No abstract

Single-crystal-to-single-crystal guest exchanges of large guest molecules [triphenylene (3a), anthracene (3b), perylene (3c), and triphenylphosphine oxide (3d)] were successfully performed in a large channel of a 3D coordination network (2) having a planar ligand, (1). Crystallographic analysis revealed efficient stackings between the planar guests (3a-c) and the ligand. The crystals of the inclusion complexes of 3a-c showed drastic color change because of strong donor-acceptor interactions between the electron-deficient ligand (1) and electron-rich guests (3a-c).

No abstract

Rational engineering and assimilation of diverse chemo‐ and biocatalytic functionalities in a single nanostructure is highly desired for efficient multistep chemical reactions but has so far remained elusive. Here, we design and synthesize multimodal catalytic nanoreactors (MCNRs) based on a mesoporous metal‐organic framework (MOF). The MCNRs consist of customizable metal nanocrystals and stably anchored enzymes in the mesopores, as well as coordinatively unsaturated cationic metal MOF nodes, all within a single nanoreactor space. The highly intimate and diverse catalytic mesoporous microenvironments and facile accessibility to the active site in the MCNR enables the cooperative and synergistic participation from different chemo‐ and biocatalytic components. This was shown by one‐pot multistep cascade reactions involving a heterogeneous catalytic nitroaldol reaction followed by a [Pd/lipase]‐catalyzed chemoenzymatic dynamic kinetic resolution to yield optically pure (>99 % ee) nitroalcohol derivatives in quantitative yields.