The Aggregation Units of J-Aggregates: Transitioning from Monomers to Hydrogen-Bonded Dimers

In recent years, J-aggregates, as supramolecular assembly structures, have increasingly attracted scientific interest. Currently, the prevailing consensus is that J-aggregates are formed through the interleaved stacking of monomers arranged in parallel. However, our findings suggest that the fundamental units constituting J-aggregates are not limited to monomers alone but also encompass molecular aggregates interconnected by noncovalent bonds, which we designate as aggregation units. We have synthesized three asymmetric pyrrolopyrrole cyanine (PPCy) dyes capable of forming hydrogen-bonded dimers and have verified that these hydrogen-bonded dimers can serve as aggregation units to generate J-aggregates. The detailed structural and optical properties revealed that the J-aggregates of these dyes exhibited a significantly red-shifted and narrowed emission in the near-infrared (NIR) fluorescence compared to the monomers.

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Publication Details

Journal
The Journal of Physical Chemistry Letters
Published
2024-08-26
DOI
https://doi.org/10.1021/acs.jpclett.4c02186
Citations
14
Primary Topic
Spectroscopy and Quantum Chemical Studies
Type
article
Field-Weighted Citation Impact
4.73

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The Aggregation Units of J-Aggregates: Transitioning from Monomers to Hydrogen-Bonded Dimers

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article

The Aggregation Units of J-Aggregates: Transitioning from Monomers to Hydrogen-Bonded Dimers

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article en
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Abstract

In recent years, J-aggregates, as supramolecular assembly structures, have increasingly attracted scientific interest. Currently, the prevailing consensus is that J-aggregates are formed through the interleaved stacking of monomers arranged in parallel. However, our findings suggest that the fundamental units constituting J-aggregates are not limited to monomers alone but also encompass molecular aggregates interconnected by noncovalent bonds, which we designate as aggregation units. We have synthesized three asymmetric pyrrolopyrrole cyanine (PPCy) dyes capable of forming hydrogen-bonded dimers and have verified that these hydrogen-bonded dimers can serve as aggregation units to generate J-aggregates. The detailed structural and optical properties revealed that the J-aggregates of these dyes exhibited a significantly red-shifted and narrowed emission in the near-infrared (NIR) fluorescence compared to the monomers.

The Journal of Physical Chemistry LettersVol. 15(35)
Dalian University of Technology (CN), Dalian University (CN)
Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 4%
Spectroscopy and Quantum Chemical Studies
4.73
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