@article{3025924,
    title = "Cooperative Self-Assembly Enables Two-Dimensional H-type Aggregation of a Sterically Crowded Perylene-Bisimide Dimer",
    author = "Pistolis, G. and Petrakis, V.S. and Kournoutas, F. and Karakostas, N. and Martinou, E. and Efthimiadou, E.K. and Fakis, M. and Mavridis, I.M.",
    journal = "Crystal Growth and Design",
    year = "2019",
    volume = "19",
    number = "8",
    pages = "4252-4263",
    publisher = "American Chemical Society",
    doi = "10.1021/acs.cgd.8b01692",
    keywords = "Aggregates;  Binding energy;  Chlorine compounds;  Crystal structure;  Dimers;  Electronic properties;  Electrostatics;  Fluorescence;  Fluorescence quenching;  Metal ions;  Metals;  Organic solvents;  Polycyclic aromatic hydrocarbons;  Self assembly;  Single crystals;  Supramolecular chemistry, Association constant;  Molecular arrangements;  Self-assembled architectures;  Single crystal x-ray structures;  Spatial arrangements;  Supramolecular assemblies;  Supramolecular interactions;  Two dimensional (2D) arrays, Structural design",
    abstract = "Identifying the role of multiple cooperative supramolecular interactions and the working mechanism underlying the formation of sophisticated, well-defined self-assembled architectures is definitely a challenging and formidable task in understanding the complexity in chemical systems and engineering the properties of advanced materials. The topological design of multifunctional tectons, capable of self-organizing into patterned supramolecular assemblies comprising stacked aromatic molecules, is of particular importance because it can lead to the predictable emergence of controlled functions with tailored electronic properties. Herein, we provide spectroscopic, structural, and mechanistic insights on metal-ion-mediated self-assembly of a charged, amphiphilic perylene-bisimide (PBI) dimer S into two-dimensional (2D) arrays consisting of parallel columnar PBI stacks with a precise spatial arrangement and pattern behavior, using a readily accessible design strategy. The building block (S), a centrosymmetric PBI homodimer bearing a disulfonated trans-stilbene core, was designed to concurrently feature high complexation directionality with a strong binding affinity through multiple supramolecular interactions. In solvents that efficiently solvate PBI, e.g., chloroform, the zinc ion interacts strongly through electrostatic interactions with the negatively charged core of S, and with the πcloud of the stilbene moiety (cation-πinteractions) forming simple 1:1 adducts. In methanol, the findings manifest the efficient formation of well-defined aggregates with H-type excitonic coupling. A single-crystal X-ray structure reveals, despite the sterically crowded bay area of PBIs constituting S, an unprecedented pattern of 2D arrays comprising face-to-face, slipped π-stacked PBI interdimers that pack in parallel columns. This molecular arrangement explains the quenched fluorescence in solution, as well as the appearance of weak excimer-like fluorescence both in solution and crystals. The spectroscopic and structural findings converge to the conclusion that the development of aggregates in solution proceeds by a cooperative growth process driven by a collection of different supramolecular interactions, i.e., electrostatic (core of S), π-πstacking (terminal PBIs), and multiple C-H···π(bay substituents). A corresponding aggregation model fits satisfactorily the experimental data in solution and allows extracting the association constants and spectra of the equilibrated species. © Copyright © 2019 American Chemical Society."
}