Dictating Packing and Interactions of Perylene Bisimides within Cyclophane Structures in the Solid State

Author:

Solymosi Iris1ORCID,Neiß Christian2,Maid Harald1,Hampel Frank1,Solymosi Thomas3,Görling Andreas2,Hirsch Andreas1,Pérez‐Ojeda M. Eugenia1ORCID

Affiliation:

1. Department of Chemistry and Pharmacy Friedrich-Alexander-University Erlangen-Nürnberg Nikolaus-Fiebiger-Straße 10 91058 Erlangen Germany

2. Department of Chemistry and Pharmacy Friedrich-Alexander-University Erlangen-Nürnberg Egerlandstraße 3 91058 Erlangen Germany

3. Helmholtz-Institute Erlangen-Nürnberg for Renewable Energy Forschungszentrum Jülich Cauerstraße 1 91058 Erlangen Germany

Abstract

AbstractCrystal packing and chromophore communication are key parameters for the performance and functionality of many applications related to light‐energy harvesting and conversion. However, obtaining crystals of flexible and very soluble structures is troublesome. Nevertheless, a crystal structure of a highly flexible perylene‐3,4 : 9,10‐tetracarboxylic acid bisimide (PBI) cyclophane was obtained and analysed to compare the chromophore arrangement in the solid state with theconfiguration in solution as well as with calculated structures. The crystal structure exhibits an intra‐ and intermolecular slip‐stack arrangement of the heterochiral PBI units, forming a unique one‐dimensional π‐stacking supramolecular polymer‐like structure. These findings emphasize that the unique solid‐state arrangement of the chromophores cannot be easily predicted by elaborate studies in solution or by theoretical calculations. Furthermore, it features the importance of controlling the crystal packing to enable specific applications based on multiexciton generation processes where the spatial dependence and relative orientation of the chromophores are decisive parameters.

Publisher

Wiley

Subject

General Chemistry

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