Abstract
Metal-organic polyhedra (MOPs) are versatile supramolecular building blocks for the design of highly porous frame-works by reticular assembly because of their diverse geometries, multiple degrees of freedom regarding functionaliza-tion, and accessible metal sites. Lipophilic functionalization is demonstrated to enable the rational assembly and crystal-lization with photoactive N-donor ligands in an aliphatic solvent to achieve multiaxially aligned photoresponsive dia-rylethene (DTE) moieties in 3D frameworks (DUT-210(M), M= Cu, Rh) featuring cooperative switchability. Combined experimental and theoretical investigations based on in situ-PXRD, UV/Vis spectroscopy and density functional theory calculations demonstrate deliberate kinetic engineering of photoswitchability based on variations in metal-linker bond strengths. The novel porous frameworks are an important step towards the knowledge-based development of photon driven motors, actuators and release systems.
Supplementary materials
Title
Supporting Information
Description
Materials and Methods, Synthetic procedure, Characterization data; spectroscopic data (1H NMR, IR, UV-Vis); in situ-PXRD and SCXRD refinement details.
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Title
Crystallographic Information Files
Description
Crystallographic Information Files for DUT-209(Cu)
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