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Six-Coordinate Zinc Porphyrins for Template-Directed Synthesis of Spiro-Fused Nanorings

[Image: see text] Five-coordinate geometry is the standard binding mode of zinc porphyrins with pyridine ligands. Here we show that pseudo-octahedral six-coordinate zinc porphyrin complexes can also be formed in solution, by taking advantage of the chelate effect. UV–vis–NIR titrations indicate that...

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Detalles Bibliográficos
Autores principales: Favereau, Ludovic, Cnossen, Arjen, Kelber, Julien B., Gong, Juliane Q., Oetterli, René M., Cremers, Jonathan, Herz, Laura M., Anderson, Harry L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2015
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4686216/
https://www.ncbi.nlm.nih.gov/pubmed/26536147
http://dx.doi.org/10.1021/jacs.5b10126
Descripción
Sumario:[Image: see text] Five-coordinate geometry is the standard binding mode of zinc porphyrins with pyridine ligands. Here we show that pseudo-octahedral six-coordinate zinc porphyrin complexes can also be formed in solution, by taking advantage of the chelate effect. UV–vis–NIR titrations indicate that the strength of this second coordination is ca. 6–8 kJ mol(–1). We have used the formation of six-coordinate zinc porphyrin complexes to achieve the template-directed synthesis of a 3D π-conjugated spiro-fused array of 11 porphyrin units, covalently connected in a nontrivial topology. Time-resolved fluorescence anisotropy experiments show that electronic excitation delocalizes between the two perpendicular nanorings of this spiro-system within the experimental time-resolution of 270 fs.