiments under dry and humid conditions corroborate the excellent CO2 selectivity under practical carbon capture conditions. Pertinently, the notable hydrolytic stability positions NbOFFIVE-1-Ni as the new benchmark adsorbent for direct air capture and CO2 removal from confined spaces.

Design of Hydrophilic Metal Organic Framework Water Adsorbents for Heat Reallocation

A new hydrothermally stable Al polycarboxylate metal-organic framework (MOF) based on a heteroatom bio-derived aromatic spacer is designed through a template-free green synthesis process. It appears that in some test conditions this MOF outperforms the heat reallocation performances of commercial SAPO-34.

Hydrolytically stable fluorinated metal-organic frameworks for energy-efficient dehydration

Drying natural gas efficiently Natural gas must be purified before it can be transported. The preparation process also includes a drying step to remove water. Microporous adsorbents such as zeolites are used for this purpose, but they often need to be heated to temperatures up to 250°C to remove the water so that they can be reused. Cadiau et al. describe a fluorinated metal-organic framework containing nickel metal centers that can remove water from gas streams but that can be regenerated by heating to only 105°C. Science, this issue p. 731 A microporous material preferentially adsorbs water over the other components in natural gas and can release it at 105°C. Natural gas must be dehydrated before it can be transported and used, but conventional drying agents such as activated alumina or inorganic molecular sieves require an energy-intensive desiccant-regeneration step. We report a hydrolytically stable fluorinated metal-organic framework, AlFFIVE-1-Ni (KAUST-8), with a periodic array of open metal coordination sites and fluorine moieties within the contracted square-shaped one-dimensional channel. This material selectively removed water vapor from gas streams containing CO2, N2, CH4, and higher hydrocarbons typical of natural gas, as well as selectively removed both H2O and CO2 in N2-containing streams. The complete desorption of the adsorbed water molecules contained by the AlFFIVE-1-Ni sorbent requires relatively moderate temperature (~105°C) and about half the energy input for commonly used desiccants.

CO2 conversion: the potential of porous-organic polymers (POPs) for catalytic CO2–epoxide insertion

Novel porous organic polymers (POPs) have been synthesized using functionalized Cr and Co–salen complexes as molecular building blocks. The integration of metalosalen catalysts into the porous polymer backbone permits the successful utilization of the resultant functionalized material as a solid-state catalyst for CO2–epoxide cycloaddition reactions with excellent catalytic performance under mild conditions of temperature and pressure. The catalysts proved to be fully recyclable and robust, thus showing the potential of POPs as smart functional materials for the heterogenization of key catalytic elements.

SMARTER crystallography of the fluorinated inorganic-organic compound Zn3Al2F12 center dot[HAmTAZ](6)

We present in this paper the structure resolution of a fluorinated inorganic-organic compound--Zn(3)Al(2)F(12)·[HAmTAZ](6)--by SMARTER crystallography, i.e. by combining powder X-ray diffraction crystallography, NMR crystallography and chemical modelling of crystal (structure optimization and NMR parameter calculations). Such an approach is of particular interest for this class of fluorinated inorganic-organic compound materials since all the atoms have NMR accessible isotopes ((1)H, (13)C, (15)N, (19)F, (27)Al, (67)Zn). In Zn(3)Al(2)F(12)·[HAmTAZ](6), (27)Al and high-field (19)F and (67)Zn NMR give access to the inorganic framework while (1)H, (13)C and (15)N NMR yield insights into the organic linkers. From these NMR experiments, parts of the integrant unit are determined and used as input data for the search of a structural model from the powder diffraction data. The optimization of the atomic positions and the calculations of NMR parameters ((27)Al and (67)Zn quadrupolar parameters and (19)F, (1)H, (13)C and (15)N isotropic chemical shifts) are then performed using a density functional theory (DFT) based code. The good agreement between experimental and DFT-calculated NMR parameters validates the proposed optimized structure. The example of Zn(3)Al(2)F(12)·[HAmTAZ](6) shows that structural models can be obtained in fluorinated hybrids by SMARTER crystallography on a polycrystalline powder with an accuracy similar to those obtained from single-crystal X-ray diffraction data.

