Accurate control of the layer number of orderly stacked 2D polymers has been an unsettled challenge in selfassembly.H erein we describe the fabrication of ab ilayer 2D supramolecular organic framework from am onolayer 2D supramolecular organic framework in water by utilizing the cooperative coordination of ar od-like bipyridine ligands to zinc porphyrin subunits of the monolayer network. The monolayer supramolecular framework is prepared from the co-assembly of an octacationic zinc porphyrin monomer and cucurbit[8]uril (CB[8]) in water through CB[8]-encapsulation-promoted dimerization of 4-phenylpyridiunium subunits that the zinc porphyrin monomer bear.T he bilayer 2D supramolecular organic framework exhibits structural regularity in both solution and the solid state,which is characterized by synchrotron small-angle X-ray scattering and high-resolution transmission electron microscopic techniques.A tomic force microscopic imaging confirms that the bilayer character of the 2D supramolecular organic framework can be realized selectively on the micrometer scale.

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Accurate control of the layer number of orderly stacked 2D polymers has been an unsettled challenge in self‐assembly. Herein we describe the fabrication of a bilayer 2D supramolecular organic framework from a monolayer 2D supramolecular organic framework in water by utilizing the cooperative coordination of a rod‐like bipyridine ligands to zinc porphyrin subunits of the monolayer network. The monolayer supramolecular framework is prepared from the co‐assembly of an octacationic zinc porphyrin monomer and cucurbit[8]uril (CB[8]) in water through CB[8]‐encapsulation‐promoted dimerization of 4‐phenylpyridiunium subunits that the zinc porphyrin monomer bear. The bilayer 2D supramolecular organic framework exhibits structural regularity in both solution and the solid state, which is characterized by synchrotron small‐angle X‐ray scattering and high‐resolution transmission electron microscopic techniques. Atomic force microscopic imaging confirms that the bilayer character of the 2D supramolecular organic framework can be realized selectively on the micrometer scale.

Different supramolecular self‐assembly between 1‐dodecyl‐3‐carboxymethylbenzotriazole (Lc12), 1‐octyl‐3‐carboxymethylbenzotriazole (Lc8) and 1‐butyl‐3‐carboxymethylbenzotriazole (Lc4) in the solid state and in aqueous solution has been investigated. For Lc12@CB[8] system, 1 : 1 host‐guest complexes were formed in aqueous solution and 2 : 2 host‐guest complexes were formed in the solid state, and the dodecyl chains adopted contorted conformations when bound to CB[8] molecules. For Lc8@CB[8] system, 1 : 1 host‐guest complexes were formed both in aqueous solution and in solid state, and the alkyl chain and benzotriazole moiety of guest Lc8 were both squeezed into the cavity of the CB[8]. The Lc4@CB[8] system was similar to Lc8@CB[8], 1 : 1 host‐guest complexes were formed in aqueous solution, the alkyl chain and benzotriazole moiety of guest Lc4 were encapsulated into the cavity of the CB[8]. Isothermal titrations in water afforded high apparent association constants for complexes Lc12@CB[8], Lc8@CB[8]and Lc4@CB[8].