Using recently reported robust porphyrinic metal–organic framework (RPM) materials, we have examined the systematic exchange of pillaring linkers/struts as a means of accessing new versions of these materials. Dipyridyl-porphyrin Zn(II) (Zn-dipy) struts were successfully replaced by M2-dipy (M2 = 2H(+), Al(III), Sn(IV)), forming crystalline solid solutions of Zn(Zn1−xMx)-RPM in variable ratios. In addition, post-synthetic metallation was demonstrated using Zn2H-RPM, again with retention of crystallinity. We examined catalytic activity for an epoxide ring-opening reaction with a series of ZnM2-RPMs. The catalytic activity depends strongly on the identity of the metal ion present in the dipyridyl-porphyrin unit.
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Takaishi et al. (2012) studied this question.
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