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Дата последнего поиска статьи во внешних источниках: 17 октября 2017 г.
Аннотация:A new cationic molecular turnstile based on a P(V) porphyrin backbone bearing two pyridyl interaction sites, one at the meso position of the porphyrin and the other on the handle connected to the porphyrin through P-O bonds, was designed and synthesized. The dynamic behavior of the turnstile 2, investigated by 1D and 2D H-1 NMR techniques, showed that in the absence of an effector, the turnstile is in its open state and undergoes a free rotation of the rotor (the handle) around the stator (the porphyrin backbone). In the presence of an external effector such as Ag+ cation or H+, the turnstile is switched to its closed states 2-Ag+ and 2-H+, respectively. The locking/unlocking process is reversible and may be achieved by precipitation of AgBr upon addition of Et4NBr in the case of the silver-locked turnstile or by addition of Et3N in the case of the proton-locked turnstile.