Synthesis of a Chiral Crystal Form of MOF-5, CMOF-5, by Chiral Induction

Chiral variants of the prototypal metal-organic framework MOF-5, ∧-CMOF-5 and -CMOF-5, have been synthesized by preparing MOF-5 in the presence of l-proline or d-proline, respectively. CMOF-5 crystallizes in chiral space group P2₁3 instead of Fm3m as exhibited by MOF-5. The phase purity of CMOF-5 was validated by single-crystal and powder X-ray diffraction, infrared spectroscopy, thermogravimetric analysis, N₂ adsorption, microanalysis, and solid-state vibrational circular dichroism. CMOF-5 undergoes a reversible single crystal-to-single crystal phase change to MOF-5 when immersed in a variety of organic solvents, although N-methyl-2-pyrrolidone (NMP) does not induce loss of chirality. Indeed, MOF-5 undergoes chiral induction when immersed in NMP, affording racemic CMOF-5.