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Article Abstract

Planar carbazole based hexaphyrin-like macrocycles with bis-coordinating cores and box-shaped cyclic BODIPYs were synthesized. Solution and solid-state structure analysis of the free macrocycles indicates an inversion of two pyrrole rings, resulting in a two-dipyrrin-like environment. The BF complexes show large Stokes shifts and exhibit excitonic coupling, fine-tuned by the -substituents.

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http://dx.doi.org/10.1039/d1cc04403fDOI Listing

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Planar carbazole based hexaphyrin-like macrocycles with bis-coordinating cores and box-shaped cyclic BODIPYs were synthesized. Solution and solid-state structure analysis of the free macrocycles indicates an inversion of two pyrrole rings, resulting in a two-dipyrrin-like environment. The BF complexes show large Stokes shifts and exhibit excitonic coupling, fine-tuned by the -substituents.

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