Substituent Size Effects on the Photophysics of 1-Aryloxy-perylene Bisimide Monomers and Aggregates: A Bay -Substitution Study

Abstract This study explores the effects of 1-substitution of perylene bisimides (PBIs) with aryloxy groups on their photophysical features and aggregation equilibria. The main variables considered for this purpose were the size of the aryloxy substituent, the solvent, and the analytical concentration. In all cases, aggregate formation was monitored by observing the concentration dependence of the spectral features. Our results led us to conclude that the resulting aggregates exhibit an H-type signature and that the substituent hinders self-assembly. Compared to the reference unsubstituted homologue, the insertion of an aryloxy group proved to be an optimal strategy for modulating the photophysical features of both monomers and aggregates. A detailed discussion is presented herein.

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Journal
The Journal of Physical Chemistry A
Published
2026-09-30
DOI
https://doi.org/10.1021/acs.jpca.6c05397
Primary Topic
Photochemistry and Electron Transfer Studies
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article
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article

Substituent Size Effects on the Photophysics of 1-Aryloxy-perylene Bisimide Monomers and Aggregates: A Bay -Substitution Study

Liliana Jiménez, Leandro D. Mena, Gustavo Ariel Pino, Andrés R. Urdaneta M.
The Journal of Physical Chemistry A
Photochemistry and Electron Transfer Studies
article

Substituent Size Effects on the Photophysics of 1-Aryloxy-perylene Bisimide Monomers and Aggregates: A Bay -Substitution Study

Liliana Jiménez, Leandro D. Mena, Gustavo Ariel Pino, Andrés R. Urdaneta M.
article en

Abstract

Abstract This study explores the effects of 1-substitution of perylene bisimides (PBIs) with aryloxy groups on their photophysical features and aggregation equilibria. The main variables considered for this purpose were the size of the aryloxy substituent, the solvent, and the analytical concentration. In all cases, aggregate formation was monitored by observing the concentration dependence of the spectral features. Our results led us to conclude that the resulting aggregates exhibit an H-type signature and that the substituent hinders self-assembly. Compared to the reference unsubstituted homologue, the insertion of an aryloxy group proved to be an optimal strategy for modulating the photophysical features of both monomers and aggregates. A detailed discussion is presented herein.

The Journal of Physical Chemistry A
Universidad Nacional de Córdoba (AR), Instituto de Investigaciones en Ciencias de la Salud (AR), Fundacion Allende (AR)
Life below water
Openalex Percentile: Top 13%
Photochemistry and Electron Transfer Studies
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Substituent Size Effects on the Photophysics of 1-Aryloxy-perylene Bisimide Monomers and Aggregates: A Bay -Substitution Study — Liliana Jiménez, Leandro D. Mena, et al. · The Journal of Physical Chemistry A (2026) | TGRS Research Map | TGRS