Control over catenation in a pillared paddlewheel metal–organic framework was achieved via solvent-assisted linker exchange. The linker exchange was demonstrated on the noncatenated structure of DO-MOF, by using 4,4′-bipyridine ( L4 ) and 4,4′-azobis(pyridine) ( L5 ) as linkers, leading to noncatenated materials SALEM-3 and SALEM-4 . The de novo synthesized analogues of SALEM-3 and SALEM-4 can only be obtained as 2-fold interpenetrated frameworks. The reaction progress of the linker exchange was monitored by NMR spectroscopy, and structure and framework catenation were characterized by powder X-ray diffraction and thermogravimetric methods.
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Bury et al. (2013) studied this question.
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