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Reaction of the chloranilate dianion with Y(NO3)3 in the presence of Et4N+ in the appropriate proportions results in the formation of (Et4N)[Y(can)2], which consists of anionic square‐grid coordination polymer sheets with interleaved layers of counter‐cations. These counter‐cations, which serve as squat pillars between [Y(can)2] sheets, lead to alignment of the square grid sheets and the subsequent generation of square channels running perpendicular to the sheets. The crystals are found to be porous and retain crystallinity following cycles of adsorption and desorption. This compound exhibits a high affinity for volatile guest molecules, which could be identified within the framework by crystallographic methods. In situ neutron powder diffraction indicates a size‐shape complementarity leading to a strong interaction between host and guest for CO2 and CH4. Single‐crystal X‐ray diffraction experiments indicate significant interactions between the host framework and discrete I2 or Br2 molecules. A series of isostructural compounds (cat)[MIII(X‐an)2] with M=Sc, Gd, Tb, Dy, Ho, Er, Yb, Lu, Bi or In, cat=Et4N, Me4N and X‐an=chloranilate, bromanilate or cyanochloranilate bridging ligands have been generated. The magnetic properties of representative examples (Et4N)[Gd(can)2] and (Et4N)[Dy(can)2] are reported with normal DC susceptibility but unusual AC susceptibility data noted for (Et4N)[Gd(can)2]. An extensive family of square grid anionic coordination polymers is formed by the combination of 8‐coordinate trivalent metal ions with bridging chloranilate ligands. Alignment of the square grid networks produces channels that are able to accommodate a variety species. The location of guest molecules within the channels has been determined using both X‐ray and neutron diffraction. [ABSTRACT FROM AUTHOR]

The need for effective CO2 capture systems remains high, and due to their tunability, metallosupramolecular architectures are an attractive option for gas sorption. While the use of extended metal organic frameworks for gas adsorption has been extensively explored, the exploitation of discrete metallocage architectures to bind gases remains in its infancy. Herein the solid state gas adsorption properties of a series of [Pd2( L)4]4+ lantern shaped coordination cages ( L = variants of 2,6-bis(pyridin-3-ylethynyl)pyridine), which had solvent accessible internal cavities suitable for gas binding, have been investigated. The cages showed little interaction with dinitrogen gas but were able to take up CO2. The best performing cage reversibly sorbed 1.4 mol CO2 per mol cage at 298 K, and 2.3 mol CO2 per mol cage at 258 K (1 bar). The enthalpy of binding was calculated to be 25-35 kJ mol−1, across the number of equivalents bound, while DFT calculations on the CO2 binding in the cage gave Δ E for the cage-CO2 interaction of 23-28 kJ mol−1, across the same range. DFT modelling suggested that the binding mode is a hydrogen bond between the carbonyl oxygen of CO2 and the internally directed hydrogen atoms of the cage. [ABSTRACT FROM AUTHOR]

Caging carbon dioxide: Self ‐ assembled discrete palladium(II) [Pd2(L)4]4+ cages with 2,6 ‐ bis(pyridin ‐ 3 ‐ ylethynyl)pyridine) ligands (L) have cavities, which bind guests containing carbonyl groups through hydrogen bonding interactions. In the solid state these cages have now been shown to bind up to four CO2 molecules, with selectivity over N2. Long ‐ range order in the packing of the molecules in powdered samples of the compound does not appear to be necessary for their activity, making their preparation easy. Additionally, the cages can be readily functionalized, opening up avenues for selective guest binding and gas separations. More information can be found in the Full Paper by B. F. Abrahams, J. D. Crowley et al. on page 10559. [ABSTRACT FROM AUTHOR]