# Multidirectional Charge Separation in Self‐Assembled Aggregates of Perylenebisimide‐Porphyrin Bola‐Supra‐Amphiphiles

**Authors:** Erik J. Schulze, Elena A. Mack, Christian L. Ritterhoff, Ufuk Borucu, Bernd Meyer, Dirk M. Guldi, Andreas Hirsch

PMC · DOI: 10.1002/anie.202523324 · Angewandte Chemie (International Ed. in English) · 2026-01-05

## TL;DR

Scientists created self-assembling structures from porphyrin and perylenebisimide molecules that can transfer charges in multiple directions.

## Contribution

A new bola-type supra-amphiphile is synthesized and shown to enable multidirectional charge separation in self-assembled aggregates.

## Key findings

- The aggregates exhibit spherical morphology with sizes between 15–100 nm.
- Fluorescence quenching in the aggregates is due to multidirectional charge separation.
- Denaturation of the aggregates restores PBI fluorescence and stops charge separation.

## Abstract

We report on the synthesis of a hydrogen‐bond mediated bola‐type supra‐amphiphile and assembly thereof in water. The assembly is based on amphiphilic porphyrins and hydrophobic perylenebisimdes (PBI), which both form the resulting bola‐form solely through the H‐bonding motif, which is shielded by the assembly of the chromophores itself. The amphiphilic porphyrin was functionalized, on one hand, with a cyanuric acid and, on the other hand, with an oligo carboxylate dendron as polar head group. Two Hamilton receptors were linked to the PBI on each imide position. Assembly was achieved by lyophilizing solutions of both components in water/THF mixtures, followed by redispersion in pure water yielding stable suspensions. Cryogenic transmission electron microscopy (cryo‐TEM) and dynamic light scattering (DLS) reveal a spherical morphology with diameters ranging from 15 – 100 nm. Once formed, the assemblies showed broadened absorptions and quenched PBI‐centered fluorescence. Using time‐resolved absorption spectroscopy, the nature of the fluorescence quenching was confirmed to be either charge separation, by which the porphyrin donates an electron to the PBI, or symmetry breaking charge separation, by which π‐π stacked PBIs donate and accept electrons. Denaturation of the supra‐amphiphile went hand‐in‐hand with a reinstation of the PBI fluorescence and suppression of charge separation.

Stable aggregates of a new hydrogen‐bond mediated porphyrin‐perylenebisimide (PBI) bola‐type supra‐amphiphile have been synthesized by lyophilization of solutions of both single molecules in THF/water mixtures, followed by redispersion in pure water. Cryogenic transmission electron microscopy verifies the spherical morphology. Femtosecond transient absorption spectroscopy unravels multi‐directional charge separation from the porphyrin to the PBI and within the PBI stacks.

## Linked entities

- **Chemicals:** porphyrin (PubChem CID 66868), cyanuric acid (PubChem CID 7956)

## Full-text entities

- **Chemicals:** Hamilton (-), THF (MESH:C018674), Porphyrin (MESH:D011166), hydrogen (MESH:D006859), Perylenebisimide (MESH:C510697), imide (MESH:D007094), cyanuric acid (MESH:C004632), water (MESH:D014867)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12955521/full.md

## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12955521/full.md

## References

73 references — full list in the complete paper: https://tomesphere.com/paper/PMC12955521/full.md

---
Source: https://tomesphere.com/paper/PMC12955521