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Terpyridine–Porphyrin Hetero‐Pacman Compounds
Authors:Dr Matthias Schwalbe  Ramona Metzinger  Thomas S Teets  Prof Dr Daniel G Nocera
Institution:1. Institut für Chemie, Humboldt‐Universit?t zu Berlin, Brook‐Taylor‐St. 2, 12489 Berlin (Germany), Fax: (+49)?30‐2093‐6966;2. Department of Chemistry, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, MA 02139‐4307 (USA)
Abstract:The two different coordination spheres afforded by Pacman architectures offer cooperativity derived from two different metal centers. A modular strategy is developed to produce a hetero‐Pacman scaffold featuring a porphyrin and terpyridine for metal‐ion binding. A double Suzuki reaction was employed to first attach a terpyridine moiety to a xanthene backbone and then attach a porphyrin. The new hetero‐Pacman scaffold has been characterized and all building blocks have been isolated and structurally characterized. The principle objective to incorporate different metal centers was confirmed by isolating a trinuclear complex comprising two porphyrinic units and a bis(terpyridine)–iron unit. The compounds described herein expand the Pacman scaffold concept by allowing for the incorporation of a terpyridine–metal complex proximate to a porphyrin‐cofactor active site for small‐molecule activation.
Keywords:carbon–  carbon coupling  coordination modes  iron  Pacman  porphyrinoids  terpyridines
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