Tetra‐armed cyclen (1) bearing two 4‐(4′‐pyridyl)benzyl and two 3,5‐difluorobenzyl groups and its Ag+ complexes were prepared and structurally characterized. The complexes formed between 1 and Ag+ undergoes a reversible structural transformation between a 2:2 dimeric complex and a 3:5 pentacyclic trefoil complex with changes in the Ag+/1 molar ratio. It was also revealed that the 3:5 trefoil complex could encapsulate benzene and [D6]benzene selectively in solid‐state. The benzene‐included structures are stabilized by C−H⋅⋅⋅F−C interactions between the benzene molecule and the ligand molecule.

A tetra-armed cyclen (L) with two substituted 3,5-difluorobenzyl and two substituted pyridine-4-yl methyl groups at the 1,4- and 7,10-positions of the cyclen ring as side arms was synthesized. When L was reacted with 1 equiv of the silver­(I), ­di­metallo­[3.3]­para­cyclophane-like 2:2 cyclic dimer, [Ag2(L)2]­(PF6)2, was obtained. The reaction of L with 2 equiv of silver­(I) gave a 3:6 cyclic trimer, [Ag6(L)3(CH3CN)3]­(OTf)6·3CH3CN. Furthermore, reversible complexation between the 2:2 cyclic dimer and 3:6 cyclic trimer was confirmed by 1H NMR and the CSI mass in the addition of silver­(I) or the [2.2.2]­cryptand.

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Tetra‐armed cyclen (1) bearing two 4‐(4′‐pyridyl)benzyl and two 3,5‐difluorobenzyl groups and its Ag+ complexes were prepared and structurally characterized. The complexes formed between 1 and Ag+ undergoes a reversible structural transformation between a 2:2 dimeric complex and a 3:5 pentacyclic trefoil complex with changes in the Ag+/1 molar ratio. It was also revealed that the 3:5 trefoil complex could encapsulate benzene and [D6]benzene selectively in solid‐state. The benzene‐included structures are stabilized by C−H⋅⋅⋅F−C interactions between the benzene molecule and the ligand molecule.