Isostructural Atomically Dispersed Rhodium Catalysts Supported on SAPO-37 and on HY Zeolite.

Zeolites are widely applied supports for metal catalysts, but molecular sieves with comparable structures-silicoaluminophosphates (SAPOs)-have drawn much less attention and been overlooked as supports for atomically dispersed metals. Now, we report SAPO-37 as a support for atomically dispersed rhodium in rhodium diethylene complexes, made by the reaction of Rh(η-CH)(acetylacetonate) with the support and anchored by two Rh-O bonds at framework tetrahedral sites, as shown by infrared and extended X-ray absorption fine structure spectra. The ethylene ligands were readily replaced with CO, giving sharp ν bands indicating highly uniform supported species.

Thermochemical evidence for strong iodine chemisorption by ZIF-8.

For the first time, using aqueous solution calorimetry, we clearly identify the chemisorption of an unusually strong iodine charge-transfer (CT) complex within the cages of a metal-organic framework. Specifically, we studied the sorption of iodine gas in zeolitic imidazolate framework-8 (ZIF-8, Zn(2-methylimidazolate)2). Two iodine-loaded ZIF-8 samples were examined.

Thermochemistry of paddle wheel MOFs: Cu-HKUST-1 and Zn-HKUST-1.

Metal-organic framework (MOF) porosity relies upon robust metal-organic bonds to retain structural rigidity upon solvent removal. Both the as-synthesized and activated Cu and Zn polymorphs of HKUST-1 were studied by room temperature acid solution calorimetry. Their enthalpies of formation from dense assemblages (metal oxide (ZnO or CuO), trimesic acid (TMA), and N,N-dimethylformamide (DMF)) were calculated from the calorimetric data.

Thermochemistry of zeolitic imidazolate frameworks of varying porosity.

The first thermochemical analysis by room-temperature aqueous solution calorimetry of a series of zeolite imidazolate frameworks (ZIFs) has been completed. The enthalpies of formation of the evacuated ZIFs-ZIF-zni, ZIF-1, ZIF-4, CoZIF-4, ZIF-7, and ZIF-8-along with as-synthesized ZIF-4 (ZIF-4·DMF) and ball-milling amorphized ZIF-4 (a(m)ZIF-4) were measured with respect to dense components: metal oxide (ZnO or CoO), the corresponding imidazole linker, and N,N dimethylformamide (DMF) in the case of ZIF-4·DMF. Enthalpies of formation of ZIFs from these components at 298 K are exothermic, but the ZIFs are metastable energetically with respect to hypothetical dense components in which zinc is bonded to nitrogen rather than oxygen.

MOF-5: enthalpy of formation and energy landscape of porous materials.

The first experimental thermodynamic analysis of a metal-organic framework (MOF) has been performed. Measurement of the enthalpy of formation of MOF-5 from the dense components zinc oxide (ZnO), 1,4-benzenedicarboxylic acid (H(2)BDC), and occluded N,N-diethylformamide (DEF) (if any) gave values of 78.64 ± 2.