From Rings to Properties: Understanding the Effect of Annelation on Pyrene

Pyrene is a central building block in organic materials chemistry, valued for its rigid aromatic core, high fluorescence, and rich capacity for structural elaboration. However, the fundamental relationship between its annelation pattern and resulting electronic properties remains underexplored. In this work, we present a comprehensive computational study of 4,766 pyrene-based polybenzenoid hydrocarbons from the COMPAS-3D data set. By systematically categorizing annelation patterns based on the positions of fused benzene rings, we uncover clear structure-property trends governing key electronic parameters, including molecular orbital energies and oxidation and reduction potentials. We find that annelations at different positions exert different effects, which combine additively, and that these trends correlate with the distribution of fixed versus migrating Clar sextets. We further show that extended linear annelation can dominate electronic behavior, superseding local pyrene effects. Additionally, we evaluate the effect of torsional strain, revealing a clear link between annelation patterns and thermodynamic molecular destabilization. These insights provide a framework for the rational design of functional pyrene-based molecules.

Authors

Institutions

Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-08-29
DOI
https://doi.org/10.1021/acs.joc.5c01401
Citations
2
Primary Topic
Synthesis and Properties of Aromatic Compounds
Type
article
Field-Weighted Citation Impact
1.87

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

From Rings to Properties: Understanding the Effect of Annelation on Pyrene

Renana Gershoni‐Poranne, Alexandra Wahab
2 citations
The Journal of Organic Chemistry
Synthesis and Properties of Aromatic Compounds
1.87
article

From Rings to Properties: Understanding the Effect of Annelation on Pyrene

Renana Gershoni‐Poranne, Alexandra Wahab
article en
2 citations

Abstract

Pyrene is a central building block in organic materials chemistry, valued for its rigid aromatic core, high fluorescence, and rich capacity for structural elaboration. However, the fundamental relationship between its annelation pattern and resulting electronic properties remains underexplored. In this work, we present a comprehensive computational study of 4,766 pyrene-based polybenzenoid hydrocarbons from the COMPAS-3D data set. By systematically categorizing annelation patterns based on the positions of fused benzene rings, we uncover clear structure-property trends governing key electronic parameters, including molecular orbital energies and oxidation and reduction potentials. We find that annelations at different positions exert different effects, which combine additively, and that these trends correlate with the distribution of fixed versus migrating Clar sextets. We further show that extended linear annelation can dominate electronic behavior, superseding local pyrene effects. Additionally, we evaluate the effect of torsional strain, revealing a clear link between annelation patterns and thermodynamic molecular destabilization. These insights provide a framework for the rational design of functional pyrene-based molecules.

The Journal of Organic ChemistryVol. 90(36)
Technion – Israel Institute of Technology (IL), ETH Zurich (CH), Institute of Catalysis and Petrochemistry (RU), Institute of Organic Chemistry (PL)
Branco Weiss Fellowship – Society in Science, Israel Science Foundation
Openalex Percentile: Top 14%
Synthesis and Properties of Aromatic Compounds
1.87
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.