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Fig. 11 Crystal structure of a metal-organic framework material Zn 2 (fma) 2 (bipy) prepared by
mechanochemical synthesis, with the structure determined directly from powder XRD data. The
structure is viewed (a) along the c -axis and (b) along the b -axis. The two (identical) interpenetrated
frameworks are indicated by yellow and purple shading . For comparison, (c) and (d) show the
corresponding views of the structure of a DMF solvate material Zn 2 (fma) 2 (bipy)(DMF) 0.5
prepared by a solvothermal route. Although there is some similarity between these structures,
there are nevertheless important structural differences between them
framework material with composition Co(dibenzoylmethanate) 2 (nicotinamide) 2 .
This material was obtained by thermal desolvation of the corresponding acetone
solvate, which was prepared under conditions of liquid-assisted grinding [ 114 ]. The
structure determined from the powder XRD data comprises “wheel-and-axle” units
of composition Co(dibenzoylmethanate) 2 (nicotinamide) 2 , which are assembled
through hydrogen-bonded amide-amide interactions involving the nicotinamide
molecules of neighbouring units, giving rise to antiparallel chains of amide
functionalities in a ladder-type motif. The structure contains tunnels with approxi-
mately hexagonal cross-section running parallel to the direction of the hydrogen-
bonded amide ladders.
Examples of other organic materials prepared by mechanochemical procedures,
for which structure determination has been carried out directly from powder XRD
data, include a hydrate cocrystal of 5-methyl-2-pyridone and trimesic acid, which
was prepared by grinding a methanol solvate cocrystal of the same components
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