Mechanical-Bond-Protected, Air-Stable Radicals

Radical templation centered around a hetero­trisradical tricationic inclusion complex <b>DB</b>^•+⊂​<b>DAPQT</b>^2(•+), assembled from an equimolar mixture of a disubstituted 4,4′-bipyridinium radical cation (<b>DB</b>^•+) and an asymmetric cyclophane bisradical dication (<b>DAPQT</b>^2(•+)), affords a symmetric [2]­catenane (<b>SC</b>·7PF₆) and an asymmetric [2]­catenane (<b>AC</b>·7PF₆) on reaction of the 1:1 complex with diazapyrene and bipyridine, respectively. Both these highly charged [2]­catenanes have been isolated as air-stable monoradicals and characterized by EPR spectroscopy. X-ray crystallography suggests that the unpaired electrons are delocalized in each case across two inner 4,4′-bipyridinium (BIPY²⁺) units forming a mixed-valence (BIPY₂)^•3+ state inside both [2]­catenanes, an observation which is in good agreement with spin-density calculations using density functional theory. Electrochemical studies indicate that by replacing the BIPY²⁺ units in homo[2]­catenane <b>HC</b>^•7+composed of two mechanically interlocked cyclobis­(paraquat-<i>p</i>-phenylene) ringswith “zero”, one, and two more highly conjugated diazapyrenium dication (DAP²⁺) units, respectively, a consecutive series of five, six, and seven redox states can be accessed in the resulting <b>SC</b>·7PF₆ (0, 4+, 6+, 7+, and 8+), <b>HC</b>·7PF₆ (0, 2+, 4+, 6+, 7+, and 8+), and <b>AC</b>·7PF₆ (0, 1+, 2+, 4+, 6+, 7+, and 8+), respectively. These unique [2]­catenanes present a promising prototype for the fabrication of high-density data memories