[2]Rotaxane End‐Capping Synthesis by Click Michael‐Type Addition to the Vinyl Sulfonyl Group

We report the application of the click Michael‐type addition reaction to vinyl sulfone or vinyl sulfonate groups in the synthesis of rotaxanes through the threading‐and‐capping method. This methodology has proven to be efficient and versatile as it allowed the preparation of rotaxanes using template approaches based on different noncovalent interactions (i.e., donor‐acceptor π–π interactions or hydrogen bonding) in yields of generally 60–80 % and up to 91 % aided by the mild conditions required (room temperature or 0 °C and a mild base such as Et3N or 4‐(N,N‐dimethylamino)pyridine (DMAP)). Furthermore, the use of vinyl sulfonate moieties, which are suitable motifs for coupling‐and‐decoupling (CAD) chemistry, implies another advantage because it allows the controlled chemical disassembly of the rotaxanes into their components through nucleophilic substitution of the sulfonates resulting from the capping step with a thiol under mild conditions (Cs2CO3 and room temperature). Another tool in the box! The click Michael‐type addition to vinyl sulfonyl groups emerges as a versatile and efficient tool for the threading‐and‐capping synthesis under mild conditions of rotaxanes based on different noncovalent interactions (see scheme). The disassembly of the interlocked structures is also possible in designs based on vinyl sulfonate moieties.