ZnAlF5·[TAZ]: an Al fluorinated MOF of MIL-53(Al) topology with cationic {Zn(1,2,4 triazole)}2+ linkers

ZnAlF5·[TAZ], the first aluminium fluorinated metal–organic framework with cationic {Zn(1,2,4 triazole)}2+ linkers has been synthesized. The structure is accurately determined by coupling direct space methods on laboratory powder X-ray diffraction data with solid-state nuclear magnetic resonance experiments and ab initio calculations, and is found to be analogous to that of MIL-53(Al).

Valuing Metal–Organic Frameworks for Postcombustion Carbon Capture: A Benchmark Study for Evaluating Physical Adsorbents

The development of practical solutions for the energy-efficient capture of carbon dioxide is of prime importance and continues to attract intensive research interest. Conceivably, the implementation of adsorption-based processes using different cycling modes, e.g., pressure-swing adsorption or temperature-swing adsorption, offers great prospects to address this challenge. Practically, the successful deployment of practical adsorption-based technologies depends on the development of made-to-order adsorbents expressing mutually two compulsory requisites: i) high selectivity/affinity for CO2 and ii) excellent chemical stability in the presence of impurities. This study presents a new comprehensive experimental protocol apposite for assessing the prospects of a given physical adsorbent for carbon capture under flue gas stream conditions. The protocol permits: i) the baseline performance of commercial adsorbents such as zeolite 13X, activated carbon versus liquid amine scrubbing to be ascertained, and ii) a standardized evaluation of the best reported metal-organic framework (MOF) materials for carbon dioxide capture from flue gas to be undertaken. This extensive study corroborates the exceptional CO2 capture performance of the recently isolated second-generation fluorinated MOF material, NbOFFIVE-1-Ni, concomitant with an impressive chemical stability and a low energy for regeneration. Essentially, the NbOFFIVE-1-Ni adsorbent presents the best compromise by satisfying all the required metrics for efficient CO2 scrubbing.

Hydrothermal synthesis, ab-initio structure determination and NMR study of the first mixed Cu-Al fluorinated MOF

Herein, the first fluorinated heterometallic metal–organic framework (MOF) containing both Cu(II) and Al(III) cations is presented. CuAlF4.5(OH)0.5(H2O)[HAmTAZ]2 (HAmTAZ = 3-amino-1,2,4-triazole) was hydrothermally synthesized. The structure of this paramagnetic compound was solved using the SDPD method (structural determination by powder diffractometry) and confirmed by 1H, 19F and 27Al solid-state nuclear magnetic resonance (NMR) experiments. The structure (space group Ima2, a = 16.306(3) A, b = 8.9356(3) A, c = 8.2884(2) A) can be described from the Cu–HAmTAZ layers connected by AlF5H2O octahedra, generating a three-dimensional network with a pcu topology. This compound illustrates that from 2D MOFs within the M(HTAZ)2(NCS)2 (M = Mn, Fe, Co, Ni, Cu, Zn) system, insertion of AlF5H2O octahedra building units between the Cu–HAmTAZ layers provides a way to generate 3D F-MOFs.

Fabrication and non-covalent modification of highly oriented thin films of a zeolite-like metal–organic framework (ZMOF) with rho topology

Here we report the fabrication of the first thin film of a zeolite-like metal–organic framework (ZMOF) with rho topology (rho-ZMOF-1, ([In48(HImDC)96]48−)n) in a highly oriented fashion on a gold-functionalized substrate. The oriented rho-ZMOF-1 film was functionalized by non-covalent modification via post-synthetic exchange of different probe molecules, such as acridine yellow, methylene blue, and Nile red. In addition, encapsulation of a porphyrin moiety was achieved via in situ synthesis and construction of the rho-ZMOF. Adsorption kinetics of volatile organic compounds on rho-ZMOF-1 thin films was also investigated. This study suggests that rho-ZMOF-1 thin films can be regarded as a promising platform for various applications such as sensing and catalysis.